ePosters

HRP0086RFC1.1

Tracing the Glucocorticoid Receptor Evolutionary Pedigree: Insights from a Comprehensive Phylogenetic Analysis of the Full NR Super-Family
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HRP0086RFC1.2

Glucocorticoid Deficiency Due to Disruption of Mitochondrial Steroidogenesis Leads to Dysregulation of Antioxidant Pathways and Nucleotide Biosynthesis
Direct

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HRP0086RFC1.3

Impaired Cardiac Function in a Mouse Model of Generalized Glucocorticoid Resistance
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HRP0086RFC1.4

Mutations of ABCD1 in 16 Vietnamese Patients with X-linked Adrenoleukodystrophy
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HRP0086RFC1.5

A Novel Animal Model to Study 21-Hydroxylase Deficiency in vivo
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HRP0086RFC1.6

Pediatric Patients with Congenital Adrenal Hyperplasia have Unfavorable Changes in their Cardiovascular Risk Profile
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HRP0086RFC1.7

The Recovery of Adrenal Function in Children with Chronic Asthma Assessed by Low Dose Short Synacthen Test (LDSST)
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HRP0086RFC1.8

Adrenal Dysfunction in HIV-Exposed Uninfected Infants Receiving Ritonavir-Boosted Lopinavir, an HIV Protease Inhibitor, for the Prevention of Breastfeeding HIV Transmission. An ANRS 12174 Substudy
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HRP0086RFC2.1

25-OH-Vitamin D Status in a Pediatric Population of Subjects Affected By Prader-Willi Syndrome Compared to Matched Obese Controls
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HRP0086RFC2.4

Results of Orthopaedic Surgery in Children with X-Linked Hypophosphatemic Rickets (XLHR)
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HRP0086RFC2.5

Growth Patterns and Fractures in Boys with Duchenne Muscular Dystrophy: Insights from Over 800 Boys in the UK North Star Cohort
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HRP0086RFC2.6

Combining COLD and MAMA-PCR Real Time Taqman Tecniques to Detect and Quantify the R201 GNAS Mutation Causing McCune-Albright Syndrome
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HRP0086RFC2.7

Effect of Paternal Loss-of-Function Mutations of GNAS on Growth During the Childhood: A Role for XL
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HRP0086RFC2.8

Final Heights and BMI in Patients Affected with Different Types of Pseudohypoparathyroidism
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HRP0086RFC3.1

Endocrinopathy in Childhood Intracranial Germ Cell Tumours is Predicted by Disease Location not Treatment: 30 year Experience from a Single Tertiary Centre
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HRP0086RFC3.2

Subfertility After Chemotherapy in PNET Tumours: 34 year Experience from a Single Centre (1980-2013)
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HRP0086RFC3.3

Unraveling the Link between Optic Nerve Hypoplasia and Pituitary Hormone Dysfunction
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HRP0086RFC3.4

Children and Adolescents with Severe TBI can Develop Late Pituitary Dysfunction Independently of the Results of the First Pituitary Evaluation
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HRP0086RFC3.5

Prospective Dynamic Evaluation of Hypothalamo-Pituitary Function in 30 Cases of Paediatric Craniopharyngioma, by Hypothalamic Injury and Treatment; A Single Centre Series
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HRP0086RFC3.6

Priority Target Conditions of Growth-Monitoring in Children: Toward Consensus
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HRP0086RFC3.7

Pituitary Structural Abnormalities in Idiopathic Isolated Growth Hormone Deficiency
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HRP0086RFC3.8

Anthropometric and Endocrine Features in Children and Adolescents with Type 1 Narcolepsy
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HRP0086RFC4.2

Adipocytokines Delay Pubertal Maturation of Human Sertoli Cells
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HRP0086RFC4.3

Early Growth Patterns are Associated with Alterations in Adipocytokine Levels and Fat Distribution Measured by DXA in 982 Children/Adolescents
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HRP0086RFC4.4

Metabolic Syndrome Markers Correlate with Gut Microbiome Activity in Children Born Very Preterm
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HRP0086RFC4.5

Steroid Metabolomic Signature of Liver Disease in Childhood Obesity
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HRP0086RFC4.6

Adipose Tissue - A Source of Hyperandrogenism in Obese Females?
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HRP0086RFC4.7

Prevalence and Characterization of Retinal Alterations in a Cohort of Overweight and Obese Children
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HRP0086RFC5.1

Adiponectin and Leptin in Children with Type 1 Diabetes for 3-5 years with or without Residual [beta] cell Function
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HRP0086RFC5.2

Limits of Agreement between HbA1c Levels Measured in Different Laboratories Following the Introduction of the International Federation of Clinical Chemistry and Laboratory Medicine Standardised Values
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HRP0086RFC5.3

Sexual Lifestyle among Young Adults with Type 1 Diabetes
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HRP0086RFC5.4

[ldquo]Transient[rdquo] Neonatal Diabetes In Adulthood: Metabolic Outcomes
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HRP0086RFC5.5

The Efficacy of Insulin Degludec in Children and Adolescents with Type 1 Diabetes
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HRP0086RFC5.6

Clinical Management of the Mitchell-Riley Syndrome Due to RFX6 Gene Mutations: Aggressive Support Results in Improved Outcome
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HRP0086RFC5.7

Early Successful Hematopoietic Cell Transplantation (HSCT) in a Boy with IPEX Syndrome Caused by Novel C.721T>C FOXP3 Mutation
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HRP0086RFC5.8

Stress Management and Health Promotion through Family Intervention Improves Metabolic Control in Children and Adolescents with Type 1 Diabetes
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HRP0086RFC6.2

RAB3IP and DGCR8 as a Potentially Pathogenic Novel Candidate Gene Involving in Growth Disorders
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HRP0086RFC6.3

Effect of Very Early Growth Hormone (GH) Treatment on Long-term Growth in Girls with Turner Syndrome (TS): A Multicenter, Open-Label, Extension Study
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HRP0086RFC6.4

Growth Hormone (GH) Treatment in Skeletal Dysplasias - Short-term Results in Prepubertal Children Reported in KIGS
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HRP0086RFC6.5

Abnormal Videofluoroscopic Swallow Studies (VFSS) in Infants with Prader-Willi Syndrome Indicate a High Rate of Silent Aspiration
Direct

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HRP0086RFC6.6

Growth Hormone (GH) Deficiency Type II: Clinical and Molecular Evidence of Impaired Regulated GH Secretion Due to an Gln181Arg GH-1 Gene Mutation
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HRP0086RFC6.7

Characteristics of Responders and Poor-responders to Increlex® Therapy - Data from Children Enrolled in the European Increlex® Growth Forum Database (EU-IGFD)
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HRP0086RFC6.8

The Actual Incidence of Small for Gestational Age (SGA) Newborns and their Catch-up Growth is Dramatically Lower than Previously Considered
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HRP0086RFC7.1

Tissue Engineered Collagen Based Tubular Scaffolds for Urethral Regeneration. A Novel Technology for the Surgical Treatment of VSD (Variation of Sex Development) Patients with Severe Hypospadias
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HRP0086RFC7.2

Reference Values for External Genitalia Size and Steroid Hormone Levels in Female Neonates
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HRP0086RFC7.3

Harmonisation of Serum Dihydrotestosterone Analysis: Establishment of an External Quality Assurance Program
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HRP0086RFC7.4

A Mutation in WT1 (Wilms' Tumor Suppressor 1) Associated with 46,XX TDSD
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HRP0086RFC7.5

Fertility Preservation in an Adolescent Boy: Inducing Puberty and Spermatogenesis Prior to Bone Marrow Transplantation
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HRP0086RFC7.6

The Hopeful Beginnings of Fertility Preservation in Children
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HRP0086RFC7.7

Clinical Decision-Making in Disorders of Sex Development (DSD): Physician Recommendations Pre- and Post-Consensus Statement
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HRP0086RFC7.8

Premature Adrenarche in Girls at Pubertal Onset is Associated with High Androgens, but Lower AMH Concentrations
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HRP0086RFC8.1

Somavaratan (VRS-317) Treatment of Children with Growth Hormone Deficiency (GHD): Results at 2 Years (NCT02068521)
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HRP0086RFC8.2

Pharmacokinetic Modelling Predicts Native hGH Levels Following Administration of a Sustained-Release Prodrug, TransCon hGH, to Children with GHD
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HRP0086RFC8.3

Batch-to-Batch Consistency of a Highly O-Glycosylated Long-Acting Human Growth Hormone (MOD-4023)
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HRP0086RFC8.4

A Hybrid Fc-fused Human Growth Hormone, GX-H9, Shows a Potential for Weekly and Semi-monthly Administration in Clinical Studies
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HRP0086RFC8.5

Optimal Sampling of IGF-1 During Weekly Administration of a Long Acting Human Growth Hormone (MOD 4023)
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HRP0086RFC8.6

A Six-Month Safety and Efficacy Study of TransCon hGH Compared to Daily hGH in Pre-Pubertal Children with Growth Hormone Deficiency (GHD)
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HRP0086RFC8.7

Safety and Tolerability of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): 24-month Complete Dataset Results of a Phase 2 Study in Children with Growth Hormone Deficiency
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HRP0086RFC8.8

Efficacy of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): 24-month Complete Database Results of a Phase 2 Study in Children with Growth Hormone Deficiency
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HRP0086RFC9.1

Neonatal Diabetes due to NKX2.2 Mutation - Genotype, Clinical Phenotype and Therapeutic Challenges in a Very Low Birth Weight Diabetic Neonate
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HRP0086RFC9.2

Missense Mutation of GLIS3 Gene Resulting in Neonatal Diabetes and Congenital Hypothyroidism
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HRP0086RFC9.3

Molecular Analysis of a Large Cohort of MODY Patients by Next Generation Sequencing
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HRP0086RFC9.4

Prevalence of Monogenic Diabetes in the Lithuanian Pediatric and Young Adult Population
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HRP0086RFC9.5

Non-Mody Monogenic Diabetes: A Very Heterogenous and Problematic Group of Diabetes
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HRP0086RFC9.6

Emerging Pitfalls of Etiological Diagnosis of Diabetes in Children and Adolescents? Analysis of a French Cohort of 310 Recent-Onset Cases
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HRP0086RFC9.7

Chronotype and Type 2 Diabetes Risk in Preadolescents
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HRP0086RFC9.8

Micro RNA and Diabetic Nephropathy
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HRP0086RFC10.1

Paternal Loss-of-Function Mutations of GNAS and Growth Retardation in a Mice Model: A Specific Placental Transcriptomic Signature?
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HRP0086RFC10.2

Dysregulation of Placental Mirna in Maternal Obesity is Associated with Pre-and Post-Natal Growth
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HRP0086RFC10.3

Vitamin D Depletion in Pregnancy Decreases Survival Time, Oxygen Saturation, Lung Weight and Body Weight in Preterm Rat Offspring
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HRP0086RFC10.4

Pharmacokinetics of Intravenous Glucagon in Children with Hyperinsulinaemic Hypoglycaemia
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HRP0086RFC10.5

Phenotype, Genotype and Short term Outcome in Congenital Hyperinsulinism (CHI)
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HRP0086RFC10.6

Increased Islet Cell Neogenesis and Endocrine Cell Differentiation in Congenital Hyperinsulinism in Infancy
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HRP0086RFC10.7

Expression of Insulin Receptor Isoforms and Type 1 Insulin-Like Growth Factor Receptor in the Placenta as a Function of Fetal Weight
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HRP0086RFC10.8

Gestational Diabetes is Associated with Changes in Placental Microbiota and Microbiome
Direct

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HRP0086RFC11.1

Central Hypothyroidism and Biallelic Defect Near the D/ERY Motif of the TRHR Gene
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HRP0086RFC11.2

The Incidence and Genetic Analysis of Congenital Hypothyroidism in Guangxi, China and the Predictors for Differentiating Permanent and Transient Congenital Hypothyroidism
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HRP0086RFC11.3

Germline and Somatic DICER1 Mutations in Familial Papillary Thyroid Carcinoma and Multinodular Goiter
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HRP0086RFC11.4

Thyroid Function in Monozygotic Twins with Intra-Twin Birth-Weight-Differences
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HRP0086RFC11.5

Novel Homozygous Mutation in the Sodium/Iodide Symporter (NIS) Gene Highlight by Next Generation Sequencing (NGS) in a Patient with Congenital Hypothyroidism
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HRP0086RFC11.6

Falsely TSH and Free Thyroid Hormone Measurements in Pediatric Patients Treated with High Dose of Biotin
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HRP0086RFC11.7

Secondary Thyroid Cancer among Childhood Cancer Survivors: A Single Institution Experience
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HRP0086RFC12.1

Molecular Genetic Diagnosis of Idiopathic Hypogonadotropic Hypogonadism by Using Targeted Next-Generation Sequencing
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HRP0086RFC12.2

A Novel Mutation of KISS1R Causing a Normosmic Isolated Hypogonadotropic Hypogonadism
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HRP0086RFC12.3

Next Generation Sequencing and Precocious Puberty: A New Diagnostic Challenge to Identify the Molecular Basis of Complex Diseases
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HRP0086RFC12.4

Molecular Screening of MKRN3, DLK1 and KCNK9 Genes in Central Precocious Puberty
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HRP0086RFC12.5

A Novel MKRN3 Nonsense Mutation Causing Familial Central Precocious Puberty
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HRP0086RFC12.6

Serum Antimullerian Hormone and Inhibin B as Potential Markers for Progressive Central Precocious Puberty in Girls
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HRP0086RFC12.7

Prevalence of Organic Lesions in Males with Central Precocious Puberty
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HRP0086RFC12.8

Circulating MKRN3 Levels Decline During Puberty in Healthy Boys
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HRP0086RFC13.1

Inhibition of Teneurin-2 (TENM2) Leads to Upregulation of UCP1 in Human White Adipocytes
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HRP0086RFC13.2

The Use of Proteomics in the Assessment of Health Status of Offspring Born after Intracytoplasmic Sperm Injection (ICSI)
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HRP0086RFC13.3

Effects of Eating Rate on Satiety Hormones, Meal Enjoyment and Memory for Recent Eating: An fMRI Study
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HRP0086RFC13.4

Which Amount of BMI-SDS Reduction is Necessary to Improve Cardiovascular Risk Factors in Overweight and Obese Children?
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HRP0086RFC13.5

Protective Potential of Metformin on Membrane Linked Functions in Diabetic Aging Female Rats
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HRP0086RFC13.6

Laparoscopic Sleeve Gastrectomy in Obese Adolescent Population
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HRP0086RFC13.7

Early Onset Obesity and Hyperphagia Associated with Defects in the GNAS Gene
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HRP0086RFC13.8

Measuring Subcutaneous Adipose Tissue Using Ultrasound in Children
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HRP0086RFC14.1

Important Contribution of GH, GHRHR and GHSR Mutations in Isolated Growth Hormone Deficiency with a Normal Location of the Posterior Pituitary -Functional Characterization of New Variants
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HRP0086RFC14.2

Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern
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HRP0086RFC14.3

Whole Exome Sequencing Identifies a GH1 Gene Mutation Causing Familial Isolated Growth Hormone Deficiency with Normal Peak Growth Hormone Concentrations
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HRP0086RFC14.4

Genetic Diagnosis of Congenital Growth Hormone Deficiency by Massive Parallel Sequencing Using a Target Gene Panel
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HRP0086RFC14.5

Gene Expression Profiling of Children with GH Deficiency (GHD) Prior to Treatment with Recombinant Human Growth Hormone (r-hGH) is Associated with Growth Response Over Five Years of Therapy
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HRP0086RFC14.6

Effect of Small Size at Birth, Adult Body Size and Growth Hormone Treatment on Telomere Length
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HRP0086RFC14.7

GH Influences Plasma Fasting Adropin Concentration in Patients with Turner Syndrome
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HRP0086RFC14.8

ACAN Mutations in Short Children Born SGA; Growth Response During GH Treatment with Additional GnRHa, and a Proposed Clinical Scoring System
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HRP0086RFC15.1

A Novel Homozygous Mutation in the Domain AF-2 of Alpha Estrogen Receptor Gene (ESR1), Generating a Bio-Inactive ER[alpha] Mutant, Resulting in Estrogen Resistance with Complex Metabolic Phenotype
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HRP0086RFC15.2

NR0B1 Frameshift Mutation in a Boy with Precocious Puberty and Normal Adrenal Function
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HRP0086RFC15.4

The Effect of Sfrp5, Wnt5a, Adiponectin, and Chemerin on Blood Pressure Regulation in Obese Children
Direct

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HRP0086RFC15.5

Effect of Melatonin on Proliferation and Differentiation of Human Dental Pulp Cells
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HRP0086RFC15.6

