ePosters

HRP0084P1-1

Evaluation of Glucose Metabolism and Cardiovascular Risk Factors and Hyperandrogenemia in Prepubertal Girls with Premature Pubarche
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HRP0084P1-2

Ontogeny of the Synchronisation between Adrenal Clock Genes, Adrenal Steroidogenesis-Related Genes and the Circadian Rhythm of the HPA Axis in Rats
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HRP0084P1-3

Are Heterozygous Carriers of CYP21A2 Less Vulnerable to Psychological Stress?
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HRP0084P1-4

Effect of CYP17A1 Inhibitors Orteronel and Galeterone on Adrenal Androgen Biosynthesis
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HRP0084P1-6

Genetic Diagnosis of Congenital Primary Adrenal Insufficiency by Massive Parallel Sequencing
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HRP0084P1-7

Carriers of 21-Hydroxylase Deficiency Demonstrate Increased Psychological Vulnerability to Stress
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HRP0084P1-8

Cortisol:Cortisone Ratio and Metalloproteinase 9 Emerging as Risk Factors Associated with Paediatrics Hypertension
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HRP0084P1-9

Founder Effect and the Clinical and Molecular Characteristics in a Cohort of Classical and Non-Classical Congenital Lipoid Adrenal Hyperplasia Due To StAR Mutations
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HRP0084P1-10

Use of a Cord Blood Fluorescein Labeled Dexamethasone Monocyte Binding Assay to Study the Glucocorticoid Receptor in Neonates
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HRP0084P1-11

Steroid 11[beta]-Hydroxylase Deficient Congenital Adrenal Hyperplasia with a Reversible Cardiomyopathy Caused by a Novel CYP11B1 Mutation: Report of Three Cases
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HRP0084P1-12

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malign Infantile Osteopetrosis
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HRP0084P1-13

Osteogenesis Imperfecta: A Pilot Trial on Treatment with the RANKL-Antibody Denosumab
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HRP0084P1-14

No Secular Trend in Vitamin D Levels Over the Past 30 Years in Swedish Children
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HRP0084P1-15

Lithium Chloride Prevents Glucocorticoid-Induced Growth Failure in Cultured Foetal Rat Metatarsal Bones
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HRP0084P1-16

Diverse Presentations of Hypophosphatasia in Paediatric Patients: A Review of the Case Literature
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HRP0084P1-17

Humanin Prevents Undesired Apoptosis of Chondrocytes without Interfering with the Anti-Inflammatory Effect of Dexamethasone in a Model of Arthritis
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HRP0084P1-18

Response to Vitamin D Replacement is Determined by Body Surface Area in Children with Vitamin D Deficiency
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HRP0084P1-21

Effects of Inorganic Phosphate and FGF23 on C2C12 Myoblast Cells
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HRP0084P1-22

Evaluation of Bone Mineral Density and Microarchitectural Parameters by DXA and HR-PQCT in 36 X-linked Hypophosphatemic Rickets Patients from a Single-Centre Study
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HRP0084P1-23

Safety and Efficacy of Treatment with Long-Acting Lanreotide Autogel® in Early Infancy in Patients with Congenital Hyperinsulinism
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HRP0084P1-24

The Influence of miR-125b in Pancreatic [beta]-Cell Apoptosis
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HRP0084P1-25

Lower Bone Mineral Density in Type 1 Diabetes Mellitus (T1DM) is Probably Associated with Wnt/[beta]-Catenin Pathway Downregulation Through Increased Dickkopf-1 Levels
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HRP0084P1-26

Human Placenta-Derived Mesenchymal Stem Cells: A Novel Protocol for Pancreatic Differentiation
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HRP0084P1-27

Activation of Insulin Signaling in Gastrocnemius after Central Leptin Infusion is Associated with an Increase in Proliferation and Muscle Fibre Size
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HRP0084P1-28

Clinical Characterisation of a Novel RFX6 Mutation - A Rare Cause of Neonatal Diabetes Syndrome
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HRP0084P1-29

Is Reduced Heart Rate Variability Associated with Arterial Stiffness in Youth with Childhood-Onset Type 1 Diabetes Mellitus?
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HRP0084P1-30

A Novel Mutation in the abcc8 Gene Causing a Variable Phenotype of Impaired Glucose Metabolism in the Same Family
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HRP0084P1-31

Type 1 Diabetes Onset: A Story of Innate and Adaptive Immune Cells?
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HRP0084P1-32

Aetiological Diagnosis of Diabetes in Italian Diabetic Children and Adolescents
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HRP0084P1-33

Improved Genetic Testing for Monogenic Diabetes in the Swiss Population by Targeted Next Generation Sequencing
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HRP0084P1-34

Low Bone Mineral Density is Associated to Poor Glycemic Control and Increased Dickkopf-1 (DKK-1) Serum Levels in Children and Adolescents with Type 1 Diabetes
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HRP0084P1-35

Effect of 6 Months Therapy with Metreleptin in an African American Boy with Congenital Generalised Lipodystrophy
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HRP0084P1-36

Somatic Paternal UPD on Chromosome 11p15 in Focal Form of Congenital Hyperinsulinism (CHI) Causes Monoallelic Expression of Mutant ABCC8 and KCNJ11
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HRP0084P1-37

Hyperthyroidism in 276 Children and Adolescents with Type 1 Diabetes from Germany and Austria
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HRP0084P1-38

Metabolic Syndrome Frequency in Longitudinally Followed Children with Premature Adrenarche During Pubertal Ages
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HRP0084P1-39

Evaluation of Ability of Urinary Podocalyxin, Nephrin and Liver type Fatty Acid Binding Protein for Early Diagnosis in Renal Injury in Adolescents with Type 1 Diabetes
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HRP0084P1-40

Efficacy and Safety of a Fixed Combination of Insulin Degludec/Insulin Aspart in Children and Adolescents with Type 1 Diabetes
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HRP0084P1-41

Current Care and Outcomes for Children and Young People with Diabetes in England and Wales: Results from the National Paediatric Diabetes Audit
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HRP0084P1-42

Dynamics Perceptions of Their Own Health in the Process of Learning Self-Control Adolescents with Type 1 Diabetes Mellitus
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HRP0084P1-43

Evaluation of Median Nerve in Children with Type1 Diabetes using Ultrasonographic Imaging and Electrophysiology
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HRP0084P1-44

Is Metabolic Control Affected by Military Service in Young Adults with Type 1 Diabetes?
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HRP0084P1-45

Immune/Inflammatory Profile in Children with Type 1 Diabetes Mellitus and Celiac Disease and/or Autoimmune Thyroiditis
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HRP0084P1-46

Trends in Insulin Therapy in 50 861 Children and Adolescents with Type 1 Diabetes from Austria and Germany Between 2000 and 2014
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HRP0084P1-47

Relative Hypoaldosteronism in a Patient with WOLCOTT-Rallison Syndrome
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HRP0084P1-48

Structured Education Programmes for Children with Type 1 Diabetes: a Systematic Review
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HRP0084P1-49

Can Hypothalamic Obesity be Treated with Stimulants? Follow Up
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HRP0084P1-50

A Feasibility Study of Intra-Gastric Balloons (Supported By a Lifestyle Programme) for the Treatment of Severe Adolescent Obesity: the (Bob) Study
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HRP0084P1-51

Distribution of Obesity Indices Among European Preschool Children and Associated Risk Factors: The ToyBox-Study
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HRP0084P1-52

A Randomised Trial of the Effects of Perinatal Education of Overweight Pregnant Women to Prevent Childhood Overweight: The ETOIG Study
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HRP0084P1-53

Perypheral Neuroblastic Tumours and Immunological Studies in ROHHADNET Syndrome (Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation and NEural Tumour)
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HRP0084P1-54

'BestPWS EU': A Phase 3 Study in Adolescent and Adult Patients With PWS in Europe
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HRP0084P1-55

Intrauterine Growth Restriction is Associated with Greater Severity in Childhood Obesity-Associated Metabolic Impairment and Poorer Adult Height Prediction
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HRP0084P1-56

Immunohistochemical Detection of Estrogen [alpha] and Androgen Receptors in Genital Tissues in Girls with Congenital Adrenal Hyperplasia
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HRP0084P1-57

Attitudes of Parents of Klinefelter Boys and Flemish Paediatricians Towards Neonatal Screening and Fertility Preservation Techniques in Klinefelter Syndrome
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HRP0084P1-58

Long-term Endocrine Outcome in Men with Partial Androgen Insensitivity Syndrome
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HRP0084P1-59

Novel Genetic Associations in Children with Disorders of Sex Development and Neurodevelopment Disorders - Insights from the Deciphering Developmental Disorders study
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HRP0084P1-60

Insight into the Human Ovarian Sex Development Networks
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HRP0084P1-62

Prediction of Germ Cell Cancer Occurrence in Postpubertal Individuals with Androgen Insensitivity Based on Pathological Findings and Cancer Predisposition SNPs
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HRP0084P1-63

Gender Identity Prediction in Adulthood by HTP Test (House-Tree-Family) in 46, XY DSD Patients
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HRP0084P1-64

MAMLD1 Mutations Seem Not Sufficient to Explain a 46, XY DSD Phenotype. What else?
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HRP0084P1-65

Subcutaneous Continuous Administration of Recombinant Human Luteinizing and Follicle-Stimulating Hormones is an Effective Treatment for Micropenis During the Mini-Puberty
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HRP0084P1-66

46, XX Ovotesticular DSD in the Absence of SRY Gene Associated to SOX3 Duplication
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HRP0084P1-67

miR-146a-Mediated Suppression of the Inflammatory Response in Human Adipocytes
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HRP0084P1-68

Leptin Resistance Alteration after Modulation of Dopamine System Funcional Activity in Rat's Diet-Induced Obesity
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HRP0084P1-70

Outcome of Adolescents Undergoing Bariatric Surgery - 1 Year Follow-Up
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HRP0084P1-71

Identifying Critical Periods for Maintaining Weight Loss in Obese Children
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HRP0084P1-72

Use of Topiramate in Severe Hyperphagia Associated to Neuropsychiatric Features in a Boy with Congenital Proopiomelanocortin Deficiency
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HRP0084P1-73

Circulating miR146a and 486-5p are Altered in Obese Children with and Without Non-Alcoholic Fatty Liver Disease (NAFLD) and Correlate with Abdominal Fat and BMI
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HRP0084P1-75

Ghrelin and Brain-Derived Neurotrophic Factor in Children with Prader-Willi Syndrome
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HRP0084P1-77

Evaluation of Adiponectin Concentrations in Obese Children and Its Correlation with Lipid and Carbohydrate Parameters
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HRP0084P1-78

Influence of Genetic Variation on the Response to Recombinant Human Growth Hormone Treatment in Children with GH Deficiency: An Analysis of 13 Single Nucleotide Polymorphisms and the GH Receptor Exon 3 Deletion
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HRP0084P1-79

Decrease of Jumping Power in Adolescents with Severe GHD After Stop of GH-Therapy
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HRP0084P1-80

Good Clinical Response to the Growth Hormone Therapy in the Patient with Familiar Short Stature Caused by Novel p.Val478Serfs*14 Mutation in ACAN Gene and Isolated Growth Hormone Deficiency
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HRP0084P1-81

The Growth Response to Growth Hormone Treatment is Greater in Patients with SHOX Enhancer Deletions Compared to SHOX Defects
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HRP0084P1-82

Assessment of Primary Cancers in Growth Hormone-Treated Paediatric Patients Compared with General Population Registries: An Epidemiological Analysis of a Large, Multinational, Prospective Observational Study
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HRP0084P1-83

Genetic Markers Contribute to the PREDICTION of Response to GH in Severe but not Mild GH Deficiency
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HRP0084P1-84

Disease and Treatment Burden in Children and Adolescents with Growth Hormone Deficiency
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HRP0084P1-85

Effects of Growth Hormone Treatment on Immunity
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HRP0084P1-86

The Growth Hormone Treatment Results in the Increase of Irisin Concentration in Plasma
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HRP0084P1-87

A Novel OTX2 Gene Mutation in a Child with Growth Hormone Deficiency
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HRP0084P1-88

The Dose Dependent Effect of Growth Hormone Therapy in Patients with IGF1 Receptor Haploinsufficiency due to Heterozygous Deletion
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HRP0084P1-89

Royal Jelly Supplementation Induces the Growth Plate Development and Increases Plasma Growth Hormone and Oestradiol Levels in Prepubertal Rats
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HRP0084P1-90

Silver-Russell Syndrome without Body Asymmetry in Three Patients with Duplications of Maternally Derived Chromosome 11p15 Involving CDKN1C
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HRP0084P1-91

Mutation in RTTN, a Regulator of Ciliary Function, Causes a Complex Syndrome Characterized by Severe Congenital Microcephaly, Lissencephaly and Profound Growth Failure in Two Siblings
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HRP0084P1-93

Severe IGF1 Deficiency and Multi-Organ Autoimmune Disease Associated with Novel Germline STAT3 Mutations
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HRP0084P1-95

Various Imprinting Disorders Underlying Silver-Russell Syndrome-Compatible Phenotype
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HRP0084P1-96

Ligase IV Deficiency Syndrome as a Cause of Microcephalic Primordial Dwarfism in Dizygotic Twins
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HRP0084P1-97

High Frequency of Hypomorphic Allelic Haplotypes of the gh1 Proximal Promoter in Patients with Proportional Undergrowth and Isolated GH Deficiency
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HRP0084P1-98

GH Excess in McCune-Albright Syndrome
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HRP0084P1-99

GH Hypersecretion in Children with NF1 and Optic Pathway Gliomas
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HRP0084P1-100

Atypical Features in Patients with Leprechaunism Suggesting a Wide Clinical Spectrum of Disease
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HRP0084P1-102

The Role of HNF1B in Human Pancreas Development and Diabetes
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HRP0084P1-103

Molecular Characterization of a Novel Non-stop KCNJ11 Mutation Associated with a Dual Focal and Diffuse Hyperinsulinaemic Hypoglycaemia Phenotype
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HRP0084P1-104

Diazoxide Responsive Congenital Hyperinsulinism in a Patient with Dual Genetic Aetiology (HNF4A and ABCC8 Mutation)
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HRP0084P1-105

Fluoxetine Induced Hypoglycaemia in a Patient with Congenital Hyperinsulinism on Lanreotide Therapy
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HRP0084P1-106

Influence of Nocturnal Glycaemia on Ventricular Repolarisation and Heart Rate Variability in Prepubertal Children with Type 1 Diabetes
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HRP0084P1-107

Changes in Serum Protein Expression in Small-for-Gestational-Age Newborn Infants at Different Gestational Ages
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HRP0084P1-108

Liver ER Stress and Intrauterine Growth Retardation in Rats
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HRP0084P1-109

Continuous Subcutaneous Infusion of Recombinant LH and FSH During Early Infancy Promotes Testicular Descent in Congenital Hypogonadotropic Hypogonadism
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HRP0084P1-110

Neonatal Screening Program for Central Congenital Hypothyroidism
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HRP0084P1-111

Serum Neurokinin B Level can be Used to Differentiate Central Precocious Puberty from Premature Thelarche
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HRP0084P1-112

Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty: A Nationwide Cohort Study
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HRP0084P1-113

Relevance of Astrocytic Signals for GnRH-Neuronal Function
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HRP0084P1-114

Screening of Mutations in Idiopathic Hypogonadotropic Hypogonadism Using a Targeted Next-Generation Sequencing Approach
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HRP0084P1-116

FSHB/FSHR Genetic Variants alter Serum FSH Levels and Prepubertal Ovarian Follicular Growth in Healthy Girls
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HRP0084P1-117

Transient Breast Budding in Healthy Girls is a Frequent Phenomenon: Description of Pubertal Progression and Associations to Gonadotropins, Estradiol and FSHB/FSHR Genetic Polymorphisms
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HRP0084P1-118

Specific Hypothalamic Activation Pattern by mGlu5 Receptor Blockade in vivo During Pubertal Development in Female Mice
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HRP0084P1-119

Lipid Profiles in Gender Dysphoric Adolescents Treated with GnRH Agonists Alone and in Combination with Cross-Sex Hormones
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HRP0084P1-120

A Novel LHX4 Mutation is Associated with Hypogonadotropic Hypogonadism, Not Combined Pituitary Hormone Deficiency
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HRP0084P1-121

A Missense Mutation in MKRN3 in a Danish Girl with Central Precocious Puberty and Her Brother with Early Puberty
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HRP0084P1-122

Congenital Hypothyroidism in Twin Couples and Triplets
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HRP0084P1-123

Th17 Cells in Children with Graves' Disease During Methimazole Treatment
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HRP0084P1-124

Thyrocytes are Particularly well Protected Against Oxidative Stress Induced by H2O2
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HRP0084P1-126

Characteristics and Outcome of Neonates with Congenital Hypothyroidism Born After In Vitro Fertilisation
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HRP0084P1-127

Transient vs Permanent Congenital Hypothyroidism: The Use of Baseline Characteristics and Long-Term Data Can Help Formulate a Practical Prognostic Algorithm
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HRP0084P1-128

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor [alpha] Mutations
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HRP0084P1-129

Intelligence and Behaviour in Children and Adolescents with Hashimoto's Thyroiditis
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HRP0084P1-130

Brain-Lung-Thyroid Syndrome - Update on the Clinical Spectrum of a Heterogeneous Disorder
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HRP0084P1-131

Increased Detection Rate of Paired Box Domain Gene Mutations by Application of Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Primary Congenital Hypothyroidism and Thyroid Dysgenesis
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HRP0084P1-132

Severe Hyperthyroidism in an Infant Revealed a Familial Non-Autoimmune Hyperthyroidism with Novel Heterozygous Thyrotropin Receptor Gene Mutation
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HRP0084P1-134

Co-Existing Variants of FOXE1 and BMP15 Genes in Young Females with Primary Ovarian Insufficiency: Evidence of Digenic Inheritance
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HRP0084P1-135

Sex Hormones and Gonadal Size in Pubertal Girls Born Small or Appropriate for Gestational Age
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HRP0084P1-136

The Eap1 Promoter is Differentially Methylated at the Onset of Puberty in Normal Weight and Obese Female Rats
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HRP0084P1-138

Weight Gain in Turner Syndrome: Association to Puberty Induction?
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HRP0084P1-139

A Study of Arterial Stiffness in Turner Syndrome Patients Using Cardio-Ankle Vascular Index
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HRP0084P1-140

Impaired Motor Function in Turner Syndrome: What is the Relationship to Performal Intelligence Scores?
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HRP0084P1-141

Adult Height after Growth Hormone Treatment and its Association with X Chromosome Dosage in Turner Syndrome: a Cross-Sectional Database Analysis of the French National Rare Disease Network
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HRP0084P1-142

Fracture Incidence is Not Associated with the Six-Year Development of Trabecular BMD in Paediatric Turner Syndrome Patients
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HRP0084P1-145

Clinical Follow-up of the First SF-1 Deficient Female Patient
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HRP0084P1-146

Salt Sensitivity of Blood Pressure at Age 7-8 Years in Preterm Born Children
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HRP0084P1-147

A New LC-MS/MS Assay for the Analysis of Sulfated Steroids in Human Serum: Quantification of Cholesterol Sulfate, Pregnenolone Sulfate, 17-Hydroxypregnenolone Sulfate and Androgen Sulfates
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HRP0084P1-148

The Analysis of Occurrence the Zinc Transporter Antibodies ZnT8 in Children with Graves' Disease and Hashimoto's Thyroiditis
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HRP0084P1-149

Recombinant Parathyroid Hormone (1-34) Replacement Treatment of Hypoparathyroidism in the Alfacalcidol-Resistant Patient with Severe Autoimmune Polyendocrinopathy Syndrome Type 1
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HRP0084P1-151

A Case of Autoimmune Polyglandular Syndrome Type I Presenting as Progressive Generalised Lipodystrophy in a 15-month-old Child
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HRP0084P1-152

