Abstracts | 0082 | ESPE2014 | 53rd Annual ESPE (ESPE 2014)

Scientific Programme, ePosters & Abstracts

Volume 82 | ESPE2014 | Next issue

53rd Annual ESPE (ESPE 2014)

Dublin, Ireland
18 Sep 2014 - 20 Sep 2014

Dublin, Ireland; 18-20 September 2014. Further information

Plenary Lectures
- Closed-Loop System: Dream or Reality?
- - Closed-Loop System: Dream or Reality?
    
    hrp0082pl1
- Immune-Based Therapies for T1D
- - Learning from Histopathology to Design Novel Immune-Therapies for Type 1 and 2 Diabetes
    
    hrp0082pl2
- Sex, Stem Cells and Decision of Cell Fate
- - Sex, Stem Cells and Decision of Cell Fate
    
    hrp0082pl3
- Gene Therapy
- - Gene Therapy
    
    hrp0082pl4
- Obesity: Novel Treatments and the Imperative for Prevention
- - Obesity: Novel Treatments and the Imperative for Prevention
    
    hrp0082pl5
- Genetics of Obesity
- - Making a Diagnosis in Severe Complex Obesity
    
    hrp0082pl6
Symposia
- Disorders of Gsalpha Signaling
- - Pseudohypoparathyroidism
    
    hrp0082s1.1
  - McCune-Albright Syndrome
    
    hrp0082s1.2
  - New Therapies in Metabolic Bone Disease: PTH
    
    hrp0082s1.3
- Endocrine Cancer Syndromes: An Update
- - PTEN: A Gene Involved in Overgrowth and Cancer
    
    hrp0082s2.1
  - MEN1 in Children and Adolescents
    
    hrp0082s2.2
  - DICER1 Syndrome: A Review of the Syndrome with a Focus on Endocrine Aspects
    
    hrp0082s2.3
- Novel Insights into Monogenic Diabetes
- - Differential Diagnosis of Monogenic Diabetes
    
    hrp0082s3.1
  - Neonatal Diabetes: New Genes, New Mechanisim, New Phenotypes
    
    hrp0082s3.2
  - Epidemiology of Monogenic Diabetes
    
    hrp0082s3.3
- Recent Advances in Our Understanding of Hypothyroidism
- - Management of Central Hypothyroidism
    
    hrp0082s4.1
  - Novel Role(s) for Immunoglobulin Superfamily, Member 1 (IGSF1) in the Hypothalamic-Pituitary-Thyroid Axis
    
    hrp0082s4.2
  - Novel Insights into Thyroid Hormone Resistance
    
    hrp0082s4.3
- Novel Insights into Hypoadrenalism
- - Aetiology of Congenital Hypoadrenalism
    
    hrp0082s5.1
  - Adrenarche: Coming of Age in the Era of Genomics and Metabolomics
    
    hrp0082s5.2
  - CAH: Health Status in Adults (CaHASE)
    
    hrp0082s5.3
- New Concepts in the Gonadotropic Axis
- - Roles of Hypothalamic microRNAs in the Regulation of Puberty
    
    hrp0082s6.1
  - New Syndromes Resulting in Secretory Pathway and Gonadotropic Axis Regulation Defects
    
    hrp0082s6.2
  - Genetic Dissection of Puberty in Mice
    
    hrp0082s6.3
- Controversies in the Surgical Management of DSD
- - Evolution of Feminising Genitoplasty
    
    hrp0082s7.1
  - Pros and Cons of Early or Late Feminising Genitoplasty
    
    hrp0082s7.2
  - Masculinising Genitoplasty
    
    hrp0082s7.3
- Novel Therapies in Paediatric Endocrinology
- - Novel Therapies Used in the Management of Congenital Hyperinsulinism
    
    hrp0082s8.1
  - Treatment of Hypophosphatasia
    
    hrp0082s8.2
  - Congenital Adrenal Hyperplasia
    
    hrp0082s8.3
- Novel Insights into Pituitary Development and Function
- - Visualizing Cell-Cell Communication Within and Between Pituitary Cell Networks
    
    hrp0082s9.1
  - Sox2+ve cells in the adult murine pituitary are stem cells with tumour-inducing potential
    
    hrp0082s9.2
  - Pax7 Dictates Alternate Pituitary Cell Fates During Development
    
    hrp0082s9.3
- Childhood Obesity: Challenges in Management
- - The Metabolically Healthy Obese Child
    
    hrp0082s10.1
  - Childhood and Adolescent Obesity: Can Treatment Response be Predicted?
    
    hrp0082s10.2
  - Natural Course of Impaired Glucose Tolerance in Obese Children
    
    hrp0082s10.3
New Perspectives
- Micro-RNAs in Health and Diseases
- - Non Coding RNA's: Introduction to Non-Coding RNAs and the Role of MicroRNAs in GnRH Neurons
    
    hrp0082np1.1
  - The Role of MicroRNAs in Diabetes
    
    hrp0082np1.2
- Regenerative Endocrinology
- - Regenerative Medicine for [beta] Cell Replacement
    
    hrp0082np2.1
  - Formation of a Thyroid Gland from Embryonic Stem Cells
    
    hrp0082np2.2
Prize Winners
- Deciphering the functional mechanisms by which MKRN3 regulates puberty initiation
- - Deciphering the Functional Mechanisms by which MKRN3 Regulates Puberty Initiation
    
    hrp0082ha1
- Pubertal onset in girls is strongly influenced by genetic variation in promoters affecting FSH action
- - Pubertal Onset in Girls is Strongly Influenced by Genetic Variation in Promoters Affecting FSH Action
    
    hrp0082ha2
Working Groups
- Bone & Growth Plate
- - Unravelling GH Actions on the Growth Plate and its Promotion of Linear Growth
    
    hrp0082wg1.1
  - The Effect of Stimulatory G Proteins on Differentiation within the Growth Plate
    
    hrp0082wg1.2
  - New Therapies in Metabolic Bone Disease: Denusomab
    
    hrp0082wg1.3
  - Abstract unavailable
    
    hrp0082wg1.4
- Global paediatric Endocrinology and Diabetes
- - Technological Horizon for the Treatment of Diabetes
    
    hrp0082wg2.1
  - Non-Insulin Glucoregulatory Therapy for Type 1 Diabetes
    
    hrp0082wg2.2
  - Debate: Should all Newly Diagnosed Patients with Diabetes Need to be Hospitalised?
    
    hrp0082wg2.3
  - Debate: Sensor/Pump Therapy from the Onset of Diabetes?
    
    hrp0082wg2.4
  - Debate: do we Need Long Acting Insulin Analogs?
    
    hrp0082wg2.5
  - Early Implementation of Insulin Pump Therapy after Diabetes Onset: is There Added Benefit?
    
    hrp0082wg2.6
  - Long Acting Insulin: Friend or Foe?
    
    hrp0082wg2.7
  - Abstract unavailable
    
    hrp0082wg2.8
- DSD
- - Genetic Variation in Human SF-1 (NR5A1): Clinical Consequences for Individuals, Families and Populations
    
    hrp0082wg3.1
  - The Potential Role of the Alternative 'Backdoor' Pathway for Androgen Synthesis and Virilisation in CAH
    
    hrp0082wg3.2
  - Long-term Outcome of Prenatal CAH Therapy
    
    hrp0082wg3.3
  - Detailed Phenotyping of DSD: External Virilisation
    
    hrp0082wg3.4
  - Imaging of the Urogenital Tract
    
    hrp0082wg3.5
  - I-DSD and I-CAH Registry Update
    
    hrp0082wg3.6
  - DSD-Life: Clinical European Study on the Outcome of DSD
    
    hrp0082wg3.7
  - DSDnet: a COST Action on the Systematic Elucidation of Differences of Sex Development
    
    hrp0082wg3.8
- Obesity
- - Abstract unavailable
    
    hrp0082wg4.1
  - Natural Course of Impaired Glucose Tolerance in Obese Children
    
    hrp0082wg4.2
  - Abstract unavailable
    
    hrp0082wg4.3
- Paediatric and adolescent gynaecology
- - New Markers of Ovarian Function in Girls
    
    hrp0082wg5.1
  - Amenorrhea and Hypothalamic-Pituitary Dysfunction
    
    hrp0082wg5.2
  - Abstract unavailable
    
    hrp0082wg5.3
  - Abstract unavailable
    
    hrp0082wg5.4
  - Contraception in Adolescence from a Public Health Perspective
    
    hrp0082wg5.5
  - Contraception in Adolescence: Current Options
    
    hrp0082wg5.6
  - Lessons Drawn from Rare Gynaecological Disorders in Relation with Ovarian Malfunction
    
    hrp0082wg5.7
- Turner
- - Liver Involvement in Tuner Syndrome
    
    hrp0082wg6.1
  - Abstract unavailable
    
    hrp0082wg6.2
  - Abstract unavailable
    
    hrp0082wg6.3
  - Motor Performance in Turner Syndrome
    
    hrp0082wg6.4
- Nurses
- - Quality of Life and Anxiety in Adolescents with Differentiated Thyroid Cancer
    
    hrp0082wg7.1
  - Evolving GH Therapy Patient Training in a Digital World
    
    hrp0082wg7.2
  - Endocrine Nursing, Social Media, and Research: Results of an International Study
    
    hrp0082wg7.3
- GPED
- - Global Pediatric Endocrinology and Diabetes: Opportunities and Call for Membership Involvement
    
    hrp0082wg8.1
  - Management of Type 1 Diabetes Mellitus in Sudanese Children: Can We Implement International Guidelines?
    
    hrp0082wg8.2
  - Global Inequalities: Limited OI Treatment Options in Indonesia
    
    hrp0082wg8.3
  - Inequities of Treatment Options in Developing Countries: Congenital Adrenal Hyperplasia
    
    hrp0082wg8.4
  - Congenital Hypothyroidism Screening Program: the Costa Rican Experience
    
    hrp0082wg8.5
  - Neonatal Screening for Congenital Hypothyroidism in Ghana: Don't Take it for Granted!
    
    hrp0082wg8.6
  - Abstract unavailable
    
    hrp0082wg8.7
Free Communications
- Adrenal
- - Molecular mechanisms of nongenomic glucocorticoid actions: the role of human glucocorticoid receptor S-palmitoylation
    
    hrp0082fc1.1
  - Clinical Phenotype of Patients with MCM4 Mutation Suggests Pubertal Delay in Males in Addition to Adrenal Failure, Absent Adrenarche, and Short Stature in Boys and Girls
    
    hrp0082fc1.2
  - Genetic Engineering Using TALENs to Study the Redox Regulation of Steroidogenesis in vivo
    
    hrp0082fc1.3
  - A Novel Non-Invasive Short Synacthen Test
    
    hrp0082fc1.4
  - Antenatal Glucocorticoid Treatment and Polymorphisms in Glucocorticoid and Mineralocorticoid Receptor Genes are Associated with Long-Term Neurodevelopmental Outcomes in Preterm Survivors
    
    hrp0082fc1.5
  - Molecular Characterization of Testicular Adrenal Rest Tumours in Congenital Adrenal Hyperplasia; Lesions with both Adrenocortical and Leydig Cell Features
    
    hrp0082fc1.6
- Bone & Mineral
- - Asfotase Alfa: Sustained Improved Growth and Function with Extended Treatment in Children with Hypophosphatasia
    
    hrp0082fc2.1
  - Hypophosphatasia: Gross Motor Function and Height Improvement in Infants and Young Children Treated with Asfotase Alfa for up to 3 Years
    
    hrp0082fc2.2
  - Calcium Homeostasis in Adolescents with [beta]-Thalassemia Major: Effect of i.m. Injection of a Megadose of Cholecalciferol
    
    hrp0082fc2.3
  - Fractures in Children with Chronic Inflammatory and/or Disabling Conditions: the SNAP Study
    
    hrp0082fc2.4
  - Pharmacokinetics and Pharmacodynamics of a Human Monoclonal Anti-Fibroblast Growth Factor 23 Antibody (KRN23) Following 4 Month Intra-Dose Escalation in Adults with X-Linked Hypophosphatemia
    
    hrp0082fc2.5
  - Efficacy and Safety Following 4 Monthly s.c. Doses of a Human Anti-Fibroblast Growth Factor 23 Antibody (KRN23) in Adults with X-linked Hypophosphatemia
    
    hrp0082fc2.6
- Diabetes
- - High Mobility Group Box-1 Serum Concentrations Increase at Onset of Diabetes in Cystic Fibrosis Patients
    
    hrp0082fc3.1
  - HbA1c Level as a Predictive Marker of Progression to Clinical Diabetes
    
    hrp0082fc3.2
  - Improved Hepatic Insulin Sensitivity in Children Randomized to CSII Treatment from Onset of Type 1 Diabetes
    
    hrp0082fc3.3
  - Genetics of Paediatric Type 2 Diabetes: ABCC8 Mutation in Obesity-Associated Insulin Secretion Defects
    
    hrp0082fc3.4
  - Pancreatic N-Methyl-D-Aspartate Receptors as Novel Drug Targets for The Treatment of Diabetes Mellitus
    
    hrp0082fc3.5
  - Alpha-Lipoic Acid and Anti-Oxidant Diet Helps to Improve Endothelial Dysfunction in Children and Adolescents with Type 1 Diabetes
    
    hrp0082fc3.6
- Growth
- - Heterozygous IGF1R Mutations Represent a Frequent Finding in Patients with Pre- and/or Postnatal Proportional Undergrowth and Low, Normal or Supranormal IGF1
    
    hrp0082fc4.1
  - The Effect of grB10-Deficiency in Zebrafish: A Translational Animal Model to Study Human Growth
    
    hrp0082fc4.2
  - Oscillations in Gene Expression Profiles Across Childhood Highlight the Relation of Growth and Specific Metabolic Functions in Both Sexes
    
    hrp0082fc4.3
  - Short Stature, Accelerated Bone Maturation, and Early Growth Cessation due to Heterozygous Aggrecan Mutations
    
    hrp0082fc4.4
  - Fetal and Postnatal Growth in Turner Syndrome and their Associations with the Dosage Effects of the X-Linked Gene: a Cross-Sectional Data Base Analysis of the French National Rare Disease Network
    
    hrp0082fc4.5
  - Longitudinal Growth of Finnish Children With Gestational Diabetes in Mothers
    
    hrp0082fc4.6
- Neuroendocrinology
- - Derivation of GnRH Neuron-Like Cells from Human Embryonic Stem Cell-Derived Neural Crest Progenitors
    
    hrp0082fc5.1
  - Mutations in the Maternally Imprinted Gene MKRN3 are a Frequent Cause of Familial Central Precocious Puberty
    
    hrp0082fc5.2
  - Loss of Function Mutations in pnpla6 Cause Hypogonadotropic Hypogonadism due to Impaired LH Release from Pituitary Gonadotropes
    
    hrp0082fc5.3
  - Reference Values for Urinary Gonadotropins in Preterm and Full-Term Infants in 'Minipuberty'
    
    hrp0082fc5.4
  - Characterization of IGFI Receptor Expression and Localization in Paediatric Gliomas Upon Diagnosis According to WHO 2007 Grading
    
    hrp0082fc5.5
  - The Diencephalic Syndrome of Emaciation in Infantile Hypothalamochiasmatic Low-Grade Gliomas : a Retrospective Case-Control Study of Diagnostic Parameters and Long-Term Outcomes Over 30 Years of Follow-Up
    
    hrp0082fc5.6
- Gonads & DSD
- - Search for Genetic Defects in the Transcription Factor Genes FOXL2, FOXE1, BMP15, NOBOX, and GDF9 in Children, Adolescents and Young Adults With Premature Ovarian Insufficiency POI
    
    hrp0082fc6.1
  - Next Generation Sequencing of the Androgen Receptor Gene in Patients With Androgen Insensitivity Syndrome and Controls
    
    hrp0082fc6.2
  - LRH1 Rescues SF1 Deficiency for Steroidogenesis in vitro but Cannot Explain the Broad Phenotype of SF1 Deficiency in men
    
    hrp0082fc6.3
  - Familial 46,XY Complete Female External Sex Development and Primary Amenorrhea Along with Hidden Gonad Tumors, Secondary to a Novel p.met64val SRY Gene Mutation
    
    hrp0082fc6.4
  - Serum Levels of AMH Reflect Ovarian Morphology by MRI in 109 Healthy Peripubertal Girls
    
    hrp0082fc6.5
  - Effects of Exposure to the Endocrine disruptor di(n-butyl) Phthalate on Testicular Dysgenesis Fetal Germ Cell Development in the Rat and in Human Fetal Testis
    
    hrp0082fc6.6
- Growth promoting therapies
- - Genetic Markers of Insulin Resistance are Associated with GH Response in Short SGA Children: the North European SGA Study
    
    hrp0082fc7.1
  - The rs1024531 GRB10 Promoter Polymorphism is Associated with Response to GH Therapy in Patients with GH Deficiency: Validation by in vitro Functional Analysis
    
    hrp0082fc7.2
  - Gene Expression Networks Associated with Changes in Serum Markers of Metabolism and Growth in GH-Treated Children with GH Deficiency
    
    hrp0082fc7.3
  - A Decade of Clinical Experience in a Swedish University Centre Using Prediction Models to Optimize GH Treatment in Prepubertal Children
    
    hrp0082fc7.4
  - Impact of GH on Adult Bone Quality in Turner Syndrome: a High Resolution Peripheral Quantitative Computed Tomography Study
    
    hrp0082fc7.5
  - Topicon[trade]ThermoMatrix[trade]-Mediated Passive Transdermal Delivery of Human GH (hGH) Across EpidermFT[trade] Full-Thickness Human Skin Equivalent (HSE): Towards an Extended-Wear hGH Patch
    
    hrp0082fc7.6
- Fat Metabolism
- - Activation of the ER Stress Response in Cultured Human Umbilical Vein Endothelial Cells by Plasma Obtained from Prepubertal Obese Children
    
    hrp0082fc8.1
  - MicroRNA-152 Promotes Hepatic Steatosis by Suppressing the Wnt Signaling Pathway
    
    hrp0082fc8.2
  - Identification of Death Ligand TNF-Related Apoptosis-Inducing Ligand as a Potent Mitogen in Human Preadipocytes
    
    hrp0082fc8.3
  - CREB-Regulated Transcription Coactivator 3: a New Adipokine Related to Childhood Obesity
    
    hrp0082fc8.4
  - Putative Gain-of-Function in Rats Carrying the Ghsr Q343X Mutation
    
    hrp0082fc8.5
  - A Novel Missense Variant in the Insulin Receptor Gene in Three Unrelated Irish Families with Severe Insulin Resistance Syndrome: Evidence for an Irish Founder Effect
    
    hrp0082fc8.6
- Beta cells
- - Inappropriately High Rates of Cell Proliferation in Diffuse Congenital Hyperinsulinism are Linked to Nuclear Expression of CDK6
    
    hrp0082fc9.1
  - Characterising the Immunohistochemical Expression of Dipeptidyl Peptidase-4 in Pancreatic Tissue from Patients with Diffuse and Focal Congenital Hyperinsulinism
    
    hrp0082fc9.2
  - In Search for New Monogenic Diabetes Genes: PCBD1
    
    hrp0082fc9.3
  - Clinical Characteristics and Molecular Genetics Analysis of 20 Patients with Neonatal Diabetes Mellitus from a Single Centre of the South-Eastern Region of Turkey
    
    hrp0082fc9.4
  - Transient Neonatal Diabetes in Adulthood: Metabolic and Neurodevelopmental Outcomes
    
    hrp0082fc9.5
  - Sulfonylurea Therapy Corrects Hypotonia, Attention Deficits, Improves Complex Neuropsychological Functions and Motricity in Patients with Neonatal Diabetes Secondary to Mutation in Potassium Channel Subunits, Through a CNS Effect
    
    hrp0082fc9.6
- Programming & Early Endocrinology
- - A Role for Delta-Like Homologue 1 in a Secretory Placental Population and Implications for Foetal Growth
    
    hrp0082fc10.1
  - Stk11 Expression in Adipose Tissue Following Fetal Growth Restriction: Relation to Catch-Up Growth and Visceral Fat Mass
    
    hrp0082fc10.2
  - Genetic and Epigenetic Defects at the GNAS Locus Lead to Opposite Patterns of Fetal and Postnatal Growth
    
    hrp0082fc10.3
  - Influence of Newborn and Maternal Factors on Neonatal Body Composition
    
    hrp0082fc10.4
  - Contrasting Associations of Maternal Smoking and Alcohol Intake in Late Pregnancy and Offspring Body Composition in Childhood
    
    hrp0082fc10.5
  - The PremAldo Study: Impaired Aldosterone Signaling Worsens Renal Sodium Loss in Preterm Infants
    
    hrp0082fc10.6
- Pituitary
- - Abnormal Sonic Hedgehog Signalling in Adamantinomatous Craniopharyngiomas and its Association with CTNNB1/[beta]-Catenin Mutations
    
    hrp0082fc11.1
  - Novel SOX2 Mutation: Identification of New Molecular Mechanisms of SOX2 Action and Interactions
    
    hrp0082fc11.2
  - Early-Onset Central Diabetes Insipidus is Associated with De Novo Arginine Vasopressin-Neurophysin II or Wolfram Syndrome 1 Gene Mutations
    
    hrp0082fc11.3
  - Management of Hyperhydration in a Child with Syndrome of Inappropriate Antidiuretic Hormone Secretion (Siadh) Using a Selective Vasopresin Receptor Agonist
    
    hrp0082fc11.4
  - Endocrine Features of a Large Cohort of Children with Septo-Optic Dysplasia and Congenital Multiple Pituitary Hormonal Deficiencies
    
    hrp0082fc11.5
  - Clinical and Neuroradiological Characteristics in Children and Adolescents with Septo-Optic Dysplasia, Multiple Pituitary Hormone Deficiencies and Optic Nerve Hypoplasia: Experience from a Single Tertiary Centre
    
