ePosters

HRP0082P1-D2-1

Allelic Frequencies of CYP21A2 Variants and Genotype-Phenotype Correlations in a Cohort of 660 CAH Patients from Germany and Austria
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HRP0082P1-D2-2

Functional Characterization of a Novel Heterozygous Point Mutation in the Human Glucocorticoid Receptor Gene Causing Primary Generalized Glucocorticoid Resistance
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HRP0082P1-D2-3

Transient Generalized Glucocorticoid Hypersensitivity: Clinical Manifestations, Endocrinologic Evaluation, and Transcriptomic Profile: the Potential Role of nf-[kappa]b
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HRP0082P1-D2-7

A Novel Founder Mutation of CYP21A2 in Patients with CAH due to 21-Hydroxylase Deficiency
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HRP0082P1-D2-8

Normal Value of Steroids in Amniotic Fluid by LC-MS/MS Method
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HRP0082P1-D2-9

Mast Cells in Human Adrenal Gland During Fetal Development
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HRP0082P1-D2-10

An Unusual Presentation of Isolated ACTH-Deficiency Secondary to TBX19 Mutation Revealed by Late Onset Hypoglycemia Seizure
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HRP0082P1-D3-12

Adrenal Rest Tumors in Patients with Primary Adrenal Insufficiency
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HRP0082P1-D3-15

Testicular Adrenal Rest Tumors and Sertoli Cell Function in Adolescents with Cah
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HRP0082P1-D3-16

A Novel Mutation in Exon 5 of TP53 Gene in a Familial Adrenocortical Carcinoma
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HRP0082P1-D3-17

Aldosterone/Renin Ratio as Key Player in the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants
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HRP0082P1-D3-18

Zenhale Inhaled Corticosteroid Therapy: Useful Second Line Therapy for Asthma in Children but be Wary of Adrenal Suppression
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HRP0082P1-D3-21

How to Interpret Cortisol Responses to Acth in Patients with Non-Classic Congenital Adrenal Hyperplasia
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HRP0082P1-D3-22

Clinical Utility of Urinary Steroid Metabolite Ratios in Children Undergoing Investigations for Suspected Disorders of Steroid Synthesis
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HRP0082P1-D2-23

Analysis of Zinc Transporter ZnT8 Autoantibodies in Children and Adolescents with Autoimmune Thyroid Diseases
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HRP0082P1-D2-24

Final Height and BMI in English and Italian Adult Survivors of Childhood Acute Lymphoblastic Leukemia Treated without Cranial Radiotherapy
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HRP0082P1-D2-25

Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy: New Insights into Phenotype and Genotype
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HRP0082P1-D2-27

Late Endocrine Effects Despite Reduced Intensity Chemotherapy for Bone Marrow Transplantation in Children
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HRP0082P1-D2-28

Immune Changes are Observed After Radioiodine Treatment for Hyperthyroidism in Graves' Disease Patients
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HRP0082P1-D2-29

Standard Population Screening for Diabetes Mellitus has Low Sensitivity in Identifying Diabetes in Adult Survivors of Childhood Bone Marrow Transplantation with Total Body Irradiation
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HRP0082P1-D2-30

Managing Children with Thickened Pituitary Stalk and/or Idiopathic Central Diabetes Insipidus: a Single Centre Experience on 63 Children
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HRP0082P1-D2-31

Primary Pancreatic Insulinomas: Clinical, Morphological, and Genetic Characteristics of 12 Children
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HRP0082P1-D2-32

Papillary Thyroid Cancer After Hematopoietic Stem Cell Transplantation in Young Age
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HRP0082P1-D2-33

Immunological Studies in Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation, and Neural Tumor (ROHHADNET) Syndrome
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HRP0082P1-D2-34

High Prevalence of Low Bone Mass in Adolescents with Non-Transfusion Dependent Hb E/[beta]-thalassemia
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HRP0082P1-D2-35

Assessment of Quality of Life Data After 4 Monthly S.C. Doses of a Human Monoclonal Anti-Fibroblast Growth Factor 23 Antibody (KRN23) in Adults with X-linked Hypophosphatemia
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HRP0082P1-D2-36

Sun Protection Habits and Calcium Intake in Children with Malignancy
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HRP0082P1-D2-39

Continuous s.c. Recombinant PTH1-34 Pump Therapy in Congenital Hypoparathyroidism Associated with Malabsorption
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HRP0082P1-D2-40

Effects and Limitations of Cinacalcet Therapy in Neonatal Severe Hyperparathyroidism
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HRP0082P1-D2-41

Young Adults with Klinefelter Syndrome and Congenital Anorchia Treated with Testosterone Have Normal Bone and Muscle Mass but Increased Central Adiposity
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HRP0082P1-D2-45

Longitudinal Changes of Bone Mineral Content in Children with Cystic Fibrosis
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HRP0082P1-D3-46

Loss of Function CYP24A1 Mutations in Patients with Hypercalcemia and Low Pth level: an Autosomal Dominant or Recessive Trait?
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HRP0082P1-D3-47

Relation Between CNP Signaling Pathway and the Effect of Combined Treatment with GnRHa and rhGH on the Linear Growth in Mid/Late Pubertal Girls at Great Bone Ages with CPP or EFP
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HRP0082P1-D3-48

Paternal Isodisomy and Sporadic Pseudohypoparathyroidism I-b
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HRP0082P1-D3-51

Bone Geometry, Volumetric Density, Microarchitecture and Estimated Bone Strength Assessed by HR-pQCT in Adult Patients with Hypophosphatemic Rickets
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HRP0082P1-D3-52

Opposing Effects of Childhood Obesity on Radial and Tibial Bone Microstructure
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HRP0082P1-D3-53

Bone Mineral Density Evaluation in Children with Gaucher Disease
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HRP0082P1-D3-54

Correlation of Sclerostin Levels with Bone Metabolism Markers and Bone Mineral Density in Children and Adolescents with Type 1 Diabetes Mellitus (T1DM)
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HRP0082P1-D3-55

Increased Osteoclast Activity in Children and Adolescents with Type 1 Diabetes Mellitus Indicated by Higher Levels of Osteoprotegerin and s-RANKL may Predispose to Lower Bone Mass
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HRP0082P1-D3-56

Effect of a Vibration Based Rehabilitation Concept On Bone and Muscle Development in Children with Osteogenesis Imperfecta
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HRP0082P1-D3-57

No Correlation Between 25OHD Status and Pro or Anti-Inflammatory Cytokines in Obese Children and Normal Weight Controls
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HRP0082P1-D1-58

A leu402pro Mutation of the Non-hla Gene il18rap in Aggressive Neonatal Type 1 Diabetes Mellitus
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HRP0082P1-D1-59

A Randomized, Crossover Pilot Study Comparing Glycemic Control and Satisfaction with an Indwelling Catheter (I-PORT Advance) for Insulin Administration in Children and Adolescents with Type 1 Diabetes on Basal-Bolus Treatment
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HRP0082P1-D1-61

Evaluation of S-100B, Antioxidant and Oxidative Capacity Before and After the Treatment in Children with Diabetic Ketoacidosis
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HRP0082P1-D1-64

Biomarkers of Subclinical Inflammation in an Infant-Juvenile Population with Type 1 Diabetes
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HRP0082P1-D1-65

Glycaemic Control and Acute Complications in European Children, Adolescents, and Young Adults With Type 1 Diabetes in the Teens Study
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HRP0082P1-D1-66

Metabolic Consequences of Antipsychotic Medication in Youths with Type 1 Diabetes: Analysis from the Prospective Nationwide German and Austrian Diabetes Survey DPV
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HRP0082P1-D1-68

Evaluation of Bone Geometry, Quality, and Bone Markers in Children with Type 1 Diabetes
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HRP0082P1-D2-69

Activation of Insulin/IGF1 Signaling Could Increase Hypothalamic Lipid Anabolism in Non-Diabetic IRS2-Deficient Mice
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HRP0082P1-D2-70

Evaluation of Subclinical Atherosclerosis by Non-Invasive Radiological Methods and its Relation with Endoglin and Nitric Oxide Levels
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HRP0082P1-D2-71

Identification of Novel Candidate Gene Variants for Mody by Whole Exome Sequencing in Korean Mody Families
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HRP0082P1-D2-73

A Novel Mutation of wfs1 Gene in a Japanese Infant of Diabetes Mellitus, Deafness, and Congenital Cataract
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HRP0082P1-D2-74

Transient Hyperglycaemia Preceded by Neonatal Hyperinsulinaemic Hypoglycaemia in an Infant with a Novel HNF1A Mutation
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HRP0082P1-D2-75

Lpl Gene Mutation and Polymorphism of Apoc2 and Apoc5 Genes in a Patient with Diabetes Mellitus Type 1
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HRP0082P1-D2-78

Hormonal and Lipid Profile in Correlation with Anthropometric Measurements Among Offspring of Diabetic Mothers
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HRP0082P1-D3-81

mHealth app for Young People with Diabetes Type 1 Transferring from Pediatric to Adult Care
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HRP0082P1-D3-82

Holding the Horses of Insulin Pump Infusion: Usage and Effectiveness of the Low Glucose Suspend Feature During Fasting in Ramadan Among Adolescents with Type 1 Diabetes Mellitus to Prevent Hypoglycemia
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HRP0082P1-D3-83

DKA During Diabetes Therapy: Multinational Comparison with 59 191 Pediatric Patients from England, Wales, The United States, Austria and Germany
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HRP0082P1-D3-85

Algorithm-Based Cholesterol Monitoring in Children with Type 1 Diabetes
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HRP0082P1-D3-86

Implementation of Effective Transition from Paediatric to Adult Diabetes Care with an Outpatient Transition Nurse
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HRP0082P1-D3-88

Improved Health-related Quality of Life with Insulin Therapy in Children with Cystic Fibrosis-related Diabetes: a Prospective Cohort Study
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HRP0082P1-D3-89

Nutritional Status and Respiratory Function in Patients Affected by Cystic Fibrosis and Glucose Metabolism Derangements after 4 Years of Insulin Therapy with Glargine
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HRP0082P1-D1-105