Noonan Syndrome-Causing SHP2 Mutants Inhibit Murine Growth Plate Chondrogenesis and Bone Development: Role of Ras/MAPK Hyperactivation
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HRP0084P1-153

Growth Curves for Height, Weight, BMI and Head Circumference in Children with Achondroplasia
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HRP0084P1-154

Novel Compound Heterozygous BMP1 Variants Associated with Osteogenesis Imperfecta
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HRP0084P1-155

Prospective Cognitive Assessment in Children with Craniopharyngioma Identifies Dysfunction at Diagnosis, After Conservative Surgery and Before Adjuvant Radiation
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HRP0084P1-156

Cushing Syndrome due to Adrenocortical Carcinoma in a 3-month-old Infant with a Large Interstitial Deletion of Chromosome 5q Including the APC Gene
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HRP0084P1-157

How do Adolescent Minors Banking Sperm Before Cancer Therapy Subsequently use the Fertility Service? A Post Banking Re-Evaluation
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HRP0084P1-158

The Expression of Related Neuroendocrine Factors with Puberty Onset in Rat at Different Developmental Stages
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HRP0084P1-159

FOXL2 Gene and Combined Pituitary Hormone Deficiency: A Possible Link
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HRP0084P1-160

Septo-Optic Dysplasia Associated with Koolen-de Vries Syndrome: A Case Report
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HRP0084P1-161

Screening of IGSF1 in Patients with Central Hypothyroidism and GH Deficiency, Participating in the Dutch HYPOPIT Study
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HRP0084P1-162

Congenital Hypothyroidism: Reduction in the Female to Male Ratio Following the Decrease of the TSH Cut-off Point Used for Neonatal Screening
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HRP0084P1-163

Paediatric Thyroid Nodule Score: Derivation and Validation of a Predictive Score for Thyroid Nodule Assessment in Children
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HRP0084P1-164

Practical Application of Elastography in the Diagnosis of Thyroid Nodules in Children
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HRP0084P1-165

Higher Urinary Iodine Levels Iodine Correlates with Lower Systolic Blood Pressure in Chilean Schoolchildren
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HRP0084P2-166

Late Diagnosis of Adrenal Insufficiency Caused by Novel Compound Heterozygous Mutations in Proopiomelanocortin
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HRP0084P2-167

Hyponatraemia Secondary to Exudative Eczema
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HRP0084P2-168

The Natural Mutant Receptor hGR[alpha]T556I Causes Primary Generalised Glucocorticoid Resistance Through Decreased Affinity for the Ligand and Impaired Interaction with the GRIP1 Coactivator
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HRP0084P2-169

References Values Under Synacthen Test for Six Steroids in Serum by LC-MS/MS
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HRP0084P2-170

Usefulness of Salivary Cortisol Levels in Secondary Adrenal Insufficiency in Paediatric Population
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HRP0084P2-171

Acute Adrenal Failure in a Term Newborn with Congenital Cytomegalovirus Infection: Case Description and Review of the Literature
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HRP0084P2-172

Resveratrol Disrupts Steroidogenesis in Human Foetal Adrenals
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HRP0084P2-174

Clinical, Biochemical and Molecular Characteristics of the Patients with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in Croatia
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HRP0084P2-176

Triple A Syndrome - the Second Most Common Cause of Chronic Adrenal Insufficiency in North Africa?
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HRP0084P2-177

Analysis the Relationship between Clinical Characteristics and Genotype of Six Cases of Bartter Syndrome and Gitelman Syndrome in Children
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HRP0084P2-178

Genotypic Heterogeneity and Clinical Phenotype in Two Patients with Triple A Syndrome (AAAS)
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HRP0084P2-179

Primary Adrenal Insufficiency: About a Paediatric Series
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HRP0084P2-180

High-Dose Hook Effect in 17- Hydroxyprogesterone Assay in 21-Hydroxylase Deficiency
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HRP0084P2-181

Baseline Cortisol Concentrations Predict Positively and Negatively Anti- and Pro- Oxidation, Respectively that are Measured Following an Acute Aerobic Exercise Bout in Pre- and Early Pubertal Normal-Weight and Obese Boys
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HRP0084P2-182

Insulin Sensitivity and Adipocytokynes in Children with Classical Congenital Adrenal Hyperplasia
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HRP0084P2-183

24-H Urinary Free Cortisol as a Screening Test for Cushing's Syndrome in Children
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HRP0084P2-184

Familial Hyporeninemic Hyperkalemia and Hypertension (Pseudohypoaldosteronism Type II) in Infancy and Childhood
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HRP0084P2-185

Severe Craniosynostosis Syndrome Associated to Salt Wasting Congenital Adrenal Hyperplasia
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HRP0084P2-186

Testicular Adrenal Cell Rest Tumours are not Associated with 21 Hydroxylase Mutations or Therapy Compliance in Boys with Classic form of CAH
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HRP0084P2-187

A Large Family with a Novel Mutation in the SCNN1A Gene Causing a Mild and Transient form of Autosomal Recessive Pseudohypoaldosteronism Type 1 (PHA1)
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HRP0084P2-188

Phosphoglucomutase-1 Deficiency Presented as Adrenal Insufficiency
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HRP0084P2-189

The Aetiological Spectrum of Congenital Adrenal Hyperplasia Based on Molecular Genetic Analyses
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HRP0084P2-190

Higher Serum DHEAS Concentration is Associated with Lower Plasma LDL Cholesterol Concentration in Children
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HRP0084P2-191

Central Adrenal Insufficiency is not a Common Feature in CHARGE Syndrome
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HRP0084P2-193

Adrenal Function in Children Born Small for Gestational Age
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HRP0084P2-194

Cushing's Syndrome in Children and Adolescents: About a Paediatric Series
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HRP0084P2-195

Serum Cortisol and Cortisone Ratio as Sensitive Tool to Identify Subjects With Severe or Partial 11[beta]-Hydroxysteroid Dehydrogenase Type 2 Deficiency
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HRP0084P2-196

The Role of the Nurse Practitioner in Optimising Care for Children with Congenital Adrenal Hyperplasia
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HRP0084P2-197

Evaluation of Medical Treatment in the First 2 Years of Life with a New Dutch National Longitudinal Registry for Children with Congenital Adrenal Hyperplasia (CAH)
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HRP0084P2-200

A Novel Mutation (c.delG209) in the Proopiomelanocortin Gene in a Child with Early-onset Obesity
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HRP0084P2-201

Improved Linear Growth in Patients with Classical Congenital Adrenal Hyperplasia
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HRP0084P2-202

Autoimmune Polyglandular Syndrome Type 1 in Russia: Clinical Experience in 112 Patients
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HRP0084P2-203

Autoimmune Encephalitis - A Newly Recognised Clinical Manifestation of Autoimmune Polyendocrine Syndrome Type 1?
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HRP0084P2-205

Mechanism of Bone Disease in Prader-Willi Syndrome
Direct

Abstract PDF
HRP0084P2-206

Hereditary Vitamin D-Resistant Rickets: Report of Four Cases with Successful Use of Intermittent Intravenous Calcium Via Peripheral Route
Direct

Abstract PDF
HRP0084P2-207

A Novel PRKAR1A Gene Mutation with Mild Brachydactyly
Direct

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HRP0084P2-208

Bone Mineral Density in Children and Adolescents with Vertical HIV Infection
Direct

Abstract PDF
HRP0084P2-209

Sclerostin and Its Associations with Energy Metabolism in Children and Adolescents
Direct

Abstract PDF
HRP0084P2-210

Genetic and Epigenetic Alterations at the GNAS Locus and Clinical Consequences in Pseudohypoparathyroidism: A New Healthcare Pathway
Direct

Abstract PDF
HRP0084P2-211

Fibrous Cortical Defects and Non-Ossifying Fibromas in Patients with Precocious Puberty
Direct

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HRP0084P2-212

The Effect of High Dose Oral 17sz Estradiol on Bone Mineralization and Body Composition in Young Women with Turner Syndrome - A 5 Year Randomized Controlled Clinical Trial
Direct

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HRP0084P2-213

Comparison of Cost Benefits and Efficacy of Zoledronic Acid and Pamidronate in the Treatment of Osteogenesis Imperfecta in Children
Direct

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HRP0084P2-214

TmP/GFR is a Useful Marker in Making a Clinical Diagnosis of X-Linked Hypophosphataemic Rickets Caused by the PHEX Gene Mutation
Direct

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HRP0084P2-215

Whole-Body Vibration Training Improves Physical Function and Increases Bone and Muscle Mass in Youngsters with Mild Cerebral Palsy
Direct

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HRP0084P2-216

A Case with Acrodysostosis and Hormone Resistance
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HRP0084P2-217

The Spectrum of Molecular Defects in 64 Patients with Hypophosphatemic Rickets Identified by Targeted Next-Generation Sequencing
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HRP0084P2-218

Nephrocalcinosis and Nephrolithiasis in 36 X-Linked Hypophosphataemic Rickets Patients: Diagnostic Imaging and Evaluation of Risk Factors in a Single-Centre Study
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HRP0084P2-220

Genotype and Phenotype Characteristics in 22 Patients with Vitamin D Dependent Rickets Type I
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HRP0084P2-221

Evidence of a Link Between Resting Energy Expenditure and Bone Remodelling, Glucose Homeostasis and Adipokine Variations in Adolescent Girls with Anorexia Nervosa
Direct

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HRP0084P2-223

Refractory Hypercalcaemia of Malignancy: Responsiveness to Denosumab and Zoledronate
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HRP0084P2-224

Fractures in Boys with Duchenne Muscular Dystrophy and their Relationship to Age
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HRP0084P2-225

Early Detection of Increased Bone Turnover among Children and Adolescents with Type 1 Diabetes Mellitus
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HRP0084P2-226

Association between Oxidative Stress and Bone Turnover Markers in the Obese Children
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HRP0084P2-227

Longitudinal Bone Development in Patients with Classical Congenital Adrenal Hyperplasia: Data Using Peripheral Quantitative Computed Tomography
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HRP0084P2-228

Online Survey to Characterise the Burden of Illness in Children with X-Linked Hypophosphatemia
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HRP0084P2-229

Comparison of the Response to Bisphosphonate Treatment between Acute Lymphoblastic Leukaemia and Osteogenesis Imperfecta Type I
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HRP0084P2-231

Cinacalcet Treatment in Girls with Hereditary Vitamin D Resistant Rickets
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HRP0084P2-232

Regulation of Bone Growth Via Ligand-Specific Activation of Oestrogen Receptor [alpha]
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HRP0084P2-233

Teriparatide (rhPTH) Therapy in a Boy with Hypoparathyroidism-Deafness-Renal Dysplasia Syndrome due to GATA3 Mutation
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HRP0084P2-234

Variable Degree of Hormonal Resistance in Patients with Progressive Osseous Heteroplasia
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HRP0084P2-235

Assessment of Foramen Magnum in Early Infancy is Efficient for Patients with Achondroplasia
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HRP0084P2-236

Body Composition Measures on Different DEXA Scanners are not the Same
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HRP0084P2-237

Intrauterine Growth Restriction, Gestational Age, Steroidal Prophylaxis and Breastfeeding Influence Bone Mass in Prepubertal Children
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HRP0084P2-238

Can Vitamin D Deficiency Cause Prolongation in Visual Evoked Potentials?
Direct

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HRP0084P2-239

Novel CYP27B1 Gene Mutations in Children with Vitamin D-Dependent Rickets Type 1A
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HRP0084P2-240

Size-Corrected Bone Mineral Density is not Affected by Haematopoietic Stem Cell Transplantation and Total Body Irradiation in Leukaemia Survivors
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HRP0084P2-241

Quantitative Sonometeric Bone Age as a Function of Height and BMI
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HRP0084P2-243

Dyslipidaemia in Children with Diabetes
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HRP0084P2-244

Diabetes Mellitus and Hypoparathyroidism in a Girl with Mitochondrial Disease
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HRP0084P2-245

Association of Ghrelin Levels and Insulin Resistance in Small for Gestational Age Rats
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HRP0084P2-247

A Case of Donohue Syndrome: New Genetic Mutation and Added Phenotypic Characteristics
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HRP0084P2-248

Genetic Analysis and Follow-Up of 23 Neonatal Diabetes Mellitus Patients in China
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HRP0084P2-250

Recombinant Human IGF1 Treatment in Patients with Insulin Receptor Mutations Resulting in Donohue Syndrome: A 10-Year Experience in a Tertiary Centre
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HRP0084P2-251

Sick Day Rule: Survey of Parents of Children with Type 1 Diabetes (Experience and Knowledge)
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Abstract PDF
HRP0084P2-252

Brachial Flow Mediated Dilation and its Relation to Osteoprotegerin in Type 1 Diabetes Mellitus
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Abstract PDF
HRP0084P2-255

Significant Impact of Nocturnal Melatonin Secretion on Obesity-Related Metabolic Disorders in Children and Adolescents
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HRP0084P2-256

Exposure to Phthalates and Phenols in Relation to Gestational Blood Glucose Homeostasis
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HRP0084P2-257

Developing a Targeted, Mobile-Health Technology (E-Book) to Promote Self-Care During Diabetes Transition
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HRP0084P2-258

Cardiac Autonomic Neuropathy is Highly Predictive for Survival in Children with Mauriac Syndrome
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HRP0084P2-259

Predictors of Cystic Fibrosis-Related Diabetes (CFRD) in Patients with cf and Pancreatic Insufficiency
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HRP0084P2-260

Adherence to Diabetes Care in Children and Adolescents with Type 1 Diabetes Mellitus in Spain: Results from the Chrystal Study
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HRP0084P2-261

Gaining from Patient Experience on a Local Level: The Introduction of Annual Questionnaires for Children and Teenagers with Diabetes
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HRP0084P2-262

Factitious Administration of Analogue Insulin to a 2-Years-Old Child
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HRP0084P2-263

Insulin Sensitivity in Adolescents with Gender Dysphoria During Puberty Suppressing Therapy with GnRH Agonists
Direct

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HRP0084P2-264

Ethnic Variation in the Correlation of Waist Circumference to Daily Insulin Requirement in Children with Type 1 Diabetes
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HRP0084P2-265

Importance of Thrombocyte Volume Parameters in Type 1 Diabetes Mellitus Patients with and without Clinical Findings of Diabetic Ketoacidosis
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HRP0084P2-266

Increased Arterial Wall Stiffness in Children with Type 1 Diabetes and Poor Metabolic Control: An Early Marker of Vascular Complications?
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HRP0084P2-267

Glycaemic Dysregulation in Transfusion Dependent Thalassaemia Patient in a Children's Hospital
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HRP0084P2-268

MODY-GCK and MODY-HNF1A in Children and Adolescents in Russian Population
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HRP0084P2-269

Clinical and Hormonal Profile in Mini-Puberty of Daughters Born after Pregnancies with Diabetes: Preliminary Report
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HRP0084P2-270

Growth and Endocrinopathy in Wolfram Syndrome: The Experience of a Nationally Commissioned Specialist Clinic
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HRP0084P2-271

Evaluation of a Novel Tool to Adjust Insulin Boluses Based on Continuous Glucose Monitoring Trend Arrows and Insulin Sensitivity (Trend Arrow Adjustment Tool[copyright]) in Children and Youth with Type 1 Diabetes Using Insulin Pump Therapy
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Abstract PDF
HRP0084P2-273

Utility of Estimated Glucose Disposal Rate and Fat Mass Percentage for Predicting Metabolic Syndrome in Children and Adolescents with Type 1 Diabetes
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HRP0084P2-274

Friedreich's Ataxia Presenting with Diabetes Mellitus in an Adolescent
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HRP0084P2-275

Do Pancreatic Functions Predict Cardiac and Liver Iron Loading in Transfusion-Dependent [beta]-Thalassemia Major Patients Using Cardiovascular and Liver T2-Star (T2*)Magnetic Resonance?
Direct

Abstract PDF
HRP0084P2-276

Determinants of Outcome of Children with Type 1 Diabetes in Cameroon
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HRP0084P2-277

Psychosocial Screening in Children with Type 1 Diabetes in Ireland
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HRP0084P2-278

Neonatal Diabetes - Experience from a Single Centre in Sri Lanka
Direct

Abstract PDF
HRP0084P2-279

Dive: A Serious Game for Diabetes Therapeutic Education in Children
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Abstract PDF
HRP0084P2-280

Glucose and Insulin Response at Standard Oral Glucose Load and Followed Submaximal Treadmill Test in Obese Adolescents
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HRP0084P2-281

Insulin Dynamics and Biochemical Markers for Predicting Impaired Glucose Tolerance in Thai Obese Youth
Direct

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HRP0084P2-282

Total-Body Irradiation is a Major Risk Factor for Young Adult Onset Diabetes Mellitus and Hyperlipidemia in Childhood Cancer Survivors after Hematopoietic Stem Cell Transplantation
Direct

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HRP0084P2-283

Variables in Diabetic Children and Adolescents Associated with High, Acceptable and Low Range of Glycosylated Haemoglobin in a DGH Setting - An Analysis
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HRP0084P2-284

In-Patient Care for Children with Type 1 Diabetes - A Regional Audit in the Yorkshire and Humber Region in the North of England
Direct

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HRP0084P2-285

Implementation of Effective Transition from Paediatric to Adult Diabetes Care: Epidemiological and Clinical Characteristics - A Pioneering Experience in North Africa
Direct

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HRP0084P2-287

Incidence of Type 1 Diabetes among Korean Children and Adolescents in 2012-2013: Analysis of Data from the Nationwide Registry of Korea
Direct

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HRP0084P2-289

Longitudinal Study of Irish Children and Adolescents on Continuous Subcutaneous Insulin Infusion
Direct

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HRP0084P2-290

C-Peptide Variation after the Diagnosis of Type 1 Diabetes in Paediatric Age
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HRP0084P2-292

Incidence of Type 1 Diabetes in Children Under 15-Years-Old in Navarre (Spain) between 1980 and 2014
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HRP0084P2-293

Quality of Life in Adolescent with Type 1 Diabetes and Its Relationship with Metabolic Control
Direct

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HRP0084P2-294

The Prevalence of Different Subtypes of Maturity-Onset Diabetes of the Young in Russian Federation as Defined by Targeted Next-Generation Sequencing
Direct

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HRP0084P2-295

Sirolimus Therapy in Infants with Congenital Hyperinsulinism after Near Total Pancreatectomy
Direct

Abstract PDF
HRP0084P2-297

GH Promotes mRNA Expression and Secretion of Progranulin in 3T3-L1 Cells
Direct

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HRP0084P2-298

Early Diagnostics of Wolfram Syndrome
Direct

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HRP0084P2-299

Improving Glycaemic Control at Diagnosis of Type 1 Diabetes: Insulin Dosing Depending on Degree of Ketonaemia at Presentation
Direct

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HRP0084P2-300

Non-Immune Diabetes Mellitus and Neurodegeneration: Two Distinct Cases of Wolfram Syndrome
Direct

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HRP0084P2-301

Evaluation of Continuous Glucose Monitoring in Cystic Fibrosis Patients
Direct

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HRP0084P2-302

The Impact of Diurnal Glycaemic Variability on the Cardiovascular System in Children with Type 1 Diabetes Mellitus
Direct

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HRP0084P2-303

Multiple Malformations Extending the Phenotypic Spectrum of Antley-Bixler Syndrome in a Patient with P450 Oxidoreductase Deficiency due to Two Novel Mutations of the POR Gene
Direct

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HRP0084P2-305

'www.steroidogenicfactor-1.info': An Online Database of Variants in Steroidogenic Factor 1 (SF-1, NR5A1) and Resource for Families and Professional Healthcare Providers
Direct

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HRP0084P2-306

Two Testes and 2X Chromosomes: Why?
Direct

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HRP0084P2-308

MAP3K1 Mutation in a Patient with Complete XY Gonadal Dysgenesis
Direct

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HRP0084P2-309

Alterations in Germ Cell Memory and Mini-Puberty Induce Infertility in Cryptorchidism
Direct

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HRP0084P2-310

Management of Gonads in Adults with Androgen Insensitivity: An International Survey
Direct