    hrp0082fc11.6
- Obesity
- - High-Fat Diet Rapidly Triggers Circadian De-Synchronization of Clock Genes, Neuropeptides and Inflammation Mediators in the Hypothalamus of C57BL Mice
    
    hrp0082fc12.1
  - Obesity in Childhood and Adolescence is Associated with Shorter Leucocyte Telomere Length
    
    hrp0082fc12.2
  - Increased Resting Energy Expenditure in Girls with Turner Syndrome
    
    hrp0082fc12.3
  - Pediatric Reference Values for Insulin from oGTT and Prevalence of Hyperinsulinemia in Obese Children
    
    hrp0082fc12.4
  - Low Circulating Levels of DKK-1 Protein in Obese Children Indicate Suppression of Canonical Wnt Signaling
    
    hrp0082fc12.5
  - Resveratrol Inhibits Inflammation-Induced Production of Cytokines in Human Adipocytes
    
    hrp0082fc12.6
- Thyroid
- - Massive Sequencing of Thyroidal Genes Reveals Unexpected Polygenic Defects in Dyshormonogenic Hypothyroidism
    
    hrp0082fc13.1
  - Thyroid Agenesis and Severe Thyroid Hypoplasia Caused by a New Inactivating TSH Receptor Mutation Ala579Val
    
    hrp0082fc13.2
  - Overexpression of Supressor Tumoral PTEN, but not DREAM, was Detected in Multinodular Goiter in Humans
    
    hrp0082fc13.3
  - The Prevalence of Congenital Malformations in Infants with TSH Elevation on Newborn Screening: the Importance of Distinguishing Between True and Transient Congenital Hypothyroidism
    
    hrp0082fc13.4
  - The Ultrastructural Changes in Thyroid Cells in the Course of Damage in Hashimoto's Thyroiditis
    
    hrp0082fc13.5
  - Abnormal Thyroid Hormone Metabolism in Patients with THRA Mutations due to Impaired Expression of the Type 3 Deiodinase
    
    hrp0082fc13.6
- Puberty
- - Brain Structure and Function in Gender Dysphoric Adolescents
    
    hrp0082fc14.1
  - Infancy Growth Rate Predicts Timing of Puberty Both in Girls and Boys
    
    hrp0082fc14.2
  - Novel Genetic Variants in a Cohort of Paediatric and Adolescent Patients with Hypogonadotrophic Hypogonadism and Kallmann Syndrome
    
    hrp0082fc14.3
  - Development of Pubertal Gynaecomastia: a Longitudinal Cohort Study
    
    hrp0082fc14.4
  - Fertility of Women Treated During Childhood for Precocious Puberty with Triptorelin: PREFER Retrospective Study
    
    hrp0082fc14.5
  - Quality of Life in Patients with Congenital Hypogonadotropic Hypogonadism
    
    hrp0082fc14.6
- Late Breaking Abstracts
- - Top Line Results of Once-Weekly, CTP-Modified Human GH (MOD-4023): Phase 2 Dose Finding Study in Children with GH Deficiency
    
    hrp0082fclb1
  - Sonic Hedgehog is Required for Cell Specification of Rathke's Pouch Progenitors During Normal Development and is Over-Expressed in Adamantinomatous Craniopharyngioma
    
    hrp0082fclb2
  - Parent-of-Origin Specific Allelic Associations Among 106 Genomic Loci for Age at Menarche
    
    hrp0082fclb3
  - Does Severity of Hypothyroidism at Birth Contribute to Abnormal Cortical Development among Children with Congenital Hypothyroidism?
    
    hrp0082fclb4
  - CB2 Polymorphism Could Modulate the Relationship Between Childhood Obesity and Age at Menarche
    
    hrp0082fclb5
  - Global Consensus Recommendations on Prevention and Management of Nutritional Rickets
    
    hrp0082fclb6
Poster Presentations
- Adrenals & HP Axis
- - Allelic Frequencies of CYP21A2 Variants and Genotype-Phenotype Correlations in a Cohort of 660 CAH Patients from Germany and Austria
    
    hrp0082p1-d2-1
  - Functional Characterization of a Novel Heterozygous Point Mutation in the Human Glucocorticoid Receptor Gene Causing Primary Generalized Glucocorticoid Resistance
    
    hrp0082p1-d2-2
  - Transient Generalized Glucocorticoid Hypersensitivity: Clinical Manifestations, Endocrinologic Evaluation, and Transcriptomic Profile: the Potential Role of nf-[kappa]b
    
    hrp0082p1-d2-3
  - Mineralo and Glucocorticoid Deficiency in Early Infancy are Caused by a Founder Novel Mutation in the Nicotinamide Nucleotide Transhydrogenase Gene
    
    hrp0082p1-d2-4
  - Carbohydrate Metabolism in Children and Adolescents with Classical Congenital Adrenal Hyperplasia due to 21-Hydoxylase Deficiency
    
    hrp0082p1-d2-5
  - Descriptive Analyses of Turner Syndrome
    
    hrp0082p1-d2-6
  - A Novel Founder Mutation of CYP21A2 in Patients with CAH due to 21-Hydroxylase Deficiency
    
    hrp0082p1-d2-7
  - Normal Value of Steroids in Amniotic Fluid by LC-MS/MS Method
    
    hrp0082p1-d2-8
  - Mast Cells in Human Adrenal Gland During Fetal Development
    
    hrp0082p1-d2-9
  - An Unusual Presentation of Isolated ACTH-Deficiency Secondary to TBX19 Mutation Revealed by Late Onset Hypoglycemia Seizure
    
    hrp0082p1-d2-10
  - Identification of a Novel Large CYP17A1 Deletion by Multiplex Ligation-Dependent Probe Amplification Analysis in Patients with Classic 17-Hydroxylase Deficiency
    
    hrp0082p1-d2-11
- Adrenals & HP Axis (1)
- - Adrenal Rest Tumors in Patients with Primary Adrenal Insufficiency
    
    hrp0082p1-d3-12
  - Assessment of Blood Pressure and Left Ventricular Parameters in Children with Classical CAH-due to 21 Hydroxylase Deficiency
    
    hrp0082p1-d3-13
  - Clinical, Biological and Genetic Characteristics of 48 Pediatric Patients with Micronodular Adrenal Hyperplasia (MAH)
    
    hrp0082p1-d3-14
  - Testicular Adrenal Rest Tumors and Sertoli Cell Function in Adolescents with Cah
    
    hrp0082p1-d3-15
  - A Novel Mutation in Exon 5 of TP53 Gene in a Familial Adrenocortical Carcinoma
    
    hrp0082p1-d3-16
  - Aldosterone/Renin Ratio as Key Player in the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants
    
    hrp0082p1-d3-17
  - Zenhale Inhaled Corticosteroid Therapy: Useful Second Line Therapy for Asthma in Children but be Wary of Adrenal Suppression
    
    hrp0082p1-d3-18
  - Development of Scotland Wide Process for Management of Acute Adrenal Insufficiency
    
    hrp0082p1-d3-19
  - Salivary Cortisol as a Diagnostic Tool of Hypercortisolism in Primary Pigmented Nodular Adrenocortical Disease (ppnad)
    
    hrp0082p1-d3-20
  - How to Interpret Cortisol Responses to Acth in Patients with Non-Classic Congenital Adrenal Hyperplasia
    
    hrp0082p1-d3-21
  - Clinical Utility of Urinary Steroid Metabolite Ratios in Children Undergoing Investigations for Suspected Disorders of Steroid Synthesis
    
    hrp0082p1-d3-22
- Autoimmune Endocrine Disease
- - Analysis of Zinc Transporter ZnT8 Autoantibodies in Children and Adolescents with Autoimmune Thyroid Diseases
    
    hrp0082p1-d2-23
  - Final Height and BMI in English and Italian Adult Survivors of Childhood Acute Lymphoblastic Leukemia Treated without Cranial Radiotherapy
    
    hrp0082p1-d2-24
  - Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy: New Insights into Phenotype and Genotype
    
    hrp0082p1-d2-25
  - Abstract unavailable
    
    hrp0082p1-d2-26
  - Late Endocrine Effects Despite Reduced Intensity Chemotherapy for Bone Marrow Transplantation in Children
    
    hrp0082p1-d2-27
  - Immune Changes are Observed After Radioiodine Treatment for Hyperthyroidism in Graves' Disease Patients
    
    hrp0082p1-d2-28
  - Standard Population Screening for Diabetes Mellitus has Low Sensitivity in Identifying Diabetes in Adult Survivors of Childhood Bone Marrow Transplantation with Total Body Irradiation
    
    hrp0082p1-d2-29
  - Managing Children with Thickened Pituitary Stalk and/or Idiopathic Central Diabetes Insipidus: a Single Centre Experience on 63 Children
    
    hrp0082p1-d2-30
  - Primary Pancreatic Insulinomas: Clinical, Morphological, and Genetic Characteristics of 12 Children
    
    hrp0082p1-d2-31
  - Papillary Thyroid Cancer After Hematopoietic Stem Cell Transplantation in Young Age
    
    hrp0082p1-d2-32
  - Immunological Studies in Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation, and Neural Tumor (ROHHADNET) Syndrome
    
    hrp0082p1-d2-33
- Bone
- - High Prevalence of Low Bone Mass in Adolescents with Non-Transfusion Dependent Hb E/[beta]-thalassemia
    
    hrp0082p1-d2-34
  - 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
    
    hrp0082p1-d2-35
  - Sun Protection Habits and Calcium Intake in Children with Malignancy
    
    hrp0082p1-d2-36
  - Vitamin D Levels and Effects of Vitamin D Replacement in Children with Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis (PFAPA) Syndrome
    
    hrp0082p1-d2-37
  - Increased Rates of Infantile Hypercalcaemia Following Guidelines for Antenatal Vitamin D3 Supplementation
    
    hrp0082p1-d2-38
  - Continuous s.c. Recombinant PTH1-34 Pump Therapy in Congenital Hypoparathyroidism Associated with Malabsorption
    
    hrp0082p1-d2-39
  - Effects and Limitations of Cinacalcet Therapy in Neonatal Severe Hyperparathyroidism
    
    hrp0082p1-d2-40
  - Young Adults with Klinefelter Syndrome and Congenital Anorchia Treated with Testosterone Have Normal Bone and Muscle Mass but Increased Central Adiposity
    
    hrp0082p1-d2-41
  - Decreased Bone Density in Boys with Klinefelter Syndrome: Results of a Placebo-Controlled Clinical Trial Using Low-Dose Androgen Treatment for 2 Years
    
    hrp0082p1-d2-42
  - Study of Mineral and Bone Metabolism in Pediatric Patients with Inflammatory Bowel Disease
    
    hrp0082p1-d2-43
  - Vitamin D Deficiency: a National Threat to Adolescent Health in Saudi Arabia
    
    hrp0082p1-d2-44
  - Longitudinal Changes of Bone Mineral Content in Children with Cystic Fibrosis
    
    hrp0082p1-d2-45
- Bone (1)
- - Loss of Function CYP24A1 Mutations in Patients with Hypercalcemia and Low Pth level: an Autosomal Dominant or Recessive Trait?
    
    hrp0082p1-d3-46
  - 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
    
    hrp0082p1-d3-47
  - Paternal Isodisomy and Sporadic Pseudohypoparathyroidism I-b
    
    hrp0082p1-d3-48
  - Vertebral Fracture Assessment in a Paediatric Population using Dual-Energy X-ray Absorptiometry
    
    hrp0082p1-d3-49
  - Genetic Study of Osteogenesis Imperfecta: Two Novel Mutations in COL1A1 and COL1A2
    
    hrp0082p1-d3-50
  - Bone Geometry, Volumetric Density, Microarchitecture and Estimated Bone Strength Assessed by HR-pQCT in Adult Patients with Hypophosphatemic Rickets
    
    hrp0082p1-d3-51
  - Opposing Effects of Childhood Obesity on Radial and Tibial Bone Microstructure
    
    hrp0082p1-d3-52
  - Bone Mineral Density Evaluation in Children with Gaucher Disease
    
    hrp0082p1-d3-53
  - Correlation of Sclerostin Levels with Bone Metabolism Markers and Bone Mineral Density in Children and Adolescents with Type 1 Diabetes Mellitus (T1DM)
    
    hrp0082p1-d3-54
  - 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
    
    hrp0082p1-d3-55
  - Effect of a Vibration Based Rehabilitation Concept On Bone and Muscle Development in Children with Osteogenesis Imperfecta
    
    hrp0082p1-d3-56
  - No Correlation Between 25OHD Status and Pro or Anti-Inflammatory Cytokines in Obese Children and Normal Weight Controls
    
    hrp0082p1-d3-57
- Diabetes
- - A leu402pro Mutation of the Non-hla Gene il18rap in Aggressive Neonatal Type 1 Diabetes Mellitus
    
    hrp0082p1-d1-58
  - 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
    
    hrp0082p1-d1-59
  - Activity of Neutral Alfa-Glucosidase in the Urine of Children and Adolescents with Type 1 Diabetes Mellitus and Diabetic Nephropathy
    
    hrp0082p1-d1-60
  - Evaluation of S-100B, Antioxidant and Oxidative Capacity Before and After the Treatment in Children with Diabetic Ketoacidosis
    
    hrp0082p1-d1-61
  - Effect of Adjunctive Therapy with Cholecalciferol on Residual [beta]-Cell Function in Recent-Onset Type 1 Diabetes Mellitus: a Prospective Pilot Study
    
    hrp0082p1-d1-62
  - Th17 Cells in Children with New Onset Type 1 Diabetes
    
    hrp0082p1-d1-63
  - Biomarkers of Subclinical Inflammation in an Infant-Juvenile Population with Type 1 Diabetes
    
    hrp0082p1-d1-64
  - Glycaemic Control and Acute Complications in European Children, Adolescents, and Young Adults With Type 1 Diabetes in the Teens Study
    
    hrp0082p1-d1-65
  - Metabolic Consequences of Antipsychotic Medication in Youths with Type 1 Diabetes: Analysis from the Prospective Nationwide German and Austrian Diabetes Survey DPV
    
    hrp0082p1-d1-66
  - Protective Effects of Combined Intervention with Adenovirus Vector Mediated il10 and igf1 Genes on Endogenous Islet [beta] Cells in Nonobese Diabetes Mice with Onset of Type 1 Diabetes Mellitus
    
    hrp0082p1-d1-67
  - Evaluation of Bone Geometry, Quality, and Bone Markers in Children with Type 1 Diabetes
    
    hrp0082p1-d1-68
- Diabetes (1)
- - Activation of Insulin/IGF1 Signaling Could Increase Hypothalamic Lipid Anabolism in Non-Diabetic IRS2-Deficient Mice
    
    hrp0082p1-d2-69
  - Evaluation of Subclinical Atherosclerosis by Non-Invasive Radiological Methods and its Relation with Endoglin and Nitric Oxide Levels
    
    hrp0082p1-d2-70
  - Identification of Novel Candidate Gene Variants for Mody by Whole Exome Sequencing in Korean Mody Families
    
    hrp0082p1-d2-71
  - Abstract unavailable
    
    hrp0082p1-d2-72
  - A Novel Mutation of wfs1 Gene in a Japanese Infant of Diabetes Mellitus, Deafness, and Congenital Cataract
    
    hrp0082p1-d2-73
  - Transient Hyperglycaemia Preceded by Neonatal Hyperinsulinaemic Hypoglycaemia in an Infant with a Novel HNF1A Mutation
    
    hrp0082p1-d2-74
  - Lpl Gene Mutation and Polymorphism of Apoc2 and Apoc5 Genes in a Patient with Diabetes Mellitus Type 1
    
    hrp0082p1-d2-75
  - Determinants of Serum Osteocalcin Concentrations in 12-Year-Old Children Born Small or Appropriate for Gestational Age
    
    hrp0082p1-d2-76
  - Molecular Genetic Analysis of Maturity Onset Diabetes of the Young (Mody) Genes in Children by Using Targeted Next-Generation Sequencing
    
    hrp0082p1-d2-77
  - Hormonal and Lipid Profile in Correlation with Anthropometric Measurements Among Offspring of Diabetic Mothers
    
    hrp0082p1-d2-78
  - Sequence Analysis of 11 Known Causative Genes in Clinically Diagnosed Children as Maturity Onset Diabetes of Youth by Next Generation Sequencing
    
    hrp0082p1-d2-79
  - Methylmalonic Acidemia (MMA) with Unusual Presentation Mimicking Diabetic Ketoacidosis
    
    hrp0082p1-d2-80
- Diabetes (2)
- - mHealth app for Young People with Diabetes Type 1 Transferring from Pediatric to Adult Care
    
    hrp0082p1-d3-81
  - 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
    
    hrp0082p1-d3-82
  - DKA During Diabetes Therapy: Multinational Comparison with 59 191 Pediatric Patients from England, Wales, The United States, Austria and Germany
    
    hrp0082p1-d3-83
  - Children and Adolescents with Type 1 Diabetes have Higher Plasma Visfatin Levels than Healthy Controls
    
    hrp0082p1-d3-84
  - Algorithm-Based Cholesterol Monitoring in Children with Type 1 Diabetes
    
    hrp0082p1-d3-85
  - Implementation of Effective Transition from Paediatric to Adult Diabetes Care with an Outpatient Transition Nurse
    
    hrp0082p1-d3-86
  - The Natural Evolution of Impaired Glucose Homeostasis Among Obese Adolescents in a High - Risk Diabetes Prone Population
    
    hrp0082p1-d3-87
  - Improved Health-related Quality of Life with Insulin Therapy in Children with Cystic Fibrosis-related Diabetes: a Prospective Cohort Study
    
    hrp0082p1-d3-88
  - Nutritional Status and Respiratory Function in Patients Affected by Cystic Fibrosis and Glucose Metabolism Derangements after 4 Years of Insulin Therapy with Glargine
    
    hrp0082p1-d3-89
  - The Relationship of Serum 25-Hydroxyvitamin D with Glucose Homeostasis in Obese Children and Adolescents in Zhejiang, China
    
    hrp0082p1-d3-90
  - Feasibility and Acceptability of Robot Assistant in Self-management of Type 1 Diabetes in Children
    
    hrp0082p1-d3-91
- Fat Metabolism & Obesity
- - TNF-Related Apoptosis-Inducing Ligand Induces a Pro-Inflammatory Secretion Profile in Human Adipocytes
    
    hrp0082p1-d1-103
  - Coexistence of Elevated Chitinase 3-Like Protein 1 and von Willebrand Levels in Prepubertal Obese Children
    
    hrp0082p1-d1-104
  - Being Overweight During the Peripubertal Period Modifies the Leptin Induced Changes in Hypothalamic Neuropeptides Involved in Metabolism but not those Involved in Pubertal Onset
    
    hrp0082p1-d1-105
  - Natural Antibiotics: New Biomarkers of Childhood Obesity
    
    hrp0082p1-d1-106
  - Evidence of Early Alterations in Adipose Tissue Biology and Function in Obese Children
    
    hrp0082p1-d1-107
  - The Impact of Antibiotic Exposure During Infancy on Weight and Height
    
    hrp0082p1-d1-108
  - Identification of Brown Adipocyte Progenitor Marker Genes in Progenitor Cells from Human Deep Neck and Subcutaneous Adipose Tissue by Gene Array Analysis
    
    hrp0082p1-d1-109
  - Free Fatty Acids Activate Hypothalamic Astrocytes in a Sexually Dimorphic Manner
    
    hrp0082p1-d1-110
  - A Multiplatform Non-targeted Metabolomics Approach to Investigate Insulin Resistance Associated to Obesity in Childhood
    
    hrp0082p1-d1-111
  - Mir-146a and -155 are Involved in FOXO1 Regulation and Non Alcoholic Fatty Liver Disease in Childhood Obesity
    
    hrp0082p1-d1-112
- Fat Metabolism & Obesity (1)
- - Prenatal Maternal Weight and Weight Status and Lipid Profile of the Offspring
    
    hrp0082p1-d2-113
  - Pro-Inflammatory (M1) and Anti-Inflammatory (M2) Profiles in Adipose Tissue of Lean and Obese Children and Adolescents
    
    hrp0082p1-d2-114
  - Important Links Between Fat Derived Proteins and Bone Remodeling Factors in Lean and Obese Girls
    
    hrp0082p1-d2-115
  - Characterizing the Metabolically Obese Normal Weight Phenotype in Youth
    
    hrp0082p1-d2-116
  - Ratio of Triglycerides to High-Density Lipoprotein Cholesterol Compared with Homeostasis Model Assessment Insulin Resistance Indexes in Screening the Metabolic Syndrome in Chinese Obese Children
    
    hrp0082p1-d2-117
  - 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
    
    hrp0082p1-d2-118
  - How Production of Vascular Endothelial Growth Factor Influences Formation of Vascular Disorders in Children with Obesity
    
    hrp0082p1-d2-119
  - RANKL and Osteoprotegerin Serum Levels in Obese Children and Adolescents
    
    hrp0082p1-d2-120
  - Sex-, Age- and Height-Specific Reference Curves for the 6-min Walk Test in Healthy Children and Adolescents
    
    hrp0082p1-d2-121
  - Predictive Value of Excess Body Weight in Childhood and Adolescence Compared to BMI and Waist to Height Ratio
    
    hrp0082p1-d2-122
  - Cardiovascular Risk Markers in Metabolically Healthy and Metabolically Unhealthy Obese Adolescents
    
    hrp0082p1-d2-123
  - A Dual Role of Fetuin A on Cardiovascular Risk in Obese Children and Adolescents
    
    hrp0082p1-d2-124
- Fat Metabolism & Obesity (2)
- - Impairment of Adipose Tissue in Prader-Willi Syndrome Rescued by GH Treatment
    
    hrp0082p1-d3-125
  - Dysautonomia and Acyl Ghrelin in Prader-Willi syndrome
    
    hrp0082p1-d3-126
  - Infancy Lipidomic Analyses and Associations with Early Nutrition and Growth
    
    hrp0082p1-d3-127
  - Acylated and Unacylated Ghrelin Levels in Children and Young Adults with Prader-Willi Syndrome
    
    hrp0082p1-d3-128
  - The Effect of Honey on Plasma Glucose and Insulin Concentrations in Obese Prepubertal Girls
    
    hrp0082p1-d3-129
  - Features of Neuroendocrine Status in Children with Different Forms of Obesity
    
    hrp0082p1-d3-130
  - Under-Diagnosed Beckwith-Wiedemann Syndrome Among Early-Onset Obese Children
    
    hrp0082p1-d3-131
  - Impact of Maternal and Fetal Inflammatory Markers on Neonatal and Infant Adiposity
    
    hrp0082p1-d3-132
  - Can We Predict the Risk of Obesity?
    