Safety of GH in Paediatrics: The GeNeSIS Prospective Observational Study Experience between 1999 and 2015 (NCT01088412)
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HRP0086RFC15.7

Long-Term Safety and Effectiveness of Daily and Weekly Growth Hormone Treatment in Pediatric GHD Patients (4-Years' Results)
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HRP0086RFC15.8

Replacement of Male Mini-Puberty
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HRP0086P1-P1

Leptin is Associated with Serum Aldosterone in Paediatric Subjects, Independently of Body Mass Index, Blood Pressure and Plasma Renin Activity
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HRP0086P1-P2

Mast Cells and Steroidogenesis in the Human Fetal Adrenal
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HRP0086P1-P3

Gender-Specific Differences in Hypothalamus-Pituitary-Adrenal Axis Activity in Children: A Meta-Analysis
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HRP0086P1-P4

Prepubertal Children Born Large for Gestational Age have Lower Serum DHEAS Concentrations than those with Lower Birth Weight
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HRP0086P1-P5

Whole Exome Sequencing in Patients with Primary Generalized Glucocorticoid Resistance, who did not have Mutations in the NR3C1 Gene
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HRP0086P1-P6

Novel CYP11A1 Mutations in 15 Patients (13 Families) with Variable Clinical Presentations
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HRP0086P1-P7

Transient Generalized Glucocorticoid Hypersensitivity Syndrome
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HRP0086P1-P8

The Effect of Obesity on the Stress Response: The Paradigm of Surgical Stress
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HRP0086P1-P9

Long-term Anthropometric Outcome of Girls with Non-classical Congenital Adrenal Hyperplasia Diagnosed in Childhood
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HRP0086P1-P10

Current Dilution Methods Cause Large Variations and Inaccuracies when Making up 1 μg Synacthen Dose
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HRP0086P1-P11

Evaluation of the Glucocorticoid, Mineralocorticoid, and Adrenal Androgen Secretion Dynamics in A Large Cohort of Patients Aged 6-18 Years with Transfusion-dependent [beta]-Thalassemia Major, with an Emphasis on the Impact of Cardiac Iron Load
Direct

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HRP0086P1-P12

Testicular Adrenal Rest Tumours in 50 Boys, Adolescents and Adult Male with Congenital Adrenal Hyperplasia
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HRP0086P1-P13

Establishment of Clinical and Lab Algorithms for the Identification Carriers of Mutations in CYP21A2 - A Study of 768 Children and Adolescents
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HRP0086P1-P14

A Unique Case of Dual Opposing Pathologies
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HRP0086P1-P15

Individualized Optimization with 17OHP-Saliva Profiles Leads to Changes in Hydrocortisone Dosing Pattern in Children with Congenital Adrenal Hyperplasia
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HRP0086P1-P16

Cortisol Response to ACTH Stimulation Test in Non-Classical Congenital Adrenal Hyperplasia
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HRP0086P1-P17

Altered Stress System Activity in Children with ADHD
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HRP0086P1-P18

Adult Individuals with Classic Congenital Adrenal Hyperplasia Exhibit Deficits in Executive Functions
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HRP0086P1-P19

Heterozygous Mutations in CYP11A1 Gene can Cause Life-Threatening Salt Wasting and Failure to Thrive
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HRP0086P1-P20

HIV Drugs as a Possible Cause for Transient 21-Hydroxylase Deficiency in a Preterm Infant
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HRP0086P1-P21

Increased Salivary and Hair Cortisol and Decreased Salivary Alpha-Amylase Concentrations in Obese Prepubertal Girls
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HRP0086P1-P22

An Assessment of the Hypothalamic-Pituitary-Adrenal Axis in Children with Prader-Willi Syndrome
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HRP0086P1-P23

The Urinary Steroidome of Children with Classic 21-Hydroxylase Deficiency Treated with Hydrocortisone
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HRP0086P1-P24

Adrenal Insufficiency in ROHHADNET Syndrome (Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation and Neural Tumor)
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HRP0086P1-P25

The Psychosocial Impact of Adrenal Insufficiency and Congenital Adrenal Hyperplasia on Children and their Parents
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HRP0086P1-P26

Sex-Specific Differences in Hypothalamus-Pituitary-Adrenal Axis Activity in Newborns with Very Low Birth Weight
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HRP0086P1-P27

Beckwith-Wiedemann Syndrome and Bilateral Phaeochromocytoma: A Diagnostic Challenge
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HRP0086P1-P28

Combined Glucocorticoid and Mineralocorticoid Deficiency Related to a New NNT Mutation: A Case Report
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HRP0086P1-P29

Testicular Adrenal Rest Tumours in Patient with X-Linked Adrenoleukodystrophy
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HRP0086P1-P30

Reference Intervals for the Steroid Hormones of 6 to 14 year Old Normal Male Children with LC-MS Method
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HRP0086P1-P31

Growth of Children with Congenital Adrenal Hyperplasia (CAH) During the First 2 years of Life - Data from the Duth Longitudinal Registry
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HRP0086P1-P32

Molecular Confirmatory Test Improves the Accuracy of Congenital Adrenal Hyperplasia Diagnosis in Newborn Screening Program
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HRP0086P1-P33

Usefulness of Corticotropin Test in Children and Adolescents with Clinical Hyperandrogenism
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HRP0086P1-P34

Primary Adrenal Insufficiency in Children: Results from a Large Nationwide Cohort
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HRP0086P1-P35

Follow-up of Growth and Puberty in Girls and Boys with Premature Adrenarche
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HRP0086P1-P36

Early Onset Hypertension with Primary Hyperaldosteronism through Mutation in the Calcium Channel CACNA1H - Case Report
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HRP0086P1-P37

DNA Methylation Signatures Associated with Prenatal Dexamethasone Treatment
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HRP0086P1-P38

Twenty Years Experience in Congenital Adrenal Hyperplasia: Clinical, Hormonal and Molecular Characteristics in a Large Cohort
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HRP0086P1-P39

Chronic Adrenal Insufficiency Due to a Mutation of Nicotinamide Nucleotide Transhydrogenase 1 (NNT1): Case Report
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HRP0086P1-P40

Cognitive Functions in Congenital Adrenal Hyperplasia
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HRP0086P1-P41

RET and TP53 Concomitant Mutations: A Challenging Approach to a Unique Association of High Tumor Predisposing Conditions
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HRP0086P1-P42

Acute Lysis of a Giant Pediatric Adrenal Cortical Carcinoma Following One Dose of op'DDD
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HRP0086P1-P43

Severe Hypertension in a Girl: Cushing Syndrome or Apparent Mineralocorticoid Excess Syndrome? Utility of Molecular Study
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HRP0086P1-P44

An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome
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HRP0086P1-P45

Polymorphisms Analyze in Gene CYP21A2 Gene Associated with Congenital Adrenal Hyperplasia
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HRP0086P1-P46

The Effect of Intrauterine Stress on Leukocyte Telomere Length in Newborns
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HRP0086P1-P47

Predictive Factors for Premature Pubarche in a Large Cohort of Italian Children
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HRP0086P1-P48

Cardiac Function in Pediatric Patients with Congenital Adrenal Hyperplasia
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HRP0086P2-P49

Evaluation of the Combination of Anti-androgen and Anti-estrogen Treatment in Classical Congenital Adrenal Hyperplasia in Boys: Retrospective Study of 11 Cases
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HRP0086P2-P50

Ovarian Cysts in a 46,XX Patient with Congenital Lipoid Adrenal Hyperplasia and with Spontaneous Puberty
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HRP0086P2-P51

Bone Health Index in Children and Adolescents with Congenital Adrenal Hyperplasia
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HRP0086P2-P52

Occasional Detection of an Adrenal Incidentaloma in a Female Adolescent Evaluated for Cardiac Arrhythmias
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HRP0086P2-P53

Final Height in Congenital Adrenal Hyperplasia: A Retrospective Study
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HRP0086P2-P54

Hyperandrogenism in a 12-year Old Girl with a Congenital Porto-Systemic Shunt and Congenital Hepatic Fibrosis
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HRP0086P2-P55

The Treatment of a Functional Adrenocortical Cancer with Mitotane
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HRP0086P2-P56

The Effect of Anti-TNF on the Metabolism of Adrenal Hormones; A Steroid Metabolomic Approach
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HRP0086P2-P57

False-Positive Increases of Steroid Hormone Precursors Mimicking 11[beta]-Hydroxylase-Deficiency in a Preterm Infant
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HRP0086P2-P58

Isthmic Spondylolisthesis in a Pre-pubertal Boy with Congenital Adrenal Hyperplasia During Aromatase Inhibitor Treatment
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HRP0086P2-P59

Hospitalisation in Children with Adrenal Insufficiency and Hypopituitarism: Is there a Differential Burden Between Boys and Girls and Between Age Groups?
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HRP0086P2-P60

A Case of Cushing's Syndrome Due to Adrenocortical Adenoma with Pubarche and Obesity
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HRP0086P2-P61

Severe Neonatal Cushing Syndrome with Multi-Organ McCune Albright Manifestations
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HRP0086P2-P62

Final Height Data in a Cohort of Patients with Congenital Adrenal Hyperplasia Treated with Tailored Doses of Hydrocortisone
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HRP0086P2-P63

The Evolution of Bone Age in Girls with Premature Adrenarche
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HRP0086P2-P64

Cushing Syndrome Due to Adrenal Adenoma in an Adolescent Patient and Successful Treatment with Laparoscopic Surgery
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HRP0086P2-P65

A Novel Mutation of DAX-1 (NR0B1) in a Boy with X-linked Adrenal Hypoplasia Congenita
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HRP0086P2-P66

Clinical-Laboratory Findings of the Cases with Premature Pubarche and the Value of Acth Stimulation Test in the Differential Siagnosis
Direct

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HRP0086P2-P67

Successful Medical Management of Severe Neonatal Cushing Syndrome with Metyrapone, Guided by Mass Spectrometry Monitoring
Direct

Abstract PDF
HRP0086P2-P68

Family Character Isolated Pheochromocytoma by Mutation in Vhl gen
Direct

Abstract PDF
HRP0086P2-P69

Exaggerated Adrenarche and Exogenous Obesity: A Diagnostic Challenge
Direct

Abstract PDF
HRP0086P2-P70

Vitamin D Insufficiency is Related to Premature Adrenarche
Direct

Abstract PDF
HRP0086P2-P71

A Case of 17-Years-Old Boy with Relapsing Cushing Disease Presenting Vertebral Compression Fracture
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Abstract PDF
HRP0086P2-P72

The ımpact of 21 Hydroxylase Deficiency on Cardiac Repolarization Changes in Children with 21-hydroxylase-deficient Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P73

Patients with Congenital Adrenal Hyperplasia have Significantly Higher Healthcare Utilisation than the General Paediatric Population
Direct

Abstract PDF
HRP0086P2-P74

Cholestasis and Hypercalcemia Secondary to Panhypopituitarism in a Newborn
Direct

Abstract PDF
HRP0086P2-P75

Clinical Management in Secondary Pseudohypoaldosteronısm: A Case Series
Direct

Abstract PDF
HRP0086P2-P77

Management Dilemmas in a Genetically Female Child with Congenital Adrenal Hyperplasia Raised as a Male
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Abstract PDF
HRP0086P2-P78

Primary Pigmented Nodular Adrenocortical Disease (PPNAD) Justifying a Pediatric Case of ACTH-independent Cushing Syndrome (CS)
Direct

Abstract PDF
HRP0086P2-P79

Three Chinese Patients from Two Kindreds with Aldosterone Synthase Deficiency: Clinical Characteristic with Mutation Analysis Report
Direct

Abstract PDF
HRP0086P2-P80

Addisonian Crisis Due to Autoimmune Adrenalitis in a 14 Year Old Boy with a History of Stem cell Transplantation (HSCT)
Direct

Abstract PDF
HRP0086P2-P81

Assessment of Cardiac Function in Children Followed up for Congenital Adrenal Hyperplasia: A Case Control Study in Cameroon
Direct

Abstract PDF
HRP0086P2-P82

A Novel Mutation of HSD3beta2 Presenting as Hypospadias with Salt-wasting in a Male Infant
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Abstract PDF
HRP0086P2-P83

Testicular Adrenal Rest Tumors in two Young Patients with Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P84

Hyperreninemic Hypoaldosteronism: Clinical and Genetic Features in Pediatric Patients
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Abstract PDF
HRP0086P2-P85

Peculiarities of Manifestation and Short-term Effects of Hormonotherapy in Children With Congenital Adrenal Cortical Hyperplasia
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Abstract PDF
HRP0086P2-P86

Congenital Adrenal Hyperplasia Revealed by Adrenal Nodules
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Abstract PDF
HRP0086P2-P87

Urosepsis or Pseudohypoaldosteronism in a Neonate?
Direct

Abstract PDF
HRP0086P2-P88

A Case Report of Adrenocortical Adenoma in a Young Girl
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Abstract PDF
HRP0086P2-P90

A Genetic Diagnosis of Familial Glucocorticoid Deficiency Resulting in Cessation of Long-term Mineralocorticoid Treatment in Three Siblings
Direct

Abstract PDF
HRP0086P2-P91

Corticosteroid-Induced Adrenal Insufficiency in a Child with T Cell Lymphoblastic Lymphoma
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Abstract PDF
HRP0086P2-P92

A Rare Endocrine Association of Dilated Cardiomyopathy with Congenital Adrenal Hyperplasia due to 11 Beta Hydroxylase Deficiency
Direct

Abstract PDF
HRP0086P2-P93

Use of an F-DEX Monocyte Binding Assay to Measure Steroid Responsiveness of Patients and their Related Donors Undergoing Stem Cell Transplant
Direct

Abstract PDF
HRP0086P2-P94

11[beta]- Hydroxylase Deficiency due to a Novel Compound Heterozygous Mutation and Literature Review
Direct

Abstract PDF
HRP0086P2-P95

Early Adrenarche: A Common Query but not Easily Resolved
Direct

Abstract PDF
HRP0086P2-P96

Assessment of Clinical Effectiveness and Safety of Using Flutamide in Children with Pre-menarche Hierperandrogenismo
Direct

Abstract PDF
HRP0086P2-P97

Congenital Adrenal Hyperplasia - Subtle Presentations with Critical Electrolyte Imbalances and Cardiac Arrhythmias. Experiences from one Hospital
Direct

Abstract PDF
HRP0086P1-P98

Knock in of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-dependent Protein Kinase A Activation: A Model of Acrodysostosis Type 1?
Direct

Abstract PDF
HRP0086P1-P99

Automated Greulich-Pyle Bone Age Determinations in Children with Chronic Endocrine Diseases
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Abstract PDF
HRP0086P1-P100

Cord 25-Hydroxyvitamin D and Infant Cranial Growth: An Odense Child Cohort Study
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Abstract PDF
HRP0086P1-P101

Effect of Bisphosphonates on Bone Fragility Due to Chronic Liver Disease in Ten Children
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Abstract PDF
HRP0086P1-P102

Radiologically Confirmed Fractures in a Scottish Nationwide Cohort of Boys with Duchenne Muscular Dystrophy
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Abstract PDF
HRP0086P1-P103

Monostotic Fibrous Dysplasia is a Single Disorder Caused by Somatic Mosaic Activating Mutations in GNAS
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Abstract PDF
HRP0086P1-P104

Clinically Significant Fracture Incidence in Czech Children: A Population-based Study
Direct

Abstract PDF
HRP0086P1-P105

Effects of Selective GPER-1 Agonist G1 on Bone Growth
Direct

Abstract PDF
HRP0086P1-P106

Bone Mineral Density, Pubertal Status and Ability to Walk are Associated to Fracture Incidence in Patients with Rett Syndrome
Direct

Abstract PDF
HRP0086P1-P107

Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome
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Abstract PDF
HRP0086P1-P108

Tolerability and Feasibility of Whole Body Vibration and its Effects on Muscle Function and Bone Health in Patients with Dystrophinopathy
Direct

Abstract PDF
HRP0086P1-P109

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta
Direct

Abstract PDF
HRP0086P1-P110

Increase in Sclerostin After Rapid Weight Loss in Children
Direct

Abstract PDF
HRP0086P1-P111

Impact of Conventional Medical Treatment on Bone Mineral Density and Bone Turnover in Adult XLH Patients: A 6 Year Cohort Study
Direct

Abstract PDF
HRP0086P1-P112

Bone Health and Body Composition in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting
Direct

Abstract PDF
HRP0086P1-P113

Extension of The Bone Health Index to Adults, and Reference Curves of Four Indices of Cortical Bone for Healthy Europeans
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Abstract PDF
HRP0086P1-P114

Extension of Automated Bone Age Determination to the End of Puberty
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Abstract PDF
HRP0086P1-P115