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HRP0084P2-311

The Localisation of Cells with XX and XY in Gonadal Tissues Associated with Ovotesticular Disorder of Sexual Development with a 46,XX/46,XY Karyotype
Direct

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HRP0084P2-312

Birth Weight in Different Aetiologies of Disorder of Sex Development
Direct

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HRP0084P2-313

A Novel Human CYP19A1 Deletion-Insertion Mutation Reveals that the C-terminus of the Aromatase Protein is Crucial for its Activity
Direct

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HRP0084P2-314

Pubertal Virilization in Two Unrelated XY Teenagers with Female Phenotype due to NR5A1/SF-1 Gene Mutation
Direct

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HRP0084P2-315

Chimerism in a Teenager with Ovotesticular Disorder of Sexual Development
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HRP0084P2-317

Next-Generation Sequencing as a Rapid Molecular Diagnosis in Patients with 46,XY Disorder of Sex Development
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HRP0084P2-319

Gonadotropin Surge During the Early Postnatal Activation Period in 46,XX Testicular/Ovotesticular Disorder of Sex Development Patients
Direct

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HRP0084P2-320

The Evaluation of AR and SRD5A2 Gene Mutations in 87 Patients with 46, XY DSD Children in Turkey
Direct

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HRP0084P2-321

Familial Mutation of NR5A1/SF-1 Gene Associated with DSD and Spleen Agenesis: A New Syndrome?
Direct

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HRP0084P2-322

Clinical Spectrum of 45,X/46,XY Mosaicism and Variants in Children
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HRP0084P2-323

Chromosomal Variations in Children and Adolescents with Gender Dysphoria: Is Routine Karyotyping Indicated?
Direct

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HRP0084P2-324

DSD 46,XY and Serum Steroid Profile Ambiguity due to Combined 17-Beta Hydroxysteroid Dehydrogenase/21-Hydroxylase Deficiencies
Direct

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HRP0084P2-325

Frequency of Cryptorchidism and Age at Operation in Helsinki Area between 2004 and 2014
Direct

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HRP0084P2-327

A Novel Mutation of Anti-Mullerian Hormone Receptor Gene in a Male with Persistent Mullerian Duct Syndrome
Direct

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HRP0084P2-328

miR-122 and Non-Alcoholic Fatty Liver Disease in Prepubertal Obese Children
Direct

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HRP0084P2-329

Meteorin-Like (METRNL) Expression in Human Adipose Tissue is Associated with Adipocyte Hypertrophy and Inflammation and is Down-Regulated During Human Adipogenesis
Direct

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HRP0084P2-330

Abdominal fat Distribution Measured by Magnetic Resonance Imaging in 197 Children Aged 10-15 Years - Correlation to Anthropometry and Dual X-Ray Absorptiometry
Direct

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HRP0084P2-331

Autonomic Nervous System Function Assessed by Heart Rate Variability in Children and Adolescents with Long Term Follow up of Craniopharyngioma
Direct

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HRP0084P2-332

SIRT1 and SIRT2 Gene Expression in Peripheral Blood Mononuclear Cells of Obese Children and Adolescents and their Relationship with Metabolic Parameters and Insulin Resistance
Direct

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HRP0084P2-334

Childhood Obesity Negatively Influences Adult Leydig Cell Function
Direct

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HRP0084P2-335

Network Coordinated Primary Care Intervention in Obese Children and Adolescents: Almost a Decade of Experience
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HRP0084P2-336

Diagnosing the Metabolic Syndrome in Survivors of Childhood Haematopoietic Stem Cell Transplantation and Total Body Irradiation
Direct

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HRP0084P2-337

Laparoscopic Sleeve Gastrectomy in Adolescents: Metabolic Consequences
Direct

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HRP0084P2-338

A Novel Melanocortin-4-Receptor Gene Mutation Associated with Early Onset Severe Obesity
Direct

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HRP0084P2-339

Hypothalamic Obesity, Hyperphagia, and Hyperinsulinaemia: Time for a Paradigm Shift in Assumptions?
Direct

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HRP0084P2-340

Prevalence of Scoliosis in a Large Cohort of Paediatric and Adolescent Prader-Willi Syndrome: A Scottish-Italian study
Direct

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HRP0084P2-341

Palmitic Acid Could Modify Cognitive and Behavioural Functions Through Sex Specific Activation of Hippocampal Astrocytes
Direct

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HRP0084P2-342

Changes in Insulin Sensitivity in Adolescents Who Underwent Bariatric Surgery: Effects of Laparoscopic Sleeve Gastrectomy and Laparoscopic Gastric Banding
Direct

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HRP0084P2-343

Chronodisruption in Obese Children
Direct

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HRP0084P2-344

Configuring a Better Estimation of Obese Children's Kidney Size
Direct

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HRP0084P2-345

Early Onset of Adiposity Rebound is Associated with Higher Leptin Concentrations in 12-Year-Old Children
Direct

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HRP0084P2-346

Metformin Treatment for Obese Children and Adolescents with Insulin Resistance
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HRP0084P2-347

A Double-Blind, Placebo-Controlled Comparison of Cinnamon Extract to Metformin Effects upon Insulin Resistance, Apolipoprotein B:Apolipoprotein A1 Ratio, and BMI of Obese Adolescent Girls with Polycystic Ovary Syndrome
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HRP0084P2-348

Pantoprazole Treatment of Exogenous Obesity and Hyperinsulinism in Childhood
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HRP0084P2-350

The Switch in Eating Behaviour in Infants with Prader-Willi Syndrome is Associated with an Increase in the Acylated:Unacylated Ghrelin Ratio: Results of a Longitudinal Study
Direct

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HRP0084P2-351

Domino Liver Transplantation for the Pre-Emptive Therapy of Compound Heterozygous Familial Hypercholesterolemia: A Case of 2-Year-Old Girl
Direct

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HRP0084P2-353

A New Mutation of PCSK1 Revealed by Neonatal Malabsorptive Diarrhoea, Panhypopituitarism, and Major Obesity
Direct

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HRP0084P2-355

Berardinelli Seip Congenital Lipodystrophy: A Light of Hope
Direct

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HRP0084P2-356

Physical and Metabolic Evolution of Obese Children and Adolescents after the Attainment of Intense Weight Reduction
Direct

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HRP0084P2-358

Elevated Serum Irisin Level is not Related to Metabolic and Anthropometric Parameters in Obese Children
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HRP0084P2-359

FTO rs9939609 Polymorphism is Associated with the Presence of Obstructive Sleep Apnoea in Obese Youth
Direct

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HRP0084P2-360

Increasing Waist/Height Ratio and BMI Z-Score are Associated with Increased Comorbidities in Obese Youth, although Neither Accurately Identifies those with Abnormal Glucose Metabolism
Direct

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HRP0084P2-362

Nonalcoholic Fatty Liver Disease and Intestinal Inflammation in Obese Children
Direct

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HRP0084P2-363

Sleep and Weight Status at 4 Years in the Inma Asturias Cohort
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HRP0084P2-364

Evaluation of Acylated Ghrelin and Obestatin Levels and Ghrelin:Obestatin Ratio in Obesity
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HRP0084P2-365

A Novel MC4R Mutation Associated with Infancy-Onset Obesity
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HRP0084P2-367

Residual Excess Weight Difference Between BMI 35-40 and Over 40 After Laparoscopic Sleeve Gastrectomy in Severely Obese Adolescents: Midterm Outcomes
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HRP0084P2-368

Effect of Visfatin on Gene Expression of Insulin Signaling Molecules in SW872 Adipocytes
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HRP0084P2-369

Childhood Obesity and Normocalcaemia with a GNAS Mutation also Present in Mother
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HRP0084P2-370

Information Technology Supported Treatment of Obese Children and Their Families: A Pilot Study
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HRP0084P2-372

The Effect of ABCA1 Gene C69T Single Nucleotide Polymorphism on Dyslipidemia and Insulin Resistance in Obese Children
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HRP0084P2-373

Obese 5 Years Old Remain Obese at Age 12
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HRP0084P2-374

Lifestyle Habits and Arterial Hypertension in Children and Adolescents
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HRP0084P2-376

Metabolic Syndrome Components of Normal Weight Central Obese Adolescents in Korea Stratified by Waist-To-Height Ratio: Results from K-NHANES 2008-2010
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HRP0084P2-377

The Effect of Exenatide on Weight and Appetite in Overweight Adolescents and Young Adults with Prader-Willi Syndrome
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HRP0084P2-378

Early-Onset Obesity and Adrenal Insufficiency Associated with a Homozygous POMC Mutation
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HRP0084P2-379

Clinical and Laboratory Differences between Metabolically Healthy and Unhealthy Obese Children
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HRP0084P2-380

Insulin Resistance and Abnormal Glucose Tolerance After Paediatric Hematopoietic Stem Cell Transplantation in Blood Cancer Survivors
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HRP0084P2-381

Metformin in Combination with Lifestyle Changes Effectively Reduces BMI and Waist Circumference in Overweight/Obese Children and Adolescents
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HRP0084P2-382

Insulin-Like Factor 5 -A Novel Orexigenic Hormone in Humans is Dysregulated in Obesity
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HRP0084P2-383

Tryptophan Supplementation as Conjunctive Therapy to Life Style Changes in Obese Adolescents
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HRP0084P2-384

Obesity in ROHHADNET Syndrome: Does Cortisol Play a Role?
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HRP0084P2-387

Biovascular Markers in Children with Kabuki Syndrome
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HRP0084P2-388

Phthalate Exposure and Metabolic Parameters in Korean Girls
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HRP0084P2-389

Childhood Craniopharyngioma with Hypothalamic Obesity - No Long-term Weight Reduction due to Rehabilitation Programs
Direct

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HRP0084P2-392

Unaltered Ratio of Circulating Levels of GH Isoforms after Administration of Different GH Provocative Tests in a Population of Short Stature Children
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HRP0084P2-393

Study of IGF1 Receptor Gene in Small for Gestational Age Patients with Short Stature Treated with RHGH
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HRP0084P2-394

Gene Expression Profiles in GH Deficient Children Relate Peak GH Levels to Circadian Clock, Chromatin Remodelling, and WNT Signalling Pathways
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HRP0084P2-395

Growth and GH in Kabuki Syndrome
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HRP0084P2-397

Silver Russell syndrome: A Cause of Partial IGF1 Resistance?
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HRP0084P2-398

The In vitro Functional Analysis of Gene Promoter Region Single Nucleotide Polymorphisms Associated with GH Response in Children with GH Deficiency
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HRP0084P2-399

Is Retesting in GH Deficient Children Really Useful?
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HRP0084P2-400

Regulation of IGF1R mRNA Expression by GnRH Agonist may be Involved in the Decrease of Height Velocity During Central Precocious Puberty Therapy
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HRP0084P2-401

GRB10 Knockdown in Zebrafish is Associated with Decreased Weight-to-length Ratio without Alterations in AKT and ERK Activity: A Model to Study Human Growth Regulation
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HRP0084P2-402

The Involvement of the Epidermal Growth Factor Receptor in the Successful GH Signalling and the Role of p21 in the Negative Regulation of the GH/GHR and EGF/EGFR Pathways, in GH Transduction Defect
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HRP0084P2-403

Homozygous Carriers of a Novel IGFALS Mutation are 1.5 SD Shorter than Heterozygous Relatives and Tend to have Lower Bone Mineral Density
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HRP0084P2-404

The Role of [beta]-TrCP, an E3 Ubiquitin Ligase, in the Signalling of the GH and Epidermal Growth Factor Pathways in Growth Hormone Transduction Defect
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HRP0084P2-405

SGA Short Stature Bearing with a Novel Nonsense Mutation (p.W1249X) in the IGF1R Gene
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HRP0084P2-406

Metabolic Health in Short Children Born Small for Gestational Age Treated with GH and GnRHa: Results of a Randomised, Dose-response Trial
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HRP0084P2-407

A Phase 2, 6-Month, Randomised, Active-Controlled, Safety and Efficacy Study of TransCon hGH Compared to Daily Human GH in Children with GH Deficiency
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HRP0084P2-408

Does Skeletal Disproportion in Children with Idiopathic Short Stature Influence Response to GH Therapy?
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HRP0084P2-409

The Influence of GH Therapy on Chemerin Concentration, Body Mass and Selected Parameters of Carbohydrate Metabolism in Prepubertal Non-Obese Children with GH Deficiency
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HRP0084P2-410

Response to GH Treatment in the Very Young with GH Deficiency
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HRP0084P2-411

Estimation of Adipsin, Omentin and Vaspin Concentration in Prepubertal Children with GH Deficiency before and after 6 Months of GH Treatment
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HRP0084P2-412

Final Height and Safety Outcomes in GH-Treated Children Born Small for Gestational Age: Experience from the Prospective GeNeSIS Observational Study
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HRP0084P2-413

Results up to January 2015 from PATRO Children, a Multi-Centre, Non-Interventional Study of the Long-Term Safety and Efficacy of Omnitrope[reg] in Children Requiring GH Treatment
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HRP0084P2-415

The Pharmacokinetics and Pharmacodynamics of TV-1106, a Once Weekly GH Supplement: Results from a Phase 2 Study of TV-1106 in Adults with GH Deficiency
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HRP0084P2-417

GH Therapy in Skeletal Dysplasias: Final Height Data
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HRP0084P2-418

Random Forest Classification Predicts Response to Recombinant GH in GH Deficient Children Using Baseline Clinical Parameters and Genetic Markers
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HRP0084P2-419

Safety Evaluation of Long-Term Recombinant GH Treatment in Childhood: Interim Analysis of the NordiNet[reg] International Outcome Study (IOS)
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HRP0084P2-420

Hypoglycaemic Adverse Events Reported in Children Enrolled in the European Increlex[reg] Growth Forum Database in Europe (5-Year Interim Data)
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HRP0084P2-421

Application of Neural Networks for Final Height Prediction Based on Pre-Treatment Data in Children with GH Deficiency Treated with GH
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HRP0084P2-423

The Accuracy of Bioelectrical Impedance Analysis to Detect the Body Composition Changes in Adolescents with Severe GHD During Transition
Direct

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HRP0084P2-424

Timing of GH Peak in Provocation Tests is Important in Predicting the Effectiveness of Treatment with rhGH in Prepubertal Children with GHD
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HRP0084P2-426

The Acid-Labile Subunit Dose Matters? Response to Human GH Treatment in Patients with Acid-Labile Subunit Deficiency
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HRP0084P2-427

rhGH Replacement Therapy Ameliorates Body Composition Substantially but has No Effect in the Quality of Life in Adolescents with GH deficiency - A Cross-Sectional Study
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Abstract PDF
HRP0084P2-428

Evaluation of the Effect of GH Treatment on Insulin Resistance and Cardiovascular Tissue
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HRP0084P2-429

Effectiveness of Recombinant IGF1 Treatment in a Patient with Isolated GH IA Deficit Producer of Anti-GH Antibodies
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HRP0084P2-430

Analysis of CD133+CD45+ Hematopoietic Progenitor/Stem Cells and CD133+/CD45- Very Small Embryonic-Like Stem Cells in Children with GH Deficiency Subjected to GH Therapy
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HRP0084P2-431

Effectiveness of rhIGF1 Treatment in a Girl with Leprechaunism
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HRP0084P2-432

A Perioperative Change of Anti-Mullerian Hormone and E2 in a Patient with Sex Cord Tumour with Annular Tubules
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HRP0084P2-435

Clinical Criteria Remain Paramount for the Diagnosis of Polycystic Ovary Syndrome in the Adolescent Age Group
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Abstract PDF
HRP0084P2-439

Markers of Fertility and Quality of Life in Adolescents with Chronic Endocrine Diseases at the Time of Transition from Paediatric to Adult Care
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HRP0084P2-440

A Novel Androgen Receptor Gene Mutation in Two Patients with a 46, XY Disorder of Sex Development
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HRP0084P2-441

The Effect and Pharmacokinetics of Percutaneous Administration of Dihydrotestosterone Gel in Chinese Children with Microphallus
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HRP0084P2-442

Differential Regulation of Serum Sex Hormone Binding Globuling in Polycystic Ovarian Syndrome Girls in Relation to Weight
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HRP0084P2-443

Usefulness of 3D Ultrasonography for Assessment of the Morphology of the Ovary in Adolescents with Hyperandrogenism
Direct

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HRP0084P2-444

An Unusual Cause of Primary Amenorrhoea Suggested by the Urine Steroid Profile
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HRP0084P2-445

The Late Effects after the Haematopoietic Stem Cells Transplantation for Patients with Non-Neoplastic Disease
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HRP0084P2-446

BMI Negatively Correlates with GH Response to GH Provocation Testing
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HRP0084P2-447

SHOX Mutation Spectrum in an Unbiased Cohort of 585 Patients Referred for Leri-Weill Dyschondrosteosis or Idiopathic Short Stature
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HRP0084P2-449

Risk for Non-Alcoholic Fatty Liver Disease in Young Adults Born Preterm
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HRP0084P2-450

Pharmacokinetics and Efficacy of a Long-Acting Human GH with Fc Fusion Protein
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HRP0084P2-452

Skeletal Dysplasia with Short Stature and a Larsen-Like Phenotype due to a Homozygous Mutation in B3GAT3
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HRP0084P2-453

Cross-Sectional and Longitudinal Follow-Up of Changes in Glucose Metabolism in Prepubertal GH-Treated SGA-Patients: Results of an Unicentric Study
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HRP0084P2-454

Growth Pattern in Children Affected of Lowe Syndrome - Descriptive Multicentre International Study: Preliminary Data
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HRP0084P2-455

Effect of Aromatase Inhibitor Treatment During Adolescence on the Final Adult Height in Males with Idiopathic Short Stature
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HRP0084P2-457

Low Plasma Ghrelin Levels in Children with Severe Protein Energy Malnutrition
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HRP0084P2-458

Sleep Apneas in Silver Russell Syndrome: A Constant Finding
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HRP0084P2-459

Heterozygous NPR2 Mutations Cause Disproportionate Short Stature, Similar to Leri-Weill Dyschondrosteosis
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HRP0084P2-460

Individuals with Cow's Milk Allergy are at Risk for not Reaching their Growth Potential
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HRP0084P2-461

French Growth Reference Charts should be Updated
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HRP0084P2-462

Advanced Bone Age and Accelerated Dental Development Associated with Elevated Retinoic Acid Levels and Haploinsufficiency of CYP26A1 and CYP26C1
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HRP0084P2-463

Recurrent IGFALS Gene Mutations p.E35Gfs*17 and p.(L409F; A475V): Hot Spot or Founder Effect?
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HRP0084P2-464

Infant with Phenotype Suggestive of Silver-Russell Syndrome and Study of Normal Methylation: Consider 12q14.3q15 Microdeletion Syndrome
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HRP0084P2-465

Making Adult Height Prediction Complete: Forecasting the Age of the Growth Spurt and the Height and Velocity Trajectories Until Adulthood
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HRP0084P2-467

Clinical and Biochemical Characteristics of a Female Patient with a Novel Homozygous STAT5B Mutation but Lack of Pulmonary Disease
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HRP0084P2-468

Novel Heterozygous ACAN Mutations in Short Stature: Expanding the Clinical Spectrum
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HRP0084P2-469

Major Improvement in Parental Perception of their Children's Height-Specific Quality of Life after 1 Year of GH Treatment: Our Experience with the QoLiSSY Questionnaire
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HRP0084P2-470

Hypomethylation within the Imprinted Dlk1 - Dio3 Domain: a Potential Regulatory Mechanism of Pre and Postnatal Growth
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HRP0084P2-473

The Pubertal Gain in Height is Inversely Related to BMI in Childhood
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HRP0084P2-474

Growth Curves for Height, Weight, BMI and Head Circumference in Children with Achondroplasia
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HRP0084P2-475

Growth Hormone Deficiency and Pituitary Dysgenesis in a Girl with Microdeletion 2q31.1
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HRP0084P2-476

One Year Screening Program for Stature Deviations - Strategy and Outcome
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HRP0084P2-477