    hrp0082p1-d3-133
  - Can Hypothalamic Obesity be Treated with Stimulants?
    
    hrp0082p1-d3-134
- Growth
- - The Association Between Adipocytes and Growth is Mediated by Growth and Differentiation Factor 5
    
    hrp0082p1-d1-135
  - A Homozygous Point Mutation in the GH1 Promoter ([mdash]161T[gt]C) Leads to Reduced GH Expression in Siblings with Isolated GH Deficiency
    
    hrp0082p1-d1-136
  - Growth Differentiation Factor 15 and Fibroblast Growth Factor 21: Novel Biomarkers for Mitochondrial Diseases
    
    hrp0082p1-d1-137
  - A Novel Homozygous Mutation of the IGF1 Receptor Gene (igf1r) in Two Siblings with Severe Short Stature, Intellectual Disability, Congenital Malformations, and Deafness
    
    hrp0082p1-d1-138
  - Functional Characterization of Three Novel Mutations in the IGF1R Gene
    
    hrp0082p1-d1-139
  - Severe Short Stature and GH Insensitivity Due to a De Novo Heterozygous STAT5B Missense Mutation
    
    hrp0082p1-d1-140
  - Whole Exome Sequencing is an Efficient Approach to Screen for Changes in Growth-Relevant Genes in Primary IGF1 Deficiency
    
    hrp0082p1-d1-141
  - Parental Gonadal Mosaicism for a BRAF Mutation in Cardiofaciocutaneous Syndrome
    
    hrp0082p1-d1-142
  - Mitochondrial DNA in Placenta: Associations with Fetal Growth and Superoxide Dismutase Activity
    
    hrp0082p1-d1-143
  - Genetics of Growth Failure in Small for Gestational Age Children
    
    hrp0082p1-d1-144
  - Genotype-Phenotype Relationship in Patients with SHOX Region Rearrangements Detected by MLPA in the French Population
    
    hrp0082p1-d1-145
  - Analysis of GH Receptor Gene Expression in Idiopathic Tall Stature Children
    
    hrp0082p1-d1-146
  - The Role of SHOX Gene in Idiopathic Short Stature: an Italian Multicenter Study
    
    hrp0082p1-d1-147
- Growth (1)
- - Beneficial Effects of Long-term GH Treatment on Adaptive Functioning in Infants With Prader-willi Syndrome
    
    hrp0082p1-d2-148
  - Early Development, Growth and Puberty before and During Treatment of Congenital IGHD
    
    hrp0082p1-d2-149
  - Cognitive Processing Speed as a Function of GH Treatment in Short Stature Children: a Multiple Regression Analysis
    
    hrp0082p1-d2-150
  - Sequential Measurements of IGFI Serum Concentrations in Patients With Severe Primary IGFI Deficiency (SPIGFD) and Growth Failure Treated With Recombinant IGFI (Increlex[reg])
    
    hrp0082p1-d2-151
  - Longitudinal Growth of Healthy Preterm Infants Born Below 37 Gestation Weeks
    
    hrp0082p1-d2-152
  - Intima Media Thickness in Children Treated With GH
    
    hrp0082p1-d2-153
  - Clinical and Laboratory Parameters Predicting a Requirement for Reevaluation of GH Status During GH Treatment
    
    hrp0082p1-d2-154
  - Clinical Characteristics and Imprinting Analysis of Chinese Silver Russell Syndrome
    
    hrp0082p1-d2-155
  - Gender Difference in Secular Trend in Sweden
    
    hrp0082p1-d2-156
  - 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
    
    hrp0082p1-d2-157
  - Effects of Methylphenidate on Growth and Appetite in Attention-Deficit Hyperactivity Patients
    
    hrp0082p1-d2-158
  - How Precisely can we Measure Increments of Bone Age and Bone Health Index with an Automated Method in Boys with Klinefelter Syndrome?
    
    hrp0082p1-d2-159
- Growth (2)
- - Final Height and Safety Outcomes in GH-Treated Children with Short Stature Homeobox-Containing Gene (SHOX) Deficiency: Experience From a Large, Multinational, and Prospective Observational Study
    
    hrp0082p1-d3-160
  - Safety and Effectiveness of Increlex[reg] Therapy in Children Enrolled in the Increlex[reg] Growth Forum Database in Europe: 4 Years Interim Results
    
    hrp0082p1-d3-161
  - Infliximab Improves Growth in Paediatric Crohn[apos]s disease Only if Commenced Early in Puberty or Prior to the Onset of Puberty
    
    hrp0082p1-d3-162
  - Six Months Follow-Up Pharmacokinetics and Pharmacodynamics Profile of Once-weekly, CTP-modified Human GH (MOD-4023;): phase 2 Dose Finding Study in Children with GHD Deficiency
    
    hrp0082p1-d3-163
  - Characterization of MOD-4023 Glycosylation, a CTP Modified Long Acting GH in Advanced Clinical Stages
    
    hrp0082p1-d3-164
  - Validating Genetic Markers of Response to Recombinant Human GH in Children with GH Deficiency or Turner Syndrome: Results From the PREDICT Validation Study
    
    hrp0082p1-d3-165
  - Short-Term Changes in Bone Formation Markers Following GH Treatment in Short Prepubertal Children with a Broad Range of GH Secretion
    
    hrp0082p1-d3-166
  - 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
    
    hrp0082p1-d3-167
  - Abstract unavailable
    
    hrp0082p1-d3-168
  - Recombinant Human GH Therapy Allows to Reach a Normal Final Adult Height in Coeliac Children with GH Deficiency due to Hypophysistis
    
    hrp0082p1-d3-169
  - The ZOMATRIP Study: 4 Year Combination Therapy of GH and GnRHa in Girls with a Short Predicted Adult Height During Early Puberty: Interim Results at the End of the Treatment Phase
    
    hrp0082p1-d3-170
  - Safety and Efficacy Results of a 6 Month, Randomized, Multi-Center Trial of a Novel Long-Acting rhGH (VRS-317) in Naive to Treatment, Pre-Pubertal Children with GH Deficiency
    
    hrp0082p1-d3-171
  - Three-Years Height Outcome During rh-GH Therapy in Subjects with Achondroplasia and Hypochondroplasia
    
    hrp0082p1-d3-172
- Perinatal and Neonatal Endocrinology
- - A Girl with Beckwith-Wiedemann Syndrome and Pseudohypoparathyroidism Type 1B, a Unique Example of Multiple Imprinting Defects
    
    hrp0082p1-d1-173
  - Use of Long Acting Somatostatin Analogue (Lanreotide) in Congenital Hyperinsulinism
    
    hrp0082p1-d1-174
  - The Role of mTORC1/RagGTPase and IGF1R/mTORC2/Akt Pathways and the Response of Diffuse Congenital Hyperinsulinism to Sirolimus
    
    hrp0082p1-d1-175
  - A Novel Mutation of the PCSK1 Gene with Surprising Enzymatic Consequences Causes Proprotein Convertase 1/3 Deficiency and Consequent Endocrinopaties
    
    hrp0082p1-d1-176
  - Growth and Puberty in Monozygotic Twins with Intra-Twin Birth-Weight Difference
    
    hrp0082p1-d1-177
  - Pubertal and Adrenal Hormones in Monozygotic Twins with Intra-Twin Birth-Weight Difference
    
    hrp0082p1-d1-178
  - Variations in Protein Expression in Small-For-Gestational-Age Newborns
    
    hrp0082p1-d1-179
  - Long-Term Cognitive Effects from Dexamethasone-Treated Pregnancies
    
    hrp0082p1-d1-180
  - The Prevalence and Outcome of Sex Chromosome Abnormalities Detected Prenatally in Scotland
    
    hrp0082p1-d1-181
  - Clinical and Histological Heterogeneity of Congenital Hyperinsulinism Due to Paternally Inherited Heterozygous ABCC8/KCNJ11 Mutations
    
    hrp0082p1-d1-182
  - Molecular Genetic Analysis of Czech Patients with Congenital Hyperinsulinism: Surprisingly High Incidence of HNF1A Mutations
    
    hrp0082p1-d1-183
  - Very Low Birth Weight [lt]1500 g is Associated with Reduced Sex-Typical Behaviour in Childhood
    
    hrp0082p1-d1-184
- Pituitary
- - Early-Onset Central Diabetes Insipidus is Associated with de novo Arginine Vasopressin-Neurophysin II or Wolfram Syndrome 1 Gene Mutations
    
    hrp0082p1-d3-185
  - A Boy with Septo-Optic Dysplasia Identified a Mutation in WDR11
    
    hrp0082p1-d3-186
  - Quality of Life and Psychosexual Function in Young Adults with Childhood-Onset Hypopituitarism
    
    hrp0082p1-d3-187
  - Butyrate Stimulates GH Secretion From Rat Anterior Pituitary Cells Via the G-Protein-Coupled Receptors GPR41 and 43
    
    hrp0082p1-d3-188
  - An Unusual Case of Hereditary Nephrogenic Diabetes Insipidus Affecting Mother and Daughter
    
    hrp0082p1-d3-189
  - A Rare Cause of Diabetes Insipidus: Congenital Proprotein Convertase 1/3 Deficiency
    
    hrp0082p1-d3-190
  - Phenotype Evaluation of Combined Pituitary Hormone Deficiency Caused By prop1 Gene Mutation in Comparison to Pituitary Deficiency Caused by Other Factors
    
    hrp0082p1-d3-191
  - Diencephalic Syndrome in Childhood Craniopharyngioma: Results of German Multicenter Studies on 485 Long-Term Survivors of Childhood Craniopharyngioma
    
    hrp0082p1-d3-192
  - A Novel Mutation of OTX2 Associated with Neonatally Diagnosed Combined Pituitary Hormone Deficiency and Bilateral Microphthalmia
    
    hrp0082p1-d3-193
  - Type 3 Congenital Multiple Pituitary Hormone Deficiency
    
    hrp0082p1-d3-194
  - Childhood Craniopharyngioma: Changes of Treatment Strategies in Multinational Trials During the Last 12 Years
    
    hrp0082p1-d3-195
  - Rathke Cleft Cysts and Endocrine Dysfunction in Children
    
    hrp0082p1-d3-196
  - Congenital Nasal Pyriform Aperture Stenosis and Pituitary Abnormalities: Case Series of 20 Patients and a Management Guideline for Early Identification of Pituitary Insufficiency
    
    hrp0082p1-d3-197
  - Spatial and Temporal Expression of Immunoglobulin Superfamily Member 1 in the Rat
    
    hrp0082p1-d3-198
- Reproduction
- - Stability Conditions in Estradiol Matrix Patches; in vitro Studies for Application in Pediatrics
    
    hrp0082p1-d1-198
  - Associations of Vascular Biomarkers and the Somatotrophic Axis with Carotid Ultrasound and Echocardiography Findings in Relation to Turner Arteriopathy
    
    hrp0082p1-d1-199
  - Testes in Infants with Prader-Willi Syndrome: hCG Treatment, Surgery, and Histology
    
    hrp0082p1-d1-200
  - The Effect of 17[beta]-Estradiol on Uterine Volume in Young Women with Turner Syndrome: a 5-Year Randomized Controlled Clinical Trial
    
    hrp0082p1-d1-201
  - Genetic Markers in the Study of Chromosome Y in the Population of Girls with Turner Syndrome
    
    hrp0082p1-d1-202
  - Girls with Turner Syndrome have Normal Muscle Force but Decreased Muscle Power
    
    hrp0082p1-d1-203
  - The Influence of GH Treatment on the Oral Disposition Index in Turner Syndrome Girls and in GH Deficient Children: 8 Years of Follow-Up
    
    hrp0082p1-d1-204
  - Abstract unavailable
    
    hrp0082p1-d1-205
  - Hypogonadotropic Hypogonadism in Patients with Congenital Adrenal Hypoplasia due to NR0B1 (DAX1) Mutations: Phenotype/Genotype Relationship
    
    hrp0082p1-d1-206
  - Analysis of the WDR11 Gene in Patients with Isolated Hypogonadotropic Hypogonadism with and without Olfactory Defects
    
    hrp0082p1-d1-207
  - GH Therapy in Turner Syndrome Patients: the Effects on Nutritional Status, Adipokines, and Aortic Dilatation
    
    hrp0082p1-d1-208
  - Evaluation of Sitting Height/Height SDS in Patients with Turner Syndrome
    
    hrp0082p1-d1-209
- Reproduction (1)
- - Messenger Ribonucleic Acid Expression of Kiss-1 and Serum Level of Kisspeptin in Rat at Different Developmental Stages
    
    hrp0082p1-d2-210
  - The Incidence of Childhood Gonadoblastoma Over 15 Years in the Republic of Ireland
    
    hrp0082p1-d2-211
  - A Novel MKRN3 Mutation Discovered in a Korean Girl with Central Precocious Puberty
    
    hrp0082p1-d2-212
  - The Association of Moebius Syndrome and Kallman Syndrome is Due to a Specific Mutation of TUBB3
    
    hrp0082p1-d2-213
  - Early Medical Treatment of Children with Gender Dysphoria: an Empirical Ethical Study on Arguments of Proponents and Opponents Concerning Early Interventions
    
    hrp0082p1-d2-214
  - Serum Inhibin-B Values in Boys with Unilateral Cryptorchidism and Boys with Unilateral Vanished Testis
    
    hrp0082p1-d2-215
  - IGSF1 Variants in Boys with Familial Delayed Puberty
    
    hrp0082p1-d2-216
  - Reference Charts for Testicular Volume in Dutch Children and Adolescents
    
    hrp0082p1-d2-217
  - High Incidence of Genetic Defects in a Cohort of 24 Male Adolescents with Persistent Pubertal Gynecomastia
    
    hrp0082p1-d2-218
  - Mutation Analysis of the KISS1, KISS1R, LIN28A, LIN28B, TAC3, and TACR3 Genes in Girls with Central Precocious Puberty
    
    hrp0082p1-d2-219
  - Successful Treatment of Male Congenital Hypogonadotropic Hypogonadism with rFSH Pretreatment Followed by GnRH
    
    hrp0082p1-d2-220
- Reproduction (2)
- - The Uterine Artery Pulsatility Index as an Accurate Index for the Assessment of Puberty
    
    hrp0082p1-d3-221
  - The Uterine Artery Pulsatility Index in Evaluation of the GnRH-Analog Treatment Efficacy in Central Precocious Puberty
    
    hrp0082p1-d3-222
  - Serum Bisphenol a Concentration and Premature Thelarche in Female Infants Aged 4-Month to 2-Year-Old
    
    hrp0082p1-d3-223
  - Test on Kisspeptin Levels in Girls with Idiopathic Central Precocious Puberty and its Significance
    
    hrp0082p1-d3-224
  - Treated and Untreated Women with Idiopathic Precocious Puberty: Long-Term General Health Status and Metabolic Outcome Between third and fifth decades
    
    hrp0082p1-d3-225
  - Serum Leptin, Ghrelin, and Adiponectin Levels in Relation to Body Composition in Rhythmic Gymnasts Entering into Puberty: a 3-year Follow-up Study
    
    hrp0082p1-d3-226
  - Impact of BMI on GnRH Stimulated LH Provocation Peak in Girls with Central Precocious Puberty
    
    hrp0082p1-d3-227
  - Impact of Bisphenol-A on the Puberty of Female Rats
    
    hrp0082p1-d3-228
  - The Role of Bisphenol A in Etiopathogenesis of Polycystic Ovary Syndrome in Adolescent Girls
    
    hrp0082p1-d3-229
  - Increasing Incidence of Premature Thelarche in the Central Denmark Region? Who Evolve into Precocious Puberty?
    
    hrp0082p1-d3-230
- Sex Development
- - Mutations Involving FIBULIN2 are a Novel Cause of 46,XY DSD
    
    hrp0082p1-d3-92
  - Ex vivo Culture of Human Fetal Gonads: Manipulation of Meiosis Regulation Affects Testis Development
    
    hrp0082p1-d3-93
  - Prenatal Exposure to Phthalates and Phenols in Relation to Anogenital Distance at Birth in Male Infants
    
    hrp0082p1-d3-94
  - Ovarian Development and Hormonal Feedback Mechanism in a 46XX Patient with cyp19a1 Deficiency Under Low Dose Estrogen Replacement
    
    hrp0082p1-d3-95
  - Isolated Hypospadias and Exposure to Endocrine Disrupting Chemicals During Pregnancy: a Multi-Institutional Controlled Study in a High Prevalence Area
    
    hrp0082p1-d3-96
  - 46, XX Ovotesticular Disorder of Sex Development: Potential Role of 13q31.1
    
    hrp0082p1-d3-97
  - A Novel NR5A1 Mutation with Preserved Fertility
    
    hrp0082p1-d3-98
  - Development of a Next Generation Sequencing Panel for Disorders of Sex Development
    
    hrp0082p1-d3-99
  - 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
    
    hrp0082p1-d3-100
  - Subjective Need for Psychological Support in Parents of Children with dsd: Results from the German Clinical Evaluation Study
    
    hrp0082p1-d3-101
  - Four Cases of Isolated Partial Gonadal Dysgenesis Due to nr0b1 (dax1) Locus Duplication Inherited in a Large Family
    
    hrp0082p1-d3-102
- Thyroid
- - The Association between rs4684677 T/A Polymorphism in Preproghrelin Gene And predisposition to Autoimmune Thyroid Diseases in Children
    
    hrp0082p1-d1-231
  - Chosen Polimorphisms in FoxP3 Gene in Children and Adolescents with Autoimmune Thyroid Diseases
    
    hrp0082p1-d1-232
  - TSH Receptor Gene Variants in Pediatric Patients with Non Autoimmune Hyperthyrotropinemia
    
    hrp0082p1-d1-233
  - Association of Toll-Like Receptor-10 Polymorphisms with Autoimmune Thyroid Disease in Korean Children
    
    hrp0082p1-d1-234
  - A Nonsense Thyrotropin Receptor Gene Mutation (R609X) is Associated with Congenital Hypothyroidism and Heart Defects
    
    hrp0082p1-d1-235
  - Genome-Wide Promoter Methylation Analysis in Cytologically Indeterminate Thyroid Nodules
    
    hrp0082p1-d1-236
  - Genetic Analysis of the Paired Box Domain Gene in a Cohort of Polish Patients with Primary Congenital Hypothyroidism
    
    hrp0082p1-d1-237
  - Homozygous Deletion of The TSH[beta] Subunit Gene Causes Congenital Secondary Hypothyroidism in a Consanguineous Family of Turkish Descent
    
    hrp0082p1-d1-238
  - Genotype and Phenotype Characterization of a Series of Italian Patients Affected with Idiopatic Central Hypothyroidism
    
    hrp0082p1-d1-239
  - A Novel Mutation in the TITF1 Gene in a Child with Benign Hereditary Chorea
    
    hrp0082p1-d1-240
  - Twin Couples and/or Triplets Discordant for Congenital Hypothyroidism at Birth: the Importance of the Re-screening at 2-4 Weeks of Life
    
    hrp0082p1-d1-241
  - Congenital Hypothyroidism and Tuberous Sclerosis: an Association or a Coincidence?
    
    hrp0082p1-d1-242
  - Evaluation of Serum Cytokines IL-6 and Osteoprotegerin Measurements in the Diagnosis of Chronic Autoimmune Thyroiditis and Graves' Disease in Children
    
    hrp0082p1-d1-243
- Thyroid (1)
- - Treatment of Graves' Disease with Methimazole in Children Alters the Proliferation of Treg Cells and T Lymphocytes
    
    hrp0082p1-d2-244
  - Thyroid Dysfunction in Children After Hematopoietic Stem Cell Transplantation: Short Term Follow-Up for 12 Months
    
    hrp0082p1-d2-245
  - The Effect of L-Thyroxine Treatment on Left Ventricular Functions in Children with Subclinical Hypothyroidism
    
    hrp0082p1-d2-246
  - Urinary Iodine Concentrations in Mothers and their Term Newborns
    
    hrp0082p1-d2-247
  - Vitamin D in Adolescents with Hashimoto's Thyroiditis
    
    hrp0082p1-d2-248
  - Capillary TSH Cut-off Levels for Congenital Hypothyroidism Screening: Evidence Against Adopting the UK Threshold of 10 mIU/l
    
    hrp0082p1-d2-249
  - In Patients with Chronic Autoimmune Thyroiditis, Investigation of the Effects of Functions of Regulatory T Cells and Vitamin D
    
    hrp0082p1-d2-250
  - Triiodothyronine-Predominant Graves' Disease (T3-P-GD): Description and Management in Childhood
    
    hrp0082p1-d2-251
  - Autoimmune Encephalopathy in a Boy with Graves' Disease
    
    hrp0082p1-d2-252
  - Maternal Hypothyroxinemia in Early Pregnancy is Associated with Poorer Arithmetic Performance in a School Test in Offspring at Age 5 Years
    
    hrp0082p1-d2-253
  - TSH: Different Normalization Methods, Very Different Normal Upper Limits
    
    hrp0082p1-d2-254
  - Usefulness of Second Screening Strategy for Congenital Hypothyroidism in LBW Neonates
    
    hrp0082p1-d2-255
  - Screening for Congenital Hypothyroidism in the Russian Federation (1997-2012)
    
    hrp0082p1-d2-256
Poster Category 2
- Adrenals & HP Axis
- - Growth Pattern in Infants with Congenital Adrenal Hyperplasia During the First Year of Life
    
    hrp0082p2-d1-257
  - ACTH and Cortisol Levels are Associated with Cardiovascular Risk in Pediatric Obesity: a Cross-Sectional Study in China
    
    hrp0082p2-d1-258
  - Inadequate Cortisol Response to Tetracosactide (Synacthen®) Test in NCCAH Patients, an Exception to the Rule?
    