A European Survey to Identify New Roads for Care, Training and Research Around Rare Metabolic Bone Diseases
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Abstract PDF
HRP0086P1-P116

Clinical and Molecular Characterization of 25-Hydroxylase Deficiency in Saudi Patients
Direct

Abstract PDF
HRP0086P1-P117

No Severe Hypercalcemia During a 12-Month High-Dose Vitamin D Intervention in Infants
Direct

Abstract PDF
HRP0086P1-P118

Management of Tracheobronchomalacia During Asfotase Alfa Treatment in Infants with Perinatal-onset Hypophosphatasia: A Case Series
Direct

Abstract PDF
HRP0086P1-P119

Novel p.Asn628Ser Heterozygous Mutation in FGFR1 is Associated with Hartsfield Syndrome and Tumoral Calcinosis
Direct

Abstract PDF
HRP0086P1-P120

Practicalities of Bisphosphonate use in UK Paediatric Tertiary Centres
Direct

Abstract PDF
HRP0086P1-P121

Computer-assisted Diagnosis of Dyschondrosteosis Based on Skeletal X-ray Geometry
Direct

Abstract PDF
HRP0086P1-P122

Bisphosphonates Therapy in Girls with Rett Syndrome and Bone Fragility
Direct

Abstract PDF
HRP0086P1-P123

Skeletal Manifestations in APECED
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Abstract PDF
HRP0086P1-P124

Two French Families with Vitamin D Dependency Rickets Type 1B Harbor Homozygous Recessive Expression Of CYP2R1 Mutations L99P and G42_L46DEL INSR
Direct

Abstract PDF
HRP0086P1-P125

Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children
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Abstract PDF
HRP0086P1-P126

Impact of Intercurrent Illness on Calcium Homeostasis and Hypoparathyroidism Management
Direct

Abstract PDF
HRP0086P1-P127

Transient Pseudohypoaldosteronism and Failiure to Thrive in A 5-Month-Old Infant
Direct

Abstract PDF
HRP0086P1-P128

Childhood Cancer Survivors (CCS) are at High Risk of Reduced Bone Mass During the Second Decade of Life
Direct

Abstract PDF
HRP0086P1-P129

Trabecular Bone Score in Children from Mexico City: Preliminary Report
Direct

Abstract PDF
HRP0086P1-P130

Triple X Syndrome: An Evaluation of Bone Mineral Status and Metabolism
Direct

Abstract PDF
HRP0086P1-P131

Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes
Direct

Abstract PDF
HRP0086P1-P132

Spinal and Forearm Bone Mineralization in Adolescents with Klinefelter Syndrome
Direct

Abstract PDF
HRP0086P1-P133

Treatment with Zoledronic Acid in Children with Duchenne Muscular Dystrophy
Direct

Abstract PDF
HRP0086P1-P134

A RCT Comparing the Effect of Three Different Vitamin D Supplementation Regimens on Se 25 OH Vit D in Asymptomatic Vit D Deficient Children
Direct

Abstract PDF
HRP0086P1-P135

Low Bone Mineral Density in Adolescents with Leukemia After Hematopoietic Stem Cell Transplantation
Direct

Abstract PDF
HRP0086P1-P136

Growth Characteristics of a Girl with Multicentric Carpo-Tarsal Osteolysis Caused by Novel Mutation in the MAFB Gene
Direct

Abstract PDF
HRP0086P1-P137

Treatment Experience and Long-Term Follow-Up Data in Two Severe Neonatal Hyperparathyroidism Cases
Direct

Abstract PDF
HRP0086P1-P138

Biochemical Parameters Associated with Serum Intact FGF23 Levels in Patients with X-Linked Hypophosphatemic Rickets
Direct

Abstract PDF
HRP0086P1-P139

Dental Effects of Intravenous Bisphosphonate When Administered in Early Infancy
Direct

Abstract PDF
HRP0086P1-P140

Bone Mass and Vitamin D Status in Children and Adolescents with Generalized Epidermolysis Bullosa
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Abstract PDF
HRP0086P1-P141

Off-Label Use of the Aromatase Inhibitor Letrozole in Pubertal Boys to Improve Final Height: Laboratory, Auxological and Bone Age Data
Direct

Abstract PDF
HRP0086P1-P142

Effect of Bisphosphonates and Denosumab on Trabecular Bone: Results of a Pilot Study in Children with Osteogenesis Imperfecta
Direct

Abstract PDF
HRP0086P1-P143

Impact of Anti-Tumour Necrosis Factor Therapy on the Insulin Like Growth Factor Axis and Bone Development in Childhood Crohn's Disease
Direct

Abstract PDF
HRP0086P1-P144

Effects of Phylloquinone and Magnesium on ATDC5 Prechondrocytes
Direct

Abstract PDF
HRP0086P1-P145

To Study the Efficacy and Safety of Growth Hormone (GH) Therapy in Children with Pycnodysostosis
Direct

Abstract PDF
HRP0086P2-P146

Bone Mineral Status and Metabolism in Patients with Williams-Beuren Syndrome
Direct

Abstract PDF
HRP0086P2-P147

The Beneficial Effect of Cinacalcet on the Treatment of vitD Resistant Rickets
Direct

Abstract PDF
HRP0086P2-P148

A Preliminary Report on Body Composition Profile of Young Patients with Chronic Hemolytic Conditions
Direct

Abstract PDF
HRP0086P2-P149

Bone Status in a Patient with IGF-I Receptor Deletion Syndrome: Bone Quality and Structure Evaluation Using DXA, pQCT, and QUS
Direct

Abstract PDF
HRP0086P2-P150

Prevalence of Vitamin D Deficiency in Haitian Infants and Children
Direct

Abstract PDF
HRP0086P2-P151

Progressive Development of PTH Resistance in Patients with Maternal GNAS Inactivating Mutations
Direct

Abstract PDF
HRP0086P2-P152

Effect of Hydroxyurea Therapy on Growth Parameters in Older Children with Sickle Cell Disease
Direct

Abstract PDF
HRP0086P2-P153

Evaluation of ALP Value in Early Prediction of the Effects of Growth Hormone Treatment in Children with Growth Hormone Deficiency (GHD)
Direct

Abstract PDF
HRP0086P2-P154

Comparison of Two Different Stoss Therapy Doses in Children with Vitamin D Deficiency or Insufficiency without Rickets
Direct

Abstract PDF
HRP0086P2-P155

Bisphosphonate Treatment of Hypercalcemia in a Child with Jansen'S Metaphyseal Chondrodysplasia
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Abstract PDF
HRP0086P2-P156

Physical Exercise Level is Associated to Peak Bone Mass in Undergraduate Students
Direct

Abstract PDF
HRP0086P2-P157

A Case with Lethal Perinatal Hypophosphatasia
Direct

Abstract PDF
HRP0086P2-P158

Anthropometric and Nutritional Parameters in Egyptian Children with Osteogenesis Imperfecta: Effect of Zoledronic Acid Therapy
Direct

Abstract PDF
HRP0086P2-P159

Low Bone Mineral Density in Adolescents with Joint Hypermobility
Direct

Abstract PDF
HRP0086P2-P160

Fractures in Children with Type 1 Diabetes are Associated with Poorer Bone Mineral Status and Glycaemic Control
Direct

Abstract PDF
HRP0086P2-P161

Identification of Predictor Factors of Growth Outcome in Children with Hypophosphatemic Rickets
Direct

Abstract PDF
HRP0086P2-P162

Effects of Socioeconomic Status on Bone Mineral Density and Vitamin D Concentrations in Healthy Female College Students
Direct

Abstract PDF
HRP0086P2-P163

Bone Health Index is Low at Diagnosis of Growth Hormone Deficiency, and Improves During Growth Hormone Therapy
Direct

Abstract PDF
HRP0086P2-P164

Vitamin D Dependent Rickets Type II in Saudi Children
Direct

Abstract PDF
HRP0086P2-P165

Bone Health and Metabolic Syndrome in Childhood Cancer Survivors
Direct

Abstract PDF
HRP0086P2-P166

Diversity in Phenotype of Two Siblings and their with X-Linked Hypophosphatemic Rickets due to PHEX Mutation
Direct

Abstract PDF
HRP0086P2-P167

Expression of Brdu, VEGF, IGF-1R and Change of the Growth Plates from Sex Hormone-Inhibited Adolescents Rats - Pilot Study
Direct

Abstract PDF
HRP0086P2-P168

A Case of Genetically Proven Carbonic Anhydrase II Deficiency
Direct

Abstract PDF
HRP0086P2-P169

Rickets as Precocious Sign of Celiac Disease
Direct

Abstract PDF
HRP0086P2-P170

Clinical and Genetic Analysis of Five Patients with Vitamin D-Dependent Rickets Type 1A
Direct

Abstract PDF
HRP0086P2-P171

About a Case of a Family of Pycnodysostose
Direct

Abstract PDF
HRP0086P2-P172

Potential Role of Vitamin D in Pathogenesis of Acute Rheumatic Fever
Direct

Abstract PDF
HRP0086P2-P173

Bartter Syndrome with Bone-Destroying Hyperparathyroidism: About Two Cases, Genetically Proved, with Long-Lasting Follow-Up
Direct

Abstract PDF
HRP0086P2-P174

Management of Hypoparathyroidism: Follow-Up of 20 Patients
Direct

Abstract PDF
HRP0086P2-P175

Assessing the Serum Levels of Ferritin and Selenium in Three Important Infections of Childhood, Compared to a Control Group
Direct

Abstract PDF
HRP0086P2-P176

A Case: Hydrocephalus Secondary to Suprasellar Arachnoid Cyst with Reset Osmostat and Isolated GH Deficiency
Direct

Abstract PDF
HRP0086P2-P177

Cinacalcet Treatment in a Child with Concurrent Juvenile Idiopathic Arthritis and Hypocalciuric Hypercalcemia
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Abstract PDF
HRP0086P2-P178

Pseudohypoparathyroidism 1a with Turner's Syndrome: A Diagnostic Dilemma
Direct

Abstract PDF
HRP0086P2-P179

Bisphosphonate Use for Control of Chronic Severe Bone Pain in Children with Malignancy Associated Bone Involvement
Direct

Abstract PDF
HRP0086P2-P180

Renal Tubular Acidosis Causing Severe Growth Delay and Rickets in Two Siblings in Haiti
Direct

Abstract PDF
HRP0086P2-P181

Pseudohypoparathyroidism Type IB Associated to Assisted Reproductive Technologies: Case Report
Direct

Abstract PDF
HRP0086P2-P182

Primary Hyperparathyroidism- A Cause of Metabolic Syndrome in Children?
Direct

Abstract PDF
HRP0086P2-P183

Hyperphosphatemic Familial Tumoral Calcinosis: Novel Indication to Sevelamer Carbonate
Direct

Abstract PDF
HRP0086P2-P184

DiGeorge Syndrome and 10p Deletion
Direct

Abstract PDF
HRP0086P2-P185

Multifocal Osteonecrosis after Short Term Methylprednysolon Therapy: A Case Report
Direct

Abstract PDF
HRP0086P2-P186

Unclear Origin of Avascular Necrosis - Clinical Case
Direct

Abstract PDF
HRP0086P2-P187

Is NOTCH-Sonic Hedgehog Signalling Pathway the Missing Link Between Hajdu-Cheney Syndrome and Syringomyelia?
Direct

Abstract PDF
HRP0086P2-P188

The Unexpected Cause of Vitamin D Deficiency in a Resource Limited Setting: A Rare Case Report of Primary Intestinal Lymphangiectasia
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Abstract PDF
HRP0086P2-P189

About a Case of Dwarfism Idiopathic
Direct

Abstract PDF
HRP0086P1-P190

The Association of HLA Class II, CTLA-4 and PTPN22 Genetic Polymorphisms and [beta]-Cell Autoantibodies in Development of Type I Diabetes in Patients with Autoimmune Thyroid Disease
Direct

Abstract PDF
HRP0086P1-P191

Insulin Pump Does Not Allow a Better Control than Injections in Childhood Type 1 Diabetes (T1d) in the ISIS-Diab Cohort
Direct

Abstract PDF
HRP0086P1-P192

Diagnostic Features of Lipodystrophy in Children with Type 1 Diabetes
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HRP0086P1-P193

Recombinant Human Insulin-Like Growth Factor 1 (rh IGF1) Treatment of a Case of Leprechaunism: A Two and a Half Year Follow-Up
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HRP0086P1-P194

Longitudinal Monitoring of Pediatric Insulin Treatment in Germany and Austria: Age-Dependent Analysis of 63 967 Children and Adolescents with Type 1 Diabetes from the DPV Registry
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Abstract PDF
HRP0086P1-P195

Two Patients with HADH (SCHAD) Hyperinsulinism without Detectable 3-Hydroxybutyrylcarnitine/3-Hydroxyglutarate
Direct

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HRP0086P1-P196

Development of Type 1 Diabetes in a Child with Inherited CD59 Deficiency Treated with Eculizumab
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HRP0086P1-P197

Diagnosis of Non-Autoimmune Paediatric Diabetes by Targeted Next Generation Sequencing (NGS): Findings in Two Families with Rare Mono- and Digenic forms of Diabetes
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HRP0086P1-P198

Neonatal Siabetes, Gallbladder Agenesis and Cholestatic Giant Cell Hepatitis: A Novel Homozygote Mutation in PDX-1 Gene
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HRP0086P1-P199

Anthropometry and Glucose Homeostasis in a Patient with Donohue Syndrome (Homozygous Insulin Receptor Mutation): Effect of Continuous s.c. rIGF-I Therapy
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Abstract PDF
HRP0086P1-P200

Driving Paediatric Diabetes Care Forward in the UK: Improvements in Outcomes in the North West Following National Initiatives
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Abstract PDF
HRP0086P1-P201

Non-Surgical Treatment of Diazoxide-Resistant of Early Diffuse Hyperinsulinism Using Long-Acting Octreotide, A Somaatostatin Analog: Follow-Up of Six Cases
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Abstract PDF
HRP0086P1-P202

Screening for Autonomic Neuropathy in Children and Adolescents with Type 1 Diabetes Mellitus
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HRP0086P1-P203

Diabetes Mellitus Caused by Bone Marrow Transplantation and Total Body Irradiation - Experience from a Regional Single Centre
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HRP0086P1-P204

A Syndrome of Permanent Neonatal Diabetes Mellitus and Neurological Abnormalities due to a Novel Homozygous Missense c.449T>A (p.I150N) Mutation in NEUROD1 Gene
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Abstract PDF
HRP0086P1-P205

Are We Screening Appropriate Age Group for Early Diagnosis of Cystic Fibrosis Related Diabetes in UK?
Direct

Abstract PDF
HRP0086P1-P206

When to Screen for Coeliac Disease in Children with Type 1 Diabetes Mellitus: The Controversy
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Abstract PDF
HRP0086P1-P207

Interrelation between ACE Gene I/D Polymorphism and Chronic Kidney Disease Severity in Uzbek Children and Adolescents with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P1-P208

Improvement of Diabetic Screening System for School Children Achieved by Close Cooperation with a Local Government of Atsugi City
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Abstract PDF
HRP0086P1-P209

Association between Hypothalamus-Pituitary Adrenal Axis Activity and Anxiety in Prepubertal Children with Type 1 Diabetes
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Abstract PDF
HRP0086P1-P210

Screening for Liver Disease in Children and Adolescents with Type 1 Diabetes Mellitus: A Cross-sectional Analysis
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Abstract PDF
HRP0086P1-P211

Exploration of Social Network, Social Integration, and Socioeconomic Status in Families with Young Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P212

Permanent Neonatal Diabetes Mellitus due to a Novel Homozygous GCK Mutation in a Premature Baby with IUGR and Its Management
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Abstract PDF
HRP0086P1-P213

The Impact of Diet on Insulin Dynamics over a 2-Year Period in Children with a Family History of Obesity
Direct

Abstract PDF
HRP0086P1-P214

Analysis of Short-Term Efficacy of MiniMed 640G with SmartGuard in Pediatric Patients with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P215

The Influence of sz-Cell Autoimmunity on Cystic Fibrosis Related Diabetes Mellitus - A DPV Registry Analysis
Direct

Abstract PDF
HRP0086P1-P216

Thyroid and Islet Autoantibodies Predict Autoimmune Thyroid Disease Already at Diagnosis of Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P217

Hemolysis in a Girl with Type 1 Diabetes Mellitus and Glucose-6-Phosphate Dehydrogenase Deficiency
Direct

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HRP0086P1-P218

Clinical Characteristics and Molecular Analysis of Patients with Neonatal Diabetes
Direct

Abstract PDF
HRP0086P1-P219

Impact of Continuous Glucose Monitoring System on Therapy of Cystic Fibrosis Related Diabetes in Children and Young Adults
Direct