Being Overweight During the Peripubertal Period Modifies the Leptin Induced Changes in Hypothalamic Neuropeptides Involved in Metabolism but not those Involved in Pubertal Onset
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HRP0082P1-D1-106

Natural Antibiotics: New Biomarkers of Childhood Obesity
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HRP0082P1-D1-107

Evidence of Early Alterations in Adipose Tissue Biology and Function in Obese Children
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HRP0082P1-D1-110

Free Fatty Acids Activate Hypothalamic Astrocytes in a Sexually Dimorphic Manner
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HRP0082P1-D1-111

A Multiplatform Non-targeted Metabolomics Approach to Investigate Insulin Resistance Associated to Obesity in Childhood
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HRP0082P1-D1-112

Mir-146a and -155 are Involved in FOXO1 Regulation and Non Alcoholic Fatty Liver Disease in Childhood Obesity
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HRP0082P1-D2-114

Pro-Inflammatory (M1) and Anti-Inflammatory (M2) Profiles in Adipose Tissue of Lean and Obese Children and Adolescents
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HRP0082P1-D2-115

Important Links Between Fat Derived Proteins and Bone Remodeling Factors in Lean and Obese Girls
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HRP0082P1-D2-118

Plasminogen Activator Inhibitor-1(Pai-1) Levels, Pai-1 Gene Polymorphism, and Family History of Cardiovascular Disease in Relation to Metabolic Parameters in a Sample of Obese Children
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HRP0082P1-D2-119

How Production of Vascular Endothelial Growth Factor Influences Formation of Vascular Disorders in Children with Obesity
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HRP0082P1-D2-120

RANKL and Osteoprotegerin Serum Levels in Obese Children and Adolescents
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HRP0082P1-D2-122

Predictive Value of Excess Body Weight in Childhood and Adolescence Compared to BMI and Waist to Height Ratio
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HRP0082P1-D2-123

Cardiovascular Risk Markers in Metabolically Healthy and Metabolically Unhealthy Obese Adolescents
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HRP0082P1-D3-128

Acylated and Unacylated Ghrelin Levels in Children and Young Adults with Prader-Willi Syndrome
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HRP0082P1-D3-129

The Effect of Honey on Plasma Glucose and Insulin Concentrations in Obese Prepubertal Girls
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HRP0082P1-D3-131

Under-Diagnosed Beckwith-Wiedemann Syndrome Among Early-Onset Obese Children
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HRP0082P1-D1-135

The Association Between Adipocytes and Growth is Mediated by Growth and Differentiation Factor 5
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HRP0082P1-D1-136

A Homozygous Point Mutation in the GH1 Promoter ([mdash]161T[gt]C) Leads to Reduced GH Expression in Siblings with Isolated GH Deficiency
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HRP0082P1-D1-137

Growth Differentiation Factor 15 and Fibroblast Growth Factor 21: Novel Biomarkers for Mitochondrial Diseases
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HRP0082P1-D1-139

Functional Characterization of Three Novel Mutations in the IGF1R Gene
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HRP0082P1-D1-140

Severe Short Stature and GH Insensitivity Due to a De Novo Heterozygous STAT5B Missense Mutation
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HRP0082P1-D1-142

Parental Gonadal Mosaicism for a BRAF Mutation in Cardiofaciocutaneous Syndrome
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HRP0082P1-D1-145

Genotype-Phenotype Relationship in Patients with SHOX Region Rearrangements Detected by MLPA in the French Population
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HRP0082P1-D1-146

Analysis of GH Receptor Gene Expression in Idiopathic Tall Stature Children
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HRP0082P1-D1-147

The Role of SHOX Gene in Idiopathic Short Stature: an Italian Multicenter Study
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HRP0082P1-D2-148

Beneficial Effects of Long-term GH Treatment on Adaptive Functioning in Infants With Prader-willi Syndrome
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HRP0082P1-D2-150

Cognitive Processing Speed as a Function of GH Treatment in Short Stature Children: a Multiple Regression Analysis
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HRP0082P1-D2-152

Longitudinal Growth of Healthy Preterm Infants Born Below 37 Gestation Weeks
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HRP0082P1-D2-153

Intima Media Thickness in Children Treated With GH
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HRP0082P1-D2-154

Clinical and Laboratory Parameters Predicting a Requirement for Reevaluation of GH Status During GH Treatment
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HRP0082P1-D2-156

Gender Difference in Secular Trend in Sweden
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HRP0082P1-D2-157

Autoantibodies Against Some Selected Appetite-Regulating Peptide Hormones and Neuropeptides are Present in Serum of Short Children with Candida Albicans Colonisation and Helicobacter Pylori Infection
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HRP0082P1-D2-158

Effects of Methylphenidate on Growth and Appetite in Attention-Deficit Hyperactivity Patients
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HRP0082P1-D3-161

Safety and Effectiveness of Increlex[reg] Therapy in Children Enrolled in the Increlex[reg] Growth Forum Database in Europe: 4 Years Interim Results
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HRP0082P1-D3-162

Infliximab Improves Growth in Paediatric Crohn[apos]s disease Only if Commenced Early in Puberty or Prior to the Onset of Puberty
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HRP0082P1-D3-165

Validating Genetic Markers of Response to Recombinant Human GH in Children with GH Deficiency or Turner Syndrome: Results From the PREDICT Validation Study
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HRP0082P1-D3-166

Short-Term Changes in Bone Formation Markers Following GH Treatment in Short Prepubertal Children with a Broad Range of GH Secretion
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HRP0082P1-D3-167

Aromatase Inhibitors in Girls: Anastrazole Combined to an LHRH Analogue is a Safe and Effective Strategy in Girls with Early or Precocious Puberty with Compromised Growth Potential
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HRP0082P1-D3-169

Recombinant Human GH Therapy Allows to Reach a Normal Final Adult Height in Coeliac Children with GH Deficiency due to Hypophysistis
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HRP0082P1-D3-172

Three-Years Height Outcome During rh-GH Therapy in Subjects with Achondroplasia and Hypochondroplasia
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HRP0082P1-D1-173

A Girl with Beckwith-Wiedemann Syndrome and Pseudohypoparathyroidism Type 1B, a Unique Example of Multiple Imprinting Defects
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HRP0082P1-D1-180

Long-Term Cognitive Effects from Dexamethasone-Treated Pregnancies
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HRP0082P1-D1-181

The Prevalence and Outcome of Sex Chromosome Abnormalities Detected Prenatally in Scotland
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HRP0082P1-D3-189

An Unusual Case of Hereditary Nephrogenic Diabetes Insipidus Affecting Mother and Daughter
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HRP0082P1-D3-190

A Rare Cause of Diabetes Insipidus: Congenital Proprotein Convertase 1/3 Deficiency
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HRP0082P1-D3-193

A Novel Mutation of OTX2 Associated with Neonatally Diagnosed Combined Pituitary Hormone Deficiency and Bilateral Microphthalmia
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HRP0082P1-D3-194

Type 3 Congenital Multiple Pituitary Hormone Deficiency
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HRP0082P1-D3-196

Rathke Cleft Cysts and Endocrine Dysfunction in Children
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HRP0082P1-D3-198

Spatial and Temporal Expression of Immunoglobulin Superfamily Member 1 in the Rat
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HRP0082P1-D1-198

Stability Conditions in Estradiol Matrix Patches; in vitro Studies for Application in Pediatrics
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HRP0082P1-D1-199

Associations of Vascular Biomarkers and the Somatotrophic Axis with Carotid Ultrasound and Echocardiography Findings in Relation to Turner Arteriopathy
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HRP0082P1-D1-200

Testes in Infants with Prader-Willi Syndrome: hCG Treatment, Surgery, and Histology
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HRP0082P1-D1-201

The Effect of 17[beta]-Estradiol on Uterine Volume in Young Women with Turner Syndrome: a 5-Year Randomized Controlled Clinical Trial
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HRP0082P1-D1-203

Girls with Turner Syndrome have Normal Muscle Force but Decreased Muscle Power
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HRP0082P1-D1-204

The Influence of GH Treatment on the Oral Disposition Index in Turner Syndrome Girls and in GH Deficient Children: 8 Years of Follow-Up
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HRP0082P1-D1-207

Analysis of the WDR11 Gene in Patients with Isolated Hypogonadotropic Hypogonadism with and without Olfactory Defects
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HRP0082P1-D1-208

GH Therapy in Turner Syndrome Patients: the Effects on Nutritional Status, Adipokines, and Aortic Dilatation
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HRP0082P1-D1-209

Evaluation of Sitting Height/Height SDS in Patients with Turner Syndrome
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HRP0082P1-D2-210

Messenger Ribonucleic Acid Expression of Kiss-1 and Serum Level of Kisspeptin in Rat at Different Developmental Stages
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HRP0082P1-D2-211

The Incidence of Childhood Gonadoblastoma Over 15 Years in the Republic of Ireland
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HRP0082P1-D2-212

A Novel MKRN3 Mutation Discovered in a Korean Girl with Central Precocious Puberty
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HRP0082P1-D2-214

Early Medical Treatment of Children with Gender Dysphoria: an Empirical Ethical Study on Arguments of Proponents and Opponents Concerning Early Interventions
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HRP0082P1-D2-216

IGSF1 Variants in Boys with Familial Delayed Puberty
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HRP0082P1-D2-217

Reference Charts for Testicular Volume in Dutch Children and Adolescents
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HRP0082P1-D2-220

Successful Treatment of Male Congenital Hypogonadotropic Hypogonadism with rFSH Pretreatment Followed by GnRH
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HRP0082P1-D3-221

The Uterine Artery Pulsatility Index as an Accurate Index for the Assessment of Puberty
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HRP0082P1-D3-222

The Uterine Artery Pulsatility Index in Evaluation of the GnRH-Analog Treatment Efficacy in Central Precocious Puberty
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HRP0082P1-D3-224

Test on Kisspeptin Levels in Girls with Idiopathic Central Precocious Puberty and its Significance
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HRP0082P1-D3-92