    hrp0082p2-d1-259
  - Genotype-phenotype Non-Concordance: How Prevalent is it? How to Explain it
    
    hrp0082p2-d1-260
  - Paradoxical Increase in Urinay Cortisol Excretion in Children with Primary Pigmented Nodular Adrenal Disease
    
    hrp0082p2-d1-261
  - Mutation Spectrum of CYP11B1 Gene in Turkish Patients with 11[beta]-hydroxylase Deficiency
    
    hrp0082p2-d1-262
  - Genotype and Phenotype Characteristics of Patients with Nonclassical Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
    
    hrp0082p2-d1-263
  - LC-MSMS Profiling of Plasma Steroids in Different Types of Congenital Adrenal Hyperplasia
    
    hrp0082p2-d1-264
  - Two Brothers with Late Onset Apparent Mineralocorticoid Excess
    
    hrp0082p2-d1-265
  - Is Basal 17-Hydroxyprogesterone a Sensitive Marker for Diagnosis of Non-Classical Congenital Adrenal Hyperplasia?
    
    hrp0082p2-d1-266
  - An adolescent with Hypertension Caused by Primary Hyperaldosteronism due to KCNJ5 Mutation
    
    hrp0082p2-d1-267
  - Analysis of Prospective Annual ACTH Stimulation Testing Among Survivors of Intracranial Tumor
    
    hrp0082p2-d1-268
  - Congenital Adrenal Hyperplasia Caused by 11[beta]-hydroxylase-Deficiency as a Rare Differential Diagnosis of Precocious Pseudo-Puberty and Hypertension
    
    hrp0082p2-d1-269
- Adrenals & HP Axis (1)
- - Osteoporosis in Triple A Syndrome: an Overlooked Symptom of Unexplained Etiolaogy
    
    hrp0082p2-d2-270
  - The Results of CYP21A2 Mutation Analysis in Adolescent with Polycystic Ovary Syndrome
    
    hrp0082p2-d2-271
  - Timing of precocious pubarche in girls: Does a contemporary subgroup exist?
    
    hrp0082p2-d2-272
  - Nonclassic Lipoid Adrenal Hyperplasia with R272C STAR Mutation: a Case Report
    
    hrp0082p2-d2-273
  - 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
    
    hrp0082p2-d2-274
  - Non-virilizing Congenital Adrenal Hyperplasia in a Female Patient: Report of a Novel HSD3B2 Mutation
    
    hrp0082p2-d2-275
  - Waist-to-Height Ratio, Waist-to-Hip Ratio, Waist Circumference, and BMI in Children and Adolescents with Classical Congenital Adrenal Hyperplasia Due to 21-Hydoxylase Deficiency (CAH)
    
    hrp0082p2-d2-276
  - Psychological and Behavioral Outcome of Female Patients with Congenital Adrenal Hyperplasia
    
    hrp0082p2-d2-277
  - Do Neonates Need a Short Synacthen Test to Investigate the Adrenal Axis?
    
    hrp0082p2-d2-278
  - Genotype-Phenotype Discordant Patients with Homozygous Intron 2 Mutation (IVS2) of CYP21 Gene
    
    hrp0082p2-d2-279
  - A 26-Day-Old Japanese Girl with Aldosterone Synthase Deficiency Caused by a Novel Mutation in the CYP11B2 Gene
    
    hrp0082p2-d2-280
  - Nonclassic CYP21A2 Deficiency: Diagnosis and Clinical Evolution
    
    hrp0082p2-d2-281
  - Steroid 11[beta]-Hydroxylase Deficiency Due to CYP11B1 Mutations in Females with Hyperandrogenemia
    
    hrp0082p2-d2-282
- Bone
- - Hypophosphatemic Rickets in Norwegian Children: Genotypes, Phenotypes, and Complications
    
    hrp0082p2-d1-283
  - Increased Fracture Rate in Children and Adolescents with Marfan Syndrome
    
    hrp0082p2-d1-284
  - Mutations in IFITM5 Leading to Prenatal and Postnatal Signs of Dominant Osteogenesis Imperfecta
    
    hrp0082p2-d1-285
  - Musculoskeletal Health in Children with Crohn's Disease at Diagnosis: Dynamic Muscle Function, Tibia Cortical and Trabecular Bone Density and Vertebral Fracture Prevalence
    
    hrp0082p2-d1-286
  - Case report: A Novel mutation in the Calcium Sensing Receptor in a Welsh Family with Hypercalcaemia
    
    hrp0082p2-d1-287
  - A New Missense Mutation in FGF23 Gene in a Male with Hyperostosis-hyperphosphatemia Syndrome
    
    hrp0082p2-d1-288
  - Pseudohypoparathyroidism Type 1A Due to Novel GNAS Mutation
    
    hrp0082p2-d1-289
  - Sleep-related Breathing Disorders in Pycnodysostosis
    
    hrp0082p2-d1-290
  - Cystinosis as a Cause of Hypophosphatemic Rickets: a Single-Center Experience
    
    hrp0082p2-d1-291
  - Pseudohypoparathyroidism Type Ib: Two Cases with Different Clinical Presentation
    
    hrp0082p2-d1-292
  - A Very Rare Case of Rickets: Fanconi-Bickel Syndrome
    
    hrp0082p2-d1-293
  - Determinants of Vitamin D Levels in Children and Adolescents with Down Syndrome
    
    hrp0082p2-d1-294
- Bone (1)
- - Determinants of Vitamin D Levels in Children, Adolescents, and Young Adults with Juvenile Idiopathic Arthritis
    
    hrp0082p2-d2-295
  - Determinants of Vitamin D Levels in Italian Children and Adolescents of Mugello, an Area of Tuscany: a Longitudinal Evaluation
    
    hrp0082p2-d2-296
  - Severe Heterotopic Ossifications in a 10-year-old Boy with PHP1a
    
    hrp0082p2-d2-297
  - Zoledronic Acid for Management of Osteopenia of Prematurity and Associated Ventilator Dependency
    
    hrp0082p2-d2-298
  - Mutation in the TBCE Gene Associated with Kenny-Caffey Type 1 Syndrome: a Rare Cause of Hypocalcemia
    
    hrp0082p2-d2-299
  - Vitamin D Levels in Children, Adolescents, and Young Adults with Juvenile onset Systemic Lupus Erythematosus: a Cross-sectional Study
    
    hrp0082p2-d2-300
  - Disproportionate Short Stature with Advanced Bone Age Due to PTHLH Mutation
    
    hrp0082p2-d2-301
  - Plasma 25-OH Vitamin D and pth Concentrations in Cord Blood: relationship with Ethnic Groups, Nutritional Habits and Degree of Maternal Sun Exposure
    
    hrp0082p2-d2-302
  - Cleidocranial Dysplasia Misdiagnosed as Rickets in Three Generations
    
    hrp0082p2-d2-303
  - Age-and Gender-Specific Reference Values of Bone Mineral Density in Korean Adolescents and Young Adults
    
    hrp0082p2-d2-304
  - Status of Vitamin D in Pregnancy to Childhood in Northern Spain: Seasonality, Sun Exposure, and Intake
    
    hrp0082p2-d2-305
  - Effects of Recombinant Human GH on Bone Mass and Body Composition in Paediatric Inflammatory Bowel Disease
    
    hrp0082p2-d2-306
- Bone (2)
- - Suppression of Bone Turnover and its Determinants in Children Receiving Bisphosphonate Therapy
    
    hrp0082p2-d3-307
  - A Case of Vitamin D Dependent Rickets Type 1 with a Novel Mutation in CYP27B1 (25-OH Vitamin D-1-[alpha]-Hydroxylase) Gene
    
    hrp0082p2-d3-308
  - Risedronate Use in Duchenne Muscular Dystrophy: a Pilot Randomised Control Trial
    
    hrp0082p2-d3-309
  - Outcomes of Vitamin D Analogues and Phosphate Supplements in Patients With Hereditary Hypophosphatemic Rickets , Comparison With Non-Treated Patients
    
    hrp0082p2-d3-310
  - Hyperostosis-Hyperphosphataemia Syndrome: Shortening a Diagnostic Odyssey
    
    hrp0082p2-d3-311
  - Severe Osteogenesis Imperfecta and Epidermolysis Bullosa Simplex Caused by FKBP10 Mutation: New Case
    
    hrp0082p2-d3-312
  - Osteogenesis Imperfecta Type I Caused by a Novel Mutation in the Start Codon of the COL1A1 Gene in a Korean Family and the Course of Pamidronate Treatment for 1 Year
    
    hrp0082p2-d3-313
  - Early Calcinosis Cutis, Short Stature and Brachydactyly: a Case Evolution
    
    hrp0082p2-d3-314
  - Does Vitamin D Affect Mean Platelet Volume Values or Not
    
    hrp0082p2-d3-315
  - Bone Size and Bone Mineral Content in Adolescents and Young Adults with Eating Disorders
    
    hrp0082p2-d3-316
  - Infantile Hypercalcemia: Still a Diagnostic and Therapeutic Enigma
    
    hrp0082p2-d3-317
- Diabetes
- - Serum Level of Osteoprotegerin and Total sRANKL in Adolescents with Type 1 Diabetes Mellitus
    
    hrp0082p2-d1-318
  - Simultaneous Changes in Trends in Incidence of Children Diabetes Type 1 in Distant Geographic Regions
    
    hrp0082p2-d1-319
  - Risk Factors for Type 2 Diabetes Mellitus in Secondary School Students in Port Harcourt Nigeria
    
    hrp0082p2-d1-320
  - Interaction of Pubertal Development and Metabolic Control in 1303 Adolescents with Diabetes Mellitus Type 1
    
    hrp0082p2-d1-321
  - Quality of Life and Glycaemic Assessment Before and After Pump School
    
    hrp0082p2-d1-322
  - Improving Paediatric Diabetes Care with the Use of an Electronic Diabetes Information Management System (Twinkle.Net) and Routine Uploading of Blood Glucose Meters and Insulin Pumps (Diasend) in Outpatient Clinic
    
    hrp0082p2-d1-323
  - Two Novel Homozygous Mutations in WFS1 Gene in Two Turkish Families with Mild Phenotypic Expression of Wolfram Syndrome
    
    hrp0082p2-d1-324
  - Imbalance Between Pro-Oxidative and Anti-Oxidative Mechanisms in Children and Adolescents with Type 1 Diabetes Mellitus
    
    hrp0082p2-d1-325
  - Trends in Incidence and Prevalence of DM Type 1 in Children in Ukraine During 2002-2012
    
    hrp0082p2-d1-326
  - Effectiveness of Insulin Pump Therapy in Children and Adolescents with Type 1 Diabetes
    
    hrp0082p2-d1-327
  - Functional Condition of the Kidneys (K/DOQI, 2002) By ACE Gene I/D Polymorphism in Children and Adolescents with Type I Diabetes Mellitus
    
    hrp0082p2-d1-328
- Diabetes (1)
- - Lipid Profile is Related to Androgen Level in Adolescent Girls with Type 1 Diabetes Mellitus
    
    hrp0082p2-d2-329
  - A Multicentre Study Evaluating the Risk and Prevalence of Diabetic Retinopathy in Children and Young People with Type 1 Diabetes Mellitus
    
    hrp0082p2-d2-330
  - ACE Gene Insertion/Deletion Polymorphism and ACE Enzymatic Activity in Egyptian Children with Type 1 Diabetes with and without Microalbuminuria
    
    hrp0082p2-d2-331
  - Game Interaction Between a Humanoid Robot and a Diabetic Teenager: Might This Improve Motivation to Fill in the Nutritional Diary?
    
    hrp0082p2-d2-332
  - A Novel AVPR2 Mutation (L161P) Causing Partial Nephrogenic Diabetes Insipidus
    
    hrp0082p2-d2-333
  - New-Onset Type 2 Diabetes Presenting with Hyperglycaemic Hyperosmolar State in a Renal Transplant Patient on GH Treatment
    
    hrp0082p2-d2-334
  - Insulin Therapy via Tubeless Patch Pump: Really an Alternative?
    
    hrp0082p2-d2-335
  - GAD Antibody Positivity is Associated with Higher Prevalence of Autoimmune Thyroiditis in Children with Type 1 Diabetes Mellitus
    
    hrp0082p2-d2-336
  - The Length of the Deletion in the Region 17q Contributes to the Individual Variability of the Phenotype of Patients with Renal Cysts and Diabetes Syndrome (RCAD, HNF1B-MODY)
    
    hrp0082p2-d2-337
  - Urinary Vitamin E Metabolites as a Biomarker of Oxidative Stress in Type 1 Diabetes
    
    hrp0082p2-d2-338
  - Direct Costs of Diabetes Care in Pediatric Patients with Type 1 Diabetes in Greece
    
    hrp0082p2-d2-339
- Diabetes (2)
- - Coated Pellets With Controlled Glucose Release in Treatment of Children with Diabetes
    
    hrp0082p2-d3-340
  - A Rare Cause of Obesity and Type 2 Diabetes: a Novel Alms1 Mutation in Two Siblings with Alstrom Syndrome
    
    hrp0082p2-d3-341
  - Prolonged Treatment with Vitamin D Supplementation and High Dose is Necessary to Treat Vitamin D Deficiency/Insufficiency (VDD/I) in Children and Adolescents with Type 1 Diabetes
    
    hrp0082p2-d3-342
  - No Association Between Serum Vitamin D and Left Ventricular Mass Index in Children and Adolescent with Type 1 Diabetes Mellitus
    
    hrp0082p2-d3-343
  - Lifestyle and Health Related Quality of Life in Adolescents with Diabetes Mellitus Type 1
    
    hrp0082p2-d3-344
  - Improvement in Type 1 Diabetes Mellitus Metabolic Control: From Conventional to Functional Insulin Therapy
    
    hrp0082p2-d3-345
  - Two Cases of 'Unknown' Lipoprotein Lipase Deficiency and Diabetes Mellitus
    
    hrp0082p2-d3-346
  - Predictors of Direct Costs of Pediatric Diabetes in Greece
    
    hrp0082p2-d3-347
  - Early Detection and Treatment of Cystic Fibrosis Related Diabetes Mellitus in a Tertiary Paediatric Centre: a Case Series
    
    hrp0082p2-d3-348
  - Retinol Binding Protein 4 and Adiponectin Levels During Oral Glucose Tolerance Test in Obese Children Newly Diagnosed of Type 2 Diabetes
    
    hrp0082p2-d3-349
  - Wellbeing of Adolescents with Type 1 Diabetes: Influence of Metabolic Control and Family Factors
    
    hrp0082p2-d3-350
  - Wolcott-Rallison Syndrome: New Mutations and Report of Two Cases
    
    hrp0082p2-d3-351
  - Socioeconomic Deprivation is Associated with Increased Hospital Admissions in Children with Type 1 Diabetes Mellitus
    
    hrp0082p2-d3-352
  - Household Unemployment and Low Levels of Education are Associated with Poor Glycaemic Control in Children and Young People with Type 1 Diabetes Mellitus
    
    hrp0082p2-d3-353
  - An Infant with a Novel Kir6.2 Mutation Causing Neonatal Diabetes and Unexplained Lack of Response to Sulphonylurea
    
    hrp0082p2-d3-354
  - Glycaemic Control and Microvascular Complications in Adolescents and Young Adults with Type 1 Diabetes: Outcome Following Transfer of Care to Adult Services
    
    hrp0082p2-d3-355
  - Diabetic Ketoacidosis at the Onset of Type I Diabetes: a Retrospective Study in a Paediatric Population
    
    hrp0082p2-d3-356
  - Early-Onset Autoinflammatory Partial Lipodystrophy Characterized by Recurrent Fever and Rash: Candle Syndrome
    
    hrp0082p2-d3-357
  - 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
    
    hrp0082p2-d3-358
  - The Sugarsquare Study: a Multicenter Randomized Controlled Trial Concerning a Web-based Patient Portal for Parents of a Child with Type 1 Diabetes
    
    hrp0082p2-d3-359
  - 'My Diabetes' Application for Android Devices as a Diabetes Management Tool
    
    hrp0082p2-d3-360
  - Comparison of HbA1c and OGTT to Diagnose Diabetes in Korean Children
    
    hrp0082p2-d3-361
- Fat Metabolism & Obesity
- - Age at Onset of Weight Gain in Prader-Willi Syndrome is Often Between 1 and 2 Years, Preceding the Hyperphagic Phase; Implications for Management
    
    hrp0082p2-d1-362
  - Novel Uncoupling Protein 1 Expression in White Adipocytes of Subcutaneous Abdominal Adipose Tissue in Children and Adolescents: A Protective Mechanism for Metabolic Equilibrium?
    
    hrp0082p2-d1-363
  - The Association Between Self-Reported Sleep Quality, Ghrelin Hormone and Obese Children and Adolescents
    
    hrp0082p2-d1-364
  - Large-Born Infants Switch from an Adipose to a Lean and Insulin-Sensitive State with Low Concentrations of Circulating Myostatin and Follistatin
    
    hrp0082p2-d1-365
  - Uric Acid and Risk for Atherosclerotic Disease Early in Life
    
    hrp0082p2-d1-366
  - Prevalence of Idiopathic Intracranial Hypertension and Related Factors in Obese Children and Adolescents
    
    hrp0082p2-d1-367
  - MAINTAIN: an Intervention Study of Weight Regain After Weight Loss in Adolescents and Children Reveals an Only Minor Role of Leptin in Weight Regain
    
    hrp0082p2-d1-368
  - The Expression of IGF Type 1 Receptor is Increased in Obese Children
    
    hrp0082p2-d1-369
  - Childhood Obesity, Renal Injury, and Future Disease Risk
    
    hrp0082p2-d1-370
  - Replacement of the Neonatal Leptin Surge During Maternal Deprivation Normalizes Some Endocrine Parameters but Exacerbates Others
    
    hrp0082p2-d1-371
  - Longitudinal Development of Adiponectin in Early Childhood and the Influence of Breastfeeding and Essential Fatty Acid Status
    
    hrp0082p2-d1-372
  - Expression Levels of the Growth-Arrest-Specific Transcript 5 in Overweight and Obese Children and Adolescents
    
    hrp0082p2-d1-373
- Fat Metabolism & Obesity (1)
- - The Role of Bone and Fat Tissue in Glucose Metabolism in Two Different Metabolic Conditions: Obesity and Diabetes Mellitus Type 1: Pilot Study
    
    hrp0082p2-d2-374
  - Family and Genetic Factors Influence the Metabolic Changes in Children
    
    hrp0082p2-d2-375
  - Non-Alcoholic Fatty Liver Disease in Children/Adolescent Affected by Prader-WIlli Syndrome
    
    hrp0082p2-d2-376
  - Short-Term Results of Single-Port Sleeve Gastrectomy in Adolescents with Severe Obesity
    
    hrp0082p2-d2-377
  - Circulating Concentrations of Fibroblast Growth Factor 21 are Undetectable in Human Infants at Term Birth and Surge within Hours After Birth
    
    hrp0082p2-d2-378
  - Severe Childhood-Onset Obesity and Testicular Function After Puberty
    
    hrp0082p2-d2-379
  - A New Case of Proopiomelanocortin Deficiency
    
    hrp0082p2-d2-380
  - Neuroendocrine and Psychological Status in Obese Children
    
    hrp0082p2-d2-381
  - Is 24-h Blood Pressure Monitoring Necessary in Obese Children and Adolescents?
    
    hrp0082p2-d2-382
  - Fetuin A Serum Levels in Children with Nonalcoholic Fatty Liver Disease
    
    hrp0082p2-d2-383
  - Ambulatory Arterial Stiffness Index in Obese Children
    
    hrp0082p2-d2-384
  - Evaluation of the Risk of Dyslipidemia in Adolescents with Obesity
    
    hrp0082p2-d2-385
- Fat Metabolism & Obesity (2)
- - Miglitol Upregulates Uncoupling Protein 1 (ucp1) by Enhancing [beta]3-Adrenergic Signaling in Mature Brown Adipocytes of Rat
    
    hrp0082p2-d3-386
  - Enhanced Liver Fibrosis Test in Obese Children with Ultrasound-Proven Steatosis
    
    hrp0082p2-d3-387
  - Metformin Treatment in Obese Children Enhances Weight Loss Related Improvement in Impaired Glucose Tolerance
    
    hrp0082p2-d3-388
  - Type and Time of Feeding in the First Year of Life are Not Associated to Circulating Multimeric Adiponectin Levels in Obese Children
    
    hrp0082p2-d3-389
  - POMC Deficiency Mimicking Neurometabolic Disease
    
    hrp0082p2-d3-390
  - The Relationship Between Weight-Related Anthropometric Parameters and Menarche in Norwegian Girls
    
    hrp0082p2-d3-391
  - HbA1c and Metabolic Parameters in a Pediatric Overweight/Obese Population
    
    hrp0082p2-d3-392
  - Comparison of FM_DXA and FM_BIA in Obese Adolescents
    
    hrp0082p2-d3-393
  - From the Need of Preventing Infantile Obesity as soon as Possible: a New Score at Birth
    
    hrp0082p2-d3-394
  - Body Composition in 10-15 Years Old Children Exposed to Pesticides Prenatally
    
    hrp0082p2-d3-395
  - D2 Dopamine Receptor Agonists Influence in the Animal Model of Dietary Obesity
    
    hrp0082p2-d3-396
  - Combined Evaluation of Glucose Levels at Fasting State and 1-H After Glucose Load Can Safely Predict Prediabetes in Obese Youth
    
    hrp0082p2-d3-397
  - Association Between Calcium Deficiency and Obesity in Children
    
    hrp0082p2-d3-398
  - Is Small for Gestational Age Status Associated with an Increase Risk of Atherogenesis?
    