Abstract PDF
HRP0086P1-P220

Effect of Allopurinol Versus Angiotensin Converting Enzyme Inhibitors in Decreasing Microalbuminuria in Type 1 Diabetic Patients
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Abstract PDF
HRP0086P1-P221

Continuous Glucose Monitoring and Hypoglycemia Unawareness in Children and Adolescents with Type 1 Diabetes
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Abstract PDF
HRP0086P1-P222

Transient, Neonatal Hyperinsulinemic Hypoglycemia May be Monogenetic, Not Only Secondary to Fetal Life Events
Direct

Abstract PDF
HRP0086P1-P223

The Relationship between the Serum Irisin Levels and the Metabolic Control in adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P224

Space-time Environmental Associations in Childhood Type 1 Diabetes (T1D). A Case-control Geographical Approach in the ISIS-Diab Cohort
Direct

Abstract PDF
HRP0086P1-P225

Association Between Vascular Endothelial Markers and Carotid Intima-media Thickness in Children and Adolescents with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P1-P227

Rising of Type 1 Diabetes Mellitus Incidence in Chilean Children Between 2006 and 2014
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Abstract PDF
HRP0086P1-P228

Frequency and Risk Factors of Depression in Type 1 Diabetes in a Developing Country
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Abstract PDF
HRP0086P1-P229

Phenotypic Variability of Identical Mutations in the ABCC8 Gene in Two Families
Direct

Abstract PDF
HRP0086P1-P230

Growth and Glucose Metabolism after Allogenic Bone Marrow Transplantation for Thalassemia Major
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Abstract PDF
HRP0086P1-P231

A Rare Form of Insulin Resistance with Pseudoacromegaly
Direct

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HRP0086P1-P232

Extrahepatic Biliary Atresia in Combination with Toxic Cholestasis Due to Glibenclamide in a Case of Neonatal Diabetes
Direct

Abstract PDF
HRP0086P1-P233

Higher-Than-Conventional Subcutaneous Regular Insulin Doses Following Diabetic Ketoacidosis are Associated with Better Short-term Glycemic Control
Direct

Abstract PDF
HRP0086P1-P234

Assessment of Selected Carbohydrate Parameters in Children Exposed to Gestational Diabetes in utero
Direct

Abstract PDF
HRP0086P1-P235

The Genetic Causes and Phenotypic Characteristics of Egyptian Patients with Neonatal Diabetes Mellitus
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Abstract PDF
HRP0086P1-P236

Does Adherence to a High HbA1c Policy Improve Outcomes in a Paediatric Diabetic Clinic Population?
Direct

Abstract PDF
HRP0086P1-P237

The Prevalence of Diabetic Ketoacidosis in Children with New-Onset Type 1 Diabetes Mellitus
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HRP0086P1-P238

Correction of Carnitine Deficiency in Children with Recent Onset Type 1 Diabetes
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Abstract PDF
HRP0086P1-P239

Fetal Growth Restriction Due to Maternal Congenital Hyperinsulinism Associated with a Novel Variant in GLUD1 and Intrauterine Diazoxide Exposure
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Abstract PDF
HRP0086P1-P240

Effect of Vitamin D Supplementation on Lipid Profile in Vitamin D Deficient T1D Patients with Dyslipidemia
Direct

Abstract PDF
HRP0086P1-P241

Renal Functional Reserve in Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P242

The Prognostic Role of Non-alcoholic Fatty Liver Disease in Children with Type 1 Diabetes Mellitus with and without Dyslipidemias
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Abstract PDF
HRP0086P1-P243

Associated and Familial Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P1-P244

Factors Affecting Dyslipidaemia in Children and Young People with Type 1 Diabetes Mellitus: A Multicentre Study
Direct

Abstract PDF
HRP0086P1-P246

Wolcott Rallison Syndrome due to a Novel Mutation in EIF2AK3 Gene
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HRP0086P1-P247

Which is the Best Site for Catheter Placement in Young Children with Type 1 Diabetes (T1D) and CSII?
Direct

Abstract PDF
HRP0086P1-P248

GCK Mutations in Chinese MODY2 Patients: A Family Pedigree Report and Review of Chinese Literature
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Abstract PDF
HRP0086P1-P249

Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P1-P250

Type 1 Diabetes (T1D) Management with Few Blood Glucose (BG) Measurements but Frequent Free Adjustment of Treatment with Cell Phones or E-mails
Direct

Abstract PDF
HRP0086P1-P251

Metabolic Impairments among Adult Survivors of Paediatric Abdominal and Pelvic Tumours in the St Jude Lifetime Cohort Study
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Abstract PDF
HRP0086P1-P252

Clinical Case of a 10-year-old Girl with Papillomatosis Due to Severe Insulin Resistance Type A
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HRP0086P1-P253

Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome
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HRP0086P1-P254

A Case-Control Search of Environmental (E) Factors for Childhood Type 1 Diabetes (T1D) Using Lifeline Questionnaires in the ISIS-Diab Cohort
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Abstract PDF
HRP0086P1-P255

Transient Neonatal Diabetes Mellitus in Hanoi, Vietnam: Clinical Feature and Outcome
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Abstract PDF
HRP0086P1-P256

The Incidence of Type 1 Diabetes in the Pediatric Population in Pomeranian Region in Poland
Direct

Abstract PDF
HRP0086P1-P257

Health-Related Quality of Life and its Associated Factors in Children With Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P1-P258

Possible Monogenic Diabetes Mellitus Including Mody is Highly Prevalent in Korean Children with Diabetes Mellitus
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Abstract PDF
HRP0086P1-P259

Phenotype and Clinical Course of Diabetes Mellitus in Individuals with Pancreatic Hypoplasia Due to a PTFA Enhancer Mutation
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Abstract PDF
HRP0086P1-P260

Microalbuminuria in Type 1 Diabetes - Audit of Management of Children and Adolescents in a Single Diabetes Centre
Direct

Abstract PDF
HRP0086P1-P261

Johansson-Blizzard Syndrome with Pan-hypopituitrism, Type 2 Diabetes and Pancreatic insufficiency: Effect of Treatment
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Abstract PDF
HRP0086P2-P262

Comparison of the Occurrence of Islet Autoantibodies in Siblings of Patients with Type 1 Diabetes Mellitus to Healthy Children
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Abstract PDF
HRP0086P2-P263

The Role of 24-h Ambulatory Blood Pressure Monitoring in Children and Adolescents with Type 1 Diabetes: Early Experience of a Single Centre
Direct

Abstract PDF
HRP0086P2-P264

Clinical, Biochemical, Genetic and Immunological Features of Mexican Recent-Onset Type 1 Diabetes Patients
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Abstract PDF
HRP0086P2-P265

Efficacy and Safety of Continuous Subcutaneous Insulin Infusion Treatment in Pre-schoolers. Long Term Experience of a Tertiary Care Centre in Spain
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HRP0086P2-P266

Gene-Environment (GxE) Interactions in Childhood Type 1 Diabetes (T1D): A Case-only Geographical Approach in the ISIS-Diab Cohort
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Abstract PDF
HRP0086P2-P267

NBAS Mutations, a New Monogenic Cause of DISOPHAL, a New Syndrome with Type 1 Diabetes (T1D)
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Abstract PDF
HRP0086P2-P268

A Patient with a Rare Monogenic Diabetes Syndrome
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Abstract PDF
HRP0086P2-P269

Which Group of Children Achieved the Best Results During Insulin Pump Therapy - Long-term Outcome in Children with Type 1 Diabetes?
Direct

Abstract PDF
HRP0086P2-P270

Seasonality of Type 1 Diabetes in Children and Adolescents According to Date of Diagnosis and Date of Birth in a Large Diabetes Centre
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Abstract PDF
HRP0086P2-P271

Abnormal Glucose Level in Patients with Thalassemia Major
Direct

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HRP0086P2-P272

A Case Report of Wolfram Syndrome due to a Novel Homozygous Mutation in WFS1 Gene
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Abstract PDF
HRP0086P2-P273

Lower Basal Insulin Dose - Better Control in Type 1 Diabetes
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Abstract PDF
HRP0086P2-P274

'Comparison of Neutrophil/Lymphocyte Ratio According to Degree of Glycemic Control in Children with Recent-onset Type 1 and Type 2 Diabetes
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Abstract PDF
HRP0086P2-P275

Pancreatic Reserve and Metabolic Control of Type 1 Diabetes in a Cohort of Spanish Children and Adolescent
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HRP0086P2-P276

The Best Practice Tariff for Paediatric Diabetes Care within England: A District General Experience
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Abstract PDF
HRP0086P2-P277

Prevalence of Cardiovascular Risk Factors and Obesity in Youth with Type 1 Diabetes in Lithuania
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HRP0086P2-P278

Childhood Type 1 Diabetes (T1D) Management with e-learning through Self-educational Tools
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Abstract PDF
HRP0086P2-P279

Mucormycosis and Type 1 Diabetes: A Case Report
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Abstract PDF
HRP0086P2-P280

Insulin Pump Therapy in Type 1 Diabetes: The Indian Experience
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Abstract PDF
HRP0086P2-P281

Child with Mutation in GATA 6 Gene - Case Report
Direct

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HRP0086P2-P282

A Case Report of a 14 Year Old Female with a Known History of Type 1 Diabetes Mellitus Who Developed Tracheal Stenosis as a Result of Prolonged Intubation from Diabetic Ketoacidosis and Subsequently Developed Acute Pancreatitis
Direct

Abstract PDF
HRP0086P2-P283

Continuous Glucose Monitoring Can Alleviate Parental Fear of Hypoglycaemia in Children with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P2-P284

The Implementation of a System of Continuous Monitoring of Blood Glucose and Open (FREE STYLE FREE) Improves Metabolic Control of Affected Children DMtipo1
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Abstract PDF
HRP0086P2-P285

Permanent Neonatal Diabetes by Gene Mutation KCNJ11. Evolution and Treatment after Three Years with Sulphonylureas
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HRP0086P2-P286

Atypical Cystic Fibrosis Adolescent Case Study (with Normal Sweat Test) Referring with Diabetes Mellitus Symptoms Found to Carry Homozygous R352Q Mutation
Direct

Abstract PDF
HRP0086P2-P287

Diabetic Ketoacidosis Risk Factors in the Initial Presentation of Type 1 Diabetes Mellitus in Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P288

Prevalence of Polycystic Ovary Symdrome and its Clinical Profile in Young Females with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P2-P289

The Frequency of Diabetic Ketoacidosis in Children and Adolescents with Newly Diagnosed Type 1 Diabetes Mellitus: A Single Centre Experience in Turkey
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Abstract PDF
HRP0086P2-P290

Wolcott-Rallison Syndrome: Clinical Case Presentation
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HRP0086P2-P291

The Story of a de novo Heterozygous HNF1A Mutation
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Abstract PDF
HRP0086P2-P292

Use of Continuous Glucose Monitoring Helps Selecting Insulin Therapy in Thalassemic Adolescents with Glycemic abnormalities
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Abstract PDF
HRP0086P2-P293

Impact of Demographic Factors on Diabetic Ketoacidosis Occurrence at Type 1 Diabetes Onset in Childhood
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Abstract PDF
HRP0086P2-P294

Differences in Hba1c among Different Ethnicities; Is it just a Matter of Mean Glycaemia?
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Abstract PDF
HRP0086P2-P295

Ischemic Intestinal Necrosis as a Rare Complication of Diabetic Ketoacidosis in a Child with New-Onset Type I Diabetes: A Case Report
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HRP0086P2-P296

Diabetes - a Rare Complication of Ataxic Telangiectasia Presenting in Childhood
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Abstract PDF
HRP0086P2-P297

Clinical and Demographic Characteristics of Patients with Type 1 Diabetes Mellitus and correlation with risk factors: A South Indian Database
Direct

Abstract PDF
HRP0086P2-P298

Insulin Response at Standard Glucose Load in Children With Normal, Low and Excessive Body Mass
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Abstract PDF
HRP0086P2-P299

Initial Presentation of Subjects with Type 1 Diabetes: A Change in Spectrum
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HRP0086P2-P300

Evaluation of the Epidemiological, Presenting and Follow-up Characteristics and their Impacts on the Glycemic Control in a Large Cohort of Pediatric Type 1 Diabetes Mellitus Patients from Southeastern Anatolian Region of Turkey
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Abstract PDF
HRP0086P2-P301

HbA1C and IGF-1 Levels in Diabetic Children Treated with Vitamin D
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Abstract PDF
HRP0086P2-P302

Long-Term Follow-Up of Non-Diabetic Obese Children and Adolescents Treated with Metformin
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Abstract PDF
HRP0086P2-P303

Understanding the Molecular and Genetic Basis of Complex Syndromes of Diabetes Mellitus
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HRP0086P2-P304

Cardiovascular Risk and Long Term Follow-up of Turkish Children with Type 2 Diabetes: Single Center Experience
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Abstract PDF
HRP0086P2-P305

Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine
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Abstract PDF
HRP0086P2-P306

Maturity-Onset Diabetes of the Young (MODY): Tracking and Clinical Follow-up
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Abstract PDF
HRP0086P2-P307

Evaluation of Autoimmune Thyroiditis Development on Onset and During Follow Up in Cases with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P308

The Autoimmune Hypothesis for Acute Bilateral Cataract in Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P309

Clinical Characteristics of Latent Autoimmune Diabetes in Youth (Type 1.5 DM)
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Abstract PDF
HRP0086P2-P310

Diabetic Ketoacidosis: Clinical Features and Precipitating Factors at DEMPU
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Abstract PDF
HRP0086P2-P311

Diabetes Distress in Adolescents and Young Adults with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P312

A Novel Glucokinase Gen Mutation: Mody Type-2 Case
Direct

Abstract PDF
HRP0086P2-P313

Congenital Hyperinsulinism in a Resource Limited Setting: Overcoming Barriers towards a Survival Path
Direct

Abstract PDF
HRP0086P2-P314

Vitamin D Levels and Relations with Clinical and Laboratory Findings in Children with Newly Diagnosed Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P315

Lipid Profile, Lipid Per-Oxidation and Trace Elements Status in Libyan Males with Type II Diabetes Mellitus
Direct

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HRP0086P2-P316

Cystic Fibrosis Related Diabetes
Direct

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HRP0086P2-P317

Type 1 Diabetes in Childhood: An 8-year Experience
Direct

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HRP0086P2-P318

A Rare Reason of Type 2 Diabetes: Alstrom Syndrome
Direct

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HRP0086P2-P319

The Relationship among Cardiac T2*, Liver T2* and Abnormal Glucose in Patients with Thalassemia Major
Direct

Abstract PDF
HRP0086P2-P320

Hyperglycaemia in a Boy of 13 years old: Not always Type 1 Diabetes Mellitus. A Case Report
Direct

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HRP0086P2-P321

Achievement of Metabolic Parameter Goals in Children and Adolescent with Type 1 Diabetes According to the Latest ADA/ISPAD Standards of Medical Care in Diabetes in a Pediatric Diabetes Clinic in North Greece
Direct

Abstract PDF
HRP0086P2-P322

Clinical and Laboratory Characteristics of Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P323

Prevalence of Acute Metabolic Complications in Children with Type I Diabetes Admitted to the Children Hospital in Qazvin, Iran (2005-2014)
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Abstract PDF
HRP0086P2-P324

Glargine versus Detemir Insulin During the Honeymoon Phase in a Child with Type1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P325

Diabetic Ketoacidosis and Multiple Organ Failure Syndrome: A Case Study
Direct

Abstract PDF
HRP0086P2-P326

Neonatal Diabetes Associated with Transaminitis in a Growth Retarded Infant
Direct

Abstract PDF
HRP0086P2-P327

Benefits of Switching Insulin from Twice Daily to Multiple Daily Injections on Glycaemic Control in Children with Type 1 Diabetes Mellitus in Sri Lanka at the Lady Ridgeway Hospital, Sri Lanka
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HRP0086P2-P328

Rapid Acting Insulin Analogue Treatment in Children and Adolescents with Type 1 Diabetes Mellitus; Insulin Glulisine Experience
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Abstract PDF
HRP0086P2-P329

The Prevalence of Dyslipidemia and Associated Factors in Children and Adolescent with Type I Diabetes
Direct

Abstract PDF
HRP0086P2-P330

Lipid Metabolism in Children with Diabetes Mellitus Type 1
Direct

Abstract PDF
HRP0086P2-P331

Prevalence of Celiac Disease in Children and Adolescents with Type 1 Diabetes Mellitus
Direct

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HRP0086P2-P332

Evaluating the Impact of the Diagnosis and Management of a Child with Type 1 Diabetes on Parents
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HRP0086P2-P333

Association Between Socioeconomic Status and Glycemic Control in Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P334