Mutations Involving FIBULIN2 are a Novel Cause of 46,XY DSD
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HRP0082P1-D3-93

Ex vivo Culture of Human Fetal Gonads: Manipulation of Meiosis Regulation Affects Testis Development
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HRP0082P1-D3-94

Prenatal Exposure to Phthalates and Phenols in Relation to Anogenital Distance at Birth in Male Infants
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HRP0082P1-D3-95

Ovarian Development and Hormonal Feedback Mechanism in a 46XX Patient with cyp19a1 Deficiency Under Low Dose Estrogen Replacement
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HRP0082P1-D3-97

46, XX Ovotesticular Disorder of Sex Development: Potential Role of 13q31.1
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HRP0082P1-D3-98

A Novel NR5A1 Mutation with Preserved Fertility
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HRP0082P1-D3-99

Development of a Next Generation Sequencing Panel for Disorders of Sex Development
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HRP0082P1-D3-100

Quality of Life in a Large Cohort of Adult Brazilian Patients with 46,XX and 46,XY Disorders of Sex Development from a Single Tertiary Centre
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HRP0082P1-D3-101

Subjective Need for Psychological Support in Parents of Children with dsd: Results from the German Clinical Evaluation Study
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HRP0082P1-D1-231

The Association between rs4684677 T/A Polymorphism in Preproghrelin Gene And predisposition to Autoimmune Thyroid Diseases in Children
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HRP0082P1-D1-233

TSH Receptor Gene Variants in Pediatric Patients with Non Autoimmune Hyperthyrotropinemia
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HRP0082P1-D1-234

Association of Toll-Like Receptor-10 Polymorphisms with Autoimmune Thyroid Disease in Korean Children
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HRP0082P1-D1-235

A Nonsense Thyrotropin Receptor Gene Mutation (R609X) is Associated with Congenital Hypothyroidism and Heart Defects
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HRP0082P1-D1-236

Genome-Wide Promoter Methylation Analysis in Cytologically Indeterminate Thyroid Nodules
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HRP0082P1-D1-237

Genetic Analysis of the Paired Box Domain Gene in a Cohort of Polish Patients with Primary Congenital Hypothyroidism
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HRP0082P1-D1-238

Homozygous Deletion of The TSH[beta] Subunit Gene Causes Congenital Secondary Hypothyroidism in a Consanguineous Family of Turkish Descent
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HRP0082P1-D1-240

A Novel Mutation in the TITF1 Gene in a Child with Benign Hereditary Chorea
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HRP0082P1-D1-242

Congenital Hypothyroidism and Tuberous Sclerosis: an Association or a Coincidence?
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HRP0082P1-D1-243

Evaluation of Serum Cytokines IL-6 and Osteoprotegerin Measurements in the Diagnosis of Chronic Autoimmune Thyroiditis and Graves' Disease in Children
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HRP0082P1-D2-245

Thyroid Dysfunction in Children After Hematopoietic Stem Cell Transplantation: Short Term Follow-Up for 12 Months
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HRP0082P1-D2-246

The Effect of L-Thyroxine Treatment on Left Ventricular Functions in Children with Subclinical Hypothyroidism
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HRP0082P1-D2-247

Urinary Iodine Concentrations in Mothers and their Term Newborns
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HRP0082P1-D2-249

Capillary TSH Cut-off Levels for Congenital Hypothyroidism Screening: Evidence Against Adopting the UK Threshold of 10 mIU/l
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HRP0082P1-D2-250

In Patients with Chronic Autoimmune Thyroiditis, Investigation of the Effects of Functions of Regulatory T Cells and Vitamin D
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HRP0082P1-D2-252

Autoimmune Encephalopathy in a Boy with Graves' Disease
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HRP0082P1-D2-253

Maternal Hypothyroxinemia in Early Pregnancy is Associated with Poorer Arithmetic Performance in a School Test in Offspring at Age 5 Years
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HRP0082P1-D2-254

TSH: Different Normalization Methods, Very Different Normal Upper Limits
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HRP0082P1-D2-255

Usefulness of Second Screening Strategy for Congenital Hypothyroidism in LBW Neonates
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HRP0082P1-D2-256

Screening for Congenital Hypothyroidism in the Russian Federation (1997-2012)
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HRP0082P2-D1-257

Growth Pattern in Infants with Congenital Adrenal Hyperplasia During the First Year of Life
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HRP0082P2-D1-259

Inadequate Cortisol Response to Tetracosactide (Synacthen®) Test in NCCAH Patients, an Exception to the Rule?
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HRP0082P2-D1-261

Paradoxical Increase in Urinay Cortisol Excretion in Children with Primary Pigmented Nodular Adrenal Disease
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HRP0082P2-D1-262

Mutation Spectrum of CYP11B1 Gene in Turkish Patients with 11[beta]-hydroxylase Deficiency
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HRP0082P2-D1-263

Genotype and Phenotype Characteristics of Patients with Nonclassical Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
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HRP0082P2-D1-265

Two Brothers with Late Onset Apparent Mineralocorticoid Excess
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HRP0082P2-D1-267

An adolescent with Hypertension Caused by Primary Hyperaldosteronism due to KCNJ5 Mutation
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HRP0082P2-D1-268

Analysis of Prospective Annual ACTH Stimulation Testing Among Survivors of Intracranial Tumor
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HRP0082P2-D2-272

Timing of precocious pubarche in girls: Does a contemporary subgroup exist?
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HRP0082P2-D2-273

Nonclassic Lipoid Adrenal Hyperplasia with R272C STAR Mutation: a Case Report
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HRP0082P2-D2-274

Severe 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia and Congenital Hypothyroidism Due to Thyroglobulin Mutations in a Single Family: Two Distinct Genetic Disorders with Phenotypic Variability within a Single Family
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HRP0082P2-D2-278

Do Neonates Need a Short Synacthen Test to Investigate the Adrenal Axis?
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HRP0082P2-D2-279

Genotype-Phenotype Discordant Patients with Homozygous Intron 2 Mutation (IVS2) of CYP21 Gene
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HRP0082P2-D2-280

A 26-Day-Old Japanese Girl with Aldosterone Synthase Deficiency Caused by a Novel Mutation in the CYP11B2 Gene
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HRP0082P2-D2-281

Nonclassic CYP21A2 Deficiency: Diagnosis and Clinical Evolution
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HRP0082P2-D1-285

Mutations in IFITM5 Leading to Prenatal and Postnatal Signs of Dominant Osteogenesis Imperfecta
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HRP0082P2-D1-287

Case report: A Novel mutation in the Calcium Sensing Receptor in a Welsh Family with Hypercalcaemia
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HRP0082P2-D1-288

A New Missense Mutation in FGF23 Gene in a Male with Hyperostosis-hyperphosphatemia Syndrome
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HRP0082P2-D1-289

Pseudohypoparathyroidism Type 1A Due to Novel GNAS Mutation
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HRP0082P2-D1-290

Sleep-related Breathing Disorders in Pycnodysostosis
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HRP0082P2-D1-291

Cystinosis as a Cause of Hypophosphatemic Rickets: a Single-Center Experience
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HRP0082P2-D1-292

Pseudohypoparathyroidism Type Ib: Two Cases with Different Clinical Presentation
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HRP0082P2-D2-299

Mutation in the TBCE Gene Associated with Kenny-Caffey Type 1 Syndrome: a Rare Cause of Hypocalcemia
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HRP0082P2-D2-301

Disproportionate Short Stature with Advanced Bone Age Due to PTHLH Mutation
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HRP0082P2-D2-302

Plasma 25-OH Vitamin D and pth Concentrations in Cord Blood: relationship with Ethnic Groups, Nutritional Habits and Degree of Maternal Sun Exposure
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HRP0082P2-D2-304

Age-and Gender-Specific Reference Values of Bone Mineral Density in Korean Adolescents and Young Adults
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HRP0082P2-D2-306

Effects of Recombinant Human GH on Bone Mass and Body Composition in Paediatric Inflammatory Bowel Disease
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HRP0082P2-D3-308

A Case of Vitamin D Dependent Rickets Type 1 with a Novel Mutation in CYP27B1 (25-OH Vitamin D-1-[alpha]-Hydroxylase) Gene
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HRP0082P2-D3-310

Outcomes of Vitamin D Analogues and Phosphate Supplements in Patients With Hereditary Hypophosphatemic Rickets , Comparison With Non-Treated Patients
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HRP0082P2-D3-311

Hyperostosis-Hyperphosphataemia Syndrome: Shortening a Diagnostic Odyssey
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HRP0082P2-D3-312

Severe Osteogenesis Imperfecta and Epidermolysis Bullosa Simplex Caused by FKBP10 Mutation: New Case
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HRP0082P2-D3-317

Infantile Hypercalcemia: Still a Diagnostic and Therapeutic Enigma
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HRP0082P2-D1-318

Serum Level of Osteoprotegerin and Total sRANKL in Adolescents with Type 1 Diabetes Mellitus
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HRP0082P2-D1-319

Simultaneous Changes in Trends in Incidence of Children Diabetes Type 1 in Distant Geographic Regions
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HRP0082P2-D1-320

Risk Factors for Type 2 Diabetes Mellitus in Secondary School Students in Port Harcourt Nigeria
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HRP0082P2-D1-321

Interaction of Pubertal Development and Metabolic Control in 1303 Adolescents with Diabetes Mellitus Type 1
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HRP0082P2-D1-322

Quality of Life and Glycaemic Assessment Before and After Pump School
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HRP0082P2-D1-326

Trends in Incidence and Prevalence of DM Type 1 in Children in Ukraine During 2002-2012
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HRP0082P2-D2-332

Game Interaction Between a Humanoid Robot and a Diabetic Teenager: Might This Improve Motivation to Fill in the Nutritional Diary?
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HRP0082P2-D2-334

New-Onset Type 2 Diabetes Presenting with Hyperglycaemic Hyperosmolar State in a Renal Transplant Patient on GH Treatment
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HRP0082P2-D2-336