    hrp0082p2-d3-399
  - Association between Lipid Profile, BMI, and Insulin Resistance Markers in Obese Prepubertal Children
    
    hrp0082p2-d3-400
  - Mannose Binding Lectin and Carotid Intima-Media Thickness in Chinese Obese Children
    
    hrp0082p2-d3-401
  - Usefulness of Hypertriglyceridemic Waist Phenotype in Obese Indian Children
    
    hrp0082p2-d3-402
  - Concomitant Changes in Full Body DXA Values and BMI-SDS During Multidisciplinary Treatment of Childhood Obesity
    
    hrp0082p2-d3-403
  - Cystic Fibrosis: Dyslipidemia in Brazilian Children
    
    hrp0082p2-d3-404
  - Do Children with Down Syndrome Show Lipid Profile Disorders?
    
    hrp0082p2-d3-405
  - Relationship Between Obesity and Platelet Indices in Children
    
    hrp0082p2-d3-406
  - Examining [beta]-Cell Reserve in Extremely Obese Children
    
    hrp0082p2-d3-407
  - SHBG Integrates the Cardiovascular Risk and Metabolic Dysfunction of Gestational Obesity
    
    hrp0082p2-d3-408
- Growth Hormone
- - Ternary Complex Formation and IGFBP3 Proteolytic Activity During Childhood: Age-Dependent Changes
    
    hrp0082p2-d1-409
  - GHR Gene Variants within Coding and Intronic Regions in Children with Idiopathic Short Stature
    
    hrp0082p2-d1-410
  - Spontaneous Baseline GH Secretion Signalling as a Regulator of Bone Metabolism in Children
    
    hrp0082p2-d1-411
  - 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)
    
    hrp0082p2-d1-412
  - A Re-Evaluation of GH Secretion with Combined Test (GHRH+ARG/PD) in Children with Prader-Willi Syndrome
    
    hrp0082p2-d1-413
  - Final Height SDS Gain of GH Treated Children with SHOX Deficiency Describing Observational and Clinical Trial Data
    
    hrp0082p2-d1-414
  - IGF1 is Associated with a More Favourable Pattern of Body Composition in Obese Children
    
    hrp0082p2-d1-415
  - Absence of GH Signaling Induces Hypothalamic Inflammation that is Reversed in Response to a High Fat Diet
    
    hrp0082p2-d1-416
  - GH Stimulated Levels in Prader-Willi Syndrome During the Transition Period between Childhood and Adulthood
    
    hrp0082p2-d1-417
  - Response to GH Treatment in Patients with Silver Russell Syndrome
    
    hrp0082p2-d1-418
  - Pubertal Development During GH Treatment with or without Additional GnRH Analogue Treatment in Short Children Born Small for Gestational Age
    
    hrp0082p2-d1-419
  - S.c. Injections of a Reversible Albumin-Binding GH Derivative (NNC0195-0092) in Adult Subjects with GH Deficiency is Well Tolerated
    
    hrp0082p2-d1-420
  - The Effects of Delaying Puberty with GnRH Agonists in Patients with Idiopathic GH Deficiency
    
    hrp0082p2-d1-421
- Growth Hormone (1)
- - Perceptions and Expectations of Patients and their Families for the Effects of GH Treatment
    
    hrp0082p2-d2-422
  - 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
    
    hrp0082p2-d2-423
  - What Dose of hGH is Adequate as a Substitution Therapy in GH Deficient Children?
    
    hrp0082p2-d2-424
  - Electronic Devices and Single-Dose Dispensing Systems GH are the Most Efficient and Less Loss of Drug
    
    hrp0082p2-d2-425
  - The Level and Conformation of Blood Plasma Carotenoids in GH Deficient Children After 1 Year of GH Therapy
    
    hrp0082p2-d2-426
  - Effects and Safety of Recombinant Human GH in GH Deficient Children with Rathke Cyst
    
    hrp0082p2-d2-427
  - The Interconnectivity Between GH Replacement Therapy and Subclinical Hypothyroidism on Growth Response in Children with Pituitary Dwarfism
    
    hrp0082p2-d2-428
  - What Should be the Diagnosis and Management of Short Children with IGF1 Deficiency, Responding to GH Administration Despite Normal GH Secretion?
    
    hrp0082p2-d2-429
  - 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
    
    hrp0082p2-d2-430
  - Vitamin D Concentrations in Children with GH Deficiency During First Year of GH Treatment
    
    hrp0082p2-d2-431
  - Growth Hormone Treatment in Children with SGA During a 5-Year Period, Assessment of Auxological Development and Insulin Resistance
    
    hrp0082p2-d2-432
  - Comparison of Measured Lean Body Mass (LBM_DXA) and Estimated LBM_BIA in Children with GH Deficiency
    
    hrp0082p2-d2-433
  - Metabolic Assessment in Children with GH Deficiency Before, During, and After Human GH Replacement Therapy
    
    hrp0082p2-d2-434
- Growth Hormone (2)
- - First-year Growth Response to GH in Relation to Final Height Outcome in Prepubertal Children with Idiopathic GH Deficiency
    
    hrp0082p2-d3-435
  - Reevaluation of GH Secretion During Puberty in Children Diagnosed as GH-deficient During Childhood
    
    hrp0082p2-d3-436
  - Long-Term Effects of GH Replacement Therapy on Thyroid Function in GH Deficiency Children
    
    hrp0082p2-d3-437
  - Does Priming with Sex Steroids Before GH Stimulation Test Increase the Diagnosis of Normal GH Secretion in Short Children?
    
    hrp0082p2-d3-438
  - GH Dosing Patterns in Short Children Born Small for Gestational Age
    
    hrp0082p2-d3-439
  - Two-Year Data from a Long-Term, Phase IV Study of Omnitrope^®, a Recombinant Human GH, in Short Children Born Small for Gestational Age
    
    hrp0082p2-d3-440
  - Effects of Gender and Gestational Age on GH Treatment in Very Young Children Born Small for Gestational Age
    
    hrp0082p2-d3-441
  - Two-Year Results from Patro Children, a Multi-Centre, Non-Interventional Study of the Long-Term Efficacy and Safety of Omnitrope^® in Children Requiring GH Treatment
    
    hrp0082p2-d3-442
  - The Effect of Two Different GH Dosages on Final Height and Bone Geometry
    
    hrp0082p2-d3-443
  - Baseline Body Composition of Children with Short Stature Diagnosed for GH Deficiency
    
    hrp0082p2-d3-444
  - GH Treatment to Final Height in Children with Idiopathic Short Stature: Evidence for an Early Therapy Initiation Effect
    
    hrp0082p2-d3-445
  - Evaluation of the Safety and Usability of FlexPro^® 30 mg/3 ml, for the Delivery of Norditropin^® in Patients Requiring GH Therapy
    
    hrp0082p2-d3-446
  - Efficacy, Adherence, and Cost Study According to Pathology and Treatment Devices in Children Treated with GHRH
    
    hrp0082p2-d3-447
- Growth
- - Isolated GH Deficiency (IGHD) may be due to Several Different Causes: mutations in the GHRH Receptor Gene Are a Relatively Rare Cause of IGHD
    
    hrp0082p2-d1-448
  - Fibroblast Growth Factor 21 is Inversely Associated with Growth Rates in Infancy
    
    hrp0082p2-d1-449
  - Identification of NPR2 Mutations in Disproportionate Short Stature
    
    hrp0082p2-d1-450
  - Eleven Years of Letrozole Treatment in a Child with 11-[beta] Hydroxylase Deficiency: Effect on Bone Age and Height Prognosis
    
    hrp0082p2-d1-451
  - Rasopathies: Assessment of Growth, Genetic Study, Genotype-Phenotype Correlation and Therapeutic Response to GH in Noonan Syndrome
    
    hrp0082p2-d1-452
  - New Reference for Height in Swedish Boys and Girls
    
    hrp0082p2-d1-453
  - Endocrine characteristics of patients with anorexia nervosa in a large paediatric study cohort
    
    hrp0082p2-d1-454
  - The Effect of Long Term GH Therapy in Discordant Twins Where One Twin is Born Small for Gestational Age: A Case Control Study
    
    hrp0082p2-d1-455
  - How Early is the Rise in Leptin Levels in Small for Gestational Age Children With Catch Up Growth
    
    hrp0082p2-d1-456
  - 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
    
    hrp0082p2-d1-457
  - Two Duplications Within PAR1 in a Family With Idiopathic Short Stature
    
    hrp0082p2-d1-458
  - Comparison Between GH assay: serum GH Cut-off Levels by ECLIA Performed in Pharmacological Estimulation Tests in Children With Short Stature
    
    hrp0082p2-d1-459
  - Skeletal Disproportion and Final Adult Height in Childhood-Onset Crohn's Disease
    
    hrp0082p2-d1-460
- Growth (1)
- - Anophthalmia, Abnormal Pituitary Development, and Suboptimal Response to GH Therapy in Two Children With Microdeletions of 14q22q23
    
    hrp0082p2-d2-461
  - Adiponectin Levels as Early Marker of Insulin Resistance in Children Born Small for Gestational Age in Our Cohort
    
    hrp0082p2-d2-462
  - Recombinant Human GH Effects on Growth and Clinical Status in Cystic Fibrosis
    
    hrp0082p2-d2-463
  - Interrelationships Between BMI and Other Overweight Related Anthropometric Variables in Childhood
    
    hrp0082p2-d2-464
  - Assessment of Omentin-1, Vaspin, and Visfatin Levels in Pediatric Patients with GH Deficiency
    
    hrp0082p2-d2-465
  - Normal Growth in Aromatase Excess Syndrome by Pharmacological Inhibition of Aromatase Activity
    
    hrp0082p2-d2-466
  - The Effect of the Environmental Factors on Growth Pattern of Turkish Children Having the Same Genetic Origin
    
    hrp0082p2-d2-467
  - Successful GH Treatment for Severe Growth Failure in Paediatric Patients with Anorexia Nervosa
    
    hrp0082p2-d2-468
  - The Analysis of Limb Segments Length and Body Proportion of Children and Adolescents Aged 6-17 Years in the Main Urban Area of Chongqing
    
    hrp0082p2-d2-469
  - Severe Short Stature due to a Heterozygous igf1r Mutation With a Good Response to rhgh Therapy: a Family Study
    
    hrp0082p2-d2-470
  - When and Why Should We Investigate the SRCAP Gene in Cases of Short Stature?
    
    hrp0082p2-d2-471
  - Body Proportions Estimated by Photometry
    
    hrp0082p2-d2-472
  - GH Deficiency in a Child With De Novo 2q31.1 Microdeletion
    
    hrp0082p2-d2-473
- Hypoglycaemia
- - Plasma Glucagon and Somatostatin Levels in Children with Congenital Hyperinsulinism During Hypoglycaemia
    
    hrp0082p2-d3-474
  - Long-Term Follow Up of Children with Congenital Hyperinsulinism on Octreotide Therapy
    
    hrp0082p2-d3-475
  - Glucagon Secretion in Response to Hypoglycemia in Patients with Congenital Hyperinsulinism
    
    hrp0082p2-d3-476
  - Opioid-Induced Endocrinopathy in a Toddler with Chronic Codeine Intoxication
    
    hrp0082p2-d3-477
  - Case Report: a Rare Cause of Hypoglycemia in a Neonate
    
    hrp0082p2-d3-478
  - The Majority of Late Presenting Congenital Hypoglycaemia Disorders are Really Missed Diagnosis: What Can we do to Improve Diagnosis in the New-Born Period?
    
    hrp0082p2-d3-479
  - The Role of Plasma C-Peptide Concentration in the Diagnosis of Congenital Hyperinsulinism
    
    hrp0082p2-d3-480
  - Presentation, Clinical and Genetic Outcomes in a Series of Infants With Congenital Hyperinsulinism
    
    hrp0082p2-d3-481
  - Feeding Issues in Children With Congenital Hyperinsulinism
    
    hrp0082p2-d3-482
  - Neurodevelopmental Outcomes in Early and Late Presenting Congenital Hyperinsulinism
    
    hrp0082p2-d3-483
  - Abstract unavailable
    
    hrp0082p2-d3-484
  - Nocturnal Hypoglycaemia in Diabetic Children: Continuous Glucose Monitoring Reveals More of the Iceberg
    
    hrp0082p2-d3-485
  - Fasting Hypoglycemia Associated With Hyperinsulinemia in a Child With Acute Lymphoblastic Leukemia and 6-Mercaptopurine Therapy
    
    hrp0082p2-d3-486
- Endocrine Oncology
- - The Cytotoxic Ability of NK Cells in Children with Autoimmune Thyroiditis
    
    hrp0082p2-d3-487
  - High Prevalence of Diabetes Mellitus Among Patients with APS Type 1 in Russia
    
    hrp0082p2-d3-488
  - Immunogenetics and Clinical Characteristics of Patients with the Most Common Organ-Specific Autoimmune Diseases: Evaluation in Respect of Gender and Autoimmunity
    
    hrp0082p2-d3-489
  - Genetic Susceptibility in Autoimmune Polyglandular Syndrome Type 3 Variant
    
    hrp0082p2-d3-490
  - Autoimunne Thyroiditis in Type 1 Diabetes Mellitus Pediatric Population
    
    hrp0082p2-d3-491
  - Autoimmune Polyglandular Syndrome in a Patient with Tuberous Sclerosis
    
    hrp0082p2-d3-492
  - Role of Metformin in the Treatment of Hypothalamic Obesity
    
    hrp0082p2-d3-493
  - 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
    
    hrp0082p2-d3-494
  - Early Occurrence of Graves' Disease After Severe Hypothyroidism in Boy Irradiated for Hodgkin's Disease
    
    hrp0082p2-d3-495
  - Endocrine Dysfunction Following Treatment of Medulloblastoma: a Single Centre Experience
    
    hrp0082p2-d3-496
  - Gonadal Tumor in 46,XY and 45,X/46,XY Female Patients: One Clinical Center Experience
    
    hrp0082p2-d3-497
  - A Rare Brain Tumor in Noonan Syndrome: Report of Two Cases
    
    hrp0082p2-d3-498
  - GH-Secreting Pituitary Adenoma with Gigantism: a Challenging Case
    
    hrp0082p2-d3-499
- Perinatal and Neonatal Endocrinology
- - The Contribution of Maternal Malaria Exposure and Metabolic Markers to Change in Blood Pressure in Nigerian Children over the First 3 Years of Life
    
    hrp0082p2-d3-500
  - Kabuki 47,XXY Syndrome: a Case Report
    
    hrp0082p2-d3-501
  - Retrospective Analysis of Cortisol Measurement in Neonates
    
    hrp0082p2-d3-502
  - Survey of Opinion on the Antenatal and Surgical Management of Disorders of Sex Development and Congenital Adrenal Hyperplasia
    
    hrp0082p2-d3-503
  - Vitamin D Deficiency as the Primary Cause of Neonatal Hypocalcemia in a Tertiary Hospital
    
    hrp0082p2-d3-504
  - Random Serial Cortisol Levels in Neonates: Does it Reduce Synacthen Testing?
    
    hrp0082p2-d3-505
  - Metabolic Profile of Neonates With Different Duration of Gestation and Different Size at Birth
    
    hrp0082p2-d3-506
  - A Couple of Naturally Conceived Twins Affected by Prader-Willi Syndrome
    
    hrp0082p2-d3-507
  - Various Presentations of X-linked Adrenoleukodystrophy: Case Reports
    
    hrp0082p2-d3-508
  - Neonatal Pituiiary-Thyroid Axis Dysregulation with Combined Thyroid Hormone and TSH Resistance in Infant with Trisomy 21 and Maternal Subclinical Hypothyroidism
    
    hrp0082p2-d3-509
  - Neonates with Acute Kidney Injury Continue to be at Risk of Iatrogenic Iodine Toxicity and Hypothyroidism with Attendant Risk to the Developing Brain
    
    hrp0082p2-d3-510
- Pituitary
- - Relationship Between Adenoid Vegetation and Neurosecretory Dysfunction (Pituitary Dysfunction)
    
    hrp0082p2-d1-511
  - Clinical Phenotype and Complications, Endocrinopathies and Neuroimaging Findings in a Case Series of Sod
    
    hrp0082p2-d1-512
  - Polyuria and Polydipsia: The Deep Waters of Diagnosis
    
    hrp0082p2-d1-513
  - Urinary Gonadotrophins for Assessment and Management of Pubertal Disorders
    
    hrp0082p2-d1-514
  - High Prevalence of PROP1 Gene Defects Among Patients with Multiple Pituitary Hormone Deficiency in Lithuania
    
    hrp0082p2-d1-515
  - Neuroendocrine Dysfunctions Following Traumatic Brain Injury in Children: a 12-Month Prospective Study
    
    hrp0082p2-d1-516
  - Could Brain MRI Replace GH Stimulation Tests in the Work-Up of GH Deficiency in the First Years of Life?
    
    hrp0082p2-d1-517
  - Goliath, a Variant of DAVID Syndrome?
    
    hrp0082p2-d1-518
  - Hyperthyroidism Due to TSH Secreting Pituitary Adenoma in a 7-Year-Old Boy
    
    hrp0082p2-d1-519
  - Hypothalamic Obesity in Children with Craniopharyngioma: Prevalence and Risk Factors of Obesity and Longitudinal Trends of BMI
    
    hrp0082p2-d1-520
- Pituitary (1)
- - Association of Pituicytoma and Cushing's Disease: a Rare Pediatric Case
    
    hrp0082p2-d2-521
  - Treatment Options in a 14-Year-Old Boy with an Atypic Cabergolin-Resistant Macroprolactinoma with Somatostatin Receptor 2 Expression and an Increased Proliferation Rate
    
    hrp0082p2-d2-522
  - Long-Term Data Including Fertility in Two Females with Hypothalamic Hamartoma Associated with Central Precocious Puberty
    
    hrp0082p2-d2-523
  - Pituitary Stalk Interruption Syndrome: a Sequential Manner to Gain Pituitary Hormone Deficiencies with Still Unknown Molecular Basis
    
    hrp0082p2-d2-524
  - Challenging Treatment of Gigantism in a Boy with McCune-Albright Syndrome
    
    hrp0082p2-d2-525
  - Child with GH Deficiency due to Remnant Craniopharyngeal Duct
    
    hrp0082p2-d2-526
  - Adolescents with Chronic Endocrine Diseases: a Multidisciplinary Approach: the Experience of the Paediatric Clinic of Palermo
    
    hrp0082p2-d2-527
  - Atypical Presentation of Hypothermia Induced Diabetes Insipidus: a Case Report
    
    hrp0082p2-d2-528
- Puberty and Neuroendocrinology
- - Is There Any Influence of TSH Serum Levels on Insulin Resistance in Euthyroid Adolescents with Polycystic Ovary Syndrome?
    
    hrp0082p2-d1-529
  - The Vaginal Maturation Index as a Marker of Local Sensitivity to Estrogens in Girls with Congenital Adrenal Hyperplasia During Puberty
    
    hrp0082p2-d1-530
  - Very Low Estradiol Levels are Independent From Duration of Amenorrhea in Girls with Severe Anorexia Nervosa
    
    hrp0082p2-d1-531
  - Evaluation of the Free Androgen Index in Adolesent Females Diagnosed with Obesity, Hirsutism, and PCOS
    
    hrp0082p2-d1-532
  - Polycystic Ovarian Syndrome in Adolescents: Metabolic Profile at Diagnosis, During and After Treatment with Oral Contraceptive
    
    hrp0082p2-d1-533
  - Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates
    
    hrp0082p2-d1-534
  - Correlation Research of Bisphenol A and Premature Thelarche in 6 Months to 2 Years Old Infant Girls
    
    hrp0082p2-d1-535
  - Monitoring GnRH Analog Treatment in Girls with Central Precocious Puberty: a Comparison of Four Methods
    
    hrp0082p2-d1-536
  - The Evaluation of Possible Role of Endocrine Disrupters in Precocious Puberty
    
    hrp0082p2-d1-537
  - Acute Exposure of Endocrine Disruptor does not Induce Oxidative Stress in the Rat's Brain
    
    hrp0082p2-d1-538
  - Dramatic Rise in the Prevalence of Precocious Puberty in Girls Over the Past 20 Years in the South of France
    
    hrp0082p2-d1-539
  - A Novel Mutation at a Splice Acceptor Site of WDR11 in a Patient with Combined Pituitary Hormone Deficiency
    
    hrp0082p2-d1-540
- Puberty and Neuroendocrinology (1)
- - Normal Minipuberty in a Patient with DAX1 Mutation: a Reliable Marker of the Function of the Hypothalamic-Pituitary-Gonadal Axis?
    