BASIC: Bone Age Study in Children
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HRP0084P2-478

Comparison of the Turkish Growth Standards with the Who Standards
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HRP0084P2-479

Moya Moya Syndrome in a Patient with Growth Hormone Deficiency and Hypergonadotropic Hypogonadism: to Treat or not to Treat with Growth Hormone Therapy?
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HRP0084P2-480

In Vitro Functional Characterization Of IGFALS Gene Variants Found In ALS Deficient or Idiopathic Short Stature (ISS) Children
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HRP0084P2-481

Klinefelter Syndrome with Short Stature and Microcephaly: An Unusual Combination
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HRP0084P2-482

Childhood Growth of Boys with Congenital Hypogonadotropic Hypogonadism
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HRP0084P2-483

Hypermethylation at the Imprinted C19mc Microrna Cluster: A New Link between Maternal Metabolism and Infant's Growth
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HRP0084P2-484

Challenged Diagnosis on Hypoglycaemia: Hirata Disease X Factitious Hypoglycaemia
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HRP0084P2-486

Transient Hyperinsulinaemic Hypoglycaemia in Association with a Novel ABCC8 Mutation: Expanding the Clinical Phenotypes
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HRP0084P2-487

Congenital Hyperinsulinism in Ukraine
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HRP0084P2-488

Unexplained Altered States of Consciousness in a Girl
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HRP0084P2-489

The Effectiveness of Sirolimus in a Newborn with Hyperinsulinaemic Hypoglycaemia
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HRP0084P2-490

Congenital Hyperinsulinism Caused by a Combination of Novel Heterozygous ABCC8 and KCNJ11 Mutations
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HRP0084P2-491

Functional Analysis of Novel ABCC8 Mutations Found in Czech Patients with Congenital Hyperinsulinism
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HRP0084P2-492

Syndromic Hypoketotic, Hypoinsulinemic Hypoglycaemia due to a Mosaic Activating Phosphatidylinositol 3-Kinase Mutation
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HRP0084P2-493

Long Acting Somatostatin Analogue (Lanreotide) Therapy in Congenital Hyperinsulinism - Pharmacokinetics and Long-Term Follow-Up Study
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HRP0084P2-494

Congenital Hyperinsulinism in Association with Poland Syndrome and Chromosome 10p11-p13 Duplication
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HRP0084P2-495

Rapid Biochemical Evaluation Aids Timely Management of Congenital Hyperinsulinism
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HRP0084P2-496

Serial 3-Dimensional Ultrasonographic Evaluation of Foetal Adrenal Volumes in the 2nd and 3rd Trimester of Pregnancy Characterises Human Adrenal Development in utero
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HRP0084P2-497

Genetic Variation in the FSH Signalling Pathway Affects Female Reproductive Hormones During Infancy
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HRP0084P2-498

Longitudinal Comparison of Inhibin B and AMH Levels and Testicular Volumes between Preterm and Full-Term Infant Boys
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HRP0084P2-499

Postnatal Catch-Down Growth is not Associated with Disturbances in Metabolic Parameters in Large-for-Gestational-Age Infants at the Age of 8 Years
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HRP0084P2-500

Birth Incidence of Prader-Willi Syndrome in France
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HRP0084P2-501

Variation of Environmental Chemicals Measured in Serum During Pregnancy
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HRP0084P2-502

Auxological Parameters, Endocrine Growth Factors and Insulin Resistance from Birth to 12 Months of Life in Children Born Small for Gestational Age
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HRP0084P2-503

Serum Fetuin-a Level for Diagnosis Hepatic Steatosis in Children with Type 1 Diabetes Mellitus
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HRP0084P2-504

Association of Dll4 Levels and VEGFR-1, VEGFR-2 in Mice Model of Oxygen-Induced Retinopathy
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HRP0084P2-505

Evaluation of Thyroid Function in Preterm Newborns of 24-30 Weeks of Gestation
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HRP0084P2-507

Fanconi Anemia Endocrine Abnormalities - Case Report
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HRP0084P2-508

The IGSF1 Deficiency Syndrome: An Unusual Case
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HRP0084P2-509

Survival, Hypothalamic Obesity, and Neuropsychological/Psychosocial Status after Childhood-Onset Craniopharyngioma: Newly Reported Long-Term Outcomes
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HRP0084P2-510

Chronic Inappropriate Antidiuresis in Childhood: Experience with Tolvaptan
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HRP0084P2-511

Pituitary Hormone Secretion Profiles in IGSF1 Deficiency Syndrome
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HRP0084P2-513

A Novel Mutation within the AVP Gene in an 18-Year-Old Male Patient with Kallmann Syndrome and Combined Pituitary Hormone Deficiency
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HRP0084P2-514

Hydrocephalus and Hypothalamic Involvement in Paediatric Patients with Craniopharyngioma or Cysts of Rathke's Pouch: Impact on Long-term Prognosis
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HRP0084P2-515

Contrasting Central Diabetes Insipidus due to preproAVP Mutations: Earlier Onset of Symptoms in Recessive than in Dominant Forms
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HRP0084P2-516

Endocrine Disorders in Children with Optic Chiasm Glioma
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HRP0084P2-517

Be Aware of Congenital Panhypopituitarism in Children with a Family History of Polydactyly
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HRP0084P2-519

Eating Behaviour, Weight Problems and Eating Disorders in 101 Long-Term Survivors of Childhood-Onset Craniopharyngioma
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HRP0084P2-520

Two Novel LHX3 Mutations in Patients with Combined Pituitary Hormone Deficiency and Sensorineural Hearing Loss
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HRP0084P2-521

A Novel Entity Characterised by GH Deficiency and Central Precocious Puberty in Two Siblings and their Father, in the Absence of Central Nervous System Defect
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HRP0084P2-523

Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes
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HRP0084P2-524

Pulsatile GnRH is Superior to hCG in Therapeutic Efficacy in Adolescent Boys with Hypogonadotropic Hypogonadodism
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HRP0084P2-525

The Lack of MKRN3 Gene Mutations in Patients with Idiopathic Sporadic GnRH-Dependent Precocious Puberty
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HRP0084P2-526

Serum AMH Levels are Lower in Healthy Boys Who Develop Pubertal Gynaecomastia
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HRP0084P2-527

Evaluation of Final Height in Girls Taking GnRH Analogue: Should the Age Limit for Precocious Puberty be Changed?
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HRP0084P2-528

Correlation of Clinical Phenotype and Genotype of Prader-Willi Syndrome and the Deletion of Paternal MKRN3 Allele in PWS Patients with Central Precocious Puberty
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HRP0084P2-529

Doppler Evaluation of the Uterine Artery for the Diagnosis and Follow-Up of Patients with Precocious Puberty
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HRP0084P2-530

Nephrogenic Diabetes Insipidus with Partial Response to Ddavp Caused by a Novel AVPR2 Splice Site Mutation
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HRP0084P2-531

Regional Brain Volume and Luteinising Hormone in Girls with Idiopathic Central Precocious Puberty
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HRP0084P2-532

Determination of Final Height in Girls with Precocious Puberty. Which is the Most Accurate Method?
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HRP0084P2-533

The Relationship between Steriod Receptors and Aromatase in the Mouse Brain
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HRP0084P2-534

Evaluation of Body Proportions in Children with Precocious or Delayed Puberty
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HRP0084P2-535

GH Deficiency with Advanced Bone Age: GHRH Receptor Mutation Detected by Exome Sequencing Associated to Non-Classical Congenital Adrenal Hyperplasia (CAH)
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HRP0084P2-536

Ultra-Deep Next-Generation Sequencing: A reliable Method for the Molecular Diagnosis of McCune Albright Syndrome
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HRP0084P2-537

Increased Ambulatory Blood Pressure in Adolescents with Gender Dysphoria Treated with Gonadotropin- Releasing Hormone Analogues
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HRP0084P2-538

Plasma Humanin Levels During Normal Childhood and Puberty. Study of Possible Correlations with Sex, Age, and Insulin Levels
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HRP0084P2-539

GnRH Infusion in Females with Hypogonadotropic Hypogonadism
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HRP0084P2-540

A Case of Familial Central Precocious Puberty Caused by a Novel Mutation in the Makorin RING Finger Protein 3 Gene
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HRP0084P2-543

The Endocrine Response to a Gonadotropin Releasing Hormone (GnRH) Test: Establishing a Reference Interval in Healthy Girls below 6 Years of Age
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HRP0084P2-544

Increasing BMI is Associated with Lower Luteinising Hormone Levels in Girls with Central Precocious Puberty at the Early Pubertal Stage
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HRP0084P2-545

Change of Growth Pattern and Bone Mineral Density in Ovariectomised Female Rats According to Oestrogen Dosage
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HRP0084P2-546

Gynecomastia with Precocious Onset in Peutz-Jeghers Syndrome: Managing the Aromatase Overexpression
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HRP0084P2-547

The Impact of Growth Hormone (GH) Therapy Combined with Estrogens on Blood Pressure (BP), Cardiac Left Ventricular (LV) Dimensions and Lipid Metabolism in Pubertal Girls with Turner's Syndrome (TS)
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HRP0084P2-548

Sensitivity of Measured Parental Height and Target Range in the Diagnosis of Turner Syndrome
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HRP0084P2-549

Balance Control in Children and Adolescent Girls with Turner Syndrome
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HRP0084P2-550

Short Stature with Neurodevelopmental Delay in Familial Variant Turner Syndrome
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HRP0084P2-551

Diagnostic Significance of Serum Concentrations of Osteoprotegerin and Proinflammatory Cytokine IL-1[beta] in Children with Autoimmune Thyroid Disease
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HRP0084P2-552

Even in the Era of Congenital Hypothyroidism Screening Mild and Subclinical Sensorineural Hearing Loss Remains a Relatively Common Complication of Severe Congenital Hypothyroidism
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HRP0084P2-553

Efficacy of Supplemental Liothyronine for Patients with Congenital Hypothyroidism and Pituitary Resistance to Thyroid Hormone
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HRP0084P2-554

Hypoceruloplasminemia as a Marker of Severe Hypothyroidism
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HRP0084P2-555

Pituitary Resistance to Exogenous Levothyroxine in Humans
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HRP0084P2-557

Potentially Excessive Levothyroxine Doses in Cases of Congenital Hypothyroidism with Eutopic Thyroid Gland
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HRP0084P2-558

Objective vs Subjective Measurement of Thyroid Volume by Ultrasound in Infants Referred with TSH Elevation on Newborn Screening
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HRP0084P2-559

Central or Primary Hypothyroidism? How to Differentiate in Patients with Low T4 but Mildly Elevated TSH Levels
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HRP0084P2-561

Analysis of Chosen Polymorphisms rs5742909 C/T - CTLA4, rs7522061 C/T - FCRL3, rs7138803 A/G - FAIM2 in Pathogenesis of Autoimmune Thyroid Diseases in Children
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HRP0084P2-562

Thyroid Dysfunction is Associated with Biochemical Markers of Non Alcoholic Fatty Liver Disease in Paediatric Population
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HRP0084P2-563

Nonautoimmune Neonatal Hyperthyroidism due to A633G Mutation in the Thyrotropin Receptor Gene
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HRP0084P2-565

Metamorphic Thyroid Autoimmunity in Down Syndrome: From Hashimoto's Thyroiditis to Graves' Disease and Beyond
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HRP0084P2-566

Analysis of B Regulatory Cells with Phenotype CD19+CD24hiCD27+IL-10+ and CD19+IL-10+ in the Peripheral Blood of Children with Graves' Disease and Hashimoto's Thyroiditis
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HRP0084P2-567

Case Report: Resistance of Thyroid Hormone due to a Novel Thyroid Hormone Receptor [beta]-Gene Mutation
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HRP0084P2-570

Goitrous Hypothyroidism of Pubertal Onset Caused by a Novel Mutation in DEHAL1 Gene
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HRP0084P2-574

Years Follow-Up of Children with Abnormal Newborn Screening Results for Congenital Hypothyroidism: Who Needs Treatment and Who Needs Permanent Treatment?
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HRP0084P2-575

Attention Deficit and Sluggish Cognitive Tempo Symptoms in Congenital Hypothyroidism: Results from a Case-Control Study
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HRP0084P2-577

Osteoprotegerin and fT4 Levels in Subclinical Hypothyroidism of Childhood
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HRP0084P2-578

Cryptorchidism is Commonly Observed in Allan Herndon Dudley Syndrome
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HRP0084P2-579

Co-Existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis; A Single-Centre Study
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HRP0084P2-580

The Diagnostic, Treatment and Follow-Up Features of Childhood Thyroid Malignancies - A Preliminary Report
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HRP0084P3-581

New Mutation Causing Systemic Pseudohypoaldosteronism
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HRP0084P3-582

Rapid Molecular Diagnosis of CAH by Strip Hybridisation Assay in DEMPU
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HRP0084P3-583

Insufficient Mineralocorticoid Replacement as a Predictor Factor for the TART in Boys with Congenital Adrenal Hyperplasia
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HRP0084P3-584

CYP11B1 Gene Mutations in Patients with Congenital Adrenal Hyperplasia in Turkey
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HRP0084P3-585

Living with Adrenal Hyperplasia for Children in Primary School between 6 and 11 Years; Educational Innovation and Design of a Learning Tool for Therapeutic Education
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HRP0084P3-587

Adrenal Atrophy Secondary to Inappropriate Oral Administration of Exogenous Steroid Presenting with Hypercalcaemia
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HRP0084P3-588

Case Report: Hypothyroidism and Acth-Deficiency Caused by TBX 19 Mutation Coincidence or Pathogenetic Correlation?
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HRP0084P3-589

Deletion Mapping in Xp21 for a Family with Complex Glycerol Kinase Deficiency Using Array-Based Comparative Genomic Hybridisation
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HRP0084P3-590

Characterisation of Ovarian Adrenal Rest Tumours in Children and Adolescent Females with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
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HRP0084P3-591

Pseudohypoaldosteronism - Subtle Presentations with Critical Electrolyte Imbalances Experiences from One Hospital
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HRP0084P3-592

Atypical Prednisone-Metabolism: Pharmacological Studies in a Boy with Classical Adrenal Hyperplasia and Suspected Malcompliance
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HRP0084P3-593

CYP21A2 Gene Mutations Analysis in 21 Chinese Patients with Salt-Wasting form of Congenital Adrenal Hyperplasia
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HRP0084P3-594

X-Linked Adrenoleucodystrophy Presenting as Addison's Disease in Childhood: A Case Report
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HRP0084P3-595

Three Siblings with Corticosterone Methyloxidase Deficiency Type 2 due to c.1175T[gt]C Mutation +a Novel c.788T[gt]A Mutation in CYP11B2 Gene
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HRP0084P3-596

Transient Pseudohypoaldosteronism as a Complication of Infected Obstructive Uropathy in Infancy, a Case Series
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HRP0084P3-597

Generalised Glucocorticoid Resistance in an Adolescent Girl with Severe Hyperandrogenia without Mutations in NR3C1 Gene
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HRP0084P3-598

Remission with Cabergolin with Recurrent Hypercortisolism after Pituitary Surgery in Cushing's Disease
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HRP0084P3-599

Phaeochromocytoma in Placental Mesenchymal Dysplasia: Who Should We Screen and for How Long?
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HRP0084P3-600

A Double Dose of Triples
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HRP0084P3-601

Central Cortisol Deficiency (Isolated ACTH Deficiency) in a Child
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HRP0084P3-602

The First Case of Primary Generalized Glucocorticoid Resistance in Serbia in an 8-Year-Old Boy with G679S Mutation of the NR3C1 Gene
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HRP0084P3-603

A Case of Phaeochromocytoma Diagnosed as Adrenal Incidentaloma
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HRP0084P3-604

Severe High Blood Pressure with Renal Failure in a Neglected Case of 11[beta]-Hydroxylase Deficient Congenital Adrenal Hyperplasia
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HRP0084P3-605

Delayed Diagnosis of Salt Wasting Congenital Adrenal Hyperplasia, without Complications of Cortisol Deficiency: A Case Report
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HRP0084P3-606

Familial Hyperaldosteronism Type 1 in an Infant without Hypertension: How Important Could be the Early Treatment with Hydrocortisone?
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HRP0084P3-608

A Prospective Evaluation of Anthropometric and Metabolic Profile Premature Adrenarche Patients
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HRP0084P3-610

Development of a Patient with Severe Pseudohypoaldosteronism due to Mutation in the [alpha] Subunit of ENaC
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HRP0084P3-611

Methodological Considerations into the Approach for Genetic Diagnostics of Congenital Adrenal Hyperplasia in a Girl with SW Form and Relatively Higher Needs of Mineral Corticoids
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HRP0084P3-612

11[beta]-Hydroxylase Deficiency: 20 Years Follow-Up
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HRP0084P3-614

Late Diagnosis of Childhood Adrenal Insufficiency and Hypogonadotropic Hypogonadism due to DAX 1 Gene Mutation
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HRP0084P3-615

Paraaortical Paragangliomas as Incidental Findings in a Female Adolescent
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HRP0084P3-616

Nephrotic Syndrome Developing in a Girl with Classic 21-Hydroxylase Deficiency - First Report
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HRP0084P3-617

Conservative Treatment Allows Substantial Improvement of Neonatal Cushing Syndrome in McCune Albright Syndrome, a 2 Year Follow-up
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HRP0084P3-618

A CYP21A2 Gene Mutation in Patients with Congenital Adrenal Hyperplasia: Molecular Genetics Report from Saudi Arabia
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HRP0084P3-620

A Rare Cause of Hypertension: Pseudophaeochromocytoma
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HRP0084P3-621

A Case of X-Linked Adrenal Hypoplasia Congenita - Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency and Duchenne Muscular Dystrophy
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HRP0084P3-622

Prenatal Treatment of Congenital Adrenal Hyperplasia: A Survey of Paediatric Endocrinologist
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HRP0084P3-623

A Case of ACTH Resistance with Generalized Hyperpigmentation at Birth
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HRP0084P3-624

Clinical and Genotypic Characterization of Simple Virilising Forms of Congenital Adrenal Hyperplasia
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HRP0084P3-625

'Reexpansion' of Testicular Tissue after Testis-Sparing Surgery in an Adolescent
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HRP0084P3-626

Exogenous Cushing's Syndrome due to Misuse of Topical Corticosteroid Therapy
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HRP0084P3-627

Familial Glucocorticoid Deficiency - A Case Report
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HRP0084P3-628

Assessment of Ovarian Function and Reserve Based on Hormonal Parameters, Ovarian Volume, and Follicle Count in Euthyroid Girls with Hashimoto Thyroiditis
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HRP0084P3-629

Early-onset Type 1 Diabetes and Multiorgan Autoimmunity in a Girl with Partial Monosomy 2q and Trisomy 10p
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HRP0084P3-630

CTLA4 A49G and C60T Genetic Polymorphism in Croatian Children and Young Adults with Autoimmune Thyroid Disease
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HRP0084P3-631

Oocyte Cryopreservation in a Patient with Premature Ovarian Failure due to Autoimmune Polyendocrine Syndrome Type 2
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HRP0084P3-632

Thyroid Function and Autoimmunity in Children with Newly Diagnosed Type 1 Diabetes Mellitus
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HRP0084P3-633

Hypercalcaemia as an Indication of Adrenal Insufficiency in a Patient with Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
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HRP0084P3-635

Radiologic Appearance is Important for Diagnosis of Autoimmune Hypophysitis
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HRP0084P3-637

About a Case of Basedow-Graves' Disease in a Infant
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HRP0084P3-638

The Autoimmune Polyendocrinopathies in Children and Adolescents
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HRP0084P3-639

Is Serum Serotonin Involved in the Bone Loss of Young Females with Anorexia Nervosa?
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HRP0084P3-640

Cranial MR Spectrometry Findings of Patients Aged 10-15 Years with Diagnosis of Rickets
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HRP0084P3-641

Evaluation of Bone Geometry, Quality and Bone Markers in Children with Type 1 Diabetes
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HRP0084P3-642