Minimally Invasive Surgical Interventions in the Treatment of Primary Persistent Hyperinsulinemic Hypoglycemia of Infancy
Direct

Abstract PDF
HRP0086P1-P335

Complete Androgen Insensitivity Syndrome Caused by a Deep Intronic Pseudoexon-Activating Mutation in the Androgen Receptor Gene
Direct

Abstract PDF
HRP0086P1-P336

Polycystic Ovary Syndrome in Adolescence: New Therapeutic Approach with Inositol and Alpha-Lipoic Acid
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Abstract PDF
HRP0086P1-P337

46,XY Partial Gonadal Dysgenesis Caused by an Xp21.2 Interstitial Duplication that Does not Encompass the NR0B1 Gene
Direct

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HRP0086P1-P338

Primary Ovarian Insufficiency in Childhood Cancer Survivors: A Report from the St Jude Lifetime Cohort (SJLIFE)
Direct

Abstract PDF
HRP0086P1-P339

Global and Sexual Quality of Life in Patients with Rokitanski Syndrome: A Comparative Study Between Surgical vs Non Surgical Management of Vaginal Agenesis in a French Cohort of 130 Patients
Direct

Abstract PDF
HRP0086P1-P340

Intrauterine Growth Restriction Affects Postnatal Testis Maturation in Rats
Direct

Abstract PDF
HRP0086P1-P341

Application of on Line Learning in Assessment of Competencies of Fellows Pediatric Endocrinology
Direct

Abstract PDF
HRP0086P1-P342

Genotype-phenotype Analysis of NR5A1/SF1 Mutations by Functional in vitro Studies
Direct

Abstract PDF
HRP0086P1-P343

Evolution of Bone Mass and Body Composition in Gender Dysphoric Adolescents Treated with Progestins to Suppress Endogenous Hormones
Direct

Abstract PDF
HRP0086P1-P344

Sertoli Cell Function During Chemotherapy in Pediatric Patients with Acute Lymphoblastic Leukemia
Direct

Abstract PDF
HRP0086P1-P345

Accuracy of Pelvic MRI in Evaluating Internal Genitalia in Patients with Disorders of Sex Development
Direct

Abstract PDF
HRP0086P1-P346

Using Public Databases, 'Virtual Controls' and Geolocalization to Search for Environmental Correlates of Hypospadias
Direct

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HRP0086P1-P347

The International AGD Consortium: A Multi-center Study of 3939 Infants and Children with Anogenital Distance Measurements
Direct

Abstract PDF
HRP0086P1-P348

Exonic Splicing Mutations by Silent Nucleotide Variation in the Androgen Receptor Gene Causes Androgen Insensitivity Syndrome
Direct

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HRP0086P1-P349

Severe 5 Alpha Reductase 2 Deficiency with Aphallia is Caused by p.Y91H SRD5A2 Mutation and is Responsive to Dihydrotestosterone Administration During Childhood
Direct

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HRP0086P1-P350

Clinical History and High Prevalence of Gonadal Tumor in 14 Patients with 46 XY Pure Gonadal Dysgenesis
Direct

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HRP0086P1-P352

A Multicenter Study on Long-Term Outcomes in 56 Males with 45,X/46,XY Mosaicism
Direct

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HRP0086P1-P353

Familial Testotoxicosis: Outcome and Possible Relation to Testicular Malignancies
Direct

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HRP0086P1-P354

Psychological Impact in Young Women of Announcement of a Utero-Vaginal Malformation (Mayer-Rokitansky-Kuster-Hauser - MRKH Syndrome) and its Treatment
Direct

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HRP0086P1-P355

Mutations at the SF-1 Ligand-Binding Domain Can Lead to Different Effects on DNA Binding: Report of Two Novel Mutations
Direct

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HRP0086P1-P356

A New International Registry Highlights the Differences in Practice for Reaching a Diagnosis of CAH - On Behalf of the I-CAH/I-DSD Registry User Group
Direct

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HRP0086P1-P357

Changes in Adrenal Steroids During Puberty Suppression and Cross Sex Hormone Treatment in Gender Dysphoric Adolescents
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HRP0086P1-P358

Do the Anti-Mullerian Hormone Levels of Adolescents with Polycystic Ovarian Syndrome (PCOS), Those Who Are at Risk for Developing PCOS, and Those Who Exhibit Isolated Oligomenorrhea Differ from those of Adolescents with Normal Menstrual Cycles?
Direct

Abstract PDF
HRP0086P1-P359

Feasibility Study for Avoiding Early Surgery in Girls with 21-Hydroxylase Deficiency (21OHD)
Direct

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HRP0086P1-P360

A Novel Familial Androgen Receptor Mutation (W752G) in Complete Androgen Insensitivity Syndrome: Use of in vitro Study According to the Nature of Amino Acid Substitution
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HRP0086P1-P361

Partial and Mixed Gonadal Dysgenesis Cannot be Distinguished by Histological Picture: Clinical Evaluation, Histological Differences and Long-Term Follow up of 61 Brazilian Patients
Direct

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HRP0086P1-P362

Aromatase Activity is Disrupted by Mutations in P450 Oxidoreductase
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HRP0086P1-P363

Mosaic Xq Partial Duplication Leading to Virilisation of an Adolescent Female
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HRP0086P1-P364

Genotyping Patients with Differences of Sex Development: 25 Years of Investigation of an Italian Population of 308 Cases (194 46,XY and 114 46,XX)
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HRP0086P1-P365

Functional Studies of a New Mutation in the LH/CG Receptor Gene Identified in 2 Sisters with 46,XY DSD
Direct

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HRP0086P1-P366

Consecutive Lynestrenol and Cross-Sex Hormone Treatment in Biological Female Adolescents with Gender Dysphoria: A Retrospective Analysis
Direct

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HRP0086P1-P367

Ovarian Reserve Assessment in Girls and Women after Hematopoietic Stem Cell Transplantation Treatment Underwent in Childhood
Direct

Abstract PDF
HRP0086P1-P368

Precocious/Early and Accelerated Puberty in a Boy with a Homozygous R192C Mutation in CYP19 (Aromatase) Gene
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HRP0086P1-P369

Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Accordingly Gender Assignment
Direct

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HRP0086P1-P370

45,X/46,XY Chromosomal Disorders of Sex Development: Experience from a Cohort of 50 Patients Followed in One Single Institution
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HRP0086P1-P371

Androgen Profile Differs to Adults in Adolescent Girls with Polycystic Ovary Syndrome
Direct

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HRP0086P1-P372

Effects and Side Effects of Cyproterone Acetate Alone and in Combination with Estrogens in Natal Male Adolescents with Gender Dysphoria
Direct

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HRP0086P1-P373

Compound Heterozygous C10orf2 Mutations in a Japanese Patient with 46,XX Ovarian Failure and Deafness
Direct

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HRP0086P1-P374

GATA Transcription Factors in Testicular Adrenal Rest Tumours
Direct

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HRP0086P1-P375

Can we Standardize Sex Assignment in 45,X/46,XY Mixed Gonadal Dysgenesis?
Direct

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HRP0086P1-P376

Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia: A Case Report
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HRP0086P1-P377

Effect and Safety Aspects of Percutaneous Administration of Dihydrotestosterone in Children with Micropenis with Different Genetic Background
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HRP0086P1-P378

Randomized Controlled Study Comparing Vitamin D and Omega 3-Fatty Acids Supplementation in Adolescents with Polycystic Ovary Syndrome
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HRP0086P1-P379

Health-Related Quality of Life and Psychological Wellbeing in Adults with Diverse Sex Development
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HRP0086P1-P380

Association of Genetic Polymorphisms Around the LIN28B Gene and Idiopathic Central Precocious Puberty Risks Among Chinese Girls
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HRP0086P1-P381

Psychological Outcomes and Quality of Life of Patients with Non-CAH DSD
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HRP0086P1-P382

Normalization of Ovulation Rate in Adolescent Girls with Hyperinsulinemic Androgen Excess
Direct

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HRP0086P2-P383

Thyroid Autoimmunity in Adolescent Girls with Polycystic Ovary Syndrome - Pilot Study
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HRP0086P2-P384

The Efficacy and Safety of Gonadotropin-Releasing Hormone Analogue Treatment to Suppress Puberty in Gender Dysphoric Adolescents
Direct

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HRP0086P2-P385

A Familial form of DSD due to NR5A1 Mutation in a Father and His Son
Direct

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HRP0086P2-P386

High Prevalence of SGA in Patients with Disorders of Sexual Development, Especially Idiopathic 46,XY DSD
Direct

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HRP0086P2-P387

Questionnaire Surveys Targeting Japanese Pediatric Endocrinologists Regarding Reproduction in Pediatric and Adolescent Cancer Patients
Direct

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HRP0086P2-P388

Fertility Outcomes after Childhood Onset Hypothalamic Hypogonadism
Direct

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HRP0086P2-P389

Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia: A Novel AMH Receptor Mutation
Direct

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HRP0086P2-P390

Three Cases of NR5A1 (SF1) Gene Mutations in DSD Patients
Direct

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HRP0086P2-P391

Sertoli-Leydig Cell Tumor as a Rare Cause of Hirsutism in a Young Adolescent
Direct

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HRP0086P2-P392

Identification of an AR Mutation in Klinefelter's Syndrome during Evaluation for Penoscrotal Hypospadias
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HRP0086P2-P393

Assessment of Sexual Identity in Patients with Congenital Adrenal Hyperplasia
Direct

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HRP0086P2-P394

Duct Ectasia, a Rare Complication of Gynaecomastia
Direct

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HRP0086P2-P395

Evaluation of Anti-Mullerian Hormone (AMH) Assay Roche® on Umbilical Cord Blood: Determination of Reference Values in Girls and Boys Newborn
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HRP0086P2-P396

Hypogonadotropic Hypogonadism in a Girl with 2p11.2-2q12.1 Duplication
Direct

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HRP0086P2-P397

A Nonvirilized form of Classic 3[beta]-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria
Direct

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HRP0086P2-P398

Nonclassic Congenital Adrenal Hyperplasia and Functional Ovarian Hyperandrogenism Diagnosed During the Transition Period: Differences in Clinical, Hormonal and Metabolic Aspects
Direct

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HRP0086P2-P399

Diagnosis of PCOS in Adolescents Using MRI
Direct

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HRP0086P2-P400

Novel CYP17A1 Mutation and CYP21 Mutations in Two Siblings
Direct

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HRP0086P2-P401

Aetiology of 46,XY DSD in Algeria; Putative Modifier Role of pV89L Polymorphism in the SRD5A2 Gene in Androgen Receptor Mutation-Negative Subjects
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HRP0086P2-P402

Children with 46,XY DSD: Etiology, Clinical Profile, Socio-Demographic Details and Sex of Rearing
Direct

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HRP0086P2-P403

Endocrine Risk Factors of Testicular Cancer of Children and Teenagers with Testicular Microlithiasis
Direct

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HRP0086P2-P404

Case Report of a Girl with Secondary Amenorrhea Associated with Aurantiasis Cutis
Direct

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HRP0086P2-P405

Maternal Ovarian Luteoma Causing Complete Virilization of a Female Fetus
Direct

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HRP0086P2-P406

The Experience of GAIA (Abuse Childhood and Adolescence Group) - AOU Meyer
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HRP0086P2-P407

State of Knowledge of Late Endocrinological Effects of Hematological Patients Who Has Undergone Chemotherapy
Direct

Abstract PDF
HRP0086P2-P408

Disorders of Sex Genitalia in Yaounde: Difficult Questions, Which Answers?
Direct

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HRP0086P2-P409

Analysis of Clinical Manifestations and Gene Mutations of 5[alpha]-Reductase Type 2 Deficiency in 16 Cases
Direct

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HRP0086P2-P410

Unusual Differential Diagnosis of Hyperandrogenism in Adolescent Female Treated for Polycystic Ovarian Syndrome
Direct

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HRP0086P2-P411

Phenotypic and Hormonal Variability in 46,XY Subjects with SF-1 Mutations
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HRP0086P2-P412

Towards the Roles of Kisspeptins in the Control of Gonadotropic Axis: Focus on Peripheral Signaling in Androgen-Dependent Tissues in the Experimentally Induced Model Hypogonadotropic Hypogonadism in Male Rats
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HRP0086P2-P413

Two Patients Presenting the Extremes of the Phenotypic Spectrum of 5 alfa Reductase Deficiency: One with at New Mutation
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HRP0086P2-P414

Disorders of Sex Development 45,X/46,XY: Clinical and Laboratory Characteristics of Patients
Direct

Abstract PDF
HRP0086P2-P415

Reproductive Function of Central Precocious Puberty in Girls: A Systematic Review
Direct

Abstract PDF
HRP0086P2-P416

Cytogenetic Variability and Phenotypic Findings in Patients with Ovotesticular Disorder of Sex development
Direct

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HRP0086P2-P417

Cytogenetic Study of Sex Chromosomal Abnormalities in Egyptian DSD Patients
Direct

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HRP0086P2-P418

Phenotype, Genotype and Gender Identity in Pubertal and Post-Pubertal Patients with Androgen Insensitivity Syndrome
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HRP0086P2-P419

XLAG Syndrome Case Accompanying a New ARX Mutation and has a Interhemispheric Cyst
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HRP0086P2-P420

Congenital Adrenal Lipoid Hyperplasia in a 30-Year-Old Female with a Tall Stature
Direct

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HRP0086P2-P421

Onset of Puberty in Healthy Boys is Associated with a Decreased BMI Compared to Values Prior to the Onset of Puberty
Direct

Abstract PDF
HRP0086P2-P422

Late Clinical Presentation, Biological Assessment and Management of PAIS in a Developing Country
Direct

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HRP0086P2-P423

Sisters with 46XY Gonadal Dysgenesis and Gonadoblastoma
Direct

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HRP0086P2-P424

Follow-up to Adulthood of Two 46,XY Siblings with 5-alpha Reductase Deficiency and Different Sex of Rearing
Direct

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HRP0086P2-P425

Constitutional Delay of Puberty: Clinical and Hormonal Characteristics of Patients
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HRP0086P2-P426

Comparison between Serum Vitamin D Levels in Precocious Pubertal Girls and Normal Girls
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Abstract PDF
HRP0086P2-P427

Complete Virilization without Salt Wasting in a 7-year-old Haitian Child with Congenital Adrenal Hyperplasia
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HRP0086P2-P428

Hematocolpos Revealed by Non-cyclic Lower-back Pain in a Pre-menarcheal Girl
Direct

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HRP0086P2-P429

Novel AMH and AMHR-II Mutations in Two Egyptian Families with Persistent Mullerian Duct Syndrome
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HRP0086P2-P430

Study of Genetics of Human Disorders of Sexual Development. Research Project.
Direct

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HRP0086P2-P431

46XX Male Syndrome
Direct

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HRP0086P2-P432

45,X/47,XYY Chromosomal Mosaicism as a Cause of 46,XY Disorder of Sex Development
Direct

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HRP0086P2-P433

46,XY Complete Gonadal Dysgenesis with Late Diagnosis
Direct

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HRP0086P2-P434

Diagnosis, Treatment and Gene Mutation Analysis of the Case with Steroid 5[alpha]-Reductase Type 2 Deficiency
Direct

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HRP0086P2-P435

An Infant with 49XXXXY Syndrome: A Case Report from Sri Lanka
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HRP0086P2-P436

Mixed Gonadal Disgenesia: Patients of Instituto da Crianca, HC-FMUSP
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HRP0086P2-P437

Primary Amenorrhea as Alarm Manifestation in a Oligosymptomatic Girl with Xq Deletion and Turner Syndrome
Direct

Abstract PDF
HRP0086P2-P438

Hypogonadotropic Hypogonadism in a Patient with Vanishing Testis Syndrome - Case Report
Direct

Abstract PDF
HRP0086P2-P439

17 Alpha Hydroxylase, 17-20 Lyase Deficiency, a Case with Hypocalcemic Symptoms
Direct

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HRP0086P2-P440

An Uncommon Case of Adolescent with POF
Direct

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HRP0086P2-P441

Trisomy 9 Syndrome in an Infant with Ambiguous Genitalia
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HRP0086P1-P442

Placental and Cord Blood DNA Methylation Profiling in Small-for-Gestational-Age Newborns from Uncomplicated Pregnancies: Relationship to Prenatal Growth and Postnatal Body Composition
Direct

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HRP0086P1-P443

The Collapse of the BDNF/POMC System in the Hypothalamus is Responsible for the Extreme Obesity with Hyperphagia Observed in Female Heterozygous MeCP2 Null Mice
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HRP0086P1-P444

Neonatal Overfeeding Alters Hepatic Insulin Sensitivity During Lactation and Leads to Long-term Insulin Resistance and Fatty Liver in Mice: Key Role of Mogat1
Direct