GAD Antibody Positivity is Associated with Higher Prevalence of Autoimmune Thyroiditis in Children with Type 1 Diabetes Mellitus
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HRP0082P2-D3-340

Coated Pellets With Controlled Glucose Release in Treatment of Children with Diabetes
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HRP0082P2-D3-344

Lifestyle and Health Related Quality of Life in Adolescents with Diabetes Mellitus Type 1
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HRP0082P2-D3-345

Improvement in Type 1 Diabetes Mellitus Metabolic Control: From Conventional to Functional Insulin Therapy
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HRP0082P2-D3-346

Two Cases of 'Unknown' Lipoprotein Lipase Deficiency and Diabetes Mellitus
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HRP0082P2-D3-349

Retinol Binding Protein 4 and Adiponectin Levels During Oral Glucose Tolerance Test in Obese Children Newly Diagnosed of Type 2 Diabetes
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HRP0082P2-D3-351

Wolcott-Rallison Syndrome: New Mutations and Report of Two Cases
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HRP0082P2-D3-352

Socioeconomic Deprivation is Associated with Increased Hospital Admissions in Children with Type 1 Diabetes Mellitus
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HRP0082P2-D3-353

Household Unemployment and Low Levels of Education are Associated with Poor Glycaemic Control in Children and Young People with Type 1 Diabetes Mellitus
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HRP0082P2-D3-354

An Infant with a Novel Kir6.2 Mutation Causing Neonatal Diabetes and Unexplained Lack of Response to Sulphonylurea
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HRP0082P2-D3-355

Glycaemic Control and Microvascular Complications in Adolescents and Young Adults with Type 1 Diabetes: Outcome Following Transfer of Care to Adult Services
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HRP0082P2-D3-357

Early-Onset Autoinflammatory Partial Lipodystrophy Characterized by Recurrent Fever and Rash: Candle Syndrome
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HRP0082P2-D3-358

Is There a Change in the Presentation of Childhood Type-1 Diabetes Mellitus in the Last 15 Years? Data from a Tertiary Care Center in Turkey
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HRP0082P2-D3-359

The Sugarsquare Study: a Multicenter Randomized Controlled Trial Concerning a Web-based Patient Portal for Parents of a Child with Type 1 Diabetes
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HRP0082P2-D3-361

Comparison of HbA1c and OGTT to Diagnose Diabetes in Korean Children
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HRP0082P2-D1-362

Age at Onset of Weight Gain in Prader-Willi Syndrome is Often Between 1 and 2 Years, Preceding the Hyperphagic Phase; Implications for Management
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HRP0082P2-D1-363

Novel Uncoupling Protein 1 Expression in White Adipocytes of Subcutaneous Abdominal Adipose Tissue in Children and Adolescents: A Protective Mechanism for Metabolic Equilibrium?
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HRP0082P2-D1-364

The Association Between Self-Reported Sleep Quality, Ghrelin Hormone and Obese Children and Adolescents
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HRP0082P2-D1-366

Uric Acid and Risk for Atherosclerotic Disease Early in Life
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HRP0082P2-D1-367

Prevalence of Idiopathic Intracranial Hypertension and Related Factors in Obese Children and Adolescents
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HRP0082P2-D1-369

The Expression of IGF Type 1 Receptor is Increased in Obese Children
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HRP0082P2-D1-370

Childhood Obesity, Renal Injury, and Future Disease Risk
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HRP0082P2-D1-371

Replacement of the Neonatal Leptin Surge During Maternal Deprivation Normalizes Some Endocrine Parameters but Exacerbates Others
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HRP0082P2-D1-373

Expression Levels of the Growth-Arrest-Specific Transcript 5 in Overweight and Obese Children and Adolescents
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HRP0082P2-D2-374

The Role of Bone and Fat Tissue in Glucose Metabolism in Two Different Metabolic Conditions: Obesity and Diabetes Mellitus Type 1: Pilot Study
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HRP0082P2-D2-375

Family and Genetic Factors Influence the Metabolic Changes in Children
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HRP0082P2-D2-377

Short-Term Results of Single-Port Sleeve Gastrectomy in Adolescents with Severe Obesity
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HRP0082P2-D2-380

A New Case of Proopiomelanocortin Deficiency
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HRP0082P2-D2-382

Is 24-h Blood Pressure Monitoring Necessary in Obese Children and Adolescents?
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HRP0082P2-D2-383

Fetuin A Serum Levels in Children with Nonalcoholic Fatty Liver Disease
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HRP0082P2-D2-384

Ambulatory Arterial Stiffness Index in Obese Children
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HRP0082P2-D3-386

Miglitol Upregulates Uncoupling Protein 1 (ucp1) by Enhancing [beta]3-Adrenergic Signaling in Mature Brown Adipocytes of Rat
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HRP0082P2-D3-387

Enhanced Liver Fibrosis Test in Obese Children with Ultrasound-Proven Steatosis
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HRP0082P2-D3-388

Metformin Treatment in Obese Children Enhances Weight Loss Related Improvement in Impaired Glucose Tolerance
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HRP0082P2-D3-390

POMC Deficiency Mimicking Neurometabolic Disease
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HRP0082P2-D3-391

The Relationship Between Weight-Related Anthropometric Parameters and Menarche in Norwegian Girls
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HRP0082P2-D3-395

Body Composition in 10-15 Years Old Children Exposed to Pesticides Prenatally
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HRP0082P2-D3-396

D2 Dopamine Receptor Agonists Influence in the Animal Model of Dietary Obesity
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HRP0082P2-D3-399

Is Small for Gestational Age Status Associated with an Increase Risk of Atherogenesis?
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HRP0082P2-D3-401

Mannose Binding Lectin and Carotid Intima-Media Thickness in Chinese Obese Children
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HRP0082P2-D3-402

Usefulness of Hypertriglyceridemic Waist Phenotype in Obese Indian Children
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HRP0082P2-D3-403

Concomitant Changes in Full Body DXA Values and BMI-SDS During Multidisciplinary Treatment of Childhood Obesity
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HRP0082P2-D3-404

Cystic Fibrosis: Dyslipidemia in Brazilian Children
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HRP0082P2-D3-405

Do Children with Down Syndrome Show Lipid Profile Disorders?
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HRP0082P2-D3-406

Relationship Between Obesity and Platelet Indices in Children
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HRP0082P2-D3-407

Examining [beta]-Cell Reserve in Extremely Obese Children
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HRP0082P2-D3-408

SHBG Integrates the Cardiovascular Risk and Metabolic Dysfunction of Gestational Obesity
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HRP0082P2-D1-412

ALS Deficiency due to a Novel and Two Already Described IGFALS Gene Mutations in an Unusual Non Consanguineous Family: Two Compound Heterozygous (Father and Son) and Two Heterozygous Carriers (Brother and Mother)
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HRP0082P2-D1-414

Final Height SDS Gain of GH Treated Children with SHOX Deficiency Describing Observational and Clinical Trial Data
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HRP0082P2-D1-415

IGF1 is Associated with a More Favourable Pattern of Body Composition in Obese Children
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HRP0082P2-D1-417

GH Stimulated Levels in Prader-Willi Syndrome During the Transition Period between Childhood and Adulthood
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HRP0082P2-D1-418

Response to GH Treatment in Patients with Silver Russell Syndrome
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HRP0082P2-D1-419

Pubertal Development During GH Treatment with or without Additional GnRH Analogue Treatment in Short Children Born Small for Gestational Age
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HRP0082P2-D1-421

The Effects of Delaying Puberty with GnRH Agonists in Patients with Idiopathic GH Deficiency
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HRP0082P2-D2-422

Perceptions and Expectations of Patients and their Families for the Effects of GH Treatment
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HRP0082P2-D2-423

Normal Onset of Clinical Puberty for Age in GH-Treated Children with Noonan Syndrome or Turner Syndrome: Data from the NordiNet® IOS and ANSWER® Program
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HRP0082P2-D2-425

Electronic Devices and Single-Dose Dispensing Systems GH are the Most Efficient and Less Loss of Drug
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HRP0082P2-D2-426

The Level and Conformation of Blood Plasma Carotenoids in GH Deficient Children After 1 Year of GH Therapy
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HRP0082P2-D2-428

The Interconnectivity Between GH Replacement Therapy and Subclinical Hypothyroidism on Growth Response in Children with Pituitary Dwarfism
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HRP0082P2-D2-429

What Should be the Diagnosis and Management of Short Children with IGF1 Deficiency, Responding to GH Administration Despite Normal GH Secretion?
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HRP0082P2-D2-430

A Reappraisal of the Cut-Off Limits of the Peak GH Response to Stimulation Tests for the Diagnosis of GH Deficiency in Children and Adolescents
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HRP0082P2-D2-431

Vitamin D Concentrations in Children with GH Deficiency During First Year of GH Treatment
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HRP0082P2-D2-433

Comparison of Measured Lean Body Mass (LBMDXA) and Estimated LBMBIA in Children with GH Deficiency
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HRP0082P2-D2-434

Metabolic Assessment in Children with GH Deficiency Before, During, and After Human GH Replacement Therapy
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HRP0082P2-D3-435

First-year Growth Response to GH in Relation to Final Height Outcome in Prepubertal Children with Idiopathic GH Deficiency
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HRP0082P2-D3-436

Reevaluation of GH Secretion During Puberty in Children Diagnosed as GH-deficient During Childhood
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HRP0082P2-D3-437

Long-Term Effects of GH Replacement Therapy on Thyroid Function in GH Deficiency Children
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HRP0082P2-D3-438

Does Priming with Sex Steroids Before GH Stimulation Test Increase the Diagnosis of Normal GH Secretion in Short Children?
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HRP0082P2-D3-439

GH Dosing Patterns in Short Children Born Small for Gestational Age
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HRP0082P2-D3-441

Effects of Gender and Gestational Age on GH Treatment in Very Young Children Born Small for Gestational Age
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HRP0082P2-D3-443

The Effect of Two Different GH Dosages on Final Height and Bone Geometry
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HRP0082P2-D3-445