    hrp0082p2-d2-541
  - GH Excess and Pseudoprecocious Puberty in a 8-Year-Old Boy with Mccune-Albright Syndrome
    
    hrp0082p2-d2-542
  - Time to Menarche After Completing GnRH Agonist in Girls with Central Precocious or Early Puberty
    
    hrp0082p2-d2-543
  - Impact of Being Born Small or Large for Gestational Age on Pubertal Onset and Progression
    
    hrp0082p2-d2-544
  - Diagnostic Spectrum of Female Pubertal Delay
    
    hrp0082p2-d2-545
  - Kallmann Syndrome: Diagnosis in Paediatric Age
    
    hrp0082p2-d2-546
  - The Triptorelin Test Compares Favourably with the GnRH Test in the Diagnosis of Central Precocious Puberty
    
    hrp0082p2-d2-547
  - Puberty in Children with Shunted Congenital Hydrocephalus with and without Myelomeningocele
    
    hrp0082p2-d2-548
  - Evaluation of Age at GnRH Analogue Treatment Discontinuation, Age at Menarche and Adult Height in Girls with Central Precocious Puberty from the Spanish Registry
    
    hrp0082p2-d2-549
  - 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
    
    hrp0082p2-d2-550
  - The Effect of Combined GH and GnRH Agonist Treatment for Near-Final Height Improvement in True Precocious Puberty and Early Puberty
    
    hrp0082p2-d2-551
  - Pubertal Development in a Cohort of Romanian School-Aged Children
    
    hrp0082p2-d2-552
- Puberty and Neuroendocrinology (2)
- - Inhibin B in the Diagnosis of Delayed Puberty
    
    hrp0082p2-d3-553
  - Predominantly Matrilineal Inheritance of Familial Precocious Puberty Suggests an Underlying Imprint Anomaly
    
    hrp0082p2-d3-554
  - Tamoxifen-Induced Hirsutism: an Unusual Side Effect in a 5 Years Old Girl with Mccune-Albright Syndrome
    
    hrp0082p2-d3-555
  - Long Term Outcomes of Precocious Puberty due to Hypothalamic Hamartomas
    
    hrp0082p2-d3-556
  - Mutational Analysis of TAC and TACR3 in Idiopathic Central Precocious Puberty
    
    hrp0082p2-d3-557
  - Pituitary-Ovarian Axis in Patients with Isolated Premature Thelarche
    
    hrp0082p2-d3-558
  - The Buserelin Stimulation Test Given as an Intranasal Spray in Diagnosing Gonadotropin Deficiency in Males with Delayed Puberty
    
    hrp0082p2-d3-559
  - Adult Height Outcome of Girls with Idiopathic Central Precocious Puberty Treated with GnRH Analogs is Irrespective of BMI
    
    hrp0082p2-d3-560
  - Delayed Puberty: Between Chronopathology and Subclinical Pathology
    
    hrp0082p2-d3-561
  - Central Precocious Puberty as the Initial Manifestation of a Pilocytic Astrocytoma with Leptomeningeal Dissemination Simulating a Hypothalamic Dysgerminoma
    
    hrp0082p2-d3-562
  - Endocrine Abnormalities in Phosphoglucomutase 1 Deficiency
    
    hrp0082p2-d3-563
- Sex Development
- - 46,XY Neonates and Infants with Ambiguous Genitalia: Who to Investigate?
    
    hrp0082p2-d1-564
  - Novel NR5A1 Gene Mutations Associated with 46,XY Disorders of Sex Development
    
    hrp0082p2-d1-565
  - The Research About sf1 Gene Abnormality in 45 Children with Micropenis
    
    hrp0082p2-d1-566
  - A New Mutation of MAMLD1 (CXorf6) Associated with NR5A1 (SF1) Variant in a Patient with 46,XY DSD
    
    hrp0082p2-d1-567
  - 46XY, DSD due to 5[alpha]-Reductase Type 2 Deficiency in 19 Chinese Patients
    
    hrp0082p2-d1-568
  - Experience of Feminizing Operations in Cases of Incomplete Sexual Development of Girls
    
    hrp0082p2-d1-569
  - Four Cases of Isolated Partial Gonadal Dysgenesis due to NR0B1 (DAX1) Locus Duplication Inherited in a Large Family
    
    hrp0082p2-d1-570
  - Identification of a Missense MAP3K1 Mutation in a Patient with Hypospadias
    
    hrp0082p2-d1-571
  - Anogenital Distance, Penis Growth, and Masculine Behaviour Evidence for Independent Neurobehavioral Effects of Foetal Versus Postnatal Androgen Exposure in Boys
    
    hrp0082p2-d1-572
  - Mutation Analysis of kdm3a (Lysine-Specific Demethylase 3a) in Patients with Hypospadias
    
    hrp0082p2-d1-573
- Sex Development (1)
- - Analysis of Steroid 5-Alpha Reductase 2 (SRD5A2) Gene in Patients with 46,XY Disorder of Sex Development
    
    hrp0082p2-d2-574
  - AMH Levels in Pediatric Girls with Chronic Disease
    
    hrp0082p2-d2-575
  - The Utility of AMH for Predicting Testosterone Response to hCG Stimulation in Children with Suspected DSD
    
    hrp0082p2-d2-576
  - A Novel Cyp19a1 Gene Mutation Identified in Three Turkish Families
    
    hrp0082p2-d2-577
  - 46,XX Ovotesticular DSD: Is it Lawful to Wait for Gonadal Surgery?
    
    hrp0082p2-d2-578
  - Mosaicism: Study of Nine Patients
    
    hrp0082p2-d2-579
  - The V89L Polymorphism in the SRD5A2 Gene in Cases with Undescended Testis
    
    hrp0082p2-d2-580
  - Rare Disease Registries: Perception of Parents and Young People
    
    hrp0082p2-d2-581
  - Down Syndrome and Disorders of Sex Development: Only Coincidence or More?
    
    hrp0082p2-d2-582
  - Novel Mutation in a Newborn with a Rare Cause of 46,XY Sex Reversal: 17[beta]- Hydroxysteroid Dehydrogenase Type 3 Deficiency
    
    hrp0082p2-d2-583
- Thyroid
- - Treatment of Pediatric Graves' Disease: Results of a Multicenter Survey in Portugal
    
    hrp0082p2-d1-584
  - Subclinical Hypothyroidism is Associated with Low IGF1 Levels and Decreased Growth Velocity
    
    hrp0082p2-d1-585
  - Thyroid Function and Autoimmunity and Their Relation to Weight Status in Healthy Children and Adolescents
    
    hrp0082p2-d1-586
  - Mutation of the TSH Receptor Gene: a Longitudinal Study in Children with Non-Autoimmune Subclinical Hypothyroidism
    
    hrp0082p2-d1-587
  - Investigation of Autoimmune Diseases Accompanying Hashimoto's Thyroiditis in Children and Adolescents and Evaluation of Cardiac Signs
    
    hrp0082p2-d1-588
  - No Difference in Cognitive Development of Young Adults and Adolescents Affected by Congenital Hypothyroidism Compared to Their Sibling Controls Despite High Dose L-Thyroxin Treatment
    
    hrp0082p2-d1-589
  - Thyroid Disorders in Siblings of CH Patients with Thyroid Dysgenesis
    
    hrp0082p2-d1-590
  - Trends in Median Age at Guthrie Sampling, Laboratory Receipt, Notification, and Start of Treatment for Infants with TSH Elevation on Newborn Screening
    
    hrp0082p2-d1-591
  - Iodine-Deficiency Levels in Schoolchildren Aged Between 6 and 12
    
    hrp0082p2-d1-592
  - Incidence of Thyroid Nodules in Children Affected by Hashimoto's Thyroiditis: a 12-Year Survey of 567 Children
    
    hrp0082p2-d1-593
  - The Evolution of Iodine Status in Schoolchildren Living in a Formerly Iodine-deficient Region of Mures County, Romania
    
    hrp0082p2-d1-594
  - Papillary Thyroid Cancer with Diffuse Pulmonary Metastasis: How to Manage?
    
    hrp0082p2-d1-595
  - Factors Useful to Distinguish between Children with Permanent Congenital Hypothyroidism and Transient or Permanent Hyperthyrotropinemia
    
    hrp0082p2-d1-596
- Thyroid (1)
- - Thyroid Nodules in Childhood and Adolescence; Clinical, Radiologic and Etiological Evaluation
    
    hrp0082p2-d2-597
  - An Unusual Presentation of Acquired Hypothyroidism: the Van Wyk-Grumbach Syndrome
    
    hrp0082p2-d2-598
  - Severe Urticaria in Graves' Disease: is Carbimazole to Blame?
    
    hrp0082p2-d2-599
  - Low Serum Free T4 Concentration in a Girl with McCune-Albright Syndrome
    
    hrp0082p2-d2-600
  - Long Term Anti-Thyroid Drug Therapy in a Paediatric Population with Down Syndrome: an Irish Experience
    
    hrp0082p2-d2-601
  - Influence of Amiodarone on Thyroid Function in Children
    
    hrp0082p2-d2-602
  - Euthyroid Sick Syndrome in Children with Diabetic Ketoacidosis
    
    hrp0082p2-d2-603
  - Levothyroxine Requirement in Congenital Hypothyroidism: 12-year Longitudinal Study
    
    hrp0082p2-d2-604
  - Abstract unavailable
    
    hrp0082p2-d2-605
  - Genetic Studies in Congenital Hypothyroidism: a Regional Study
    
    hrp0082p2-d2-606
  - Premature Menarche Associated with Hashimoto Thyroiditis at 2 Years 9 Months: Case Report
    
    hrp0082p2-d2-607
  - Iodine Nutrition and Neonatal Thyrotropin Levels in Lucknow, India
    
    hrp0082p2-d2-608
  - Auxological Pattern, BMI and Endocrine Follow Up in Children with Congenital Hypothiroidism: the Data of the Pediatric Clinic of Palermo
    
    hrp0082p2-d2-609
- Turner Syndrome
- - Therapeutic Effects of GH Combined with Low-Dose Stanozolol on Growth Velocity and Final Height of Girls with Turner Syndrome
    
    hrp0082p2-d3-610
  - Epidemiology of Turner Syndrome in Iceland 1968-2012
    
    hrp0082p2-d3-611
  - Anti-Mullerian Hormone: a Marker of Premature Ovarian Insufficiency in Girls with Turner Syndrome
    
    hrp0082p2-d3-612
  - Nationwide Study of Turner Syndrome During Childhood in Turkey: Evaluation of Associated Problems
    
    hrp0082p2-d3-613
  - Aortic Dilation in a Large Cohort of Paediatric and Young Adult Patients with Turner Syndrome
    
    hrp0082p2-d3-614
  - Aortic Dimensions and Cardiac Anomalies in a Cohort of Children with Turner Syndrome
    
    hrp0082p2-d3-615
  - Improvements in Bone Mineral Density in Girls of Prepubertal Age with Turner Syndrome
    
    hrp0082p2-d3-616
  - Early Occurrence of Gonadoblastoma Found at Elective Gonadectomy in Turner Syndrome Mosaic for Y Chromosome
    
    hrp0082p2-d3-617
  - GH Deficiency as a Cause of Persistent Hypoglycaemia in a Child with Turner Mosaic and Kabuki Syndrome
    
    hrp0082p2-d3-618
  - A Child with Clinical and Cytogenetic Features of Male Edward Syndrome and Turner Syndrome with Bilateral Gonadoblastoma in Infancy
    
    hrp0082p2-d3-619
  - Turner Syndrome: Analysis of Changes in the Age at Diagnosis and Phenotypic and Genotypic Description of 174 Patients
    
    hrp0082p2-d3-620
Poster Category 3
- Adrenals & HP Axis
- - The Effect of Working in a Children's Hospital on Urinary Catecholamine Excretion Rates in Male and Female Physicians
    
    hrp0082p3-d1-621
  - Body Composition Analysis in Girls With Premature Adrenarche
    
    hrp0082p3-d1-622
  - Pseudohypoaldosteronism Type 1: Role of Urinary Steroid Profiling in Specific and Early Diagnosis: Lessons in Differential Diagnosis of PHA1 vs PHA2 (Renal Tract Anomaly)
    
    hrp0082p3-d1-623
  - Genotype-Phenotype Correlations in Bulgarian Patients with c.293-13A/C[gt]G Splice Mutation of 21CYPA2 Picked up by Neonatal Screening (NS)
    
    hrp0082p3-d1-624
  - A Pediatric Case of Cushing's Disease Presenting with Diabetic Ketoacidosis
    
    hrp0082p3-d1-625
  - Cyp21a2 Mutation Spectrum in Bulgarian Cah Patients
    
    hrp0082p3-d1-626
  - A Rare Cause of Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency: a Case Report
    
    hrp0082p3-d1-627
  - Familial Glucocorticoid Deficiency: Masked Diagnosis by Hydrocortisone Life-Saving Treatment
    
    hrp0082p3-d1-628
  - Clinical and Genetic Diagnosis of Allgrove Syndrome
    
    hrp0082p3-d1-629
  - Clinical Case of Cushing Syndrome in Secreting NET
    
    hrp0082p3-d1-630
  - Homozygous c.923dupT Combined with Heterozygous c.334G[gt]A CYP21A2 Mutation: a Case Report from the Bulgarian CAH Screening Programme
    
    hrp0082p3-d1-631
  - Secondary Pseudohypoaldosteronism Type 1: the Role of a Urinary Steroid Profile
    
    hrp0082p3-d1-632
  - Steroid 11[beta] Hydroxylase Deficiency in Egyptian Children
    
    hrp0082p3-d1-633
- Adrenals & HP Axis (1)
- - Prenatal Dexamethasone Use for the Prevention of Virilization in Pregnancy at Risk for Classical Congenital Adrenal Hyperplasia
    
    hrp0082p3-d2-634
  - Congenital Adrenal Hyperplasia: Survey of the Management in Children Across UK
    
    hrp0082p3-d2-635
  - Neonatal Hypercalcaemia Associated with Congenital Adrenal Hyperplasia
    
    hrp0082p3-d2-636
  - Abstract unavailable
    
    hrp0082p3-d2-637
  - Addison Disease and Atrophic Gastritis: High Persistent ACTH Levels Although an Adequate Treatment
    
    hrp0082p3-d2-638
  - Four Cases of Ovarian Adrenal Rest Tumors in Chinese Girls with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
    
    hrp0082p3-d2-639
  - Therapeutic Troubles of Cushing's Disease in Adolescence: Report of a Case
    
    hrp0082p3-d2-640
  - Congenital Hypoaldosteronism of Unknown Etiology in Five Half-Siblings
    
    hrp0082p3-d2-641
  - X-Linked Adrenoleukodystrophy in eight Patients
    
    hrp0082p3-d2-642
  - The Ganglioneuromas: About Eight Cases
    
    hrp0082p3-d2-643
  - Cushings Syndrome without Origin
    
    hrp0082p3-d2-644
  - Untreated Congenital Hyperplasia with Central Precocious Puberty
    
    hrp0082p3-d2-645
- Autoimmune Endocrine Disease
- - Hypothyroidism in Anorexia Nervosa due to Primary Autoimmune Pathogenesis
    
    hrp0082p3-d3-646
  - Autoimmune Disease and Arnold Chiari Syndrome: Any Correlation?
    
    hrp0082p3-d3-647
  - Genetically Proven APS Type 1 in Two Siblings
    
    hrp0082p3-d3-648
  - Rare Association of Diabetes Insipidus with Autoimmune Thyroiditis
    
    hrp0082p3-d3-649
  - Coexistence of Unusual and Distinctive Initial Clinical Manifestations of Systemic Lupus Erythematosus (SLE): a Child Case Presentation and Evaluation of Polyglandular Autoimmune Syndrome in SLE
    
    hrp0082p3-d3-650
  - Diabetes Mellitus after Hematopoietic Stem Cell Transplantation
    
    hrp0082p3-d3-651
  - Preservation of Ovarian Function in Young Females Cancer Survivors with Risk of Ovarian Failure
    
    hrp0082p3-d3-652
  - Late Endocrine Effects in Children and Adolescentes Submitted to Allogenic Bone Marrow Transplantation
    
    hrp0082p3-d3-653
  - Adrenocortical Tumor: a Case Report
    
    hrp0082p3-d3-654
  - A Conservative Approach to the Management of Endocrine Neoplasia in Carney Complex in an Adolescent Male
    
    hrp0082p3-d3-655
  - Two Cases of Thyroid Carcinoma in Children
    
    hrp0082p3-d3-656
  - Is There Any Correlation Between Height and Pediatrics' Malignancy
    
    hrp0082p3-d3-657
  - Increasing Testicular Size due to Bilateral Large Cell Calcifying Sertoli Cell Tumours in a Peri-Pubertal Child with Carney Complex
    
    hrp0082p3-d3-658
  - Evaluation of the Relation between Thyroid Dysfunction and Oxidant/Antioxidant Status in Obese Children
    
    hrp0082p3-d3-659
- Bone
- - Normal Serum Calcium Levels and Vitamin-D Dependent Rickets Type 2 (VDDR-II): a Novel Vitamin D Receptor Mutation
    
    hrp0082p3-d1-660
  - No Gene Alterations in 11 Genes Associated with Isolated Hypoparathyroidism
    
    hrp0082p3-d1-661
  - Hypercalcemia due to Subcutaneous Fat Necrosis in a Newborn Successfully Treated with Pamidronate Infusion Therapy
    
    hrp0082p3-d1-662
  - Hypovitaminosis D: Factors Affecting in Spanish Children and Adolescents
    
    hrp0082p3-d1-663
  - Abstract unavailable
    
    hrp0082p3-d1-664
  - Survey of Vitamin D Status in Breastfeeding Infants Under the Age of 6 Months Attending the Growth Monitoring Clinic at Rubaga Hospital
    
    hrp0082p3-d1-665
  - Hypercalciuria in Patients with Coexisting Osteogenesis Imperfecta and Renal Tubular Acidosis
    
    hrp0082p3-d1-666
  - Metabolic and Bone Disorders in Vertically HIV-Infected Children
    
    hrp0082p3-d1-667
  - Lumbar Spine Areal Bone Mineral Density and 25-Hydroxyvitamin D Serum Concentrations at 2-Year Follow-up in Patients with Osteogenesis Imperfecta
    
    hrp0082p3-d1-668
  - Achondroplasia and Neurological Disorders
    
    hrp0082p3-d1-669
  - Primary Hypomagnesaemia with Secondary Hypocalcaemia (HSH): an Uncommon Diagnosis for a 2 Month Old Afro-Caribbean Formula Fed Infant Presenting with Seizures
    
    hrp0082p3-d1-670
  - A Challenging Diagnosis of Pseudohypoparathyroidism Type 1a and Practical Management: a Case Report
    
    hrp0082p3-d1-671
  - Obese Adolescent with Gait and Depression
    
    hrp0082p3-d1-672
- Bone (1)
- - Normal Bone Mineral Acquisition in Korean Adolescents; Korea National Health and Nutrition Examination Surveys
    
    hrp0082p3-d2-673
  - Klippel-Trenaunay-Weber Syndrome: the First Case Report in an African Child
    
    hrp0082p3-d2-674
  - FGFR3 Gene: a Very Rare Mutation
    
    hrp0082p3-d2-675
  - Abstract unavailable
    
    hrp0082p3-d2-676
  - Risk Factors Affecting the Development of Nephrocalcinosis, the Most Common Complication of Hypophosphatemic Rickets
    
    hrp0082p3-d2-677
  - When is Epilepsy Not Epilepsy
    
    hrp0082p3-d2-678
  - Evaluation of Patients with Stunting in Armenia
    
    hrp0082p3-d2-679
  - Fluctuation in Cerebral Calcification in a Patient with Pseudohypoparathyroidism Type 2
    
    hrp0082p3-d2-680
  - Variability in Clinical and Genetic Spectrum in Hypophosphatasia: Natural History in Two Patients
    
    hrp0082p3-d2-681
  - Cautionary Tales in the Management of Transient Neonatal Hypoparathyroidism
    
    hrp0082p3-d2-682
  - Two Different Diagnosis of Pseudohypoaldosteronism
    
    hrp0082p3-d2-683
  - Clinical Phenotype and Molecular Studies in Patients with Hypophosphatemic Rickets
    
    hrp0082p3-d2-684
  - Autosomal-Dominant Hypocalcaemia, New Clinical Features
    
    hrp0082p3-d2-685
  - I.V. Zolendronic Acid: Experience of Treatment of Children with Osteogenesis Imperfecta in Indonesia
    
    hrp0082p3-d2-686
- Bone (2)
- - Bone Health in a Cohort of Irish Spinal Muscular Atrophy Patients
    
    hrp0082p3-d3-686
  - Endocrinological Assessment of Children with Bronchiectasis
    
    hrp0082p3-d3-687
  - Infantile Hypophosphatasia
    
    hrp0082p3-d3-688
  - Vitamin D Levels in Short Prepubertal Children Born Small for Gestational Age
    
    hrp0082p3-d3-689
  - Prospective Evaluation of Bone Mineralization, PTH Regulation, and Metabolic Profile in Adult Patients with Hereditary Hypophosphatemic Rickets
    
    hrp0082p3-d3-690
  - Bone Mineral Density and Vitamin D Status in Girls and Adolescents with Turner Syndrome
    
    hrp0082p3-d3-691
  - Vitamin D Deficiency in Children
    
    hrp0082p3-d3-692
  - The Use of Pamidronate in Pediatric Patients with Disease of Other than Osteogenesis Imperfecta: the Experience of Our Center
    
    hrp0082p3-d3-693
  - McCune-Albright Syndrome Associated to Hypophosphatemic Rickets
    
    hrp0082p3-d3-694
  - Clinical Effects of Vitamin D in Asthma
    
    hrp0082p3-d3-695
  - A Korean Boy with Pseudohypoparathyrodism Type Ia Presenting with Congenital Megacolon and Spinal Stenosis: Identification of a Novel GNAS Gene Mutation
    
    hrp0082p3-d3-696
  - A Case with Odontohypophosphatasia and Family Investigation
    
    hrp0082p3-d3-697
  - TSH/fT4 Ratio as a Marker of TSH Resistance in Pseudoparathyroidism 1A and Obesity
    
    hrp0082p3-d3-698
  - Infantile Hypophosphatasia
    
    hrp0082p3-d3-699
- Diabetes
- - Efficacy and Safety of CSII Treatment in Paediatric Age: Long Term Experience of a Tertiary Care Centre in Spain
    
    hrp0082p3-d1-699
  - Diabetic Ketoacidosis in Children with T1DM: an Italian Multicentre Survey
    
    hrp0082p3-d1-700
  - Changing Presentation of Type 1 Diabetes to a Tertiary Paediatric Centre
    
    hrp0082p3-d1-701
  - Abnormal Blood Glucose as a Prognostic Factor for Adverse Clinical Outcome Among Children with Acute Medical Conditions in Ghana
    