Abstract PDF
HRP0086P1-P445

The Impact of Activating PIK3CA Mutations and PTEN Haploinsufficiency on Human Adipocyte Phenotype and Biology
Direct

Abstract PDF
HRP0086P1-P446

Bioinactive Leptin is not Frequently Detected in Severe Early Onset Childhood Obesity
Direct

Abstract PDF
HRP0086P1-P447

Neonatal Overnutrition Causes Sex and Age Dependant Long-Term Effects on Body Weight, Body Composition and Serum Triglyceride and Free Fatty Acid Levels
Direct

Abstract PDF
HRP0086P1-P448

Laparoscopic sleeve gastrectomy in adolescents with morbid and dynamic obesity. A controlled monocentric study.
Direct

Abstract PDF
HRP0086P1-P449

Efficacy, Safety and Metabolic Effects of Carbohydrate Restriction in the Treatment of Obese Adolescents
Direct

Abstract PDF
HRP0086P1-P450

Severe Hypertriglyceridemia in Pediatric Oncology Patient
Direct

Abstract PDF
HRP0086P1-P451

The Frequencies of 5-HTTLPR Locus in Promotor Part of Serotonine Transporter Gene (SLC6A4) Polymorphism in Children with Different Forms of Obesity
Direct

Abstract PDF
HRP0086P1-P452

High Predictability of Impaired Glucose Tolerance by Combining Diagnostic Parameters in Obese Children
Direct

Abstract PDF
HRP0086P1-P453

The Effect of Subclinical Hypothyroidism (SH) and Treatment of SH with L-T4 on Basal Metabolic Rate in Obese Children: A Prospective Study
Direct

Abstract PDF
HRP0086P1-P454

Influence of Television Viewing During Meals on Eating Patterns
Direct

Abstract PDF
HRP0086P1-P455

Seven-year Follow-up of Mothers from a Randomized Controlled Trial of Exercise in Pregnancy and their Offspring
Direct

Abstract PDF
HRP0086P1-P456

E-Health: A National Registry and Therapeutic Algorithm for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece
Direct

Abstract PDF
HRP0086P1-P457

Premature Adrenarche and Metabolic Risk: Differences by Gender
Direct

Abstract PDF
HRP0086P1-P458

Association of miR-34a and mir-149 with Obesity and Insulin Resistance in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P1-P459

Erythropoietin Activates Classical Brown Adipose Tissue Through the Erythropoietin Receptor/STAT3 Pathway, Improving Obesity and Glucose Homeostasis in High Fat Diet-induced Obese Mice
Direct

Abstract PDF
HRP0086P1-P460

The Association between Insulin Resistance and Lower Extremity Muscle Strength, Static and Dynamic Standing Balances in Obese Adolescents
Direct

Abstract PDF
HRP0086P1-P461

Adiponectin and IL-6 in Simple Childhood Obesity with and without Hepatic Steatosis
Direct

Abstract PDF
HRP0086P1-P462

Determinants of Advanced Bone Age in Childhood Obesity
Direct

Abstract PDF
HRP0086P1-P463

Exposure to Phthalates Is Associated with Overweight or Obesity in 4-Year-Old Children
Direct

Abstract PDF
HRP0086P1-P464

Central Obesity among European Preschool Children: The ToyBox-Study
Direct

Abstract PDF
HRP0086P1-P465

Changes in Waist-to-Height Ratio during Preschool Years Differ between Children being Obese or Overweight at Five Years of Age Compared with not Overweight Children
Direct

Abstract PDF
HRP0086P1-P466

Remarkable Increase in the Prevalence of Overweight and Obesity among School Age Children in Antalya, Turkey, between 2003 and 2015
Direct

Abstract PDF
HRP0086P1-P467

The Peculiarities of Neurotransmitters Levels in Children with Obesity and Different Genotypes of COMT Gene
Direct

Abstract PDF
HRP0086P1-P468

Association of Fasting Triglycerides to High-Density Lipoprotein Ratio with Risk for Metabolic Disorders in Children
Direct

Abstract PDF
HRP0086P1-P469

Assessment of Adherence to Mediterranean Diet during a Weight Loss Intervention in Children with Cardiometabolic Risk
Direct

Abstract PDF
HRP0086P1-P470

Brain Structure, Executive Function and Appetitive Traits in Adolescent Obesity
Direct

Abstract PDF
HRP0086P1-P471

Improved Clinical and Laboratory Changes after 12 Months of Use of Metformin in Obese Insulin Resistant Children and Adolescents
Direct

Abstract PDF
HRP0086P1-P472

Risk factors for Atherosclerosis after Anticancer Treatment in Childhood: The Assessment of Lipid Parameters and Indicators of Susceptibility to Atherosclerosis in a Group of Pediatric Patients after Anticancer Treatment
Direct

Abstract PDF
HRP0086P1-P473

Inherited Duplication (X) (p11.4) Associated with Obesity, Autoaggressive Behaviour and Delayed Speech Development
Direct

Abstract PDF
HRP0086P1-P474

Switching Patients with Congenital Hyperinsulinism from Standard Octreotide to Long-Acting Release Octreotide Preserves Blood Glucose Control and Improves Quality of Life of Their Caregivers
Direct

Abstract PDF
HRP0086P1-P475

Reduction of Body Mass and Change in Body Composition of the Participants of the PoZdro! - Programme for Prevention of Diabetes and Civilisation Diseases by Medicover Foundation - Preliminary Results, after the First Year of Interventions
Direct

Abstract PDF
HRP0086P1-P476

Polysomnography in Obese Children with and without Prader-Willi
Direct

Abstract PDF
HRP0086P1-P477

Renal Involvement ın Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P1-P478

BMI Correlates Positively with Hair Cortisol, whereas Excessive Body Fat Correlates Positively with Hair Cortisol: Salivary Cortisol and Fasting Insulin Concentrations in Prepubertal Girls
Direct

Abstract PDF
HRP0086P1-P479

Hepatic Steatosis and Cardiovascular Risk in Overweight Children: Preliminary Results of the Study EFIGRO
Direct

Abstract PDF
HRP0086P1-P480

Associations of Different Appetite Hormones with Physical Activity and Cardiorespiratory Fitness in Adolescent Boys with Different BMI Values
Direct

Abstract PDF
HRP0086P1-P481

The Relation of Glycaemic Variability Obtained by Continuous Subcutaneous Glucose Monitoring with IL-6 and Adiponectin Levels in Obese Children with Metabolic Syndrome and Insulin Resistance
Direct

Abstract PDF
HRP0086P1-P482

Changes in Urine and Plasma Metabolomics Profiles after a Lifestyle Intervention Program in Obese Prepubertal Children
Direct

Abstract PDF
HRP0086P1-P483

The Effectiveness of a Stress Management Intervention Program in the Management of Overweight and Obesity in Childhood and Adolescence
Direct

Abstract PDF
HRP0086P1-P484

Fetuin-A as an Alternative Marker for Insulin Resistance and Cardiovascular Risk in Prepubertal Children
Direct

Abstract PDF
HRP0086P1-P485

What are Early Predictors of Impaired Glucose Tolerance in Children Born SGA?
Direct

Abstract PDF
HRP0086P1-P486

Multidisciplinary Intervention Programme in Childhood Obesity- Review of Service
Direct

Abstract PDF
HRP0086P1-P487

Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report
Direct

Abstract PDF
HRP0086P1-P488

Glucose Metabolism In Children with Prader-Willi Syndrome: The Effect Of Gh Therapy
Direct

Abstract PDF
HRP0086P1-P489

Impact of a Group-based Treatment Program on Adipocytokines, Oxidative status, Inflammatory Cytokines, and Pulse Wave Velocity in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P490

Matsuda Index in Correlation with Clinical Indicators of Insulin Resistance in Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P491

Anthropometric, Biological and Imagistical Methods For Assessing the Cardiovascular Risk in Obese Children
Direct

Abstract PDF
HRP0086P2-P492

Trends of Nutrition of Ukrainian Children from Kharkiv Region: Tendency to Overweight, Dehydration, Impaired Social Adaptation
Direct

Abstract PDF
HRP0086P2-P493

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P494

Comparison between CDC (Centers for Disease Control and Prevention) and Italian Growth Charts in the Characterization of Pediatric Obesity
Direct

Abstract PDF
HRP0086P2-P495

The Cutoff Values of Indirect Indices for Measuring Insulin Resistance in Korean Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P496

Intensive Exercise Intervention for Long-term Adolescent and Young Adult Survivors of Oncology-Related Cranial Insult: A Pilot Study
Direct

Abstract PDF
HRP0086P2-P497

Cardiometabolic Effect of Sugar-Sweetened Beverages Reduction in Obese Children
Direct

Abstract PDF
HRP0086P2-P498

A Comprehensive and Multidisciplinary Management Plan is Extremely Effective at Reducing the Prevalence of Overweight and Obesity in Childhood and Adolescence
Direct

Abstract PDF
HRP0086P2-P499

Multidisciplinary Care Management of Pediatric Obesity and Factors Associated with Better Outcomes
Direct

Abstract PDF
HRP0086P2-P500

Prevalence and Characteristics of Polycystic Ovary Syndrome in Obese Adolescents
Direct

Abstract PDF
HRP0086P2-P501

Efficacy of the Treatment for Childhood Obesity in Specialist Care: Age Over 10 Years at Baseline and Acanthosis Nigricans Predict a Worse Outcome
Direct

Abstract PDF
HRP0086P2-P502

Metabolic Syndrome in Prepubertal Obese Children: Inclusion of the Triglyceride/Hdl Ratio as an Alternative Diagnostic Criterion
Direct

Abstract PDF
HRP0086P2-P503

The relationship between Subclinical Hypothyroidism and Iodine Deficiency, Serum Leptin Levels and Metabolic Syndrome in Obese Children
Direct

Abstract PDF
HRP0086P2-P504

Analysis of Circulating miRNAs in Obese Children Born Small for Gestational Age
Direct

Abstract PDF
HRP0086P2-P505

Irisin and Abdominal Obesity in Preschool Age
Direct

Abstract PDF
HRP0086P2-P506

Long Term Outcomes after Hospital Based, Life-Style Weight Loss Intervention During Childhood
Direct

Abstract PDF
HRP0086P2-P507

Implications of Insulin Resistance in Obese and Overweight Children: A Cohort Analysis
Direct

Abstract PDF
HRP0086P2-P508

Effects of Highly Mineralized Water on Weight and Metabolism - A Randomized Controlled Blinded Trial in a Pediatric Hospital Staff
Direct

Abstract PDF
HRP0086P2-P509

Which Marker is the Most Reliable One for the Detection of NAFLD in Outpatient Clinic?
Direct

Abstract PDF
HRP0086P2-P510

Nonalcoholic Fatty Liver Disease: Evolution after 1 year of Follow-Up with Different Therapies
Direct

Abstract PDF
HRP0086P2-P511

Lifestyle Survey of Doctors, Medical Residents and Medical Students in Latvia
Direct

Abstract PDF
HRP0086P2-P512

Weight Status in Children at 8 Years: A Prospective Cohort Study
Direct

Abstract PDF
HRP0086P2-P513

Low Birth Weight is not Associated with Increased Risk of Metabolic Syndrome in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P514

Prader Willi Syndrome in Brazil: 6 months Follow-up in a Reference Center
Direct

Abstract PDF
HRP0086P2-P515

Early Blood Pressure Abnormalities Related to Cardiovascular Risk in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P516

4G Polymorphism of Plasminogen Activator Inhibitor-1 (PAI-1), PAI-1 Plasma Levels, and Lipid Profiles in Overweight/Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P517

Polycystic Ovarian Syndrome in a Population of Obese Adolescents
Direct

Abstract PDF
HRP0086P2-P518

Vitamin D Deficiency in Obese Children and the Relationship with Insulin Resistance and Metabolic Syndrome
Direct

Abstract PDF
HRP0086P2-P519

Dietary Habits of Children and Adolescents Attending an Out-Patient Clinic for the Prevention and Management of Overweight and Obesity in Greece
Direct

Abstract PDF
HRP0086P2-P520

Preliminary Findings on Nutrition Care Competence in Health Care Professionals Using a Standardized Questionnaire NUTCOMP Korean Version
Direct

Abstract PDF
HRP0086P2-P521

Construction of Remote Monitoring System of Children with Tall or Short Stature and Overweight or Poor Weight Gain from the Elementary School Health Checkup Data
Direct

Abstract PDF
HRP0086P2-P522

The Effect of Demographic and Lifestyle Factors on One-year BMI Increments in 776 Norwegian Children Aged 6-15 Years
Direct

Abstract PDF
HRP0086P2-P523

Body Image Perception Changes in Obese and Lean Children
Direct

Abstract PDF
HRP0086P2-P524

Non-Alcoholic Hepatic Steatosis in Obese Children and the Relationship with Insulin Resistance
Direct

Abstract PDF
HRP0086P2-P525

Prevalence of Melanocortin 4 Receptor Mutations in Turkish Obese Children
Direct

Abstract PDF
HRP0086P2-P526

Prevalence of Overweight and Obesity in Children and Adolescents in Izmir, Western Turkey
Direct

Abstract PDF
HRP0086P2-P527

Arbitrary Cutoffs Lead to Underestimation of Metabolic Abnormalities in Obese Children: The Value of Age- and Sex-adjusted Normative Values
Direct

Abstract PDF
HRP0086P2-P528

Breasts Diseases in Adolescent Girls With Obesity
Direct

Abstract PDF
HRP0086P2-P529

Insulin Resistance Correlates to Cognitive Fatigue Dimensions in Non-diabetic Obese Children
Direct

Abstract PDF
HRP0086P2-P530

Vascular Endothelial Growth Factor as The Predictor Microangiopathy in Obese and Diabetic Children
Direct

Abstract PDF
HRP0086P2-P531

Associations of Serum 25-Hydroxyvitamin D and Components of the Metabolic Syndrome in an Egyptian Cohort
Direct

Abstract PDF
HRP0086P2-P532

Retrospective Evaluation of the Efficiency of Metformin Therapy in Obese Children with Insulin Resistance
Direct

Abstract PDF
HRP0086P2-P533

Parental Obesity can Trigger Obesity in Children
Direct

Abstract PDF
HRP0086P2-P534

Value of BMI-SDS, Waist Circumference-SDS and Waist-to-Height Ratio in the Identification of Obese Children and Adolescents at an Increased Risk for Cardio-Metabolic Complications
Direct

Abstract PDF
HRP0086P2-P535

Thyroid Dysfunction and Formation of Dyslipoproteiniaemias: Gender Differences in Children with Obesity
Direct

Abstract PDF
HRP0086P2-P536

How Early is Insulin Resistance in Our Pediatric Population with Metabolic Syndrome
Direct

Abstract PDF
HRP0086P2-P537

Insulin Resistance for Adolescents with Obesity in Latvia
Direct

Abstract PDF
HRP0086P2-P538

Parental Obesity can Trigger Obesity in Children
Direct

Abstract PDF
HRP0086P2-P539

Cerebrotendinous Xanthomatosis: A Case Report of Rare Lipid Storage Disorder
Direct

Abstract PDF
HRP0086P2-P540

Analysing Child Obesity Risk Factors: Adenotonsillectomy
Direct

Abstract PDF
HRP0086P2-P541

Non-Medicament Treatment of Severe Obese Children, Using the One-Year Courses
Direct

Abstract PDF
HRP0086P2-P542

Obstructive Sleep Apnea Syndrome in Early Childhood: Case Report
Direct

Abstract PDF
HRP0086P2-P543

25-Hydroxyvitamin D Concentrations in Pubertal Children with Obesity
Direct

Abstract PDF
HRP0086P2-P544

Management Preschool Children of Prader-Willi Syndrome
Direct

Abstract PDF
HRP0086P2-P545

Prevalence of Acanthosis Nigricans and Related Factors in Iranian Obese Children
Direct

Abstract PDF
HRP0086P1-P546

Higher Risk of Low Birth Weight and Multiple Nutritional Deficiencies in Neonates from Mothers after Gastric Bypass: A Case Control Study
Direct

Abstract PDF
HRP0086P1-P547

Laboratory Findings of 302 Patients with Hyperinsulinemic Hypoglycemia at Hypoglycemia
Direct

Abstract PDF
HRP0086P1-P548

Recognition of a Sequence: More Growth before Birth, Longer Telomeres at Birth, More Lean Mass after Birth
Direct

Abstract PDF
HRP0086P1-P549

Congenital Hyperinsulinism in Infancy: The Profiles of Insulin Secretory Granules are Markedly Different in Focal- and Diffuse [beta]-Cells
Direct

Abstract PDF
HRP0086P1-P550

Persistent Ketotic Hypoglycemia as an Atypical Presentation of Heterozygous HNF4A Mutation
Direct