Comparison of Treatment Alternatives for Hypercalcemia due to Vitamin D Intoxication in Children
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HRP0084P3-643

Influence of Birth Weight and Total Body Less Head Bone Mineral Contents in 10-18 Korean Adolescents: Results from the Korea National Health and Nutrition Examination Surveys 2008-2010
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HRP0084P3-644

Clinical and Molecular Characterisation of Patients with Pseudohypoparathyroidism
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HRP0084P3-645

Long Term Effects of Bisphosphonate Treatment in a Case with Infantile Onset Severe form of Juvenile Paget's Disease
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HRP0084P3-646

Diagnosis and Management of Gorham-Stout Disease: A Protocol Proposal
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HRP0084P3-647

Vitamin D Dependent Rickets Type 1A with Genetic Analysis in Three Chinese Children
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HRP0084P3-648

A Novel Mutation in CYP24A1 Gene in an Infant with Severe Hypercalcaemia and Unique Neurological Presentation
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HRP0084P3-649

Continuous 1-34 rhPTH Therapy in a Girl with a PTH-Gene Defect
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HRP0084P3-650

Prevalence of Vitamin D Deficiency in Sickle Cell Anaemic Children in Jos, Nigeria
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HRP0084P3-652

Endocrine Function, Vitamin D and Bone Mass Status in [beta]-Thalassemia Major
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HRP0084P3-653

Late Sequel of Meningococcemia: Presenting as Skeletal Dysplasia
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HRP0084P3-655

A Longitudinal, Prospective, Long-Term Registry of Patients with Hypophosphatasia
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HRP0084P3-656

Retrospective Evaluation of Patients Diagnosed as Nutritional Rickets: A Single Centre Study
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HRP0084P3-657

Discrepancy in Bone Age Rating Using Tanner-Whitehouse Rating and Automated Bone Age Determination in a Child Who was Later Diagnosed with Metaphyseal Dysplasia
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HRP0084P3-658

Vitamin Levels in Pregnant Women and in Cord Blood in Newborn in Our Area - Preliminary Results
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HRP0084P3-659

Vitamin D Status in Romanian Children 0-18 Years - Should we be More Careful Regarding Supplementation?
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HRP0084P3-660

4 Years Follow-Up for 25OHD and iPTH in Vitamin D Substituted Patients with Diabetes Mellitus 1: An Unicentric Prospective Study
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HRP0084P3-661

Bone Mineral Density in Prader-Willi Females During the Transition Phase
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HRP0084P3-662

Seasonal Differences in Plasma 25-OH Vitamin D Concentrations in Cord Blood
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HRP0084P3-663

Spondyloenchondrodysplasia with Immune Dysregulation and without Neurological Involvement: Report of Two Siblings with ACP5 Gene Mutation
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HRP0084P3-664

Short Stature in Osteogenesis Imperfecta is not Caused by Deficiencies in IGF1 or IGF-BP3
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HRP0084P3-665

Vitamin D Status in Children in the Western Part of Turkey
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HRP0084P3-666

Parathyroid Adenoma Should be Considered in the Management of Hypophosphataemic Rickets
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HRP0084P3-667

Neurological Clinic Delays the Diagnosis of Pseudohypoparathyroidism
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HRP0084P3-668

Treatment of Life Threatening Hypercalcaemia in Two Infants
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HRP0084P3-669

Comparison of the Levels of Vitamin D in Children in Northern Spain (Domestic or Foreign)
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HRP0084P3-671

How are we Using Bisphosphonates in Children with Secondary Osteoporosis in a Tertiary Centre?
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HRP0084P3-672

Pseudohypoparathyroidism: Clinical Heterogeneity Illustrated by Three Different Cases
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HRP0084P3-673

Successful Treatment of Severe Hypercalcemia in an Infant with Williams Syndrome Using a Single Infusion of Pamidronate Followed by Low Calcium Diet
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HRP0084P3-674

25-Hydroxy Vitamin D Levels in Patients with Chronic Diseases on Corticosteroid Treatment
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HRP0084P3-675

Pseudohypoparathyroidism Type 1b, a Rare Diagnosis in Adolescents
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HRP0084P3-676

What Lies Beneath: An Enigma of Missed Opportunities and Calcium Problem
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HRP0084P3-677

A Novel Homozygous Six Nucleotide Deletion in GLUT2 Gene in a Fanconi-Bickel Syndrome Family
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HRP0084P3-678

Final Height in a Patient with Fanconi Syndrome and GH Deficiency Treated with GH
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HRP0084P3-679

Carpal Spasm in Hypophosphataemic Patient
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HRP0084P3-683

Hypocalcaemia by Parathyroid Dysfunction in Children and Adolescents
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HRP0084P3-684

VDR Gene Analysis Results of Four Patients with Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets
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HRP0084P3-686

A Rare Reason of Hyperinsulinism: Munchausen Syndrome by Proxy
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HRP0084P3-687

Correlation of Vitamin D Levels with Glycaemic Control, Total Daily Insulin Dose, BMI, and Ethnicity in Paediatric Patients with Type 1 Diabetes Mellitus
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HRP0084P3-688

Management of Children with Type 1 Diabetes During Illness (Sick Days): Is There a Need for National Consensus Guideline?
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HRP0084P3-689

Incretin Secretion was not Impaired in Obese Korean Children and Adolescents with Type 2 Diabetes
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HRP0084P3-690

Neonatal Diabetes Mellitus: Clinical Feature and Outcome
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HRP0084P3-691

Acute Kidney Injury as a Severe Complication of Diabetic Ketoacidosis
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HRP0084P3-692

BMI in Children and Young People with Type 1 Diabetes in England and Wales
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HRP0084P3-693

Blood vs Urine Ketone Monitoring in a Pediatric Cohort of Patients with Type 1 Diabetes: a Crossover Study
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HRP0084P3-694

Elastargene 3C Helps to Improve HbA1c in Children and Adolescents with Type 1 Diabetes Using Insulin Pump Therapy
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HRP0084P3-695

Intraosseous Infusion: Sometimes the Only Way to Treat Severe Diabetic Ketoacidosis
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HRP0084P3-696

Influence of hypoglycemic episodes on attention and behavioural abnormalities in diabetic children
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HRP0084P3-697

Recurrent Ketosis after Prolonged Exercise in Type 1 Diabetes: The Need for Glycogen Replacement Strategies: Case Report
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HRP0084P3-698

Adherence to Diabetic Ketoacidosis Management Protocol: a Paediatric Centre Experience
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HRP0084P3-699

Continuous Intersticial Glucose Monitoring in Early Detection of Glucose Tolerance Abnormalities in Adolescents with Cystic Fibrosis
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HRP0084P3-700

Health-Related Quality of Life in Children and Adolescents with Type 1 Diabetes Mellitus in Spain: Results From the CHRYSTAL Study
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HRP0084P3-701

HbA1c Rather Than BMI Lifestyle and Adherence to Mediterranean Diet is the Major Determinant of Triglyceride/HDL Cholesterol Ratio in Adolescents with Type 1 Diabetes
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HRP0084P3-702

Non-HDL Cholesterol in Diabetic Children: Treatment Recommendations Considering Glycaemic Control, BMI, Age, Gender, and Generally Accepted Cut Points
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HRP0084P3-703

A 1-year Follow-up Study to Evaluate Efficacy and Compliance of Continuous Glucose Monitoring in Children with Type 1 Diabetes Mellitus
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HRP0084P3-704

Diabetic Ketoacidosis Treatment: Experience from a Paediatric Tertiary Centre (2004-2014)
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HRP0084P3-705

Treatment of Dyslipidemia in Children and Adolescents with Diabetes Mellitus Type 1
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HRP0084P3-706

Hearing Changes in Children and Adolescents with Type 1 Diabetes Mellitus
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HRP0084P3-707

A Novel Genetic Mutation in a Turkish Family with GCK-MODY
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HRP0084P3-709

Elevated HbA1c and Cardiometabolic Risk Factors in Korean Children and Adolescents: Data from the Korean National Health and Nutrition Examination Survey, 2011-2012
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HRP0084P3-710

How Appropriate are the Lengths of Syringe Needles Used for Subcutaneous Injections to the Children at School Age
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HRP0084P3-711

Heterogeneous Presentation of Paediatric Hyperglycaemic Hyperosmolar State - A Case Series
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HRP0084P3-712

A Novel Compound Heterozygous Mutation in an Adolescent with Insulin-dependent Diabetes: A Case Report of Wolfram Syndrome
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HRP0084P3-713

Sirolimus Therapy in an Infant with Persistent Hyperinsulinaemic Hypoglycaemia
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HRP0084P3-714

Permanent Neonatal Diabetes Mellitus in Beckwith Wiedemann Syndrome: An Unusual Co-Occurrence
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HRP0084P3-715

Prevalence of Vascular Complications in Children with Type 1 Diabetes in Ireland
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HRP0084P3-716

Hyperglycaemia During Chemotherapy for Acute Lymphoblastic Leukaemia Among Taiwanese Children
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HRP0084P3-717

Seip-Berardinelli Syndrome in a Patient Referred by Low Weight Gain
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HRP0084P3-718

Effect of Reward-based Motivation on Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus
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HRP0084P3-719

Fanconi-Bickel Syndrome due to a Novel SLC2A2 Mutation Presenting with Transient Neonatal Diabetes
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HRP0084P3-721

GAD Antibodies Negative Type 1 Diabetes and Dravet Syndrome
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HRP0084P3-722

Social Risk Assessment in Children with Diabetes Mellitus to Plan Medical and Social Care
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HRP0084P3-724

Study of Adiponectin Level in Diabetic Adolescent Girls in Relation to Glycaemic Control and Complication of Diabetes
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HRP0084P3-725

Frequent and Prolonged Daytime Hypoglycemia in Diabetic Children Detected by Continuous Glucose Monitoring: A Problem of Hypoglycaemia Unawareness?
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HRP0084P3-726

Neonatal Diabetes Mellitus due to Insulin Gene Mutation
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HRP0084P3-727

Single Centre Experience of Neonatal Diabetes
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HRP0084P3-728

Assessment of the Effect of the Diagnosis of Type 1 Diabetes Mellitus in the Nutritional Habits of Unaffected Family Members
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HRP0084P3-729

Lifestyle and Metabolic Control in Adolescents with Type 1 Diabetes
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HRP0084P3-730

[beta]-Cells' Functional Exhaustion at Type 1 Diabetes Onset may Lead to Early Microvascular Complications
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HRP0084P3-731

Influence of Pancreatic Autoinmunity in the Onset and Progression of Diabetes in Paediatric Population
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HRP0084P3-732

Severe Insulin Resistance and Dyslipidaemia with Unremarkable Fat Distribution in an Adolescent Girl due to Mutation in the PPARG Gene (Familial Partial Lipodystrophy Type 3)
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HRP0084P3-733

Use of Smartphone, a Cellular Glucometer and Social Media App in the Management of Type 1 DM in the Adolescent Population: The Future of Diabetes Care
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HRP0084P3-734

A Boy with Wolfram Syndrome
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HRP0084P3-735

Cardiovascular Risk Factors in Children and Adolescents with Type 1 diabetes
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HRP0084P3-736

Megaloblastic Anaemia and Diabetes in a Young Girl
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HRP0084P3-737

Audit Assessing Glycaemic Control in Children Aged Less than 16 Years with Type 1 Diabetes in Malta Over the Period 2013-2014
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HRP0084P3-739

Assessment of Quality of Life in Adolescents with Type 1 Diabetes; a Pilot Study
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HRP0084P3-740

Mody3 Early Identification and Diagnosis
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HRP0084P3-741

Low fT3 Syndrome due to Metabolic Acidosis/Ketoacidosis in Type 1 Diabetes Mellitus (Type 1 DM)
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HRP0084P3-742

Coping Styles of Adolescents with Type 1 Diabetes and their Parents: Association with Metabolic Control and Disease Duration
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HRP0084P3-744

Transition During Adolescence, is there Room to Improve?
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HRP0084P3-745

Vitamin D Status in Egyptian Children with T1D and the Role of Vitamin D Replacement on Glycaemic Control
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HRP0084P3-746

Residual C-Peptide in Paediatric Patients with Type 1 Diabetes
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HRP0084P3-747

A Novel Nonsense Mutation in the WFS1 Gene Causes Wolfram Syndrome
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HRP0084P3-748

Health Literacy of Caregivers of Children with Type 1 Diabetes: A Pilot Study on Impact on Glycaemic Control in an Arabic-Speaking Population
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HRP0084P3-751

Fasting the Holy Month of Ramadan in Older Children and Adolescence with Type 1 Diabetes in Kuwait
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HRP0084P3-752

The Long-Term Insulin Management with Premixed Insulin in Neonates and Infants with Diabetes
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HRP0084P3-754

Thyroid Function and Prevalence of Celiac Disease in Children with T1D in Lithuanian Pediatric Population
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HRP0084P3-755

Severe Hypertriglyceridaemia in a Child with Severe Diabetic Ketoacidosis
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HRP0084P3-756

Factors Related to Progression to Macroalbuminuria in Type 1 Diabetic Children with Microalbuminuria
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HRP0084P3-757

Acute Painful Neuropathy in a Teenager with Type 1 Diabetes (T1D) and Eating Disorders
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HRP0084P3-758

A Case of Tacrolimus Related Posttranslated Diabetes Mellitus (PTDM)
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HRP0084P3-759

Short-Term Use of Continuous Glucose Monitoring System in Paediatric Patients with Type 1 Diabetes Mellitus and Correlation with Short-Term Improvement in Glycaemic Control
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HRP0084P3-760

Neonatal Diabetes - the Great Masquerader: Experiences from One Hospital
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HRP0084P3-762

Metabolic Control and Glycemic Variability in Pediatric Patients with Type 1 Diabetes in Multiple Daily Injections Therapy Using Automated Bolus Calculator Glucometer
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HRP0084P3-763

Maturity Onset Diabetes of the Young: Just Think about It
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HRP0084P3-764

The Role of KCNJ11 Gene in Neonatal Diabetes
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HRP0084P3-765

A Case of DEND (Developmental Delay, Epilepsy, and Neonatal Diabetes) Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea Therapy
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HRP0084P3-766

Two Permanent Neonatal Diabetes Mellitus Cases due to Mutation in abcc8 Genes in Vietnam: Clinical Features and Long - Term Outcome in Treating by Sulfonylurea (2008-2014)
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HRP0084P3-767

Type 1 Diabetes in Pediatric Patients: Demographic and Clinical Characterisation
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HRP0084P3-768

The Missing Link in Neonatal Diabetes
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HRP0084P3-769

Cutaneous Manifestations among Type 1 Diabetic Patients in DEMPU
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HRP0084P3-770

Particularites de la prise en charge du diabete Type 1 chez des enfants dont la revelation est survenue avant l'age de five ans
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HRP0084P3-771

Evaluation of Boluses Delivered by Insulin Pump in Type 1 Diabetes Mellitus Paediatric Patients
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HRP0084P3-773

Mauriac Syndrome, a Rare Complication of Type 1 Diabetes Mellitus
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HRP0084P3-774

Is Autoimmunity on the Increase in Type 1 Diabetes Mellitus? Presentation of Multiple Auto-Immune Disorders at Diagnosis of Type 1 Diabetes Mellitus
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HRP0084P3-775

Type 1 Diabetes Mellitus and Precocious Puberty: Rare Association
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HRP0084P3-776

School Aged Presentation of Diabetes Mellitus Type 1 with Repeat Hyperglycaemia, Positive Pancreatic Autoimmunity and Related Genetic Risks
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HRP0084P3-777

Clinical Changes Observed After System Implementation of JUNIORSTAR Systems in Children with Dm1a
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HRP0084P3-778

Metabolic Control in Children in Northern Spain DM1A with Deficit of Vitamin D
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HRP0084P3-779

Effects of Educational Interventions for Children and Adolescents with Type 1 Diabetes Mellitus
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HRP0084P3-780

Clinical Findings, Endocrine Profile and Genetic Features of 5[alpha]-Reductase-2 Deficiency
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HRP0084P3-781

Aromatase Deficiency due to Novel CYP19A1 Mutation in an Egyptian Patient with Ambiguous Genitalia
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HRP0084P3-782

The Time of First Presentation at the Department of Paediatric Endocrinology of Patients with 46, XY DSD
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HRP0084P3-784

A Cross-Sectional Growth Reference and Chart of Stretched Penile Length for Japanese Boys Aged 0-7 Years: Ethnic Differences and Secular Changes
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HRP0084P3-785

Recurrent Orchitis in a Patient with True Hermaphroditism
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HRP0084P3-786

Isolated Persistent Pubertal Gynecomastia in Three Adolescent Males as the Only Phenotypic Expression of PAIS with Androgen Receptor Gene Mutations
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HRP0084P3-787

Identical Twins Raised as Sister and Brother
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HRP0084P3-788

Persistent Mullerian Duct Syndrome Associated with Anorchia Caused by a Compound Heterozygous Mutation in the AMHR-II Gene
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HRP0084P3-789

A Novel Mutation in Steroidogenic Factor Gene in a Patient with 46, XY DSD without Adrenal Insufficiency
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HRP0084P3-790

Evaluation of Two New Anti-Mullerian Hormone Assays for the Investigation of Disorders of Sexual Development in Neonates
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HRP0084P3-791

'Female', 'Male', or 'Between' in a 46, XY-Patient with a 17sz-HSD3-Mutation
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HRP0084P3-792

Physical Assessment and Growth Curve of 46, XY Disorders of Sex Development Children Who Aged 0-16-Years-Old
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HRP0084P3-794

A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
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HRP0084P3-795

Polymorphisms and Mutations of the Genes INSL3 and HOXD13 in the Pathogenesis of Isolated Cryptorchidism in Greece
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HRP0084P3-797

Screening for Y Microdeletions in Patients with Hypergonadotropic Hypogonadism due to Disorder of Sexual Development
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HRP0084P3-798

'I am a Boy Since 8-Years-Old': Female During Childhood, Virilization at Puberty
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HRP0084P3-799

A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty
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HRP0084P3-800

A Novel Mutation of the AMH in an Egyptian Male with Persistent Mullerian Duct Syndrome
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HRP0084P3-801

Pseudo-Precocious Puberty in Androgen Insensitivity Syndrome Secondary to a Prepubertal Oestrogen Producing Sertoli Cell Tumour
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HRP0084P3-802

Gender Reassignment in Muslim Communities
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HRP0084P3-803

A Case of Klinefelter Syndrome with an Atypical Presentation
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HRP0084P3-805

Patient with Primary Amenorrhea and Glomerular Nephropathy
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HRP0084P3-806

The Advent of Disorders of Sexual Differentiation Team at a Major Teaching Nigeria: Impact on Patient Management and Outcome
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HRP0084P3-808

Characteristic of Children with Mixed Gonadal Dysgenesis
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HRP0084P3-809

A 19-Year-Old Adolescent with Short Stature and Scrotal Tumour
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HRP0084P3-810

An Atypical Case of Mayer-Rokitansky-Kuster-Hauser Syndrome with Hyperandrogenemia
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HRP0084P3-811

Cushing's Syndrome due to Ectopic ACTH Secretion by a Germline Tumour in the Cross-tail Area in a 7 Month Old Female Infant
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HRP0084P3-812

Uterine Bleeding: A Rare Side Effect of Mitotane Treatment for Recurrent Adrenal Carcinoma
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HRP0084P3-813

Metabolic Syndrome in Childhood Acute Lymphoblastic Leukaemia Survivors
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HRP0084P3-814

Results of GH Treatment in Childhood Brain Tumours Survivors
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HRP0084P3-815

Craniopharyngioma - Symptoms, Treatment and Follow Up - An Analysis of 100 Cases
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HRP0084P3-816

Von Hippel-Lindau Disease in an Adolescent with a Newly Described Alteration in the VHL Gene
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HRP0084P3-817

Two Synchronous Central Nervous System Tumors in a Child with Neurofibromatosis Type 1
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HRP0084P3-818