GH Treatment to Final Height in Children with Idiopathic Short Stature: Evidence for an Early Therapy Initiation Effect
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HRP0082P2-D3-446

Evaluation of the Safety and Usability of FlexPro® 30 mg/3 ml, for the Delivery of Norditropin® in Patients Requiring GH Therapy
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HRP0082P2-D3-447

Efficacy, Adherence, and Cost Study According to Pathology and Treatment Devices in Children Treated with GHRH
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HRP0082P2-D1-448

Isolated GH Deficiency (IGHD) may be due to Several Different Causes: mutations in the GHRH Receptor Gene Are a Relatively Rare Cause of IGHD
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HRP0082P2-D1-449

Fibroblast Growth Factor 21 is Inversely Associated with Growth Rates in Infancy
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HRP0082P2-D1-451

Eleven Years of Letrozole Treatment in a Child with 11-[beta] Hydroxylase Deficiency: Effect on Bone Age and Height Prognosis
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HRP0082P2-D1-453

New Reference for Height in Swedish Boys and Girls
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HRP0082P2-D1-455

The Effect of Long Term GH Therapy in Discordant Twins Where One Twin is Born Small for Gestational Age: A Case Control Study
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HRP0082P2-D1-456

How Early is the Rise in Leptin Levels in Small for Gestational Age Children With Catch Up Growth
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HRP0082P2-D1-457

Relation Between CNP and the Effect of Combined Treatment With GnRHa and GH on the Linear Growth in Mid/Late Pubertal Girls with Central Precocious Puberty or Early and Fast Puberty at Great Bone Ages
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HRP0082P2-D1-458

Two Duplications Within PAR1 in a Family With Idiopathic Short Stature
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HRP0082P2-D1-459

Comparison Between GH assay: serum GH Cut-off Levels by ECLIA Performed in Pharmacological Estimulation Tests in Children With Short Stature
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HRP0082P2-D2-461

Anophthalmia, Abnormal Pituitary Development, and Suboptimal Response to GH Therapy in Two Children With Microdeletions of 14q22q23
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HRP0082P2-D2-462

Adiponectin Levels as Early Marker of Insulin Resistance in Children Born Small for Gestational Age in Our Cohort
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HRP0082P2-D2-464

Interrelationships Between BMI and Other Overweight Related Anthropometric Variables in Childhood
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HRP0082P2-D2-466

Normal Growth in Aromatase Excess Syndrome by Pharmacological Inhibition of Aromatase Activity
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HRP0082P2-D2-470

Severe Short Stature due to a Heterozygous igf1r Mutation With a Good Response to rhgh Therapy: a Family Study
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HRP0082P2-D2-472

Body Proportions Estimated by Photometry
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HRP0082P2-D2-473

GH Deficiency in a Child With De Novo 2q31.1 Microdeletion
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HRP0082P2-D3-475

Long-Term Follow Up of Children with Congenital Hyperinsulinism on Octreotide Therapy
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HRP0082P2-D3-476

Glucagon Secretion in Response to Hypoglycemia in Patients with Congenital Hyperinsulinism
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HRP0082P2-D3-477

Opioid-Induced Endocrinopathy in a Toddler with Chronic Codeine Intoxication
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HRP0082P2-D3-478

Case Report: a Rare Cause of Hypoglycemia in a Neonate
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HRP0082P2-D3-480

The Role of Plasma C-Peptide Concentration in the Diagnosis of Congenital Hyperinsulinism
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HRP0082P2-D3-481

Presentation, Clinical and Genetic Outcomes in a Series of Infants With Congenital Hyperinsulinism
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HRP0082P2-D3-483

Neurodevelopmental Outcomes in Early and Late Presenting Congenital Hyperinsulinism
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HRP0082P2-D3-486

Fasting Hypoglycemia Associated With Hyperinsulinemia in a Child With Acute Lymphoblastic Leukemia and 6-Mercaptopurine Therapy
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HRP0082P2-D3-487

The Cytotoxic Ability of NK Cells in Children with Autoimmune Thyroiditis
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HRP0082P2-D3-490

Genetic Susceptibility in Autoimmune Polyglandular Syndrome Type 3 Variant
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HRP0082P2-D3-491

Autoimunne Thyroiditis in Type 1 Diabetes Mellitus Pediatric Population
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HRP0082P2-D3-493

Role of Metformin in the Treatment of Hypothalamic Obesity
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HRP0082P2-D3-494

Three Year Experience of a National Interdisciplinary Initiative to Improve Outcomes for Children with Hypothalamic Pituitary Axis Tumours (HPATs) Using Multi-site Videoconferencing for Decision Making on Behalf of the UK HPAT Interest Group
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HRP0082P2-D3-496

Endocrine Dysfunction Following Treatment of Medulloblastoma: a Single Centre Experience
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HRP0082P2-D3-499

GH-Secreting Pituitary Adenoma with Gigantism: a Challenging Case
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HRP0082P2-D3-500

The Contribution of Maternal Malaria Exposure and Metabolic Markers to Change in Blood Pressure in Nigerian Children over the First 3 Years of Life
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HRP0082P2-D3-501

Kabuki 47,XXY Syndrome: a Case Report
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HRP0082P2-D3-502

Retrospective Analysis of Cortisol Measurement in Neonates
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HRP0082P2-D3-504

Vitamin D Deficiency as the Primary Cause of Neonatal Hypocalcemia in a Tertiary Hospital
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HRP0082P2-D3-506

Metabolic Profile of Neonates With Different Duration of Gestation and Different Size at Birth
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HRP0082P2-D3-508

Various Presentations of X-linked Adrenoleukodystrophy: Case Reports
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HRP0082P2-D3-509

Neonatal Pituiiary-Thyroid Axis Dysregulation with Combined Thyroid Hormone and TSH Resistance in Infant with Trisomy 21 and Maternal Subclinical Hypothyroidism
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HRP0082P2-D3-510

Neonates with Acute Kidney Injury Continue to be at Risk of Iatrogenic Iodine Toxicity and Hypothyroidism with Attendant Risk to the Developing Brain
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HRP0082P2-D1-511

Relationship Between Adenoid Vegetation and Neurosecretory Dysfunction (Pituitary Dysfunction)
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HRP0082P2-D1-512

Clinical Phenotype and Complications, Endocrinopathies and Neuroimaging Findings in a Case Series of Sod
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HRP0082P2-D1-513

Polyuria and Polydipsia: The Deep Waters of Diagnosis
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HRP0082P2-D1-514

Urinary Gonadotrophins for Assessment and Management of Pubertal Disorders
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HRP0082P2-D1-517

Could Brain MRI Replace GH Stimulation Tests in the Work-Up of GH Deficiency in the First Years of Life?
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HRP0082P2-D1-518

Goliath, a Variant of DAVID Syndrome?
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HRP0082P2-D1-519

Hyperthyroidism Due to TSH Secreting Pituitary Adenoma in a 7-Year-Old Boy
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HRP0082P2-D2-521

Association of Pituicytoma and Cushing's Disease: a Rare Pediatric Case
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HRP0082P2-D2-524

Pituitary Stalk Interruption Syndrome: a Sequential Manner to Gain Pituitary Hormone Deficiencies with Still Unknown Molecular Basis
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HRP0082P2-D2-526

Child with GH Deficiency due to Remnant Craniopharyngeal Duct
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HRP0082P2-D2-528

Atypical Presentation of Hypothermia Induced Diabetes Insipidus: a Case Report
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HRP0082P2-D1-529

Is There Any Influence of TSH Serum Levels on Insulin Resistance in Euthyroid Adolescents with Polycystic Ovary Syndrome?
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HRP0082P2-D1-530

The Vaginal Maturation Index as a Marker of Local Sensitivity to Estrogens in Girls with Congenital Adrenal Hyperplasia During Puberty
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HRP0082P2-D1-531

Very Low Estradiol Levels are Independent From Duration of Amenorrhea in Girls with Severe Anorexia Nervosa
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HRP0082P2-D1-533

Polycystic Ovarian Syndrome in Adolescents: Metabolic Profile at Diagnosis, During and After Treatment with Oral Contraceptive
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HRP0082P2-D1-540

A Novel Mutation at a Splice Acceptor Site of WDR11 in a Patient with Combined Pituitary Hormone Deficiency
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HRP0082P2-D2-542

GH Excess and Pseudoprecocious Puberty in a 8-Year-Old Boy with Mccune-Albright Syndrome
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HRP0082P2-D2-543

Time to Menarche After Completing GnRH Agonist in Girls with Central Precocious or Early Puberty
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HRP0082P2-D2-545

Diagnostic Spectrum of Female Pubertal Delay
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HRP0082P2-D2-547

The Triptorelin Test Compares Favourably with the GnRH Test in the Diagnosis of Central Precocious Puberty
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HRP0082P2-D2-548

Puberty in Children with Shunted Congenital Hydrocephalus with and without Myelomeningocele
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HRP0082P2-D2-549

Evaluation of Age at GnRH Analogue Treatment Discontinuation, Age at Menarche and Adult Height in Girls with Central Precocious Puberty from the Spanish Registry
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HRP0082P2-D2-550

Final Height in a Boy with McCune-Albright Syndrome and Precocious Puberty Treated with Ketoconazole, Cyproterone Acetate, and Leuprolide Acetate Depot for More than 5 Years
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HRP0082P2-D2-552

Pubertal Development in a Cohort of Romanian School-Aged Children
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HRP0082P2-D3-553

Inhibin B in the Diagnosis of Delayed Puberty
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HRP0082P2-D3-555

Tamoxifen-Induced Hirsutism: an Unusual Side Effect in a 5 Years Old Girl with Mccune-Albright Syndrome
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HRP0082P2-D3-558

Pituitary-Ovarian Axis in Patients with Isolated Premature Thelarche
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HRP0082P2-D3-560

Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI
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HRP0082P2-D3-562

Central Precocious Puberty as the Initial Manifestation of a Pilocytic Astrocytoma with Leptomeningeal Dissemination Simulating a Hypothalamic Dysgerminoma
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HRP0082P2-D3-563