    hrp0082p3-d1-702
  - Urinary c-Peptid/Creatinine Ratio in Children and Adolescents Diagnosed with Maturity-Onset Diabetes of the Young
    
    hrp0082p3-d1-703
  - A Case with Neonatal Diabetes and Congenital Hypothyroidism due to Glis3 Gene Deletion
    
    hrp0082p3-d1-704
  - Glycemic Control of Patients with Type 1 Diabetes Using Automated Bolus Calculator Glucometerr
    
    hrp0082p3-d1-705
  - Congenital Hyperinsulinism Linked to INS-R Mutation: Case Report
    
    hrp0082p3-d1-706
  - The Lung Endothelin System: a Potent Therapeutic Target with Bosentan for the Amelioration of Lung Alterations in a Rat Model of Diabetes Mellitus
    
    hrp0082p3-d1-707
  - Clinical Significance of Typing Fulminant Type 1 Diabetes in Children and Adolescents
    
    hrp0082p3-d1-708
  - Continuous Subcutaneous Insulin Infusion Therapy in Preschool Children with Type 1 Diabetes Mellitus
    
    hrp0082p3-d1-709
  - Health-Related Quality of Life Among Turkish Children and Adolescents with Type 1 Diabetes
    
    hrp0082p3-d1-710
  - Autoimmune Thyroiditis in Georgian Children and Adolescents with Type 1 Diabetes Mellitus
    
    hrp0082p3-d1-711
- Diabetes (1)
- - Audit of the Use of Integrated Care Pathway in the Management of Diabetic Keto Acidosis in Children
    
    hrp0082p3-d2-712
  - Development of Diabetes Mellitus after Hematopoietic Stem Cell Transplantation for Childhood Leukemia
    
    hrp0082p3-d2-713
  - Case of Family Neonatal Diabetes with KCNJ11 Gene Mutation
    
    hrp0082p3-d2-714
  - Insulin Pump Therapy in One Case of 6q24 Transient Neonatal Diabetes for 3 Years
    
    hrp0082p3-d2-715
  - 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
    
    hrp0082p3-d2-716
  - Diabetes Mellitus a Late Complication in Glycogen Storage Disease Type 1b
    
    hrp0082p3-d2-717
  - Incidence of Diabetes Mellitus and Associated Complications Among Children: Results from Azerbaijan Diabetes Registry 1997-2007
    
    hrp0082p3-d2-718
  - Arabic Translation and Validation of the Newest Vital Sign Health Literacy Tool: a Pilot Project to Test Health Literacy of Caregivers of Children with Type 1 Diabetes in Kuwait
    
    hrp0082p3-d2-719
  - Anti-Cyclic Citrullinated Peptide Antibodies are not Frequent in Children with Type 1 Diabetes
    
    hrp0082p3-d2-720
  - Glycemic Variability and Metabolic Control in Pediatric Patients with Type 1 Diabetes Mellitus
    
    hrp0082p3-d2-721
  - Knowledge Base and Attitudes of Senior Medical Staff to Insulin Therapy in Children with Diabetes
    
    hrp0082p3-d2-722
  - Estimation of Compensation and Prevalence of Chronic Complications of Type 1 DM in Children According to the Screening Data
    
    hrp0082p3-d2-723
- Diabetes (2)
- - Prevalence of Impaired Glucose Tolerance and Insulin Resistance in a Sample of the 6- to 16-Year-Old Overweight or Obese Pediatric Population
    
    hrp0082p3-d3-724
  - Differences in Pubertal Development and Anthropometry Between Normal Population and Type 1 Diabetic Child at Debut in Spain
    
    hrp0082p3-d3-725
  - Effect of Vitamin D Treatment on Glucose and Insulin Metabolism, and Bone Turnover in Children with Symptomatic Vitamin D Deficiency
    
    hrp0082p3-d3-726
  - Evaluation of HbA1c Measurement in Trinidad and Tobago
    
    hrp0082p3-d3-727
  - The Result of Sulphonylureas Treatment in Patients with Neonatal Diabetes Mellitus due to kcnj11/abcc8 Gene Mutations in Vietnam
    
    hrp0082p3-d3-728
  - Prevalence of Secondary Diabetes and Related Factors in China Hospitalized Children
    
    hrp0082p3-d3-729
  - Wolcott-Rallison Syndrome in Two Siblings with no Implication of EIF2AK3 Mutation
    
    hrp0082p3-d3-730
  - Prevalence of Atopic Diseases in Diabetic Children and Adolescents
    
    hrp0082p3-d3-731
  - The Pattern of Body Composition Change in Type 1 Diabetes by Gender
    
    hrp0082p3-d3-732
  - Transient Neonatal Diabetes and Intermediate DEND Phenotype with KCNJ11 Mutation
    
    hrp0082p3-d3-733
  - Offspring of Parents with Obesity, Complex Investigations Risk of Carbohydrate Disturbances and Diabetes
    
    hrp0082p3-d3-734
  - Metabolic Control in a Pediatric Population with Type 1 Diabetes Mellitus
    
    hrp0082p3-d3-735
- Diabetes (3)
- - Metabolic Compensation Correlation with Chronic Complications of Type 1 Diabetes in Children in Latvia
    
    hrp0082p3-d2-736
  - IGF1 Levels in Children with Type 1 Diabetes are Primarily Related to Glycemic Control and Residual [beta] Cell Mass, and not Affected by Different Modalities of Insulin Therapy
    
    hrp0082p3-d2-737
  - When Should We Suspect Maturity Onset Diabetes of the Young in Children and Adolescents
    
    hrp0082p3-d2-738
  - Cystic Fibrosis-Related Diabetes in Children and Adolescents in the Russian Federation
    
    hrp0082p3-d2-739
  - Continuous Glucose Monitoring System in the Diagnosis of Early Glycemic Abnormalities in High-Risk Groups
    
    hrp0082p3-d2-740
  - Incidence of Dyslipidemia and its Association with Glycemic Control in Adolescents and Young Adults with Type 1 Diabetes
    
    hrp0082p3-d2-741
  - 'Learning by Doing Approach': Use of Multimedia Applications in Type 1 Diabetic Children
    
    hrp0082p3-d2-742
  - Seip Berardinelli Syndrome Case Report
    
    hrp0082p3-d2-743
  - Nine-Year-Old Boy with Wolfram Syndrome: Case Report
    
    hrp0082p3-d2-744
  - A Case of Type 2 Diabetes Associated with Ichthyosis: Chanarin-Dorfman Syndrome
    
    hrp0082p3-d2-745
  - 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?
    
    hrp0082p3-d2-746
  - Comparison the Clinical Efficacy of Autologous Hematopoietie Stem Cell Transplantation and Traditional Insulin Therapy in Newly Diagnosed Primary Childhood Type 1 Diabetes
    
    hrp0082p3-d2-747
- Diabetes (4)
- - Monogenic Diabetes in a Paediatric Population: Finding the Needle in the Haystack
    
    hrp0082p3-d3-748
  - Hyperglycemia: MODY: a Diagnosis to Remember
    
    hrp0082p3-d3-749
  - A Case of Type 1 Diabetes Associated with Cerebellar Ataxia: Stiff-Person Syndrome
    
    hrp0082p3-d3-750
  - 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
    
    hrp0082p3-d3-751
  - The Psychological Impact of Diabetes on Glycaemic Control in Affected Saudi Children at Different Developmental Age Groups
    
    hrp0082p3-d3-752
  - Type 1 Diabetes Mellitus in Pediatric Population: Chronic Complications and Associated Diseases
    
    hrp0082p3-d3-753
  - Ketoacidosis-Associated Stroke: Cerebral Infarction
    
    hrp0082p3-d3-754
  - Multiple Daily Injections Since the Diagnosis of Type 1 Diabetes Mellitus in Children and Adolescents: Assessment of 3 Years
    
    hrp0082p3-d3-755
  - Haemolysis and Acute Pancreatitis During Diabetic Ketoacidosis Treatment in a 14-Year-Old Boy with Unknown Glucose-6-Phosphate Dehydrogenase Deficiency
    
    hrp0082p3-d3-756
  - Pneumothorax, Pneumomediastinum, and Subcutaneous Emphysema: Complications of Severe DKA in T2DM Obese Patient
    
    hrp0082p3-d3-757
  - Diabetes Insipidus in Pediatric Practice
    
    hrp0082p3-d3-758
  - Diabetes Mellitus Type 2 in Pediatrics: an Emerging Reality in Our Country: First Described in Spain
    
    hrp0082p3-d3-759
- Fat Metabolism & Obesity
- - Association of Ghrelin Gene Polymorphisms with Obesity in Japanese Children
    
    hrp0082p3-d1-760
  - 25-Hydroxy Vitamin D Deficiency and its Relationship to Obesity and Other Risk Factors in a Group of Iranian Children and Adolescents
    
    hrp0082p3-d1-761
  - 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
    
    hrp0082p3-d1-762
  - Association of Lifestyle with Metabolic Syndrome in Children
    
    hrp0082p3-d1-763
  - Prevalence of Metabolic Syndrome and Insulin Resistance Among Aged 3-9 Children
    
    hrp0082p3-d1-764
  - The Relation of Serum Leptin and Soluble Leptin Receptor Levels with Metabolic and Clinical Parameters in Obese and Healthy Children
    
    hrp0082p3-d1-765
  - Positive Association of Pro-Oxidative Stress Markers with Adipose Mass in Pre- and Early-Pubertal Boys
    
    hrp0082p3-d1-766
  - Prevalence Metabolic Syndrome and Its Components Among Children with Obesity
    
    hrp0082p3-d1-767
  - Serum Omentin-1 and Vaspin Levels in Obese Children and Their Correlation with Lipid Metabolism
    
    hrp0082p3-d1-768
  - The Importance of Weight for Height for Prediction of Metabolic Syndrome in Obese Children and Adolescents: Impact of Gender and Pubertal Status
    
    hrp0082p3-d1-769
  - Understanding How Race Influences Plasma Peptide YY in the Aging Population
    
    hrp0082p3-d1-770
  - Level of Non-HDL Cholesterol and its Related Factors in Chinese Han Students
    
    hrp0082p3-d1-771
  - Do Children with Down Syndrome Show Lipid Profile Disorders?
    
    hrp0082p3-d1-772
- Fat Metabolism & Obesity (1)
- - Trends in Obesity Prevalence and BMI among Pre-Pubertal Bulgarian Children, 1990-2007
    
    hrp0082p3-d2-773
  - The Prevalence of 25-Hydroxyvitamin D Insufficiency and Deficiency Among Overweight and Obese Children and Adolescents in Greece
    
    hrp0082p3-d2-774
  - Metabolic and Lifestyle Correlates of Health-Related Quality of Life Among Taiwanese Obese Adolescents
    
    hrp0082p3-d2-775
  - Prevalence of Dyslipidemia and Associated Factors Among Obese Turkish Children
    
    hrp0082p3-d2-776
  - The Interaction of Exophtalmos with Obesity in Turkish Children and Adolescents
    
    hrp0082p3-d2-777
  - Reproducibility of the Glucose Tolerance Test in Overweight Children
    
    hrp0082p3-d2-778
  - Younger Age and BMI [gt]3SD are Risk Factors for Mortality in Children with Hypothalamic Obesity
    
    hrp0082p3-d2-779
  - Age-Related Characteristics of Nutritional Status in Children with Alimentary Obesity
    
    hrp0082p3-d2-780
  - Relationship Between Adiposity Degree and Physical Activity and Inactivity Among Children and Adolescents
    
    hrp0082p3-d2-781
  - Antenatal and Early Childhood Determinants of the Development of Obesity in Children
    
    hrp0082p3-d2-782
  - The Association Hypothyroidism: Obesity in a Group of Children and Adolescents
    
    hrp0082p3-d2-783
  - A New Lipodystrophy Syndrome?
    
    hrp0082p3-d2-784
  - Prevalence of Excessive Body Mass and Obesity Among Children and Adolescents Residing in Tashkent, Uzbekistan
    
    hrp0082p3-d2-785
- Fat Metabolism & Obesity (2)
- - Hypothalamic Obesity in Children and Adolescents: a Multi-Disciplinary Approach and Novel Therapeutic Tools
    
    hrp0082p3-d3-786
  - Obese Teenagers and Risk of Injuries During School Physical Activity
    
    hrp0082p3-d3-787
  - Erythrocyte Sedimentation Rate and CRP Levels in Childhood Obesity
    
    hrp0082p3-d3-788
  - Bone Age Advancement in Prepubertal Children with Overweight and Obesity
    
    hrp0082p3-d3-789
  - Obesity Correlates in Adolescence
    
    hrp0082p3-d3-790
  - Correlation Between Fasting Blood Glucose and Glucose Tolerance Test in Overweight Children
    
    hrp0082p3-d3-791
  - Frequency of Vegetable and Fruit Consumption in Overweight Children and Their Parents
    
    hrp0082p3-d3-792
  - Prevalence of Abnormalities of Glucose Metabolism in Obese Greek Children and Adolescents
    
    hrp0082p3-d3-793
  - Prader-Willi Syndrome: Reports of Two Patients with Congenital Abnormalities of Kidney and Urinary Tract
    
    hrp0082p3-d3-794
  - Response to Treatment in a Group of Patients with Childhood Obesity
    
    hrp0082p3-d3-795
  - Prevalence of Overweight and Obesity in Children and Adolescents at Public and Private Schools from Uberaba Brazil
    
    hrp0082p3-d3-796
  - Gene Mutation and Clinical Characteristics Analysis in Progressive Familial Intrahepatic Cholestasis
    
    hrp0082p3-d3-797
  - Characteristics of a Population of Obese Children and Adolescents: Suggesting a New Paradigm
    
    hrp0082p3-d3-798
- Gonads and Gynaecology
- - Effects of GNRH Analogue Treatment on Internal Genitales of Girls with Central Precocious
    
    hrp0082p3-d3-799
  - Ovarian Tumors Observed in Endocrinology
    
    hrp0082p3-d3-800
  - The Usefulness of the Leuprolide Stimulation Test as a Diagnostic Method of Idiopathic CPP in Girls
    
    hrp0082p3-d3-801
  - The Effects of Rhythmical Massage Therapy and Heart Rate Variability-Biofeedback on Primary Dysmenorrhea a Qualitative Study
    
    hrp0082p3-d3-802
  - Menstrual Regularity Among Early Menarche Girls and CPP or EFP Girls Treated with GnRHa
    
    hrp0082p3-d3-803
  - Complete Blood Count Parameters in Girls with Polycystic Ovary Syndrome
    
    hrp0082p3-d3-804
  - The Genotypic and Phenotypic Variability of Mixed Gonadal Dysgenesis
    
    hrp0082p3-d3-805
  - A Rare Cause for 46,XX Ovarian Dysgenesis: Perrault Syndrome
    
    hrp0082p3-d3-806
  - A Rare Cause of Ovarian Failure; Ovarioleucodystrophy
    
    hrp0082p3-d3-807
  - Phenotypic and Genotypic Characteristics of Patients with Turner Syndrome
    
    hrp0082p3-d3-808
  - Three Siblings with Gonadal Dysgenesis
    
    hrp0082p3-d3-809
- Growth
- - The Role of IGF1R Gene Mutation in the Development of Oligodendrocytes
    
    hrp0082p3-d1-810
  - A Novel GHR Mutation, c.439+1g[gt]a; in a Family with Laron Syndrome
    
    hrp0082p3-d1-811
  - 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
    
    hrp0082p3-d1-812
  - BMI, IGF1-SDS, and rhGH Treatment
    
    hrp0082p3-d1-813
  - A Novel GH1 Functional Mutation in a Family with Isolated GH Deficiency
    
    hrp0082p3-d1-814
  - Insulin Tolerance Test and GHRH Plus Arginine in the Reassessment of Pituitary Function at Adult Height Achievement
    
    hrp0082p3-d1-815
  - The Level and Conformation of Blood Plasma Carotenoids in Girls with Turner Syndrome After 1 Year of GH Therapy
    
    hrp0082p3-d1-816
  - Increased Required Dose of GH in Children with Inborn Panhypopituitarism
    
    hrp0082p3-d1-817
  - Assessment of Compliance with GH Therapy
    
    hrp0082p3-d1-818
  - Body Composition in GH Deficient Children: Effects of GH Therapy and Comparison Between DXA and Anthropometric Data
    
    hrp0082p3-d1-819
  - Socioeconomic Factors Influence rhGH Treatment Adherence and its Response in Children
    
    hrp0082p3-d1-820
  - Study of GH Receptor exon 3 Polymorphism in Children With Prader-Willi Syndrome
    
    hrp0082p3-d1-821
  - Auxological Evaluation of 'Non-Identical Twins'
    
    hrp0082p3-d1-822
  - Three-Years Height Outcome During rhGH Therapy in Severe Short Subjects Affected by Skeletal Dysplasias
    
    hrp0082p3-d1-823
- Growth (1)
- - Correlation Between Initial Treatment Effect of Recombinant Human GH and Exon 3 Polymorphism of GH Receptor in Chinese GH Deficiency Children
    
    hrp0082p3-d2-823
  - GH Deficiency in a Case with Neurofibromatosis-Noonan Syndrome
    
    hrp0082p3-d2-824
  - 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
    
    hrp0082p3-d2-825
  - Usability and Safety of FlexPro[reg] PenMate[reg] in Patients, Caregivers and Healthcare Professionals (HCPs)
    
    hrp0082p3-d2-826
  - Impairment of Glucose Metabolism in GH Deficient Children Under GH Replacement
    
    hrp0082p3-d2-827
  - Growth Response After 1 Year of GH Treatment in Children Born Small for Gestational (SGA) Without GH Deficiency: our Experience
    
    hrp0082p3-d2-828
  - Cross-Sectional and Prospective Study of the Effects of GH Therapy on Metabolic Panel in Children with GH Deficiency
    
    hrp0082p3-d2-829
  - Prader-Willi Syndrome and GH Therapy: valuable Effects and Adverse Events
    
    hrp0082p3-d2-830
  - Recovery of Central Fever After GH Therapy in a Patient with GH Deficiency Secondary to Posttraumatic Brain Injury
    
    hrp0082p3-d2-831
  - The Impact of GH Replacement Therapy in Children Born Small-for-Gestational-Age: growth Response and Safety Profile
    
    hrp0082p3-d2-832
  - GH Treatment in 50 Child with Short Stature: Lebanese Experience
    
    hrp0082p3-d2-833
  - Effectiveness of GH Therapy in Children with Short Stature and Decreased GH Peak in Stimulating Tests is Independent from GH Secretion After Falling Asleep
    
    hrp0082p3-d2-834
  - An Unusual Case of a Child with GH Deficiency and Arnold-Chiari Malformation Type I
    
    hrp0082p3-d2-835
- Growth (2)
- - What is the Profile of Gigantism: Seven Observations
    
    hrp0082p3-d3-836
  - GH Treatment in Dent's Disease: a Case Report
    
    hrp0082p3-d3-837
  - Analysis of the Effectiveness of Treatment with GH in a Tertiary Hospital in the Last 30 Years
    
    hrp0082p3-d3-838
  - A Rare Syndrome Benefits from GH Therapy: Hypotonia-Cystinuria Syndrome
    
    hrp0082p3-d3-839
  - Changes in BMI in GHD and SGA Children in the First Year of Treatment
    
    hrp0082p3-d3-840
  - Study of the Effect of GH Treatment on Growth in Patients Affected by the Inherited Metabolic Disease Methylmalonic Acidemia
    
    hrp0082p3-d3-841
  - Pubertal Development of Isolated GH Deficient Patients
    
    hrp0082p3-d3-842
  - Two Years of GH Therapy in Children with Growth Deficiency
    
    hrp0082p3-d3-843
  - WHO Growth Charts Replacing National Reference Data: Their Influence on Screening for Over- or Underweight and of Growth Disorders
    
    hrp0082p3-d3-844
  - Skeletal Maturity of Radius, Ulna, and Short Bones in TW3 Method for Children in Korea
    
    hrp0082p3-d3-845
  - Design and Recruitment of a Longitudinal Cohort Study of Growth and Puberty in Russian Boys
    
    hrp0082p3-d3-846
  - Multiple Endocrinopathies in a Case with H Syndrome due to a Novel slc29a3 Mutation
    
    hrp0082p3-d3-847
  - Severe Short Stature with Features of Achondroplasia, Later Diagnosed as Panhypopituitarism: a Case Report
    
    hrp0082p3-d3-848
- Growth (3)
- - GH Therapy in Prepubertal Children: Results After 4 Years
    
    hrp0082p3-d2-849
  - 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
    
    hrp0082p3-d2-850
  - Growth pattern of the nigerian child compared to international references
    
    hrp0082p3-d2-851
  - Evaluation of Potential Waste of GH Across Available GH Pen Devices and an Electronic GH Delivery Device
    
    hrp0082p3-d2-852
  - Switching From the Original to the Biosimilar Recombinant Human GH - Omnitrope[reg]: an Experience of a Single Paediatric Centre in Spain
    
    hrp0082p3-d2-853
  - Descriptive Analysis of Medication Adherence for Patients Treated with GH Therapy
    
    hrp0082p3-d2-854
  - Effect of Cyanotic and Acyanotic Congenital Heart Disease on Placental and Birth Size
    
    hrp0082p3-d2-855
  - Anthropometric Evaluation of a Cohort of School-Aged Children: the Need for National Growth References in Romania
    
    hrp0082p3-d2-856
  - Differences in Personality of Monozygotic Twins can be Predicted by Difference in Birth Weight in Teen Monozygotic Twins
    
    hrp0082p3-d2-857
  - The Growth Speed of Late Pretem Infants Aged 1 Year
    
    hrp0082p3-d2-858
  - Response of GH Therapy in Six Children with Achondroplasia
    
    hrp0082p3-d2-859
  - Clinical Expression of Familial Williams-Beuren Syndrome in a Turkish Family
    
    hrp0082p3-d2-860
  - Abstract unavailable
    
    hrp0082p3-d2-861
- Growth (4)
- - Muccopolysacharidose and Hypopituitarism: a Case Report
    
    hrp0082p3-d3-862
  - Costello Syndrome: What About GH Treatment?
    