Endocrine Evaluation in Children and Adolescents Submitted to Allogeneic Bone Marrow Tranplantation
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HRP0084P3-819

Early Endocrine Complications in Survivors of Childhood Malignant Tumours
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HRP0084P3-820

AIP Polymorphism in Familiar Isolated Pituitary Adenomas: Case Report
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HRP0084P3-821

Primary Hypogonadism after Haematopoietic Stem Cell Transplant in Paediatric Patients with Cancer
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HRP0084P3-822

Galactocele: A Rare Case of Breast Enlargement Among Children
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HRP0084P3-823

LHRH Analogues Successfully Suppress Menstruation During Chemotherapy in Teenagers and Young Adults
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HRP0084P3-824

Suprasellar Brain Tumours Related Endocrinopathies
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HRP0084P3-825

GH and Prolactin Secreting Adenoma in an Adolescent Boy
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HRP0084P3-826

The Evaluation of Bone Mass Density in Patients after Therapy of Solid Tumours
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HRP0084P3-827

The Pathway to the True Diagnosis
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HRP0084P3-828

Long-Term Effects of a Ketogenic vs a Hypocaloric Diet in Children and Adolescents with Obesity
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HRP0084P3-829

Metabolically Unhealthy Obese Children Under the Risk of Exercise Induced Chronotropic Incompetence
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HRP0084P3-830

Determinants of Serum Interleukin 1 - Receptor Antagonist Concentrations in 12-Year-Old Children Born Small or Appropriate for Gestational Age
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HRP0084P3-831

Evaluation of Renal Functions in Obese Children and Adolescents with Cystatin-C and Creatinin Based GFR: is Increasing GFR Reflected Hyperfiltration and Possible Renal Damage in Future?
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HRP0084P3-832

The French Experience in Bariatric Surgery 'Laparoscopic Adjustable Gastric Banding' in Adolescence
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HRP0084P3-833

Correlation of Serum FGF-21 Levels with Metabolic Parameters in Korean Obese Children
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HRP0084P3-834

Liver Steatosis in Obese Children Courses with Enhanced Insulin Resistance and Dyslipidaemia, Which are Influenced by Gender, Puberty, Race and Body Fat Distribution
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HRP0084P3-835

How Early are Vascular Changes in Obese Children Among North Indian Population?
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HRP0084P3-836

Prader-Willi Syndrome - A General Picture of 51 Cases
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HRP0084P3-837

Comparison of Two Family-Intervention (Parents Only vs Parent and Child) in the Treatment of Childhood Obesity
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HRP0084P3-838

Bioavailable Vitamin D in Obese Children: The Role of Insulin Resistance
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HRP0084P3-839

Age at Menarche in Relation to BMI. Data from the Hellenic Action Plan for the Assessment, Prevention and Treatment for Childhood Obesity
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HRP0084P3-840

Are Age and Initial BMI-SDS in Obese Children and Adolescents Associated with the BMI-SDS Courses During and after the Attendance of an Inpatient Weight-Loss Program (LOGIC-Trial)?
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HRP0084P3-841

Turn off and Turn in: The Influence of Television Viewing and Sleep on Lipid Profiles in Children
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HRP0084P3-842

Hepatic Steatosis Influences Significantly the Cardiovascular Risk in Children with Metabolic Syndrome
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HRP0084P3-844

The Risk of Metabolic Syndrome among Dyslipidemic Children and Adolescents
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HRP0084P3-845

RNAi as Tool to Study Molecular Mechanisms of Metabolic Adverse Reactions in Caenorhabditis Elegans
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HRP0084P3-846

Hypertriglicerydaemia in a Boy with Bardet-Biedl Syndrome - Case Report
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HRP0084P3-847

Uric Acid and Triglycerides/HDL Ratio as a Predisposing Factor for Metabolic Syndrome in Children
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HRP0084P3-848

Increased Prevalence of 25-Hydroxyvitamin D Insufficiency and Deficiency among Overweight and Obese Children and Adolescents in Greece
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HRP0084P3-849

The Triglyceride-to-High Density Lipoprotein Cholesterol Ratio in Overweight Korean Children
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HRP0084P3-850

Waist Height Ratio as a Marker of Obesity and Insulin Resistance in Adolescents
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HRP0084P3-851

Genotype and Clinical Characteristics in Korean Patients with Prader-Willi Syndrome: A Single Centre Study
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HRP0084P3-853

Nonalcoholic Steatohepatitis Leading to Cirrhosis of the Liver as a Complication of Hypothalamic Disorders in a Course of Craniopharyngioma - Case Report
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HRP0084P3-854

Association of Sleep Habits and Risk Factors for Metabolic Disorders in Children
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HRP0084P3-855

Plasminogen Activator Inhibitor-1 as a Marker of Insulin Resistance in Obese Adolescents
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HRP0084P3-856

Relationship between Visceral Obesity and Plasma Fibrinogen in Obese Children
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HRP0084P3-858

Prevalence of Asthma Symptoms and Association with Obesity, Sedentary Lifestyle and Sociodemographic Factors: Data from the Hellenic National Plan for the Assessment, Prevention and Treatment of Childhood Obesity
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HRP0084P3-859

Long-Term Effects of Neonatal Over-Nutrition on Metabolic Equilibrium are Age and Sex Dependant
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HRP0084P3-860

Metabolic Syndrome in Greek Adolescents and the Effect of 6-Month Educational/Behavioural School Interventions
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HRP0084P3-862

Diagnosis and Treatment of Familial Hypercholesterolemia in Children - A Preliminary Report
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HRP0084P3-864

A Systemic Approach for the Management of the Program Entitled 'Development of a National System for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece'
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HRP0084P3-865

Waist Circumference to Body Height is a Suitable Measure of Cardiovascular Risk in Overweight and Obese Children
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HRP0084P3-866

The Effectiveness of a Comprehensive and Personalized Plan of Action in the Prevention and Management of Overweight and Obesity in Childhood and Adolescence
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HRP0084P3-867

Insulin Resistance in Adolescents with Screen Addiction and Attention-Deficit/Hyperactivity Disorder
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HRP0084P3-868

Ketogenic Diet in Paediatrics: Work in Progress
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HRP0084P3-869

Severe Hypothalamic Obesity in a Girl with Craniopharyngioma - Case Report
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HRP0084P3-871

Body Composition and Metabolic Risk Factors in Preschool Children
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HRP0084P3-872

Evaluation of Alternatives to OGTT to Assess Glucose Intolerance and Diabetes in an Obese Paediatric Population
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Abstract PDF
HRP0084P3-873

Sex Differences in the Pubertal Response to High-Fat Diet
Direct

Abstract PDF
HRP0084P3-874

Relation between Thyroid Function Tests and Cardiometabolic Risk Factors in Childhood Obesity
Direct

Abstract PDF
HRP0084P3-876

Obesity has a Significant Impact on Hyperandrogenemia Only after Puberty in Korean Girls
Direct

Abstract PDF
HRP0084P3-877

Higher Hb1Ac in Obese Prader-Willi Syndrome Patients vs Obese Controls
Direct

Abstract PDF
HRP0084P3-878

Obese Children and Adolescents: Reasons for Non-compliance with Follow-up Scheduling
Direct

Abstract PDF
HRP0084P3-879

Cardiometabolic Risk Factors in Overweight/Obese Children and Adolescents and Family History of Cardiovascular Disease
Direct

Abstract PDF
HRP0084P3-880

Healthcare Professionals' Perception of Overweight in Preschool-aged Children
Direct

Abstract PDF
HRP0084P3-881

Evaluation of the Relationship between Serum Adropin Levels and Blood Pressure in Obese Children
Direct

Abstract PDF
HRP0084P3-882

Adipocyte Fatty Acid Binding Protein is Related to Weight Status and Metabolic Risk Markers in Childhood Obesity
Direct

Abstract PDF
HRP0084P3-883

Investigating Predisposing Factors for Childhood Obesity
Direct

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HRP0084P3-884

Vitamin D Status in Iranian Obese and Non-obese Children
Direct

Abstract PDF
HRP0084P3-885

Is vitamin D Important Player in Hepatosteatosis in Childhood Obesity?
Direct

Abstract PDF
HRP0084P3-886

Obesity in School Children of Zahedan-Iran; Double Burden of Weight Disorders
Direct

Abstract PDF
HRP0084P3-887

Sports Regulated and Lipid Profile in Children and Adolescents with Overweight
Direct

Abstract PDF
HRP0084P3-888

Weight and the Factors Influencing it in a Cohort of School Aged Children
Direct

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HRP0084P3-889

Dietary Patterns in a Group of Obese Children
Direct

Abstract PDF
HRP0084P3-890

Does Vitamin D Influence Energy Metabolism in Children and Adolescents?
Direct

Abstract PDF
HRP0084P3-891

Bone Age Assessment and Glucose Metabolism in Overweight and Obese Children
Direct

Abstract PDF
HRP0084P3-892

The Triglyceride-to-HDL Cholesterol Ratio is Associated with Insulin Resistance in Obese Boys But Not in Obese Girls
Direct

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HRP0084P3-893

Experience with Sleeve Gastrectomy in Adolescent Obese Subjects and in Prader-Willi Syndrome
Direct

Abstract PDF
HRP0084P3-894

Metabolic Syndrome and Inflammatory Markers in Obese Children at Chiang Mai University Hospital
Direct

Abstract PDF
HRP0084P3-896

Prevalence of Excess Weight in Adolescents at Primary Health Care Units in South Brazil
Direct

Abstract PDF
HRP0084P3-898

A Case of Rapid Onset Obesity, Hypoventilation, Hypothalamic Dysregulation and Neuroendocrine Tumours-ROHHADNET Syndrome
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Abstract PDF
HRP0084P3-899

The Influence of Physical Activity and Physical Fitness in the Metabolic Profile and Microcirculation of Eutrophic, Overweight and Obese Children 5-12 Years of Age
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Abstract PDF
HRP0084P3-900

Predicting Early Cardiovascular Risk in Obese Children Based on Anthropometry
Direct

Abstract PDF
HRP0084P3-901

Metabolic Syndrome Rates Among Adolescents of the Greek School Community
Direct

Abstract PDF
HRP0084P3-902

Identification and Management of Obesity by General Paediatricians in the UK
Direct

Abstract PDF
HRP0084P3-903

Genotype and Phenotype Characterisation in Two Patients with MEHMO Syndrome
Direct

Abstract PDF
HRP0084P3-904

Generalized Idiopathic Benign Acanthosis Nigricans in Childhood
Direct

Abstract PDF
HRP0084P3-905

Potential Connection of Dyslipidaemia with BMI and Associated Disorders in Obese Children and Adolescents
Direct

Abstract PDF
HRP0084P3-906

Deficiency of 25-(OH) D-Vitamin in Adolescents with Obesity
Direct

Abstract PDF
HRP0084P3-908

The Prevalence of Obesity in Children and Adolescents in the Udmurt Republic
Direct

Abstract PDF
HRP0084P3-909

Survey Serum 25-Hydroxyvitamin D Concentration in Obese Children and Clinical Significance in Chinese Population
Direct

Abstract PDF
HRP0084P3-910

Clinico-Biochemical Correlation Among Children with Obesity and Metabolic Syndrome
Direct

Abstract PDF
HRP0084P3-912

In Different Method of the Evaluation of State of Feeling of Obese Children; Goodenough Harris 'the Draw-a-person' Test
Direct

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HRP0084P3-913

Phenotypic Study of Obesity in Children and Adolescents
Direct

Abstract PDF
HRP0084P3-914

Association of Serum Levels of 25(OH) Cholecalciferol and Childhood Obesity
Direct

Abstract PDF
HRP0084P3-916

Vitamin D Deficiency can Modulate GH/IGF1 Axis in GH Deficient Children
Direct

Abstract PDF
HRP0084P3-917

Serum IGFI Concentration and Growth During Infancy Correlate to Polyunsaturated Fatty Acid Pattern
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Abstract PDF
HRP0084P3-918

Are Short Children with Low GH Secretion Metabolically Different from Children of Normal Height?
Direct

Abstract PDF
HRP0084P3-919

Familial Short Stature Associated to Terminal Microdeletion of 15q26.3: Variable Phenotype not Involving the IGF1 Receptor Gene
Direct

Abstract PDF
HRP0084P3-920

Is the Insulin Secretion in Pancreatic Beta Cells Related with IGF-1/IGFBP-1 Axis in Korean Children?
Direct

Abstract PDF
HRP0084P3-921

Severe Isolated Growth Hormone Deficiency and Myopathy in Two Brothers with RNPC3 Mutation
Direct

Abstract PDF
HRP0084P3-922

Gigantism Secondary to Growth Hormone Secreting Pituitary Macrodenoma
Direct

Abstract PDF
HRP0084P3-923

IGFI and Relation to Growth in Infancy and Early Childhood in Very-Low-Birth-Weight Infants and Term Appropriate for Gestational Age Infants
Direct

Abstract PDF
HRP0084P3-924

Severe Isolated Growth Hormone Deficiency and Myopathy in Two Brothers With RNPC3 Mutation
Direct

Abstract PDF
HRP0084P3-925

Influence of the -202 A/C IGFBP3 Promoter Polymorphism on Individual Variation in Body Height in Korean Girls
Direct

Abstract PDF
HRP0084P3-927

Comparison of Two IGF1 Assays in Patients Treated with GH
Direct

Abstract PDF
HRP0084P3-928

Acute Effects of a Training Session on IGF1 and IGFBP3 Concentrations in Brazilian Jiu-Jitsu Fighters
Direct

Abstract PDF
HRP0084P3-929

Biochemical Profiles Differentials by SGA Children Catch Up
Direct

Abstract PDF
HRP0084P3-930

IGF1 Deficiency: An Important Differential Diagnosis in Severe Growth Failure and Its Excellent Response to rhIGF1 Replacement Therapy
Direct

Abstract PDF
HRP0084P3-931

5-Year Response to GH in Children with Noonan Syndrome and GH Deficiency: Our Experience and Review of the Literature
Direct

Abstract PDF
HRP0084P3-932

Modification of Cardiovascular Risk Factors in Children Treated with GH
Direct

Abstract PDF
HRP0084P3-933

Adult Height in Children Born Small for Gestational Age and Treated with GH: Data from the French KIGS Database
Direct

Abstract PDF
HRP0084P3-934

Psychosocial Functioning and Self-Perception of Children and Adolescents Treated with GH
Direct

Abstract PDF
HRP0084P3-935

Do IGF1 Generation Test Results Predict 1st-Year Growth Response to GH Treatment in Idiopathic Short Stature?
Direct

Abstract PDF
HRP0084P3-936

Adherence to GH Treatment: Impact of Actual Height, Treatment Duration, and Puberty
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Abstract PDF
HRP0084P3-937

The Blood Oxidant System and Insulin Resistance in Girls with Turner Syndrome after 1 Year of GH Therapy
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Abstract PDF
HRP0084P3-938

An Open-Label Phase 2 Dose-Finding Study Comparing Three Different Doses of Weekly TV-1106 and Daily Recombinant Human GH (Genotropin[reg]) in Treatment-Naive, Pre-Pubertal, GH-Deficient Children
Direct

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HRP0084P3-939

Increasing Lean Body Mass, Phase Angle, and Total Body Water But Decreasing Body Fat Among Short-statured Children Born Small-for-Gestational Age on GH Treatment
Direct

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HRP0084P3-940

GH Dosing Patterns in Children with Isolated GH Deficiency and Multiple Pituitary Hormone Deficiency Enrolled in the NordiNet[reg] International Outcome Study
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Abstract PDF
HRP0084P3-941

Decrease of Small Dense LDL and Lipoprotein-Associated Phospholipase A2 due to Human GH Treatment in Short Children with GH Deficiency and Small for Gestational Age Status
Direct

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HRP0084P3-942

Long-Term Insulin Sensitivity and [beta]-Cell Function in Short Children Born Small for Gestational Age Treated with GH and GnRHa: Results of a Randomised, Dose-response Trial
Direct

Abstract PDF
HRP0084P3-943

Influence of the Application of the POI Score on the Results of GH Therapy in Prader-Willi
Direct

Abstract PDF
HRP0084P3-944

The Impact of GH Therapy in Noonan Syndrome Children with Identified Mutations in RAS/MAPK Pathway
Direct

Abstract PDF
HRP0084P3-945

As Great Intra as Interindividual Variability in Uptake of s.c. GH Injections in Longitudinally Followed GH Treated Children
Direct

Abstract PDF
HRP0084P3-946

The Correlation between the Increase in IGF1 and the Growth Improvement Induced by GH Treatment in Short Children Born Small for Gestational Age
Direct

Abstract PDF
HRP0084P3-947

Medical and Biochemical Effects of Intervention Program in Patients with Poor Adherence to rhGH Treatment
Direct

Abstract PDF
HRP0084P3-948

Favourable GH Treatment Response in a Young Boy with Achondroplasia
Direct

Abstract PDF
HRP0084P3-949

Plexiform Neurofibroma and Demielinisant Lesions in a Patient with GH Deficiency Treated with rGH
Direct

Abstract PDF
HRP0084P3-950

Growth, Development and Puberty of Patients with Congenital Multiple Pituitary Hormone Deficiencies
Direct

Abstract PDF
HRP0084P3-952

Linear Regression Model of Final Height Prediction Based on Pre-Treatment Data in Children with GH Deficiency Treated with GH
Direct

Abstract PDF
HRP0084P3-953

Vitamin D Levels and not Vitamin A are Correlated with Height Velocity in Children with GH Deficiency Who are Under GH Treatment
Direct

Abstract PDF
HRP0084P3-954

Long-Term Effects of GH Replacement Therapy on Hematopoiesis in GH Deficient Children
Direct

Abstract PDF
HRP0084P3-955

Thyroid Function in Children Treated with rhGH for GH Deficiency
Direct

Abstract PDF
HRP0084P3-956

A 5-year Follow-up of Adults, with Childhood-Onset GH Deficiency, Treated with GENOTONORM[reg] in France
Direct

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HRP0084P3-957

Somatotropic Pituitary Insufficiency in Kearns-Sayre Syndrome - The Clinical Picture, Genetic Diagnosis and Efficacy of rhGH Therapy
Direct

Abstract PDF
HRP0084P3-958

The Correlation between the Increase in IGF1 24 h after the First Injection of GH and the Improved Growth
Direct

Abstract PDF
HRP0084P3-959

Late Diagnosis of a Type II/III Mucolipidoses Treated with GH Replacement Therapy
Direct

Abstract PDF
HRP0084P3-960

Does Applying Regular Questionnaire to Patients on GH Increase the Compliance?
Direct

Abstract PDF
HRP0084P3-961

Characterisation of Children Born Small for Gestational Age within the Australian Indications for GH (GH) Therapy: An OZGROW Analysis
Direct

Abstract PDF
HRP0084P3-962

Effectiveness of rhGH Treatment in a Boy with Nephrogenic Diabetes Insipidus
Direct

Abstract PDF
HRP0084P3-963

The Easypod[trade] Connect Observational Study: Comparison of Results from Interim Analyses
Direct

Abstract PDF
HRP0084P3-964

Evaluation of the Facility of Use of a New GH Administration Device - Study DAGH2014
Direct

Abstract PDF
HRP0084P3-965

Effect of Human Growth Hormone on Growth Rate of Short Stature Children with Low Birth Weight
Direct

Abstract PDF
HRP0084P3-966

GH Treatment and First Year Response: A Retrospective Study
Direct

Abstract PDF
HRP0084P3-967

Usefulness of Reevaluation of Growth Hormone Secretion During Puberty
Direct

Abstract PDF
HRP0084P3-969

Evaluating First Year Response and Final Height to Growth Hormone Treatment in Growth Hormone Deficiency Based on Peak GH Levels on Testing
Direct

Abstract PDF
HRP0084P3-970

Growth Hormone Therapy in Children: Predictive Factors and Short-Term and Long-Term Response Criteria in an Italian Cohort
Direct