Endocrine Abnormalities in Phosphoglucomutase 1 Deficiency
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HRP0082P2-D1-566

The Research About sf1 Gene Abnormality in 45 Children with Micropenis
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HRP0082P2-D1-567

A New Mutation of MAMLD1 (CXorf6) Associated with NR5A1 (SF1) Variant in a Patient with 46,XY DSD
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HRP0082P2-D1-568

46XY, DSD due to 5[alpha]-Reductase Type 2 Deficiency in 19 Chinese Patients
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HRP0082P2-D1-571

Identification of a Missense MAP3K1 Mutation in a Patient with Hypospadias
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HRP0082P2-D1-572

Anogenital Distance, Penis Growth, and Masculine Behaviour Evidence for Independent Neurobehavioral Effects of Foetal Versus Postnatal Androgen Exposure in Boys
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HRP0082P2-D1-573

Mutation Analysis of kdm3a (Lysine-Specific Demethylase 3a) in Patients with Hypospadias
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HRP0082P2-D2-579

Mosaicism: Study of Nine Patients
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HRP0082P2-D2-581

Rare Disease Registries: Perception of Parents and Young People
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HRP0082P2-D2-582

Down Syndrome and Disorders of Sex Development: Only Coincidence or More?
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HRP0082P2-D2-583

Novel Mutation in a Newborn with a Rare Cause of 46,XY Sex Reversal: 17[beta]- Hydroxysteroid Dehydrogenase Type 3 Deficiency
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HRP0082P2-D1-584

Treatment of Pediatric Graves' Disease: Results of a Multicenter Survey in Portugal
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HRP0082P2-D1-585

Subclinical Hypothyroidism is Associated with Low IGF1 Levels and Decreased Growth Velocity
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HRP0082P2-D1-586

Thyroid Function and Autoimmunity and Their Relation to Weight Status in Healthy Children and Adolescents
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HRP0082P2-D1-587

Mutation of the TSH Receptor Gene: a Longitudinal Study in Children with Non-Autoimmune Subclinical Hypothyroidism
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HRP0082P2-D1-590

Thyroid Disorders in Siblings of CH Patients with Thyroid Dysgenesis
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HRP0082P2-D1-591

Trends in Median Age at Guthrie Sampling, Laboratory Receipt, Notification, and Start of Treatment for Infants with TSH Elevation on Newborn Screening
Direct

Abstract PDF
HRP0082P2-D1-593

Incidence of Thyroid Nodules in Children Affected by Hashimoto's Thyroiditis: a 12-Year Survey of 567 Children
Direct

Abstract PDF
HRP0082P2-D1-595

Papillary Thyroid Cancer with Diffuse Pulmonary Metastasis: How to Manage?
Direct

Abstract PDF
HRP0082P2-D1-596

Factors Useful to Distinguish between Children with Permanent Congenital Hypothyroidism and Transient or Permanent Hyperthyrotropinemia
Direct

Abstract PDF
HRP0082P2-D2-597

Thyroid Nodules in Childhood and Adolescence; Clinical, Radiologic and Etiological Evaluation
Direct

Abstract PDF
HRP0082P2-D2-601

Long Term Anti-Thyroid Drug Therapy in a Paediatric Population with Down Syndrome: an Irish Experience
Direct

Abstract PDF
HRP0082P2-D2-602

Influence of Amiodarone on Thyroid Function in Children
Direct

Abstract PDF
HRP0082P2-D2-604

Levothyroxine Requirement in Congenital Hypothyroidism: 12-year Longitudinal Study
Direct

Abstract PDF
HRP0082P2-D2-606

Genetic Studies in Congenital Hypothyroidism: a Regional Study
Direct

Abstract PDF
HRP0082P2-D3-611

Epidemiology of Turner Syndrome in Iceland 1968-2012
Direct

Abstract PDF
HRP0082P2-D3-612

Anti-Mullerian Hormone: a Marker of Premature Ovarian Insufficiency in Girls with Turner Syndrome
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HRP0082P2-D3-613

Nationwide Study of Turner Syndrome During Childhood in Turkey: Evaluation of Associated Problems
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HRP0082P2-D3-617

Early Occurrence of Gonadoblastoma Found at Elective Gonadectomy in Turner Syndrome Mosaic for Y Chromosome
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HRP0082P2-D3-618

GH Deficiency as a Cause of Persistent Hypoglycaemia in a Child with Turner Mosaic and Kabuki Syndrome
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Abstract PDF
HRP0082P2-D3-619

A Child with Clinical and Cytogenetic Features of Male Edward Syndrome and Turner Syndrome with Bilateral Gonadoblastoma in Infancy
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HRP0082P2-D3-620

Turner Syndrome: Analysis of Changes in the Age at Diagnosis and Phenotypic and Genotypic Description of 174 Patients
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Abstract PDF
HRP0082P3-D1-622

Body Composition Analysis in Girls With Premature Adrenarche
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Abstract PDF
HRP0082P3-D1-623

Pseudohypoaldosteronism Type 1: Role of Urinary Steroid Profiling in Specific and Early Diagnosis: Lessons in Differential Diagnosis of PHA1 vs PHA2 (Renal Tract Anomaly)
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Abstract PDF
HRP0082P3-D1-624

Genotype-Phenotype Correlations in Bulgarian Patients with c.293-13A/C[gt]G Splice Mutation of 21CYPA2 Picked up by Neonatal Screening (NS)
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HRP0082P3-D1-625

A Pediatric Case of Cushing's Disease Presenting with Diabetic Ketoacidosis
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Abstract PDF
HRP0082P3-D1-626

Cyp21a2 Mutation Spectrum in Bulgarian Cah Patients
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Abstract PDF
HRP0082P3-D1-627

A Rare Cause of Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency: a Case Report
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Abstract PDF
HRP0082P3-D1-628

Familial Glucocorticoid Deficiency: Masked Diagnosis by Hydrocortisone Life-Saving Treatment
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Abstract PDF
HRP0082P3-D1-629

Clinical and Genetic Diagnosis of Allgrove Syndrome
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HRP0082P3-D1-631

Homozygous c.923dupT Combined with Heterozygous c.334G[gt]A CYP21A2 Mutation: a Case Report from the Bulgarian CAH Screening Programme
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HRP0082P3-D2-634

Prenatal Dexamethasone Use for the Prevention of Virilization in Pregnancy at Risk for Classical Congenital Adrenal Hyperplasia
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HRP0082P3-D2-635

Congenital Adrenal Hyperplasia: Survey of the Management in Children Across UK
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HRP0082P3-D2-636

Neonatal Hypercalcaemia Associated with Congenital Adrenal Hyperplasia
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Abstract PDF
HRP0082P3-D2-641

Congenital Hypoaldosteronism of Unknown Etiology in Five Half-Siblings
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HRP0082P3-D2-642

X-Linked Adrenoleukodystrophy in eight Patients
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HRP0082P3-D2-645

Untreated Congenital Hyperplasia with Central Precocious Puberty
Direct

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HRP0082P3-D3-648

Genetically Proven APS Type 1 in Two Siblings
Direct

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HRP0082P3-D3-651

Diabetes Mellitus after Hematopoietic Stem Cell Transplantation
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Abstract PDF
HRP0082P3-D3-655

A Conservative Approach to the Management of Endocrine Neoplasia in Carney Complex in an Adolescent Male
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HRP0082P3-D3-658

Increasing Testicular Size due to Bilateral Large Cell Calcifying Sertoli Cell Tumours in a Peri-Pubertal Child with Carney Complex
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HRP0082P3-D1-660

Normal Serum Calcium Levels and Vitamin-D Dependent Rickets Type 2 (VDDR-II): a Novel Vitamin D Receptor Mutation
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Abstract PDF
HRP0082P3-D1-662

Hypercalcemia due to Subcutaneous Fat Necrosis in a Newborn Successfully Treated with Pamidronate Infusion Therapy
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HRP0082P3-D1-668

Lumbar Spine Areal Bone Mineral Density and 25-Hydroxyvitamin D Serum Concentrations at 2-Year Follow-up in Patients with Osteogenesis Imperfecta
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HRP0082P3-D1-672

Obese Adolescent with Gait and Depression
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Abstract PDF
HRP0082P3-D2-681

Variability in Clinical and Genetic Spectrum in Hypophosphatasia: Natural History in Two Patients
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HRP0082P3-D2-682

Cautionary Tales in the Management of Transient Neonatal Hypoparathyroidism
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HRP0082P3-D2-684

Clinical Phenotype and Molecular Studies in Patients with Hypophosphatemic Rickets
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HRP0082P3-D3-690

Prospective Evaluation of Bone Mineralization, PTH Regulation, and Metabolic Profile in Adult Patients with Hereditary Hypophosphatemic Rickets
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HRP0082P3-D3-693

The Use of Pamidronate in Pediatric Patients with Disease of Other than Osteogenesis Imperfecta: the Experience of Our Center
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HRP0082P3-D3-696

A Korean Boy with Pseudohypoparathyrodism Type Ia Presenting with Congenital Megacolon and Spinal Stenosis: Identification of a Novel GNAS Gene Mutation
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HRP0082P3-D3-697

A Case with Odontohypophosphatasia and Family Investigation
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Abstract PDF
HRP0082P3-D3-698

TSH/fT4 Ratio as a Marker of TSH Resistance in Pseudoparathyroidism 1A and Obesity
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Abstract PDF
HRP0082P3-D1-699

Efficacy and Safety of CSII Treatment in Paediatric Age: Long Term Experience of a Tertiary Care Centre in Spain
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Abstract PDF
HRP0082P3-D1-700

Diabetic Ketoacidosis in Children with T1DM: an Italian Multicentre Survey
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Abstract PDF
HRP0082P3-D1-702

Abnormal Blood Glucose as a Prognostic Factor for Adverse Clinical Outcome Among Children with Acute Medical Conditions in Ghana
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HRP0082P3-D1-707

The Lung Endothelin System: a Potent Therapeutic Target with Bosentan for the Amelioration of Lung Alterations in a Rat Model of Diabetes Mellitus
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Abstract PDF
HRP0082P3-D1-708