    hrp0082p3-d3-863
  - The Establishment of a New Paediatric Endocrinology Training Programme in South Africa
    
    hrp0082p3-d3-864
  - Side Effect of Treatment with rGh
    
    hrp0082p3-d3-865
  - GH Treatment Adherence in Children in Latvia
    
    hrp0082p3-d3-866
  - The Effect of GH and Pubertal Induction Therapy in Turner Syndrome
    
    hrp0082p3-d3-867
  - Hearing Loss in Turner Syndrome
    
    hrp0082p3-d3-868
  - Genotype-Phenotype Correlation in Turner Syndrome
    
    hrp0082p3-d3-869
  - Primary Amenorrhea with Normal Stature: Why Not Turner Syndrome?
    
    hrp0082p3-d3-870
  - The Causes of Short Stature in Turner Syndrome
    
    hrp0082p3-d3-871
  - Descriptive Analyses of Turner Syndrome
    
    hrp0082p3-d3-872
  - Phenotypic and Genotypic Characteristics of Patients with Turner Syndrome
    
    hrp0082p3-d3-873
- Perinatal and Neonatal Endocrinology
- - Clinical Characteristics and Phenotype-Genotype Analysis in Turkish Patients with Congenital Hyperinsulinism; Predominance of Recessive KATP Channel Mutations
    
    hrp0082p3-d1-874
  - Clinical Remission in a Patient with Congenital Hyperinsulinism due to Paternally Inherited Two Novel Mutations in KCJN11 Gene
    
    hrp0082p3-d1-875
  - Biochemical Studies in Patients with Hyperinsulinaemic Hypoglycaemia
    
    hrp0082p3-d1-876
  - Congenital Hyperinsulinism: Clinical and Molecular Characteristics of Brazilian Patients
    
    hrp0082p3-d1-877
  - Clinical and Genetic Analysis of 95 Cases of Congenital Hyperinsulinism
    
    hrp0082p3-d1-878
  - Congenital Hyperinsulinism: a Single-Center Experience
    
    hrp0082p3-d1-879
  - Persistent Hyperinsulinemic Hypoglycemia of an Infancy Carrying abcc8 arg598stop Mutation
    
    hrp0082p3-d1-880
  - A Case of Hyperinsulinism/Hyperammonemia Syndrome
    
    hrp0082p3-d1-881
  - Project Episga: PreMeb Presentation, Subject Recruitment, and Initial Data
    
    hrp0082p3-d1-882
  - Iodine Status in Pregnant, Lactating Mothers and their Infants and Effects of Iodine Supplementation
    
    hrp0082p3-d1-883
  - Gender Differences in Sex Steroids and IGF1 at Birth and at 5 Years of Age
    
    hrp0082p3-d1-884
  - Neonatal Seizures Neonatal due to Hypocalcemia Secondary to Maternal Vitamin D Deficiency
    
    hrp0082p3-d1-885
  - 3-Ketothiolase Deficiency Induced by ACAT1 Gene Mutation
    
    hrp0082p3-d1-886
- Perinatal and Neonatal Endocrinology (1)
- - Permanent Neonatal Diabetes Mellitus in China
    
    hrp0082p3-d2-887
  - Neonatal Neurogenic Diabetes Insipidus: a Case Report
    
    hrp0082p3-d2-888
  - Evolution and Epidemiological Assessment of the Influence of Sociological Variables of Children Born SGA in the Last Decade in Basque Country
    
    hrp0082p3-d2-889
  - A Novel Mutation Causing Pseudohypoaldosteronsim
    
    hrp0082p3-d2-890
  - A Novel Mutation in the NR3C2 Gene Causing Pseudohypoaldosteronism Type 1
    
    hrp0082p3-d2-891
  - Subcutaneous Fat Necrosis Causing Prolonged Hypercalcaemia in a Neonate: an Unusual Case
    
    hrp0082p3-d2-892
  - Severe Vitamin D Deficiency Among Pregnant Women and Their Newborns in Turkey
    
    hrp0082p3-d2-893
  - 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
    
    hrp0082p3-d2-894
  - 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
    
    hrp0082p3-d2-895
  - Cord Blood Vitamin D Concentrations in Native and Immigrant Population from a Mediterranean Area in Spain
    
    hrp0082p3-d2-896
  - Transient Neonatal Diabetes Mellitus: New Case
    
    hrp0082p3-d2-897
  - Marfan Neonatal Syndrome: a Case Report
    
    hrp0082p3-d2-898
  - Iodine Status in the Neonate and the Effect on Thyroid Function
    
    hrp0082p3-d2-899
- Pituitary
- - Effect of Pubertal Status, Age and Gender on Cortisol Response to Insulin Induced Hypoglycaemia in Children and Adolescents
    
    hrp0082p3-d1-900
  - Music Benefits on Postoperative Distress and Pain in Pediatric Day Care Surgery
    
    hrp0082p3-d1-901
  - A Case of Congenital Isolated ACTH Deficiency due to tbx19 Gene Mutation
    
    hrp0082p3-d1-902
  - Xanthogranulomatous Hypophysitis: a Rare but Mistaken Pituitary Lesion
    
    hrp0082p3-d1-903
  - Long-Term Endocrinological Follow-Up in Diencephalic Syndrome
    
    hrp0082p3-d1-904
  - Key-Role of TSH Deficiency in Disclosing Craniopharyngioma Diagnosis in a Short Girl with Hashimoto's Thyroiditis
    
    hrp0082p3-d1-905
  - Pituitary Dysfunctiona with Associated Lesions in the Hypothalamo-Pituitary Region: Histiocytosis or Dysgerminoma?
    
    hrp0082p3-d1-906
  - A Case of Combined Pituitary Hormone Deficiency in a Patient Affected by Osteogenesis Imperfecta
    
    hrp0082p3-d1-907
  - Macroprolactinoma in Adolescence: a Case Report
    
    hrp0082p3-d1-908
  - Idiopathic Central Diabetes Insipidus: a Case of Pediatric Xhantogranuloma
    
    hrp0082p3-d1-909
  - Central Diabetes Insipidus Caused by Congenital Cytomegalovirus: a Rare Association?
    
    hrp0082p3-d1-910
  - Primary Polydipsia in a Family with Mutation in the AVP Gene and Proven Central Diabetes Insipidus
    
    hrp0082p3-d1-911
- Pituitary (1)
- - Screening for SOX2 Mutations in Bulgarian Patients with Congenital Hyposomatotropism: First Results
    
    hrp0082p3-d3-912
  - Follow Up for Adult Height of Girl with the Onset of Puberty at 6 or 7 Years Old
    
    hrp0082p3-d3-913
  - The Influence of Specimen pH on Urinary LH and FSH by Immunochemiluminometric Assays
    
    hrp0082p3-d3-914
  - Thickened Pituitary Stalk with Central Diabetes Insipidus: What Diagnosis?
    
    hrp0082p3-d3-915
  - Polyuria Syndrome Associated with Visual Disorders in Children: Discuss at First Craniopharyngioma, the Primary Polydypsia is an Exclusion Diagnosis
    
    hrp0082p3-d3-916
  - Multiple Pituitary Hormone Deficiency with Transitory Pituitary Enlargement due to Prop1 Mutation (Case Presentation)
    
    hrp0082p3-d3-917
  - MRI in Children with GH Deficiency
    
    hrp0082p3-d3-918
  - Dynamic Stimulation Testing in Pediatric Endocrinology: Experience of a Pediatric Endocrine Unit in a Developing Country
    
    hrp0082p3-d3-919
  - A Case of Hypopituitarism Caused by Traumatic Brain Injury in Infancy
    
    hrp0082p3-d3-920
  - Severe Features of Central Hypothyroidism und Hypoadrenalism Effectively Resolved by Treatment with Somatropin in a Boy with Panhypopituitarism
    
    hrp0082p3-d3-921
  - A Case of Combined Pituitary Hormone Deficiency (CPHD) due to Anterior Pituitary Hypoplasia
    
    hrp0082p3-d3-922
  - Think Histiocytosis X Facing Insipidus Diabetes with Thickened Pituitary Stalk
    
    hrp0082p3-d3-923
- Puberty and Neuroendocrinology
- - Leptin Levels in Boys with Pubertal Gynecomastia
    
    hrp0082p3-d1-924
  - The Timing and Evolution of Puberty in a Sample of School-Aged Children in a Brazilian City
    
    hrp0082p3-d1-925
  - The Significance of GnRH Stimulation Test, Leptin, and Pelvic Ultrasound Findings for Differentiating Idiopathic Central Precocious Puberty from Premature Telarche
    
    hrp0082p3-d1-926
  - Basal LH Combined with the Tanner Stage of Breast Development can Predict the Gonadotropin Response Following GnRH Stimulation Test
    
    hrp0082p3-d1-927
  - Characteristics of Children Treated with Leuprolide Acetate
    
    hrp0082p3-d1-928
  - Long-Term Consequences of Indirect Topical Exposure to Testosterone Gel in Young Children
    
    hrp0082p3-d1-929
  - Final Height in Girls with Idiopathic Central Precocious Puberty Treated with GNRH Analog: Comparison with Untreated Controls
    
    hrp0082p3-d1-930
  - X-Linked Recessive Form of Nephrogenic Diabetes Insipidus in a 7-Year-Old Boy
    
    hrp0082p3-d1-931
  - Idiopathic Hypogonadotropic Hypogonadism due to a GNRH1 Mutation
    
    hrp0082p3-d1-932
  - Effect on BMI of GnRH Analogue Treatment in Central Precocious Puberty or Early and Fast Puberty Girls
    
    hrp0082p3-d1-933
  - An Unusual Combination of Premature Ovarian Failure and a History of GNRH Treatment for Idiopathic Precocious Puberty
    
    hrp0082p3-d1-934
  - An Unusual Case of Early and Accelerated Puberty
    
    hrp0082p3-d1-935
  - Association of Van Wyk Grumbach and Debre Semelaigne Syndromes in Two Cases with Severe Hypothroidism
    
    hrp0082p3-d1-936
  - Van Wyk Grumbach Syndrome: Case Report from Georgia
    
    hrp0082p3-d1-937
- Puberty and Neuroendocrinology (1)
- - Hyperandrogenism Doesn't Increase the Insulin Resistance in Overweight and Obese Adolescent Girls with Polycystic Ovary Syndrome
    
    hrp0082p3-d3-938
  - Precocious Puberty due to Duplication of the Pituitary Gland
    
    hrp0082p3-d3-939
  - Inhibin B in the Boys with Constitutional Delay of Puberty: Relationship with Gonadotropins, Testosterone, and Anti-Mullerian Factor
    
    hrp0082p3-d3-940
  - A Rare Cause of Peripheric Precocious Puberty: Adrenocortical Tumor
    
    hrp0082p3-d3-941
  - A Severe LHRH-Independent Precocious Puberty in a 26-Month-Old Girl with a Clinical Diagnosis of McCune-Albright Syndrome
    
    hrp0082p3-d3-942
  - Triptorelin Test in the Diagnosis of Precocious Puberty
    
    hrp0082p3-d3-943
  - Central Precocious Puberty and Autism: Three Cases Report
    
    hrp0082p3-d3-944
  - Precipitated Puberty: Correlations with Embarrassed Ovarian Function
    
    hrp0082p3-d3-945
  - Impact of Bisphenol-A on the Puberty of Female Rats
    
    hrp0082p3-d3-946
  - The Etiology of Central Precocious Puberty and Effect of GnRH Agonist for 2 years in Korean Boys
    
    hrp0082p3-d3-947
  - Hypothalamic Hamartoma as a Cause of Central Precocious Puberty in 4.5-Year-Old Girl: Case Report
    
    hrp0082p3-d3-948
  - The Perception of Body Image and Self-Esteem in Girls with Precocious Puberty, Being Treatment with GnRH Analogue
    
    hrp0082p3-d3-949
  - Leydig Cell Hyperplasia Mimicking Tumor: a Rare Cause of Isosexual Precoccious Puberty
    
    hrp0082p3-d3-950
  - Impact of Different Doses of Bisphenol-A on the Puberty of Female Rats
    
    hrp0082p3-d3-951
- Sex Development
- - Discordant Genotypic Sex and Concordant Phenotypes in Two Spanish Siblings with 17[alpha]-Hydroxylase/17, 20-Lyase Deficiency Carrying the Most Prevalent Mutated Alleles in Brazilian Patients
    
    hrp0082p3-d1-952
  - The Development of Gonadoblastoma in a 3-Year-Old Girl with 46,Xdel(Y)p11.3, Gonadal Dysgenesis and Associated Congenital Anomalies
    
    hrp0082p3-d1-953
  - 46,XX DSD: Bilateral Ovotestis with SOX9
    
    hrp0082p3-d1-954
  - Severe Undervirilisation in a 46,XY Case due to a Novel Mutation in HSD17B3 Gene
    
    hrp0082p3-d1-955
  - Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Syndrome
    
    hrp0082p3-d1-956
  - 5[alpha]-Steroid Reductase 2 Deficiency in a Large Family
    
    hrp0082p3-d1-957
  - 17[beta]HSD-3 Enzyme Deficiency in Newborn Due to a Novel Mutation in HSD17B3 Gene
    
    hrp0082p3-d1-958
  - Partial Androgen Insensitivity Syndrome in a Boy with Inactivating Androgen Receptor Mutation and Somatic Mosaicism
    
    hrp0082p3-d1-959
  - Clinical Characteristics of 30 Patients with 45,X/46,XY Mosaicism
    
    hrp0082p3-d1-960
  - Three Siblings Extremely Androgen Insensitivity Syndrome Due to an AR Mutation with Differing Phenotypes
    
    hrp0082p3-d1-961
  - 46,XY Female with Turner Syndrome, Crohn's Disease and Low Level Mosaicism for Monosomy X
    
    hrp0082p3-d1-962
- Sex Development (1)
- - Hypospadias in a Male Patient with 21-Hydroxylase Deficiency and Atypical Clinical Course: Presentation of Two Brothers
    
    hrp0082p3-d2-963
  - An Ovulating Testis
    
    hrp0082p3-d2-964
  - Mosaicism Ratios of 45,X to 46,X IdicY Explained a Phenotype in a Case with Mixed Gonadal Dysgenesis
    
    hrp0082p3-d2-965
  - A Rare Case of Swyer Syndrome with Spontaneous Breast Development and Menstruation
    
    hrp0082p3-d2-966
  - Phenotypic and Genotypic Variability of Patients with 5-[alpha] Reductase Type 2 Deficiency
    
    hrp0082p3-d2-967
  - The Novel Mutation in the Steroidogenic Acute Regulatory Protein in 46,XY Case with Adrenal Insufficiency and Complete Sex Reversal
    
    hrp0082p3-d2-968
  - A Challenging Diagnosis in Three 46,XY Females from Two Related Families
    
    hrp0082p3-d2-969
  - A Familial Case of Complete Androgen Insensitivity Syndrome
    
    hrp0082p3-d2-970
  - A Case of 46,Y,dup(x)(p21.2p22.2) DSD Caused by Overexpressed DAX1
    
    hrp0082p3-d2-971
  - Disorders of Sexual Differentiation Observed in Endocrinology
    
    hrp0082p3-d2-972
  - Incidens of Sex Differentione Disorder: 46,XY
    
    hrp0082p3-d2-973
- Thyroid
- - Increasing Incidence of Congenital Hypothyroidism in Neonatal Screening Program in Central Serbia: 30 Years of Experience
    
    hrp0082p3-d1-974
  - Prevalence of Additional Autoimmune Diseases in Autoimmune's Thyroiditis Children and Their First- and Second-Degree Relatives: Results from a Large, Single-Center Study
    
    hrp0082p3-d1-975
  - Adiposity and Pubertal Status Effects on Thyroid Function in Overweight Children and Adolescents
    
    hrp0082p3-d1-976
  - Neonatal Thyrotoxicosis in Maternal Grave's Disease: a Case Series and Review of the Literature
    
    hrp0082p3-d1-977
  - Treatment the Resistance to Thyroid Hormones in Girl
    
    hrp0082p3-d1-978
  - Free T3/free T4 Ratios in Children with Hypothyroidism Treated with Levothyroxine Monotherapy
    
    hrp0082p3-d1-979
  - Diagnostic challenges of thyroid dysfunction in eating disorders
    
    hrp0082p3-d1-980
  - Kocher-Debre-Semelaigne Syndrome with Rhabdomyolysis and Increased Creatinine: a Case Report
    
    hrp0082p3-d1-981
  - Preliminary Result and Normative TSH Values for Healthy Nigerian Newborn Children
    
    hrp0082p3-d1-982
  - Resistance to Thyroid Hormone Syndrome from Childhood to Adulthood: Variation in Symptoms and Thyroid Function
    
    hrp0082p3-d1-983
  - Thyroid Disorders After Oncologic Treatment in Children
    
    hrp0082p3-d1-984
  - Trends in Incidence of Permanent and Transient Congenital Hypothyroidism in Shanghai China
    
    hrp0082p3-d1-985
  - Klippel-Feil Syndrome and Thyroiditis: a Case Report
    
    hrp0082p3-d1-986
- Thyroid (1)
- - The Association of Thyroid Dysfunction and Blood Pressure in Korean Children
    
    hrp0082p3-d2-987
  - Thyrotoxicosis in Childhood and Adolescents
    
    hrp0082p3-d2-988
  - Aetiology and Different Clinical Conditions of Hyperthyroidism in Children and Adolescents
    
    hrp0082p3-d2-989
  - Bmi and Auxological Follow Up in Children with Hashimoto Thyroiditis: Utility of a Phisical Activity Program
    
    hrp0082p3-d2-990
  - Missed Cases of Congenital Hypothyroidism Detected By Screening Program in Central Serbia (1983-2014)
    
    hrp0082p3-d2-991
  - Thyroid Pathology Among 14-Year-Old Adolescents
    
    hrp0082p3-d2-992
  - Raised Free Thyroxine Levels in a Boy with Hypertension
    
    hrp0082p3-d2-993
  - The Evaluation of Transient Hypothyroidism in Patients Diagnosed with Congenital Hypothyroidism
    
    hrp0082p3-d2-994
  - Optimizing Treatment in Congenital Hypothyroidism
    
    hrp0082p3-d2-995
  - Report of a Hurthle Cell Neoplasm in a Boy
    
    hrp0082p3-d2-996
  - Delayed Diagnosis of Congenital Hypothyroidism and Consequences: a Case Series
    
    hrp0082p3-d2-997
  - Importance of Early Indemnification of Hashimoto Thyroiditis at Pregnant Women in Conditions of Iodine Deficiency in Republic of Uzbekistan
    
    hrp0082p3-d2-998
  - Improvement of Hematological Values with Stabilization of STH
    
    hrp0082p3-d2-999
  - Changes of Laboratory Findings Before and After Thyroid Hormone Replacement in a Naive 19.24 Year-Old Female Case of Ectopic Thyroid
    
    hrp0082p3-d2-1000
Late Breaking Posters
- (1)
- - Histological Evaluation of Patients with Partial Gonadal Dysgenesis and NR5A1 Mutations: Review in Leydig and Germ Cell Pattern
    
    hrp0082lbp-d3-1001
  - Pseudoexon Activation in Nicotinamide Nucleotide Transhydrogenase in Two Siblings with Familial Glucocorticoid Deficiency
    
    hrp0082lbp-d3-1002
  - Increasing Incidence of Infants Born Small and Large for Gestational Age Over 20 Years
    
    hrp0082lbp-d3-1003
  - Methyl Donor Deficiency Impairs Pre-Osteoblast Differentiation Through PGC-1[alpha] Hypomethylation and Increased ERR[alpha]
    
    hrp0082lbp-d3-1004
  - 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
    
    hrp0082lbp-d3-1005
  - Abstract unavailable
    
    hrp0082lbp-d3-1006
  - Hepatic NAD Metabolism is Dysregulated by an Excessive Supply of Lipids
    
    hrp0082lbp-d3-1007
  - Long-Term Impact of Childhood-Onset Type 1 Diabetes: Social Insertion, Quality of Life, Sexuality
    
    hrp0082lbp-d3-1008
  - Family Studies of CYP21A2 Gene Identify Different Haplotypes for Nonclassical 21-Hydroxylase Deficiency in Brazilian Population
    
    hrp0082lbp-d3-1009
  - Effect of Triptorelin 3.75 mg Subcutaneously Injection Every 6 Weeks on Adult Height in Girls with Idiopathic Central Precocious Puberty
    
    hrp0082lbp-d3-1010
  - The Circulating miRNAs Expression in Simple Obese Children
    
    hrp0082lbp-d3-1011
  - Total and Acylated Ghrelin Levels in Children and Adolescents with Growth Retardation
    
    hrp0082lbp-d3-1012
  - Copy Number Determination of CYP21A2 Gene Supplements the Molecular Biological Analysis of Hungarian Patients with 21-Hydroxylase Deficiency
    
    hrp0082lbp-d3-1013
  - CpG Methylation Changes within the INS, HLA-G and PTPN-22 Promoters in Childhood Type 1 Diabetes
    
    hrp0082lbp-d3-1014
  - A Secular Trend for Pubertal Timing in Swedish Men Born 1946-1991: The BEST Cohort
    
    hrp0082lbp-d3-1015
  - The Diverse Phenotype of Mutations in T₃ Receptor Alpha (TR[alpha])
    
    hrp0082lbp-d3-1016
  - Exploring the Pathogenesis of Hypothalamic Obesity: the Interaction of Hormonal, Neuronal and Psychological Factors
    
    hrp0082lbp-d3-1017

Bioscientifica Abstracts is the gateway to a series of products that provide a permanent, citable record of abstracts for biomedical and life science conferences.

Find out more

ESPE Abstracts

53rd Annual ESPE (ESPE 2014)

Contents

BiosciAbstracts