Abstract PDF
HRP0086P1-P551

Enhanced Mitochondrial Densities Associate with the Pathobiology of [beta]-Cells in Congenital Hyperinsulinism in Infancy
Direct

Abstract PDF
HRP0086P1-P552

Congenital Adrenal Hyperplasia Newborn Screening: Improving the Effectiveness of the Neonatal 17OH-Progesterone and Serum Confirmatory Tests
Direct

Abstract PDF
HRP0086P1-P553

Neonatal Diabetes in Ukraine
Direct

Abstract PDF
HRP0086P1-P554

Clinical and Molecular Characteristics of Turkish Patients with Congenital Hyperinsulinism: A Single-Center Experience
Direct

Abstract PDF
HRP0086P1-P555

Islet of Langerhans in Congenital Hyperinsulinism in Infancy are Disrupted and with Decreased Expression of Collagen (IV) [alpha]1 Chain in Basement Membranes
Direct

Abstract PDF
HRP0086P1-P556

Pancreatic Glucagon Secretion is Severely Impaired and Somatostatin Secretion Unchanged in Patients with Hyperinsulinaemic Hypoglycaemia
Direct

Abstract PDF
HRP0086P1-P557

Mutations in MODY Genes: About Four Cases of Congenital Hyperinsulinism
Direct

Abstract PDF
HRP0086P1-P558

Cerebral Outcome of Children with Congenital Hyperinsulism
Direct

Abstract PDF
HRP0086P1-P559

Recognition of the Fetal and Perinatal Features of the Prader-Willi Syndrome is Required to Avoid Delay in Diagnosis
Direct

Abstract PDF
HRP0086P1-P560

Congenital Hyperinsulinism Due to Compound Heterozygous Mutation in ABCC8 and KCNJ11 GENES: 20 Years Experience of A National Referral Centre
Direct

Abstract PDF
HRP0086P1-P561

A Case of Hyperinsulinemic Hypoglycemia, Associated with Insulin Autoimmune Syndrome (IAS) in 3.5 Year Old Girl
Direct

Abstract PDF
HRP0086P1-P562

Effectiveness of Calcium Channel Blocker Nifedipine in Children with Hyperinsulinaemic Hypoglycaemia Due to Genetically Proven Mutations in the ABCC8/KCNJ11/GCK Genes
Direct

Abstract PDF
HRP0086P1-P563

Hyponatremia in Infants Under 100 Days Old: Frequently Overlooked and Multifactorial
Direct

Abstract PDF
HRP0086P1-P564

Long-Term Effects of Differences in Fetal Environment: Endocrine Influences on Cognitive Function and Personality in Teen Monozygotic Twins
Direct

Abstract PDF
HRP0086P1-P565

Different Long-term Neurodevelopmental Outcomes in Very Preterm Versus Very-low-birth-weight Infants
Direct

Abstract PDF
HRP0086P1-P566

Challenging Management of Costello Syndrome with Severe Congenital Hyperinsulinaemic Hypoglycaemia
Direct

Abstract PDF
HRP0086P1-P567

Risk Factors and Clinical Features of a Large Cohort of Patients with Transient Hyperinsulinemic Hypoglycaemia
Direct

Abstract PDF
HRP0086P1-P568

A Rare Case of Neonatal Hypothyroidism
Direct

Abstract PDF
HRP0086P1-P569

Maternal Nutritional Risk Factors Associated with Neonatal Hyperinsulinism
Direct

Abstract PDF
HRP0086P2-P570

Genotype and Phenotype of 99 Vietnamese Patients with Congenital Hyperinsulinism
Direct

Abstract PDF
HRP0086P2-P571

The Effects of Serum Insulin, Leptin, Ghrelin, Adiponectin and Resistin Levels on Early Postnatal Growth in Small for Gestational Age Newborns
Direct

Abstract PDF
HRP0086P2-P572

Sirolimus Therapy in Infant with Congenital Hyperinsulinemic Hypoglycemia Unresponsive to Diaxoside
Direct

Abstract PDF
HRP0086P2-P573

IPEX Syndrome Caused by A Novel Mutation in Foxp3 Gene: A Case Report
Direct

Abstract PDF
HRP0086P2-P574

Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Sensitivity in Premature Neonates
Direct

Abstract PDF
HRP0086P2-P575

Persistent Hyperinsulinemic Hypoglycemic of Infancy
Direct

Abstract PDF
HRP0086P2-P576

The Postnatal Effect of Serum Vitamin D Binding Protein on Serum Vitamin D Level
Direct

Abstract PDF
HRP0086P2-P577

Endocrinologists Have A Role in Moderating Adverse Metabolic Consequences of Early Over Feeding of Children Born IUGR
Direct

Abstract PDF
HRP0086P2-P578

Primary Hyperparathyroidism in Children and Adolescents: About a Series of Ten Patients
Direct

Abstract PDF
HRP0086P2-P579

The Effects of Serum Leptin, Ghrelin, Adiponectin and Resistin Levels on Early Postnatal Growth in Infants of Diabetic Mothers
Direct

Abstract PDF
HRP0086P2-P580

Newborns of Mothers Affected by Autoinmune Thyroid Disease
Direct

Abstract PDF
HRP0086P2-P581

Missense Mutation of GLIS3 Gene Resulting Inneonatal Diabetes and Congenital Hypothyroidism
Direct

Abstract PDF
HRP0086P2-P582

Birth Chest Circumference Relations to Circulating Insulin-Like Growth Factor-I in the Not-life-threatened Newborn: Relevance of Birthweight to Birth Crown-Heel Length Ratio Beyond The Presence of a Small Birthweight for Gestational Age and of Respiratory Support Measures
Direct

Abstract PDF
HRP0086P2-P583

Neonatal Failure to Thrive and Dyselectrolytemia - Not Always a Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P584

A Unique IL2RA Mutation Presenting as Neonatal Diabetes, Congenital Hypothyroidism and Sepsis
Direct

Abstract PDF
HRP0086P2-P585

Change Level of TRAb in Newborn Leads to Thyroid Dysfunction - Case Report
Direct

Abstract PDF
HRP0086P2-P586

Hyperthyrotropinemia of the Preterm Newborn: Treat or Not to Treat?
Direct

Abstract PDF
HRP0086P2-P587

Permanent Neonatal Diabetes Mellitus Due to a G32S Heterozygous Mutation in the Insulin Gene
Direct

Abstract PDF
HRP0086P2-P588

Case Report on Hyperinsulinism/hyperammonaemia Syndrome: An Easily Treatable Cause of Postprandial Hypoglycaemia
Direct

Abstract PDF
HRP0086P2-P589

Severe Systemic Pseudohypoaldosteronism Type 1: 5 Years of Evolution
Direct

Abstract PDF
HRP0086P2-P590

Birth Chest Circumference Relations to Circulating Insulin-Like Growth Factor Binding Protein-3 in The Not-Life-Threatened Newborn: Relevance of Birthweight to Birth Crown-Heel Length Ratio After Control for A Small Birthweight for Gestational Age, for Respiratory Support Measures and for Circulating Insulin-Like Growth Factor-I
Direct

Abstract PDF
HRP0086P2-P591

Renal form of Pseudohypoaldosteronism Type I in Sucking: Clinical Case
Direct

Abstract PDF
HRP0086P2-P592

Neonatal Hyperparathyroidism with Homozygous Missense Mutation in the CASR Gene
Direct

Abstract PDF
HRP0086P1-P593

The Mechanistic Role of Fibroblast Growth Factor 21 (FGF21) in Growth Hormone Resistance Secondary to Chronic Childhood Conditions
Direct

Abstract PDF
HRP0086P1-P594

Somapacitan, a Once-Weekly Reversible Albumin-Binding Growth Hormone (GH) Derivative, Is Well Tolerated and Convenient in Adults with GH Deficiency (AGHD): Results from a 26-Week Randomised, Controlled Phase 3 Trial
Direct

Abstract PDF
HRP0086P1-P595

The Diagnostic Value of IGF-II, IGF-I and IGFBP-3 in Silver-Russell Syndrome
Direct

Abstract PDF
HRP0086P1-P596

Functional in vitro Characterization of Two Novel Germinal STAT3 Mutations Associated with Short Stature, Immunodeficiency and Autoimmune Disease
Direct

Abstract PDF
HRP0086P1-P598

Human Phase1 Clinical Data of ALT-P1 (hGH-NexP) by Healthy Korean Males
Direct

Abstract PDF
HRP0086P1-P599

Validation of Prediction Models for Near Final Adult Height in Children with Idiopathic Growth Hormone Deficiency Treated with Growth Hormone for 1 Year
Direct

Abstract PDF
HRP0086P1-P600

The Influence of Recombinant Human Growth Hormone Treatment on Very Small Embryonic/Epiblast Like Stem Cells
Direct

Abstract PDF
HRP0086P1-P601

A Lipid-Based System for the Oral Delivery of Growth Hormone
Direct

Abstract PDF
HRP0086P1-P602

Prediction of First Year Response to Growth Hormone Treatment in Neural Network Models
Direct

Abstract PDF
HRP0086P1-P603

Pediatric Phase 2 Data Demonstrate that TransCon hGH Has an Anti-hGH Immunogenic Profile that is Comparable to Daily hGH
Direct

Abstract PDF
HRP0086P1-P604

The Exon3-Deleted Growth Hormone Receptor Gene Polymorphism (d3-GHR) is Associated with Increased Spontaneous Growth and Impaired Insulin Sensitivity in Prepubertal Short SGA Children (NESGAS)
Direct

Abstract PDF
HRP0086P1-P605

A New Case of Intragenic Deletion in IGF1R with Very Mild Phenotype
Direct

Abstract PDF
HRP0086P1-P606

The Role of IGF-1R Gene Polymorphisms with Regard to Susceptibility to Idiopathic Short Stature Risk in the Chinese Population of Jiangxi Area
Direct

Abstract PDF
HRP0086P1-P607

Effects of the Addition of Metformin to Recombinant Human GH on Bone Maturation and Pubertal Progression in Short Children Born Small-for-Gestational-Age
Direct

Abstract PDF
HRP0086P1-P608

Pubertal Height Gain in Females with Isolated Growth Hormone Deficiency Treated with rhGH Alone or in Combination with GnRHan
Direct

Abstract PDF
HRP0086P1-P609

Cognitive Abilities and Academic Achievement Among Youths with Short Stature Receiving Growth Hormone Therapy
Direct

Abstract PDF
HRP0086P1-P610

One Year Use of Anastrazole Improves the Predicted Adult Height of Male Adolescents with and without Associated GH Therapy
Direct

Abstract PDF
HRP0086P1-P611

IGFALS Gene Deletion in a Family with Short Stature
Direct

Abstract PDF
HRP0086P1-P612

Adherence with Twice-Monthly, At-Home Dosing Schedule of Somavaratan (VRS-317) Long-Acting Growth Hormone Treatment in Children with Growth Hormone Deficiency (GHD) (NCT02068521)
Direct

Abstract PDF
HRP0086P1-P613

Glucose Dysregulation in Children with Growth Hormone Deficiency (GHD), Turner Syndrome (TS) or Born Small for Gestational Age (SGA) Treated with GH: A Report from the NordiNet International Outcome Study (IOS)
Direct

Abstract PDF
HRP0086P1-P614

Serum [alpha]-Klotho Levels are not Informative for the Evaluation of GH Secretion in Short Children
Direct

Abstract PDF
HRP0086P1-P615

Immunogenicity Results of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): A Phase 2 Study in Children with Growth Hormone Deficiency
Direct

Abstract PDF
HRP0086P1-P616

Serum IGF-I, IGFBP-3 and Als Concentrations and Physical Performance in Young Swimers During a Training Season
Direct

Abstract PDF
HRP0086P1-P617

The Blood Antioxidant System in Adult Growth Hormone Deficient Patients after Concluded Childhood Growth Hormone Therapy
Direct

Abstract PDF
HRP0086P1-P618

Design and Clinical Development of TransCon Growth Hormone for Growth Hormone Deficiency (GHD)
Direct

Abstract PDF
HRP0086P1-P619

Mutations in PROP1 Gene in Combination with 47,XYY Karyotype: Case Report
Direct

Abstract PDF
HRP0086P1-P620

Efficacy of Growth Hormone Treatment in Patients with Type 1 Diabetes Mellitus and Growth Hormone Deficiency
Direct

Abstract PDF
HRP0086P1-P621

Final Height after Growth Hormone Treatment in Children with Chronic Renal Failure
Direct

Abstract PDF
HRP0086P1-P622

Major Plasma Carotenoids Levels in Growth Hormone Deficient Children
Direct

Abstract PDF
HRP0086P1-P623

Autosomal Dominant Growth Hormone Deficiency due to a Novel Mutation in the gh1 Gene
Direct

Abstract PDF
HRP0086P1-P624

A Novel GH1 Mutation in a Family with Autosomal-Dominant Type II Isolated Growth Hormone Deficiency
Direct

Abstract PDF
HRP0086P1-P625

2nd Year Pharmacokinetic and Pharmacodynamic Modeling of Long-Acting Human Growth Hormone (MOD 4023) in Growth Hormone Deficient Children
Direct

Abstract PDF
HRP0086P1-P626

Significance of IGF-I Generation Test in Diagnosing Primary and Non-Primary IGF-I Deficiency - Clinical Considerations
Direct

Abstract PDF
HRP0086P1-P627

Change of Growth Pattern and Thickness of Epiphyseal Plate in Female Rats According to Injected Estrogen Dosage
Direct

Abstract PDF
HRP0086P1-P628

Height Gain and Safety Outcomes in Growth Hormone (GH)-Treated Girls and Boys with Idiopathic Short Stature (ISS): Experience from the Prospective GeNeSIS Observational Study
Direct

Abstract PDF
HRP0086P1-P629

Treatment of Resistant Paediatric Somatotropinomas due to AIP Mutation with Pegvisomant
Direct

Abstract PDF
HRP0086P1-P630

GH-Pattern with High Trophs are Often Found after Daily sc rhGH-Injection in Children
Direct

Abstract PDF
HRP0086P1-P631

Are the GH Treatment Doses in Use within Secretion Rates of Healthy Children?
Direct

Abstract PDF
HRP0086P1-P632

The Influence of Growth Hormone Treatment on Fat-free Mass in Prepubertal Children with Kabuki Syndrome
Direct

Abstract PDF
HRP0086P1-P633

Evaluation of Prepubertal Patients with Suspected Neurosecretory Dysfunction of Growth Hormone Secretion: Diagnostic Steps and Treatment Response
Direct

Abstract PDF
HRP0086P1-P634

Four-Year Results from PATRO Children, a Multi-Centre, Non-Interventional Study of the Long-Term Safety and Efficacy of Omnitrope® in Children Requiring Growth Hormone Treatment
Direct

Abstract PDF
HRP0086P1-P635

Glucagon vs Clonidine Stimulation for Testing Growth Hormone Secretion in Children and Adolescents: Which is Better?
Direct

Abstract PDF
HRP0086P1-P636

The Use of Tissue Doppler Imaging in Assessing Right and Left Ventricle Diastolic Function in Children with Growth Hormone Deficiency before and after 1-Year Therapy with Growth Hormone
Direct

Abstract PDF
HRP0086P1-P637

Diagnosing GH Deficiency in Children by Arginine Hydrochloride Infusion Test: Relationship between Auxiological Characteristics, Arginine Plasma Profile and Arginine-Stimulated GH Release
Direct

Abstract PDF
HRP0086P1-P638

Retrospective Analysis of Growth Hormone (GH) Treatment Results in Children with Idiopathic Growth Hormone Deficiency (IGHD), Turner Syndrome (TS) and Small for Gestational Age (SGA) using iGRO* in a Pediatric Endocrine Practice
Direct

Abstract PDF
HRP0086P1-P639

Spanish ECOS Study Analysis: Socioeconomic Data, Adherence and Growth Outcomes with Case Studies
Direct

Abstract PDF
HRP0086P1-P640

Analysis of Correlation between Stem Cells (CD133+/CD45+ and CD133+/CD45−) and Anthropometric Parameters of Children with Growth Hormone/Primary Insulin-Like Growth Factor 1 Deficiency
Direct

Abstract PDF
HRP0086P2-P641

Hypochondroplasia (HC) Treatment with rGH: Actualization of Pilot Observations
Direct

Abstract PDF
HRP0086P2-P642

The Influence of Growth Hormone Treatment on the Basal Metabolism in Prepubertal Children with Kabuki Syndrome
Direct

Abstract PDF
HRP0086P2-P643

An Analysis of the Safety of Childhood Growth Hormone (GH) Therapy: Data from the NordiNet® International Outcome Study (IOS)
Direct