Abstract PDF
HRP0084P3-971

Patients with Childhood Onset Growth Hormone Deficiency Treated with rhGH - Reevaluation in the Transition Period between Childhood and Adulthood - Preliminary Study
Direct

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HRP0084P3-972

Time Trends in Baseline Characteristics (2006-2014) in Short Children with Growth Hormone Deficiency (GHD), Born Small for Gestational Age (SGA) and with Ullrich-Turner Syndrome (TS) Enrolled in Nordinet[reg] International Outcomes Study (IOS) in Germany and Czech Republic
Direct

Abstract PDF
HRP0084P3-973

A Patient with an 13q Deletion Syndrome, Important Growth Delay and Somatotropine Insufficiency Undergoing Growth Hormone Therapy-Case Report.
Direct

Abstract PDF
HRP0084P3-974

Linear Growth in a Child with Ellis Van Creveld Syndrome: Positive Effect of Growth Hormone Therapy
Direct

Abstract PDF
HRP0084P3-975

Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome
Direct

Abstract PDF
HRP0084P3-976

Thyroid Function in Children with Prader-Willi Syndrome, the First 12 Months of GH Therapy
Direct

Abstract PDF
HRP0084P3-977

Congenital Hypopituitarism and Severe Developmental Delay Associated with Homozygous POU1F1 Mutation
Direct

Abstract PDF
HRP0084P3-978

GH Therapy in Lery-Weill Syndrome: Report of Three Cases
Direct

Abstract PDF
HRP0084P3-979

The Assessment of Quality of Life and New Technologies for Therapeutic Monitoring in a Cohort of Paediatric Patients Treated with GH
Direct

Abstract PDF
HRP0084P3-980

Final Height in Patients with Isolated GH Deficiency and Multiple Pituitary Hormone Deficiencies, Treated with GH
Direct

Abstract PDF
HRP0084P3-981

Current Practice in Diagnosis and Treatment of GH Deficiency in Childhood: A Survey from Turkey
Direct

Abstract PDF
HRP0084P3-983

GH Therapy in Kuwait: First Report on Characteristics and Response in Treated Children
Direct

Abstract PDF
HRP0084P3-984

Management of Prepubertal Gynecomastia in Two Patients with Peutz-Jeghers Sydrome: Use of Aromatase Inhibitors
Direct

Abstract PDF
HRP0084P3-985

Age at Menarche in Chronic Respiratory Disease: Cystic Fibrosis and Asthma - Comparison with a Large Cohort of Healthy Girls Living in Verona
Direct

Abstract PDF
HRP0084P3-986

Optimal Strategy for Ovarian Function Assessment in Girls with Central Precocious Puberty before and During GnRH Analogue Treatment
Direct

Abstract PDF
HRP0084P3-987

From Prepuberty to Adulthood: Semen Quality and Its Predictors in a Prospective Cohort Study of Russian Young Men
Direct

Abstract PDF
HRP0084P3-988

Further Expansion of the CHARGE Geno-Phenotype: A Girl with a Novel Deletion of CHD7 and with the Combination of Hypogonadotropic Hypogonadism and Agenesis of Internal Genitalia
Direct

Abstract PDF
HRP0084P3-989

Metabolism and Gonadal Axis of Early Menarche Girls and Girls Treated with GnRHa During Puberty
Direct

Abstract PDF
HRP0084P3-990

The Consequences of Polycystic Ovary Syndrome in Adolescent Girls
Direct

Abstract PDF
HRP0084P3-991

Pelvic MRI as Alternative to Pelvic us for the Diagnosis of PCOS in Overweight and Obese Adolescent Girls
Direct

Abstract PDF
HRP0084P3-993

The Effect of Aromatase Inhibitor in a Pubertal Patient with Aromatase Excess Syndrome
Direct

Abstract PDF
HRP0084P3-994

Homozygous CYP17A1 Mutation Identified in a Chinese Family with 46, XX and 46, XY 17[alpha]-Hydroxylase Deficiency
Direct

Abstract PDF
HRP0084P3-995

Puberty and Gonadal Function in Adolescents Girls after Renal Transplantation
Direct

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HRP0084P3-996

Endocrine Disruptor and Premature Puberty, is There Any Association?
Direct

Abstract PDF
HRP0084P3-998

The Changes of Body Fat and Metabolic Parameters During GnRHa Treatment in Central Precocious Puberty or Early and Fast Puberty Girls
Direct

Abstract PDF
HRP0084P3-999

Sertoli Cell Tumour in a Case of Androgen Insensitivity Syndrome
Direct

Abstract PDF
HRP0084P3-1000

Final Height of Children with SGA Treated with Biosynthetic GH: About a Series of 30 Children
Direct

Abstract PDF
HRP0084P3-1001

Anti-Mullerian Hormone is a Useful Marker of Gonadotoxicity in Girls Treated for Cancer: A Prospective Study
Direct

Abstract PDF
HRP0084P3-1002

Leydig-Cell Tumour, a Rare Cause of LH-Independent Sexual Precocity in Boys
Direct

Abstract PDF
HRP0084P3-1003

Antimullerian Hormone and Inhibin B Markers of the Ovarian Reserve After Ovariectomy
Direct

Abstract PDF
HRP0084P3-1006

Early and Sever Manifestation of McCune-Albright Syndrome with GNAS Mutation in the Liver Tissue
Direct

Abstract PDF
HRP0084P3-1007

Depth and Timing of Hypoglycaemia Achieved During Insulin Tolerance Test in Children
Direct

Abstract PDF
HRP0084P3-1008

Presenting Characteristics, Auxological, and Aetiologic Evaluation of 364 Patients with GH Deficiency
Direct

Abstract PDF
HRP0084P3-1009

Nutritional Supplementation, Sleep Patterns and Growth in Short and Lean Prepubertal Children
Direct

Abstract PDF
HRP0084P3-1010

Disease-Specific Growth Charts of Marfan Syndrome in Korea
Direct

Abstract PDF
HRP0084P3-1011

Targeted Birth Length and Parental Height Measurement in Babies with Birthweight[le]9th Centile; Improved Uptake During Second Study During 1 Calendar Year in a Single Newborn Unit
Direct

Abstract PDF
HRP0084P3-1012

Case Report of Wolf-Hirschhorn Syndrome by Chromosomal Microarray Analysis: Importance of the Molecular Investigation for the Aetiological Diagnosis of Short Stature
Direct

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HRP0084P3-1013

Achondroplasia Reference as Background Matrix for Following Children with Extreme Short Stature
Direct

Abstract PDF
HRP0084P3-1014

Altered Gene-Expression in Human Growth Plate Cartilage Tissue Exposed to Dexamethasone
Direct

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HRP0084P3-1015

Reversible GH Excess in Two Girls with Neurofibromatosis Type 1 and Optic Pathway Glioma
Direct

Abstract PDF
HRP0084P3-1016

Autosomal Recessive Omodysplasia: A Rare Cause of Disproportionate Short Stature
Direct

Abstract PDF
HRP0084P3-1017

The Growth Characteristics of Patients with Noonan Syndrome, and First 2 Years Results of GH Treatment: A Nationwide Multicentre Study
Direct

Abstract PDF
HRP0084P3-1018

Vitamin D in Short Children on GH Therapy: Effects of Vitamin D Status and Vitamin D Supplementation on Glucose Homeostasis
Direct

Abstract PDF
HRP0084P3-1021

Response to rhGH Treatment in Patients with Transient or Permanent GH Deficiency
Direct

Abstract PDF
HRP0084P3-1022

Postnatal Growth and Biochemical Markers of Late Preterm Infants: Prospective Birth Cohort
Direct

Abstract PDF
HRP0084P3-1023

Alterations of SHOX and Its Enhancers as a Cause of Short Stature: Evolution of Our Cases
Direct

Abstract PDF
HRP0084P3-1024

Vitamin D Status in Pre-Pubertal Children with Isolated Idiopathic GH Deficiency: Effect of GH Therapy
Direct

Abstract PDF
HRP0084P3-1025

New Point Mutation in Short Stature Homeobox Gene Leads to Phenotype of Lery-Weill Dyschondrosteosis
Direct

Abstract PDF
HRP0084P3-1026

Fasting and Post-Meal Levels of Appetite Regulating Hormones, before and Following GH Treatment, in Children with Idiopathic Short Stature
Direct

Abstract PDF
HRP0084P3-1027

Impact of Using WHO vs National Growth Charts on the Clinical Performance of a Decision Rule for Growth Monitoring
Direct

Abstract PDF
HRP0084P3-1028

Comparison of the Performance of Algorithms Proposed to Standardize Growth Monitoring
Direct

Abstract PDF
HRP0084P3-1029

Evaluation of 207 Danish Girls with Constitutional Tall Stature: Diagnostic Characteristics and Effects of Oral Administration of 17-[beta] Oestradiol
Direct

Abstract PDF
HRP0084P3-1030

Sitting Height/Height Ratio: An Indicator for Genetic Study of the SHOX Gene in Children with Disharmonic Short Stature - An In-House Analysis
Direct

Abstract PDF
HRP0084P3-1031

Final Height in Survivors of Childhood Acute Leukaemia
Direct

Abstract PDF
HRP0084P3-1032

Impact of Recombinant Human GH on Height in Children with Chronic Kidney Disease
Direct

Abstract PDF
HRP0084P3-1033

Birth Length and Metabolic Syndrome in Obese Children
Direct

Abstract PDF
HRP0084P3-1034

Birth Characteristics Influence the Male to Female Diagnostic Prevalence of Idiopathic GH Deficiency
Direct

Abstract PDF
HRP0084P3-1035

Two Cases with Decelerated Linear Growth, Normal GH - IGF1 Axis with an Exceptional Response to GH Therapy
Direct

Abstract PDF
HRP0084P3-1036

Impact of GH Treatment in Children Final Height and Weight Status
Direct

Abstract PDF
HRP0084P3-1038

Short Stature in a Rare 15q Duplication - is hGH Treatment Beneficial?
Direct

Abstract PDF
HRP0084P3-1040

Psychomotor Development in Children Born Small for Gestational Age During Early Infancy
Direct

Abstract PDF
HRP0084P3-1041

Patient with Classic Phenotype of Hypochondroplasia and Deletion of the Gene SHOX
Direct

Abstract PDF
HRP0084P3-1042

GH Treatment in Survivors of Paediatric Brain Tumors
Direct

Abstract PDF
HRP0084P3-1043

GH Deficiency in a Patient with 4p16 Deletion: An Infrequent Association with Wolf-Hirschhorn Syndrome
Direct

Abstract PDF
HRP0084P3-1044

Value of Alkaline Phosphatase Assay in Short Stature Exploration
Direct

Abstract PDF
HRP0084P3-1045

Small for Gestational Age Incidence in One of the Regions of the Russian Federation
Direct

Abstract PDF
HRP0084P3-1046

Final Height in Patients with and without Pituitary Abnormalities Detected by MRI and/or CT Treated with GH
Direct

Abstract PDF
HRP0084P3-1048

A Rare Cause of Short Stature: the Floating Harbor Syndrome
Direct

Abstract PDF
HRP0084P3-1049

Correlations Between IGF1 Levels and Anthropometrical Parameters in Children Under GH Therapy
Direct

Abstract PDF
HRP0084P3-1050

BMI and Total Cholesterol are Negative Predictors of Peak Stimulated GH in Han Children with Short Stature
Direct

Abstract PDF
HRP0084P3-1051

A 4-Month-Old Boy with Beckwith Wiedemann Syndrome
Direct

Abstract PDF
HRP0084P3-1052

MEGHA: Observational Study on Prescription of the GH Saizen in Adults in France
Direct

Abstract PDF
HRP0084P3-1053

Comparative Study of Low-Dose GH Treatment in Children with Idiopathic Short Stature and GH Deficiency
Direct

Abstract PDF
HRP0084P3-1054

To Investigate the Changes of Hormone Levels and Body Composition in Pubertal Children with Growth Retardation: a Clinical Controlled Study
Direct

Abstract PDF
HRP0084P3-1055

The Effect of BMI in Reducing Risk of Refractory Seizure due to Probable Lipoid Tissue Factors
Direct

Abstract PDF
HRP0084P3-1056

GH Treatment for Idiopathic Short Stature
Direct

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HRP0084P3-1057

The Frequency Study and the Aetiological Profile of Short Stature in 2-15 Years Old Children Admitted in Endocrinology Clinic of 17 Shahrivar Hospital, Rasht, Between 2008 and 2013
Direct

Abstract PDF
HRP0084P3-1058

Cystic Encephalomalacia and Infantile Spasm as a Complication of Transient and Mild Hyperinsulinemic Hypoglycemia
Direct

Abstract PDF
HRP0084P3-1059

Hyperglycemia Preceded by Neonatal Hyperinsulinemic Hypoglycemia in Infants with Novel HNF1A Mutations
Direct

Abstract PDF
HRP0084P3-1060

Transient Congenital Hyperinsulinism and Renal Fanconi Syndrome
Direct

Abstract PDF
HRP0084P3-1061

Clinical Characteristics and Molecular Analysis of Turkish Patients with Congenital Hyperinsulinism: a Single-Centre Experience with 15 Cases
Direct

Abstract PDF
HRP0084P3-1062

Congenital Hyperinsulinaemic Hypoglycaemia of Infancy, Renal Fanconi Syndrome and Hepatopathy due to a Mutation in the hnf4a Gene
Direct

Abstract PDF
HRP0084P3-1063

Genotype-Phenotype Associations in 90 Children with Congenital Hyperinsulinism
Direct

Abstract PDF
HRP0084P3-1065

Glycogen-Storage Disease Type VI in a Girl Presenting with Recurrent Ketotic Hypoglycaemia but No Hepatomegaly
Direct

Abstract PDF
HRP0084P3-1066

Congenital Hyperinsulinism in a Newborn with a Novel Paternally Inherited Heterozygous Mutation (p.E1517G) in the ABCC8 Gene
Direct

Abstract PDF
HRP0084P3-1067

Discontinuation of Diazoxide Therapy in Children with Hyperinsulinaemic Hypoglycaemia with no Identified Genetic Aetiology: a Long-term Follow-up Study
Direct

Abstract PDF
HRP0084P3-1068

Pancreatic Hormones in Children with Hyperinsulinaemic Hypoglycaemia
Direct

Abstract PDF
HRP0084P3-1069

Experience Based on 193 18F-DOPA PET CTs in Patients with Congenital Hyperinsulinism: Pearls and Pitfalls in Imaging Diagnostics in Patients with CHI
Direct

Abstract PDF
HRP0084P3-1070

Severe Neonatal Hypoglycemia in the Newborn Despite Prenatal Diagnosed Cerebral Midline Malformations: a Review of Three Cases
Direct

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HRP0084P3-1071

A Case of Mild Congenital Hyperinsulinaemia Presenting with Developmental Delay, Complicated by Diazoxide-induced Transient Neutropenia
Direct

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HRP0084P3-1072

Failure of Sirolimus Response on Three More Cases with a Diffuse Type of Congenital Hyperinsulinism
Direct

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HRP0084P3-1073

Auxological Characteristics of Persistent Hyperinsulinemic Hypoglycemia at Birth
Direct

Abstract PDF
HRP0084P3-1074

Congenital Hyperinsulinism in Siblings: Case Report
Direct

Abstract PDF
HRP0084P3-1075

Genetic Causes of Congenital Hyperinsulinism in Slovakia
Direct

Abstract PDF
HRP0084P3-1076

Hyperinsulinism Secondary to Congenital Portosystemic Shunt in a Neonate
Direct

Abstract PDF
HRP0084P3-1077

Clinical Presentation of a Patient with a Novel Homozygous Mutation in the TRPM6 Gene
Direct

Abstract PDF
HRP0084P3-1078

Long Acting Somatostatin Analogues in the Management of Congenital Hyperinsulinism in Cases with Poor Compliance to Conventional Therapy
Direct

Abstract PDF
HRP0084P3-1079

Isolated Postprandial Hyperinsulinaemic Hypoglycaemia
Direct

Abstract PDF
HRP0084P3-1080

Severe Congenital Hyperinsulinism in a Neonate Homozygous for Two Novel Missense Mutations in the KCNJ11 Gene
Direct

Abstract PDF
HRP0084P3-1081

Congenital Glucose-Galactose Malabsorption in a Male Infant
Direct

Abstract PDF
HRP0084P3-1083

Cholestatic Hepatopathy and Hypoglycaemic Seizures as Primary Manifestation of Hypocortisolism in Infancy
Direct

Abstract PDF
HRP0084P3-1084

Plasma Kisspeptin Levels of Infants Breast Growth in Neonatal Period
Direct

Abstract PDF
HRP0084P3-1085

Circadian Variation in Cortisol Concentration in Mother's Milk
Direct

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HRP0084P3-1087

Differences in Leptin Levels Between Newborns with and without Intrauterine Growth Restriction Born in the Hospital Gineco Obstetrico 'Isidro Ayora' of Quito-Ecuador. Year 2013-2014
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HRP0084P3-1088

Leptin and Neuropeptide Y Levels in Newborns
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Abstract PDF
HRP0084P3-1089

Cord Blood and Maternal Serum IGF1,2, IGFBP3 Levels in Overweight Pregnants
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Abstract PDF
HRP0084P3-1090

Crystal Formation in the Meibomian Glands as Diagnostic Proof of Pseudohypoaldosteronism Type I
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Abstract PDF
HRP0084P3-1091

Transient Neonatal Hypoparathyroidism Secondary to an Unknown Maternal Parathyroid Adenoma
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Abstract PDF
HRP0084P3-1092

Relations of Birth Chest Circumference to Blood Serum IGF1 in the Newborn Free of Life-threatening Disease: Possible Role of Birth Body Weight in Addition to Respiratory Supportive Treatment
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HRP0084P3-1093

Relations of Birth Chest Circumference to Blood Serum IGFBP3 in the Newborn Free of Life-threatening Disease: Possible Role of Birth Body Weight Beyond Blood Serum IGF1 and Respiratory Supportive Treatment
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Abstract PDF
HRP0084P3-1094

EPIPEG-PREMEB Proyect. Clinical Situation before 12 months go on a SGA Population
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Abstract PDF
HRP0084P3-1095

McCune-Allbright Syndrome in a Male Newborn with Hyperthiroydism
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Abstract PDF
HRP0084P3-1096

Role of Notch1-Dll4 Signalling Pathway in Mice Model of Oxygen-induced Retinopathy
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Abstract PDF
HRP0084P3-1098

Case Presentation; a Neonate Presenting to a District General Hospital with Isolated Cranial Diabetes Insipidus Evolving to Partial Hypopituitarism
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Abstract PDF
HRP0084P3-1099

Isolated GH Deficiency (IGHD) Associated with 7q11.23 Duplication Syndrome: a Case Report
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Abstract PDF
HRP0084P3-1100

Cushing Disease in a Patient with Beckwith-Wiedemann: an Unusual Association
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Abstract PDF
HRP0084P3-1101

Baseline Characteristics, GH Response, and Long term Evolution in 67 Patients with Pituitary Stalk Interruption According to the Initial Presentation
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Abstract PDF
HRP0084P3-1102

Clinical Characteristics of Children with Congenital Combined GH Deficiency without Associated Syndrome in Belgium
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HRP0084P3-1103

Pitfalls in Reporting of Paediatric Pituitary Scans
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HRP0084P3-1104

Long term Follow-up of a Child Treated with CyberKnife Radiosurgery for ACTH-secreting Pituitary Adenoma after Bilateral Adrenalectomy
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HRP0084P3-1105

Off-label Use of Vaptans in Children with Severe Symptomatic Hyponatremia due to SIADH
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HRP0084P3-1106

Acquired Long QT Syndrome in a 14-year-old Boy with Panhypopituitarism
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HRP0084P3-1107

Between 3 to 4 Years after Severe Traumatism Brain Injury 22% at Least of Children and Adolescents do have Persistent Pituitary Dysfunction
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HRP0084P3-1108