Clinical Significance of Typing Fulminant Type 1 Diabetes in Children and Adolescents
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HRP0082P3-D1-710

Health-Related Quality of Life Among Turkish Children and Adolescents with Type 1 Diabetes
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HRP0082P3-D2-714

Case of Family Neonatal Diabetes with KCNJ11 Gene Mutation
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HRP0082P3-D2-716

Uptake of a Novel Tool to Adjust Insulin Boluses, Based on CGM Trend Arrows and Insulin Sensitivity (Trend Arrow Adjustment Tool); in Children with Type 1 Diabetes, Who are Using Insulin Pump Therapy and Continuous Glucose Monitoring
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HRP0082P3-D2-720

Anti-Cyclic Citrullinated Peptide Antibodies are not Frequent in Children with Type 1 Diabetes
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Abstract PDF
HRP0082P3-D2-722

Knowledge Base and Attitudes of Senior Medical Staff to Insulin Therapy in Children with Diabetes
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Abstract PDF
HRP0082P3-D3-724

Prevalence of Impaired Glucose Tolerance and Insulin Resistance in a Sample of the 6- to 16-Year-Old Overweight or Obese Pediatric Population
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HRP0082P3-D3-725

Differences in Pubertal Development and Anthropometry Between Normal Population and Type 1 Diabetic Child at Debut in Spain
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HRP0082P3-D3-727

Evaluation of HbA1c Measurement in Trinidad and Tobago
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HRP0082P3-D3-728

The Result of Sulphonylureas Treatment in Patients with Neonatal Diabetes Mellitus due to kcnj11/abcc8 Gene Mutations in Vietnam
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HRP0082P3-D3-735

Metabolic Control in a Pediatric Population with Type 1 Diabetes Mellitus
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HRP0082P3-D2-740

Continuous Glucose Monitoring System in the Diagnosis of Early Glycemic Abnormalities in High-Risk Groups
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Abstract PDF
HRP0082P3-D2-741

Incidence of Dyslipidemia and its Association with Glycemic Control in Adolescents and Young Adults with Type 1 Diabetes
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Abstract PDF
HRP0082P3-D2-744

Nine-Year-Old Boy with Wolfram Syndrome: Case Report
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HRP0082P3-D2-746

Current Status of Diabetes Management, Glycemic Control and Complications in Children and Adolescents with Diabetes: a Registry-Based Study in Egypt: Where Do We Stand Now? and Where Do We Go from Here?
Direct

Abstract PDF
HRP0082P3-D3-749

Hyperglycemia: MODY: a Diagnosis to Remember
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Abstract PDF
HRP0082P3-D3-751

Continuous Glucose Monitoring vs Oral Glucose Tolerance Test and HbA1C in the Evaluation of Glycemic Abnormalities in an Obese Adolescent Before vs After Partial Gastrectomy
Direct

Abstract PDF
HRP0082P3-D3-752

The Psychological Impact of Diabetes on Glycaemic Control in Affected Saudi Children at Different Developmental Age Groups
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HRP0082P3-D3-753

Type 1 Diabetes Mellitus in Pediatric Population: Chronic Complications and Associated Diseases
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Abstract PDF
HRP0082P3-D3-759

Diabetes Mellitus Type 2 in Pediatrics: an Emerging Reality in Our Country: First Described in Spain
Direct

Abstract PDF
HRP0082P3-D1-760

Association of Ghrelin Gene Polymorphisms with Obesity in Japanese Children
Direct

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HRP0082P3-D1-762

A Rare Case of Sea-Blue Histiocytosis Associated with Niemann-Pick Disease Type B in a 8-year and 9-month Old Boy with Hypertension
Direct

Abstract PDF
HRP0082P3-D1-765

The Relation of Serum Leptin and Soluble Leptin Receptor Levels with Metabolic and Clinical Parameters in Obese and Healthy Children
Direct

Abstract PDF
HRP0082P3-D1-766

Positive Association of Pro-Oxidative Stress Markers with Adipose Mass in Pre- and Early-Pubertal Boys
Direct

Abstract PDF
HRP0082P3-D1-769

The Importance of Weight for Height for Prediction of Metabolic Syndrome in Obese Children and Adolescents: Impact of Gender and Pubertal Status
Direct

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HRP0082P3-D2-773

Trends in Obesity Prevalence and BMI among Pre-Pubertal Bulgarian Children, 1990-2007
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Abstract PDF
HRP0082P3-D2-774

The Prevalence of 25-Hydroxyvitamin D Insufficiency and Deficiency Among Overweight and Obese Children and Adolescents in Greece
Direct

Abstract PDF
HRP0082P3-D2-776

Prevalence of Dyslipidemia and Associated Factors Among Obese Turkish Children
Direct

Abstract PDF
HRP0082P3-D3-789

Bone Age Advancement in Prepubertal Children with Overweight and Obesity
Direct

Abstract PDF
HRP0082P3-D3-790

Obesity Correlates in Adolescence
Direct

Abstract PDF
HRP0082P3-D3-793

Prevalence of Abnormalities of Glucose Metabolism in Obese Greek Children and Adolescents
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Abstract PDF
HRP0082P3-D3-796

Prevalence of Overweight and Obesity in Children and Adolescents at Public and Private Schools from Uberaba Brazil
Direct

Abstract PDF
HRP0082P3-D3-799

Effects of GNRH Analogue Treatment on Internal Genitales of Girls with Central Precocious
Direct

Abstract PDF
HRP0082P3-D3-803

Menstrual Regularity Among Early Menarche Girls and CPP or EFP Girls Treated with GnRHa
Direct

Abstract PDF
HRP0082P3-D3-804

Complete Blood Count Parameters in Girls with Polycystic Ovary Syndrome
Direct

Abstract PDF
HRP0082P3-D3-805

The Genotypic and Phenotypic Variability of Mixed Gonadal Dysgenesis
Direct

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HRP0082P3-D3-806

A Rare Cause for 46,XX Ovarian Dysgenesis: Perrault Syndrome
Direct

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HRP0082P3-D3-807

A Rare Cause of Ovarian Failure; Ovarioleucodystrophy
Direct

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HRP0082P3-D3-809

Three Siblings with Gonadal Dysgenesis
Direct

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HRP0082P3-D1-811

A Novel GHR Mutation, c.439+1g[gt]a; in a Family with Laron Syndrome
Direct

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HRP0082P3-D1-812

Maternal Inheritance of an Heterozygous Exon 4 IGF1 Gene Mutation (g.65941 G[gt]A) in an IUGR Child with Mild Post Natal Growth Retardation
Direct

Abstract PDF
HRP0082P3-D1-814

A Novel GH1 Functional Mutation in a Family with Isolated GH Deficiency
Direct

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HRP0082P3-D1-816

The Level and Conformation of Blood Plasma Carotenoids in Girls with Turner Syndrome After 1 Year of GH Therapy
Direct

Abstract PDF
HRP0082P3-D1-817

Increased Required Dose of GH in Children with Inborn Panhypopituitarism
Direct

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HRP0082P3-D1-818

Assessment of Compliance with GH Therapy
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Abstract PDF
HRP0082P3-D1-819

Body Composition in GH Deficient Children: Effects of GH Therapy and Comparison Between DXA and Anthropometric Data
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Abstract PDF
HRP0082P3-D1-820

Socioeconomic Factors Influence rhGH Treatment Adherence and its Response in Children
Direct

Abstract PDF
HRP0082P3-D1-822

Auxological Evaluation of 'Non-Identical Twins'
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Abstract PDF
HRP0082P3-D2-824

GH Deficiency in a Case with Neurofibromatosis-Noonan Syndrome
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HRP0082P3-D2-825

Monitoring of GH Treatment by the Electronic Auto-Injection Device Easypod[trade] Allows to Improve the Outcome and Maximize Adherence in Patients with Generally High Adherence Rates
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Abstract PDF
HRP0082P3-D2-826

Usability and Safety of FlexPro[reg] PenMate[reg] in Patients, Caregivers and Healthcare Professionals (HCPs)
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HRP0082P3-D2-828

Growth Response After 1 Year of GH Treatment in Children Born Small for Gestational (SGA) Without GH Deficiency: our Experience
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HRP0082P3-D2-830

Prader-Willi Syndrome and GH Therapy: valuable Effects and Adverse Events
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HRP0082P3-D2-831

Recovery of Central Fever After GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury
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HRP0082P3-D2-833

GH Treatment in 50 Child with Short Stature: Lebanese Experience
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HRP0082P3-D3-836

What is the Profile of Gigantism: Seven Observations
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HRP0082P3-D3-839

A Rare Syndrome Benefits from GH Therapy: Hypotonia-Cystinuria Syndrome
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HRP0082P3-D3-841

Study of the Effect of GH Treatment on Growth in Patients Affected by the Inherited Metabolic Disease Methylmalonic Acidemia
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HRP0082P3-D3-843

Two Years of GH Therapy in Children with Growth Deficiency
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HRP0082P3-D3-846

Design and Recruitment of a Longitudinal Cohort Study of Growth and Puberty in Russian Boys
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HRP0082P3-D3-848

Severe Short Stature with Features of Achondroplasia, Later Diagnosed as Panhypopituitarism: a Case Report
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HRP0082P3-D2-850

A Follow-up Study up to Adult Height of the Patients Included in the Phase iii Clinical Trial with the Biosimilar Human Recombinant GH (omnitrope®) on the Treatment of Spanish Children with GH Deficit
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HRP0082P3-D2-851

Growth pattern of the nigerian child compared to international references
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HRP0082P3-D2-853

Switching From the Original to the Biosimilar Recombinant Human GH - Omnitrope[reg]: an Experience of a Single Paediatric Centre in Spain
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HRP0082P3-D2-855

Effect of Cyanotic and Acyanotic Congenital Heart Disease on Placental and Birth Size
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HRP0082P3-D2-856

Anthropometric Evaluation of a Cohort of School-Aged Children: the Need for National Growth References in Romania
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HRP0082P3-D3-867

The Effect of GH and Pubertal Induction Therapy in Turner Syndrome
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Abstract PDF
HRP0082P3-D1-874

Clinical Characteristics and Phenotype-Genotype Analysis in Turkish Patients with Congenital Hyperinsulinism; Predominance of Recessive KATP Channel Mutations
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HRP0082P3-D1-875

Clinical Remission in a Patient with Congenital Hyperinsulinism due to Paternally Inherited Two Novel Mutations in KCJN11 Gene
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HRP0082P3-D1-881

A Case of Hyperinsulinism/Hyperammonemia Syndrome
Direct

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HRP0082P3-D1-882

Project Episga: PreMeb Presentation, Subject Recruitment, and Initial Data
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HRP0082P3-D1-884

Gender Differences in Sex Steroids and IGF1 at Birth and at 5 Years of Age
Direct

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HRP0082P3-D1-885

Neonatal Seizures Neonatal due to Hypocalcemia Secondary to Maternal Vitamin D Deficiency
Direct

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HRP0082P3-D2-889

Evolution and Epidemiological Assessment of the Influence of Sociological Variables of Children Born SGA in the Last Decade in Basque Country
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HRP0082P3-D2-890

A Novel Mutation Causing Pseudohypoaldosteronsim
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HRP0082P3-D2-892

Subcutaneous Fat Necrosis Causing Prolonged Hypercalcaemia in a Neonate: an Unusual Case
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HRP0082P3-D2-894

Relationship of Birth Gestational Age with IGF Binding Protein 3 Beyond Influences of Gender, Small-For-Gestational-Age Status, Caesarean Section, Caloric Intake, Parenteral Nutirtion, and Predominant Breast Milk Feeding in the Not-Life Threatened Newborn: Relevance of Not-Brain-Related Birth Body Weight
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HRP0082P3-D2-895

Relationship of Birth Gestational Age with the Ratio between IGF2 and IGF Binding Protein 3 in Blood Serum Beyond Influences of Gender, Small-For-Gestational-Age Status, Caesarean Section, Caloric Intake, and Predominant Breast Milk Feeding in the Not-Life-Threatened Newborn: Relevance of Parenteral Nutrition
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HRP0082P3-D2-897

Transient Neonatal Diabetes Mellitus: New Case
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HRP0082P3-D1-902

A Case of Congenital Isolated ACTH Deficiency due to tbx19 Gene Mutation
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HRP0082P3-D1-903

Xanthogranulomatous Hypophysitis: a Rare but Mistaken Pituitary Lesion
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HRP0082P3-D1-904

Long-Term Endocrinological Follow-Up in Diencephalic Syndrome
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HRP0082P3-D1-905

Key-Role of TSH Deficiency in Disclosing Craniopharyngioma Diagnosis in a Short Girl with Hashimoto's Thyroiditis
Direct

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HRP0082P3-D1-906

Pituitary Dysfunctiona with Associated Lesions in the Hypothalamo-Pituitary Region: Histiocytosis or Dysgerminoma?
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HRP0082P3-D1-907

A Case of Combined Pituitary Hormone Deficiency in a Patient Affected by Osteogenesis Imperfecta
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HRP0082P3-D1-911

Primary Polydipsia in a Family with Mutation in the AVP Gene and Proven Central Diabetes Insipidus
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HRP0082P3-D3-912

Screening for SOX2 Mutations in Bulgarian Patients with Congenital Hyposomatotropism: First Results
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HRP0082P3-D3-920

A Case of Hypopituitarism Caused by Traumatic Brain Injury in Infancy
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HRP0082P3-D3-923

Think Histiocytosis X Facing Insipidus Diabetes with Thickened Pituitary Stalk
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HRP0082P3-D1-925

The Timing and Evolution of Puberty in a Sample of School-Aged Children in a Brazilian City
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HRP0082P3-D1-926

The Significance of GnRH Stimulation Test, Leptin, and Pelvic Ultrasound Findings for Differentiating Idiopathic Central Precocious Puberty from Premature Telarche
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HRP0082P3-D1-927

Basal LH Combined with the Tanner Stage of Breast Development can Predict the Gonadotropin Response Following GnRH Stimulation Test
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HRP0082P3-D1-932

Idiopathic Hypogonadotropic Hypogonadism due to a GNRH1 Mutation
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HRP0082P3-D1-933

Effect on BMI of GnRH Analogue Treatment in Central Precocious Puberty or Early and Fast Puberty Girls
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HRP0082P3-D1-934

An Unusual Combination of Premature Ovarian Failure and a History of GNRH Treatment for Idiopathic Precocious Puberty
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HRP0082P3-D1-936

Association of Van Wyk Grumbach and Debre Semelaigne Syndromes in Two Cases with Severe Hypothroidism
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HRP0082P3-D3-938

Hyperandrogenism Doesn't Increase the Insulin Resistance in Overweight and Obese Adolescent Girls with Polycystic Ovary Syndrome
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HRP0082P3-D3-941

A Rare Cause of Peripheric Precocious Puberty: Adrenocortical Tumor
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HRP0082P3-D3-947

The Etiology of Central Precocious Puberty and Effect of GnRH Agonist for 2 years in Korean Boys
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HRP0082P3-D3-948

Hypothalamic Hamartoma as a Cause of Central Precocious Puberty in 4.5-Year-Old Girl: Case Report
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HRP0082P3-D3-949

The Perception of Body Image and Self-Esteem in Girls with Precocious Puberty, Being Treatment with GnRH Analogue
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HRP0082P3-D1-954

46,XX DSD: Bilateral Ovotestis with SOX9
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HRP0082P3-D1-955

Severe Undervirilisation in a 46,XY Case due to a Novel Mutation in HSD17B3 Gene
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HRP0082P3-D1-957

5[alpha]-Steroid Reductase 2 Deficiency in a Large Family
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HRP0082P3-D1-960

Clinical Characteristics of 30 Patients with 45,X/46,XY Mosaicism
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HRP0082P3-D1-961

Three Siblings Extremely Androgen Insensitivity Syndrome Due to an AR Mutation with Differing Phenotypes
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HRP0082P3-D2-963

Hypospadias in a Male Patient with 21-Hydroxylase Deficiency and Atypical Clinical Course: Presentation of Two Brothers
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HRP0082P3-D2-964

An Ovulating Testis
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HRP0082P3-D2-965

Mosaicism Ratios of 45,X to 46,X IdicY Explained a Phenotype in a Case with Mixed Gonadal Dysgenesis
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HRP0082P3-D2-966

A Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation
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HRP0082P3-D2-967

Phenotypic and Genotypic Variability of Patients with 5-[alpha] Reductase Type 2 Deficiency
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HRP0082P3-D2-968

The Novel Mutation in the Steroidogenic Acute Regulatory Protein in 46,XY Case with Adrenal Insufficiency and Complete Sex Reversal
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HRP0082P3-D2-969

A Challenging Diagnosis in Three 46,XY Females from Two Related Families
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HRP0082P3-D2-970

A Familial Case of Complete Androgen Insensitivity Syndrome
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HRP0082P3-D2-971

A Case of 46,Y,dup(x)(p21.2p22.2) DSD Caused by Overexpressed DAX1
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HRP0082P3-D1-974

Increasing Incidence of Congenital Hypothyroidism in Neonatal Screening Program in Central Serbia: 30 Years of Experience
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HRP0082P3-D1-975

Prevalence of Additional Autoimmune Diseases in Autoimmune's Thyroiditis Children and Their First- and Second-Degree Relatives: Results from a Large, Single-Center Study
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HRP0082P3-D1-976

Adiposity and Pubertal Status Effects on Thyroid Function in Overweight Children and Adolescents
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HRP0082P3-D1-977

Neonatal Thyrotoxicosis in Maternal Grave's Disease: a Case Series and Review of the Literature
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HRP0082P3-D1-978

Treatment the Resistance to Thyroid Hormones in Girl
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Abstract PDF
HRP0082P3-D1-981

Kocher-Debre-Semelaigne Syndrome with Rhabdomyolysis and Increased Creatinine: a Case Report
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HRP0082P3-D1-982

Preliminary Result and Normative TSH Values for Healthy Nigerian Newborn Children
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HRP0082P3-D1-984

Thyroid Disorders After Oncologic Treatment in Children
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HRP0082P3-D2-988

Thyrotoxicosis in Childhood and Adolescents
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HRP0082P3-D2-991

Missed Cases of Congenital Hypothyroidism Detected By Screening Program in Central Serbia (1983-2014)
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HRP0082P3-D2-993

Raised Free Thyroxine Levels in a Boy with Hypertension
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HRP0082P3-D2-994

The Evaluation of Transient Hypothyroidism in Patients Diagnosed with Congenital Hypothyroidism
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HRP0082P3-D2-1000

Changes of Laboratory Findings Before and After Thyroid Hormone Replacement in a Naive 19.24 Year-Old Female Case of Ectopic Thyroid
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HRP0082LBP-D3-1002

Pseudoexon Activation in Nicotinamide Nucleotide Transhydrogenase in Two Siblings with Familial Glucocorticoid Deficiency
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HRP0082LBP-D3-1005

A 2-Year Multi-Centre, Open Label, Randomized Two Arm Study of Genotropin Treatment in Very Young Children Born Small for Gestational Age: Early Growth and Neurodevelopment
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HRP0082LBP-D3-1008

Long-Term Impact of Childhood-Onset Type 1 Diabetes: Social Insertion, Quality of Life, Sexuality
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HRP0082LBP-D3-1010

Effect of Triptorelin 3.75 mg Subcutaneously Injection Every 6 Weeks on Adult Height in Girls with Idiopathic Central Precocious Puberty
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HRP0082LBP-D3-1012

Total and Acylated Ghrelin Levels in Children and Adolescents with Growth Retardation
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HRP0082LBP-D3-1013

Copy Number Determination of CYP21A2 Gene Supplements the Molecular Biological Analysis of Hungarian Patients with 21-Hydroxylase Deficiency
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ESPE Abstracts

53rd Annual ESPE (ESPE 2014)

EPosters

BiosciAbstracts