Causes and Consequences of Thickened Pituitary Stalk Found by MRI in Children and Adolescents with Central Diabetes Insipidus
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Abstract PDF
HRP0084P3-1109

Acute Phase Proteins and Endocrine Dysfunction after Traumatic Brain Injury in Childhood
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Abstract PDF
HRP0084P3-1110

Two Cases of Combined Pituitary Hormone Deficiency Proven to have Mutations of GLI2
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HRP0084P3-1111

AVP-NPII Gene Mutations and Clinical Characteristics of the Patients with Autosomal Dominant Familial Central Diabetes Insipidus
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Abstract PDF
HRP0084P3-1112

A Boy with Combined Pituitary Hormone Deficiency and Agenesis of Right Internal Carotid Artery: A Rare Association or a Simple Coincidence?
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Abstract PDF
HRP0084P3-1113

A Rare case of Congenital Hyperinsulinism Associated with Hypopituitarism due to Pituitary Stalk Interruption Syndrome
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Abstract PDF
HRP0084P3-1114

Management of Risperidone Induced Hyperprolactinemia in an Adolescent with Severe Autism
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Abstract PDF
HRP0084P3-1116

Hormone Disorder and Vitamin Deficiency in Attention Deficit Hyperactivity Disorder (adhd) and Autism Spectrum Disorders (ASD)
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HRP0084P3-1117

Two Novel Mutations in GLI2 Gene in Two Unrelated Argentinean Prepuberal Patients, One with Isolated Growth Hormone Deficiency, and Another with Multiple Pituitary Hormone Deficiency, Both with Developmental Defects in Posterior Pituitary Gland
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HRP0084P3-1118

Pituitary Stalk Interruption Syndrome Presenting with Normogonadotropic Amenorrhea and Hypoprolactinemia
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HRP0084P3-1119

Paediatric CNS Germ Cell Tumours: Endocrine Outcome
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HRP0084P3-1120

Description of Patients Diagnosed with Central Diabetes Insipidus, 14 Year Experience at the National Children's Hospital, Costa Rica
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HRP0084P3-1121

Pegvisomant in Child Acromegaly
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HRP0084P3-1122

Case Series; Central Diabetes Insipidus Presenting to a District General Hospital
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HRP0084P3-1123

A 5-Year-Old Patient with Cushing's Disease
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HRP0084P3-1124

Sequelae in Giant Prolactinoma in a Teenage Boy
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HRP0084P3-1125

Combined Pituitary Hormone Deficiency
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HRP0084P3-1126

Outstanding Growth Response to Growth Hormone Replacement Therapy in 3 Different Cases of Growth Hormone Deficiency
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HRP0084P3-1127

Pituitary Stalk Interruption Syndrome: A Case of an Infant
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HRP0084P3-1129

Thickened Pituitary Stalk with Central Diabetes Insipidus: What Diagnosis?
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HRP0084P3-1130

Clinical Features and Pubertal Timing in Girls with Premature Adrenarche
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HRP0084P3-1131

Growth Outcomes in Childhood Craniopharyngioma: A Longitudinal Assessment of 21 Cases at a Single Centre
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Abstract PDF
HRP0084P3-1132

Effects of GnRH Agonists and Antagonists on Danazol-Induced Precocious Puberty Rat
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HRP0084P3-1133

Clinical Characteristics of Girls with Atypical Precocious Puberty
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HRP0084P3-1134

Paraphilic Compulsion Secondary to Dopamine Replacement Therapy and Successful Treatment with GnRH Analogues
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HRP0084P3-1135

Cardiovascular Disease Risk Factors in Girls with Isolated Premature Pubarche
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Abstract PDF
HRP0084P3-1136

Menstruation Pattern in Idiopathic Central Precocious Puberty Girls after Discontinuing GnRH Agonist Therapy
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HRP0084P3-1137

Age of Menarche and Near Final Height after Long-Term Use of GNRH Agonist or Combined with GH in Idiopathic Central Precocious Girls
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HRP0084P3-1138

Psychosocial Changes after GnRH Agonist Treatment in Girls with Idiopathic Central Precocious Puberty
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Abstract PDF
HRP0084P3-1139

Multicentre Study of Early Screening and Prevention of Prader-Willi Syndrome
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Abstract PDF
HRP0084P3-1140

A Novel GLUT1 Mutation in a Patient with Apparently Normal Cerebrospinal Fluid Glucose Level
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Abstract PDF
HRP0084P3-1141

Does Treatment with GnRH Analogues Affect BMI in Children with Precocious or Early Puberty?
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Abstract PDF
HRP0084P3-1142

Qualitative Assessment of Precocious Puberty-Related UCC (User Created Contents) on YouTube
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Abstract PDF
HRP0084P3-1143

Premature Adrenarche is Associated to Precocious Thelarche but not to Precocious Gonadarche or Pubarche in Chilean Adolescents
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Abstract PDF
HRP0084P3-1144

Central Precocious Puberty in Cerebral Palsy
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HRP0084P3-1145

Changes in BMI During GNRH Agonist Treatment in Girls with Idiopathic Central Precocious Puberty and Early Puberty
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HRP0084P3-1146

An Elevated Tumour Marker and Adrenarche in a Child Using Lavender Oil: A Case Report
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HRP0084P3-1147

Persistent Isolated Cyclical Vaginal Bleeding (Premature Menarche) not Associated with GnRH Pubertal Response or Endometrial Echo Should be Considered for Examination Under General Anaesthesia
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Abstract PDF
HRP0084P3-1148

Endocrine Dysfunction in Hypothalamic Hamartoma Depends on Presentation (Endocrine or Epileptogenic), Radiological Characteristics and Surgery
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Abstract PDF
HRP0084P3-1149

Idiopathic Central Precocious Puberty - Treatment Criteria
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Abstract PDF
HRP0084P3-1150

Physiological Dose Reverse Rhythm Testosterone Treatment Abolishes the Development of Permanent Gynaecomastia in Adolescent Boys with 47,XXY Klinefelter Syndrome
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Abstract PDF
HRP0084P3-1151

Urinary Bisphenol A and Its Relation with Kisspeptin in Girls with Idiopathic Central Puberty Precocious and Premature Telarche
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HRP0084P3-1152

Prevalence of Parental Consanguinity in Children with Precocious Puberty and Kisspeptin Gene Polymorphisms
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Abstract PDF
HRP0084P3-1153

Effects of Nutrition and Vitamin D Deficiency on Central Puberty Precocious
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Abstract PDF
HRP0084P3-1155

Familial Precocious Puberty: Clinical Characteristics and GnRH Agonist Response
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HRP0084P3-1156

Eating Disorders in Greek Adolescents: Frequency and Characteristics
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Abstract PDF
HRP0084P3-1158

Evaluation of the Effect of Two Different GnRH-Agonist Therapies on the Anthropometric Measurements in Girls with Idiopathic Central Precocious Puberty
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Abstract PDF
HRP0084P3-1159

Testotoxicosis: Be Careful to Predict the Final Height!
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HRP0084P3-1160

Central Precocious Puberty Presented due to Late Started Treatment for Familial Testotoxicosis
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HRP0084P3-1162

Delayed Puberty in Girl: Clinical and Aetiologic Study
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HRP0084P3-1163

Pubertal Development Anticipation
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Abstract PDF
HRP0084P3-1164

The Relationship between Xenoestrogens Exposure and Early Puberty among Young Females Living in Jeddah, Saudi Arabia
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HRP0084P3-1165

One Year Follow-Up of Asymptomatic Precocious Puberty; Clinical and Laboratory Characteristics
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Abstract PDF
HRP0084P3-1168

Endocrinopathies in a 17-Year-Old Girl with Diamond-Blackfan Anemia and Transfusion-Associated Iron Overload
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Abstract PDF
HRP0084P3-1169

Large Goitre in a Patient with Congenital Hypothyroidism
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Abstract PDF
HRP0084P3-1170

Topical Iodine Induced Thyrotoxicosis in a Newborn with Giant Omphalocele
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HRP0084P3-1171

A Familial Case of Congenital Hypothyroidism due to a Mutation in the Thyroglobulin Gene Detected by Next Generation Sequencing
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HRP0084P3-1172

Central Hypothyroidism and GH Deficiency in a Boy with Williams-Beuren Syndrome
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HRP0084P3-1173

Avoidable Thiamazole-Induced Omphalomesenteric Duct Remnants: 20-Year Retrospective Study in Our Hospital
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HRP0084P3-1174

The Impact on Families of Receiving a Diagnosis of Congenital Hypothyroidism
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HRP0084P3-1175

Final Height in Italian Patients with Congenital Hypothyroidism Detected by Neonatal Screening: An Observational Study Over 20 Years
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Abstract PDF
HRP0084P3-1176

Graves' Disease in Childhood and Adolescence: Clinical Manifestations, Adverse Effects, and Predictive Factors for Response to Antithyroid Drugs
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Abstract PDF
HRP0084P3-1177

The Correlation between TSH Levels and BMI Percentiles in Hypothyroid Children Who are Chemically Euthyroid on Levothyroxine Treatment
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Abstract PDF
HRP0084P3-1178

Short Stature with Lipodystrophy: Reminder of a Forgotten Syndrome
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Abstract PDF
HRP0084P3-1179

Plasma Visfatin Level and Its Association with Apolipoproteins A1 and B in Hypothyroid Children
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Abstract PDF
HRP0084P3-1180

Outcome of Thyrotoxicosis in Childhood and Adolescence in a Geographically Define Area; a 24-Year Experience
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Abstract PDF
HRP0084P3-1181

Early Discrimination between Transient and Permanent Congenital Hypothyroidism in Children with Eutopic Gland
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Abstract PDF
HRP0084P3-1182

The Role of Early Thyroid Imaging in Children with Congenital Hypothyroidism
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Abstract PDF
HRP0084P3-1183

Effect of Marijuana Use on Thyroid Function and Autoimmunity
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Abstract PDF
HRP0084P3-1184

Paediatric Thyroid Disease: About a Series of 48 Cases
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HRP0084P3-1185

Neonatal Hyperthyroidism with Craniolacunia
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HRP0084P3-1186

Is Transient Hypothyroidism in Preterm Infants True?
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Abstract PDF
HRP0084P3-1187

The Benefits of Preterm Neonate Development by Early Replacement Therapy with Levothyroxine: Longitudinal Prospective Study
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Abstract PDF
HRP0084P3-1188

Intrathyroidal Ectopic Thymic Tissue Mimicking a Thyroid Nodule: A Report of Three Paediatric Cases
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HRP0084P3-1189

Simultaneous Occurrence of Thyroid Storm, Diabetic Ketoacidosis, and Multiple Cerebral Infarction in a 16-Year-Old Girl
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HRP0084P3-1190

Two Patients with Allen-Herndon-Dudley Syndrome: a Novel Mutation on MCT8 Gene
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HRP0084P3-1191

Audit of Thyroid Carcinoma in Children, Adolescents, and Adults
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HRP0084P3-1193

NKX2-1 p.Asp266Argfs142X De Novo Mutation in a Girl with Congenital Hypothyroidism (CH): Phenotypic Description
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HRP0084P3-1194

Development and Risk Factors of Thyroid Dysfunction in Patients with Positive TPO Antibodies
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HRP0084P3-1195

The Evaluation of CD8+CD122+T Cells in Children with Autoimmune Thyroiditis
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HRP0084P3-1196

Hoffmann Syndrome in a Boy with Severe Acquired Primary Hypothyroidism
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HRP0084P3-1197

Congenital Hypothyroidism Incidence and Dysgenesis or Dyshormonogenesis Prevalence in a Large Infants Cohort from South of France
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HRP0084P3-1198

Thyroid Function in a Large Group of Obese Children: Causes and Consequences
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HRP0084P3-1199

Thyroid Nodules in Children and Adolescents
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HRP0084P3-1200

Trisomy 21 and Thyroid Dysfunction: About 50 Paediatric Cases
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HRP0084P3-1201

NKX2-1 (TTF-1) Germline Mutations are not a Frequent Cause of Congenital Hypothyroidism due to Dysgenesis
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HRP0084P3-1202

A Curious Case of Thyrotoxic Crisis and Lower Extremity Weakness in a 15 year-Old Female with Graves' Disease
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HRP0084P3-1203

Newborns of Mothers with Graves' Disease: Survey of 14 Years
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HRP0084P3-1204

Use of Liothyronine in a Case of Consumptive Hypothyroidism Caused by Hepatic Hemangiomas
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HRP0084P3-1205

Subclinical Hypothyroidism in Children and Adolescents - A 5-year Single-center Follow-up Study
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HRP0084P3-1206

The Difference between Cord and Filter Paper TSH Level in Congenital Hypothyroidism Screening Programme
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HRP0084P3-1207

Neonatal Hyperthyrotropinaemia - Watchful Waiting vs Treatment: Experiences from a Tertiary Centre
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HRP0084P3-1208

Congenital Central Hypothyroidism due to a Homozygous Mutation in the TSHB Gene - Just Think about It!
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HRP0084P3-1209

A Case of Acute Suppurative Thyroiditis with Piriform Sinus Fistula Treated with Chemocauterization Using Trichloroacetic Acid
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HRP0084P3-1210

Thyroid Dysfunction in Children with Trisomy 21: When Subclinical Hypothyroidism should be Treated?
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HRP0084P3-1211

Rectal Diluted Levothyroxine for the Treatment of Neonatal Hypothyroidism: An Alternative Route of Administration
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HRP0084P3-1213

Hyperthyroidism in Children and Adolescents: Causes, When and How to Treat - A Tunisian Experience
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HRP0084P3-1214

Massive Pericardial Effusion and Short Stature Caused by Autoimmune Hypothyroidism in 9-Years-Old Dyspneic Girl
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HRP0084P3-1215

Prevalence of Goitre and Thyroid Nodule and Analysis of the Association between Anthropometric Measurements and Thyroid Volume in Children
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HRP0084P3-1216

Hyperfunctioning Thyroid Nodule in an Adolescent
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HRP0084P3-1217

Subclinical Hypothyroidism in Children and Adolescents: About a Study of 25 Cases
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Abstract PDF
HRP0084P3-1218

Effects of Subclinically Hypothyroidism on Haemorheological Parameters in Paediatric Population
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Abstract PDF
HRP0084P3-1219

Unilateral Graves' Disease in an Adolescent: Case Report
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HRP0084P3-1220

Transient Hyperthyroidism Associated with a Thyroid Nodule
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HRP0084P3-1221

Hyalinizing Trabecular Tumour of Thyroid Gland in 17-Year-Old Boy - Case Report
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HRP0084P3-1222

Seven Cases with Williams Beuren Syndrome: Endocrine Evaluation and Long-Term Follow-Up
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HRP0084P3-1223

Clinical Course in a Girl with hTPO Mutation R161I in Exon 5: 18 Years of Follow-Up
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HRP0084P3-1224

Transient Polyarthritis with Carbimazole Treatment
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HRP0084P3-1226

A Rare Adverse Effect of Radioactive Iodine Therapy in a Child with Graves' Disease
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HRP0084P3-1227

A 7 Month-Old Male Infant with Spontaneous Transient Graves' Thyrotoxicosis
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HRP0084P3-1228

Sex and Age Differences in the Incidence of Thyroid Disease in Children with Obesity
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HRP0084P3-1229

Euthyroid Sick Syndrome in Children Presenting with Diabetic Ketoacidosis
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HRP0084P3-1230

The Role of Thyroid Fine-Needle Aspiration Cytology in the Treatment and Follow-Up of Thyroid Nodules in the Paediatric Population
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Abstract PDF
HRP0084P3-1231

Angioneurotic Oedema with Antithyroid Drugs in Thyroid Storm: What is the Best Therapeutic Option
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HRP0084P3-1232

Malabsorption of Levothyroxine in a Child Affected by Short Bowel Syndrome
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Abstract PDF
HRP0084P3-1233

Growth Curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
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HRP0084P3-1234

Cardiovascular Assessment in Turner Syndrome: Current Practice in the United Kingdom
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HRP0084P3-1235

Turner Syndrome in Iceland 1968-2012: Congenital Anomalies and Clinical Outcomes
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HRP0084P3-1237

Clinical Features and Genetic Considerations of Turner Syndrome: A Review of Our Cases
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HRP0084P3-1238

Growth Characteristics of Patient with Turner Syndrome Different Age and Karyotypes by the Ukrainian National Register
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HRP0084P3-1239

Nationwide Study of Turner Syndrome in Ukraine
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HRP0084P3-1240

Patients with Turner's Syndrome Should Have Ophthalmological Examination before Commencing Recombinant GH Treatment
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HRP0084P3-1241

Renal Problems in Early Adult Patients with Turner Syndrome
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HRP0084P3-1242

To Predict Ovarian Function is a Single Determination of AMH Useful in Patients with Turner Syndrome?
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HRP0084P3-1243

Anthropometric Findings from Birth to Adulthood in Turkish Girls with Turner Syndrome and Association with Karyotpye Distribution
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HRP0084P3-1244

GH Therapy in Turner Syndrome
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HRP0084P3-1245

A Rare Variant of Turner Syndrome: First Clinical Report from Kuwait
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HRP0084P3-1246

Turner Syndrome with Breast Development: Case Report
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HRP0084P3-1247

The Association between Selected Endocrinopathies and Central Arterial Pressure in Children and Adolescents
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Abstract PDF
HRP0084P3-1248

The Development of a Publication Presentation Workshop: Enhancing the Publication of African Paediatric Endocrinological Research
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Abstract PDF
HRP0084P3-1249

Telomere Length in Young Adults Born Preterm and the Risk for Cardiovascular Disease; Support for Accelerated Biological Ageing in Subjects Born Preterm
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Abstract PDF
HRP0084P3-1250

A Survival Analysis Approach to Assess the Association between Maternal Prepregnancy Overweight and Childhood Overweight: Results of the Ulm Birth Cohort Study (UBCS)
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Abstract PDF
HRP0084P3-1251

Sexually Dimorphic Methylation of SF-1 in Rat Placenta after Gestational Exposure to BPA
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Abstract PDF
HRP0084P3-1253

Newborns with Longest Telomeres are Big at Birth and Have Most Lean Mass: Not Most Fat: in Late Infancy
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HRP0084P3-1254

Untargeted Plasma Metabolomics in Prepubertal ICSI and Naturally Conceived Children Unravels Gender: Dimorphic Metabolic Trajectories After ICSI
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HRP0084P3-1255

Analysis of Gene Methylation Difference and Evaluation the Effect of GH in Silver-Russell Syndrome
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Abstract PDF
HRP0084LBP-1256

Higher Expression of the Oncogene YAP1, a Wnt/[beta]-Catenin Target, is associated with Poor Outcome in Pediatric Patients with Adrenocortical Tumors
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Abstract PDF
HRP0084LBP-1258

A Distinct Population of Islet Cells Defines Diffuse Congenital Hyperinsulinism in Infancy but not Other Forms of the Disease
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Abstract PDF
HRP0084LBP-1259

Adrenal Steroid Precursors Accumulating in Congenital Adrenal Hyperplasia lead to Transactivation of the Glucocorticoid Receptor
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Abstract PDF
HRP0084LBP-1262

The Existence of an Androgen Responsive Transcriptome in the Peripheral Blood of Boys Extends the Utility of the HCG Stimulation Test
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Abstract PDF
HRP0084LBP-1266

Determining the Effects of Race, Skin Colour, and Genotype on the Response to Vitamin D Therapy
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Abstract PDF
HRP0084LBP-1267

Safety and Efficacy of Long-Acting GH (VRS-317) in Children with GHD: Effects of Dose Change in the Second Treatment Year
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Abstract PDF
HRP0084LBP-1268

Genetic Causes of Disproportional Short Stature Identified by Whole Exome Sequencing
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Abstract PDF
HRP0084LBP-1269

Reduced Humanin Levels in Children with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0084LBP-1270

Long-Term Safety and Effectiveness of Daily and Weekly GH Treatment in Pediatric Patients
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Abstract PDF

ESPE Abstracts

54th Annual ESPE (ESPE 2015)

EPosters

BiosciAbstracts