Abstract PDF
HRP0086P2-P644

Adverse Effects after Priming with Testosterone in Short Statured Boys before Growth Hormone Stimulation Test
Direct

Abstract PDF
HRP0086P2-P645

Effect of One-Year Growth Hormone Therapy on Serum Levels of Ghrelin and Leptin in Children with Growth Hormone Deficiency and their Correlations with Cardiac Functions and Dimensions
Direct

Abstract PDF
HRP0086P2-P646

Metabolic Parameters and Glucose Homeostasis in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting
Direct

Abstract PDF
HRP0086P2-P647

Final Adult Height (FAH) in Patients with PROR-1 Gene Mutations during GH Long-Term Therapy
Direct

Abstract PDF
HRP0086P2-P648

Congenital Hypopituitarism: Genotypic-Phenotypic-Neuroradiological Correlation
Direct

Abstract PDF
HRP0086P2-P649

A Case of Hypopituitarism in a Patient with Cantu Syndrome
Direct

Abstract PDF
HRP0086P2-P650

Delaying Puberty with GnRHa does not Promote Adult Height in GH Treated Children Who Enters Puberty at Average Age
Direct

Abstract PDF
HRP0086P2-P651

Estimation of FGF21 Concentration in Prepubertal Children with Growth Hormone Deficiency before and after 6 Months of Growth Hormone Treatment
Direct

Abstract PDF
HRP0086P2-P653

Improving the 'Gold Standard': The Insulin Tolerance Test Revisited
Direct

Abstract PDF
HRP0086P2-P654

Adherence to Growth Hormone Therapy: Comparison of Electronic Auto-Injection to Non-Electronic Injection Devices
Direct

Abstract PDF
HRP0086P2-P655

Factors Influencing Peak GH Response During Insulin and Clonidine Stimulation Tests
Direct

Abstract PDF
HRP0086P2-P656

Improved Growth Outcomes with Jet Delivery of Growth Hormone in Children are Maintained Over Long-Term Treatment
Direct

Abstract PDF
HRP0086P2-P657

Septo-Optic Dysplasia and Excellent Growth with Low Growth Hormone Dose: Our Experience
Direct

Abstract PDF
HRP0086P2-P658

Early Diagnosis and Treatment of a Newborn with POU1F1 Mutation
Direct

Abstract PDF
HRP0086P2-P659

Influences of GHR-Exon 3 and -202 A/C IGFBP3 Polymorphisms on 1 Year Follow-Up Outcome of Growth Hormone Treatment in Korean Children with Growth Hormone Deficiency
Direct

Abstract PDF
HRP0086P2-P660

Comparison between Effects of Oral Iron and Vitamin A with Oxandrolone upon Height and Puberty of Children with Constitutional Delay of Growth and Puberty
Direct

Abstract PDF
HRP0086P2-P661

'First Do No Harm': Growth Hormone (hGH) Treatment in a Case of Recurrent Craniopharyngioma
Direct

Abstract PDF
HRP0086P2-P662

High Efficacy Growth Hormone Therapy in Patient with Homozygous Mutation in Growth Hormone Gene (GH-1) During 3 Years
Direct

Abstract PDF
HRP0086P2-P663

A Case of GH Deficiency in a Female with 3M Syndrome
Direct

Abstract PDF
HRP0086P2-P664

Case Report of SHOX Gene Haploinsufficiency Diagnosed in Early Infancy
Direct

Abstract PDF
HRP0086P2-P665

Association between IGF-1 (Insulin-Like Growth Factor) SD Levels and Children with Growth Hormone Deficiency with and without Pituitary Morphological Abnormalities
Direct

Abstract PDF
HRP0086P2-P666

Usefulness of Growth Hormone Transient Treatment Suspension in Prepubertal Children Treated with Growth Hormone
Direct

Abstract PDF
HRP0086P2-P667

Birth Length, Weight and Head Circumference of Neonates with IGF-I Receptor Mutations
Direct

Abstract PDF
HRP0086P2-P668

A Rare Cause of Growth Delay: Jacobsen Syndrome
Direct

Abstract PDF
HRP0086P2-P669

A GH-1 Mutation Diagnosed in a Preadolescent Obese Girl with Only Mild Reduced Height
Direct

Abstract PDF
HRP0086P2-P670

A New Reusable Manual Pen Device for Injection of Human Growth Hormone: Results of a Convenience and Functionality Evaluation Study
Direct

Abstract PDF
HRP0086P2-P671

Assessing Disease and Treatment Burden for Young Children with Growth Hormone Deficiency (GHD)
Direct

Abstract PDF
HRP0086P2-P672

Long-Term Results of GH Therapy in GH-Deficient Children Treated in Albania
Direct

Abstract PDF
HRP0086P2-P674

Did Growth Hormone Treatment Associated with Psychological Status in Children with Short Stature?
Direct

Abstract PDF
HRP0086P2-P675

The Effects and Safety of Recombinant Human GH (rhGH) Treatment on Growth Hormone Deficiency in Children with Rathke's Cleft Cyst
Direct

Abstract PDF
HRP0086P2-P676

Is the Growth Hormone Deficiency the Cause of Short Stature in Floating Harbor Syndrome?
Direct

Abstract PDF
HRP0086P2-P677

LHX-4 Gene Mutation in a Boy with Hypopituitarism and Severe Congenital Myopathy
Direct

Abstract PDF
HRP0086P2-P678

Prevalence and Causes of Short Stature and Impact of GH Therapy among Preschool Children at King Abdul-Aziz Medical City for National Guard in Riyadh, Saudi Arabia
Direct

Abstract PDF
HRP0086P2-P679

Association between Growth Hormone Peak at a Stimulation Test and Pituitary Morphological Findings in Children with Growth Hormone Deficiency
Direct

Abstract PDF
HRP0086P2-P680

A Case of Growth Hormone Deficiency with Combined Encephalocraniocutaneous Lipomatosis and Jaffe-Campanacci Syndrome
Direct

Abstract PDF
HRP0086P2-P681

Evaluation of GH Deficient Pre Pubertal Children Treated with Omnitrope® Using the AuxoLog Computer Program
Direct

Abstract PDF
HRP0086P2-P682

Calcaneal Apophysitis (Sever's Disease) Development in a Case Using Growth Hormone
Direct

Abstract PDF
HRP0086P2-P683

Bone Health Index: A Potential Discriminator between Growth Hormone Deficiency and Constitutional Delay in Growth and Puberty in Adolescent Children
Direct

Abstract PDF
HRP0086P2-P684

Growth Effects of Somatropin during the Treatment Congenital Hypopituitarism in Children after the Start of Puberty
Direct

Abstract PDF
HRP0086P2-P685

Congenital Hypopituitarism and Giant Cell Hepatitis in a Two-Months-Old Boy
Direct

Abstract PDF
HRP0086P2-P686

Neonatal Characteristics of GH Deficiency in 107 Children
Direct

Abstract PDF
HRP0086P2-P687

Diagnostic Value of Growth Hormone Stimulation Test for Growth Hormone Deficiency in Short Children
Direct

Abstract PDF
HRP0086P1-P688

Thyrotoxicosis, Nephrogenic Syndrome of Inappropriate Antidiuresis, Tall Stature and Mental Retardation Caused by a Novel GNAS Gain of Function Mutation
Direct

Abstract PDF
HRP0086P1-P689

Novel Germline Mutations in DICER1 Gene in Patients with Different Pediatric Hereditary Tumors
Direct

Abstract PDF
HRP0086P1-P690

Fludrocortisone: A Treatment for Tubulopathy Post Paediatric Renal Transplantation - A Scottish Study
Direct

Abstract PDF
HRP0086P1-P691

Neonatal Diabetes and Congenital Hypothyroidism, a Rare Condition: Report of 2 Cases with Different Genetic Causes
Direct

Abstract PDF
HRP0086P1-P692

Access to Medicines in Pediatric Endocrinology and Diabetes in Africa: Insights from the WHO and National Lists of Essential Medicines
Direct

Abstract PDF
HRP0086P1-P693

Is it Cautious to Wait for Serum Basal Calcitonin Levels Rise in Patients with Ret Codon C634 Mutation?
Direct

Abstract PDF
HRP0086P1-P695

CANDLE Syndrome: A New Autoinflammatory Lipodystrophic Disorder with Challenging Diagnosis and Limited Therapeutic Options
Direct

Abstract PDF
HRP0086P1-P696

Variable Phenotype and Genetic Findings in a Cohort of Patients with Pseudohypoparathyroidism
Direct

Abstract PDF
HRP0086P1-P697

Contiguous Gene Syndrome Involving DAX1 Deletion with Congenital Adrenal Insufficiency
Direct

Abstract PDF
HRP0086P1-P698

Clusters of Autoinmune Diseases in Children
Direct

Abstract PDF
HRP0086P1-P699

Role of PTPN22 C1858T Gene Polymorphism in Pediatric Polyautoimmunity
Direct

Abstract PDF
HRP0086P2-P700

Effects of 2 Years of Growth Hormone Treatment on Glucose Tolerance in Young Adults with Prader-Willi Syndrome
Direct

Abstract PDF
HRP0086P2-P701

TPIT Mutation may be Involved in Multiple Pituitary Deficiencies
Direct

Abstract PDF
HRP0086P2-P702

Clinical Analysis of 24 Cases of Rathke's Cleft Cysts in Children
Direct

Abstract PDF
HRP0086P2-P703

French National Healthcare Network for Rare Endocrine Diseases (FIRENDO): The First Year of Activity to Monitor Patients with Rare Endocrine Diseases
Direct

Abstract PDF
HRP0086P2-P704

Autoimmune Diseases and Metabolic Outcome in Turner Syndrome - Comparison between 45,X0 and other X Chromosome Abnormalities
Direct

Abstract PDF
HRP0086P2-P705

Endocrinological Disorders in Children with Neurofibromatosis Type 1 and Optic Pathway Gliomas
Direct

Abstract PDF
HRP0086P2-P706

Nephrogenic Syndrome of Inappropriate Antidiuresis (NSIAD) Managed with Fluid Restriction and Salt Supplementation
Direct

Abstract PDF
HRP0086P2-P707

The Triglyceride to High-Density Lipoprotein Cholesterol Ratio and Non-High-Density Lipoprotein Cholesterol Reference Data for Korean Children and Adolescents: Results of the 2007-2013 Korean National Health and Nutrition Examination Surveys (KHANES)
Direct

Abstract PDF
HRP0086P2-P708

Inhibition of NAMPT Increases the Sensitivity of Leukemia Cells for Etoposide
Direct

Abstract PDF
HRP0086P2-P709

Neonatal Endocrinological Problems in Collodion Babies
Direct

Abstract PDF
HRP0086P2-P710

Endocrine Dysfunction in Children and Adolescents with CHARGE Syndrome
Direct

Abstract PDF
HRP0086P2-P711

Growth and Pubertal Patterns in Young Survivors of Childhood Acute Lymphoblastic Leukemia
Direct

Abstract PDF
HRP0086P2-P712

Clinical Assessment of Hypercalciuria and Hypomagnesemia in Patients with Bartter Syndrome and Gitelman Syndrome
Direct

Abstract PDF
HRP0086P2-P713

Wolfram Syndrome: Three Cases
Direct

Abstract PDF
HRP0086P2-P714

Autoimmune Hypoparathyroidism and Celiac Disease: A Rare Paediatric Association Outside an Autoimmune Polyglandular Syndrome
Direct

Abstract PDF
HRP0086P2-P715

Management of Endocrine Complications of Thalassemia
Direct

Abstract PDF
HRP0086P2-P716

Endocrine Disorders in Children with Thalassemia Major - A Hospital Based Retrospective Study
Direct

Abstract PDF
HRP0086P2-P717

15-Year Old Girl with APS Type IIIc, with Post-Thymectomy Remission - Case Report
Direct

Abstract PDF
HRP0086P2-P718

Endocrine and Metabolic Evaluation of Children with Neurodevelopmental Disability
Direct

Abstract PDF
HRP0086P2-P719

Endocrine Complication in Survivors of Childhood Cancers
Direct

Abstract PDF
HRP0086P2-P720

Familial Williams Syndrome
Direct

Abstract PDF
HRP0086P2-P721

Stanazolol Abuse: Diagnostic Dilemma in an Adolescent with Persistent Hypoglycemia
Direct

Abstract PDF
HRP0086P1-P722

Role of the Metabotropic mGlu5 Glutamate Receptor in the Initiation of Puberty and Reproduction in Female Mice
Direct

Abstract PDF
HRP0086P1-P723

Effect of Dietary Control on Pubertal Onset and Immunoreactivity of Kisspeptin and Neurokinin B in Female Offspring Rats Fed High Fat Diet During Perinatal Period
Direct

Abstract PDF
HRP0086P1-P724

Estimating the Psychosocial Impact of Idiopathic Central Precocious Puberty (ICPP) in Girls Aged 6 to 8 Years: A Qualitative Study
Direct

Abstract PDF
HRP0086P1-P725

Metabolic and Pubertal Alterations in Children with Narcolepsy-Cataplexy
Direct

Abstract PDF
HRP0086P1-P726

Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case
Direct

Abstract PDF
HRP0086P1-P727

Changes of Serum AMH and Inhibin B Levels in Girls with Central Precocious Puberty before and During Treatment with GnRH Agonists
Direct

Abstract PDF
HRP0086P1-P728

FGFR1 Loss-of-Function Mutations of in Three Japanese Patients with Isolated Hypogonadotropic Hypogonadism and Split Hand/Foot Malformation
Direct

Abstract PDF
HRP0086P1-P729

Clinical and Mutational Spectrum in Slovenian Patients with Hypogonadotropic Hypogonadism
Direct

Abstract PDF
HRP0086P1-P730

MKRN3 Mutations and Central Precocious Puberty
Direct

Abstract PDF
HRP0086P1-P731

Precocious Puberty in Patients with Primary Adrenal Insufficiency due to Melanocortın Receptor 2 Mutation
Direct

Abstract PDF
HRP0086P1-P732

Association between Estrogen Receptor Gene Polymorphisms and Premature Thelarche
Direct

Abstract PDF
HRP0086P1-P733

The Influences of Circulating Leptin, Kisspeptin, and Neurokinin B Levels to Precocious Puberty in Obese Girls
Direct

Abstract PDF
HRP0086P1-P734

Pseudopuberty in a Young Girl with Adrenocortical Carcinoma During Mitotane Therapy
Direct

Abstract PDF
HRP0086P1-P735

Prolactinomas in Children and Young Adults: 10 Year Experience in a Tertiary Regional Paediatric - Young Adult - NeuroEndocrine Surgical Centre
Direct

Abstract PDF
HRP0086P1-P736

Cut-Off Values for Nocturnal Salivary Testosterone to Enable Detection of Early Puberty
Direct

Abstract PDF
HRP0086P1-P737

Screening of PROP-1, LHX2 and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland
Direct

Abstract PDF
HRP0086P1-P738

Oxytocin Deficiency is Associated with Hyperphagia and Weight Gain in Hypothalamic and Common Obesity: A First-in-Humans Proof-of-Concept Study
Direct

Abstract PDF
HRP0086P1-P739

Evaluation of Puberty in Children with Sickle Cell Anemia: A Case Control Study in Yaounde, Cameroon
Direct

Abstract PDF
HRP0086P1-P740

Standard Triptorelin Therapy May Not Fully Suppress Pubertal Progress in Adolescents with Gender Dysphoria
Direct

Abstract PDF
HRP0086P1-P741

Serum Anti-Mullerian Hormone Levels in Precocious Puberty Girls According to the Timing of GnRH Agonist Treatment
Direct

Abstract PDF
HRP0086P1-P742

Precocious Puberty in Septo-Optic Dysplasia Syndrome - Presentation of 2 Cases
Direct

Abstract PDF
HRP0086P1-P743

Proton Therapy as a Promising Therapeutic Option for Children with Aggressive and Uncontrolled Pituitary Macro Adenoma: A Case Report
Direct

Abstract PDF
HRP0086P1-P744

A Prospective Evaluation of Urinary Gonadotrophins for Assessment and Management of Pubertal Disorders
Direct

Abstract PDF
HRP0086P1-P745

Constitutional Delay of Puberty or Hypogonadotropic Hypogonadism: Diagnostic Value of Inhibin B and AMH Measurements
Direct

Abstract PDF
HRP0086P1-P746

Prognostic Significance of the Proliferative Index Ki67 for Patients with Craniopharyngiomas
Direct

Abstract PDF
HRP0086P1-P747

Etiology, Differential Diagnosis and Clinical Course of Delayed Puberty: A Single Center Experience
Direct

Abstract PDF
HRP0086P1-P748

GH Therapy Assessment in GH Deficient Patients During the Transition Period
Direct

Abstract PDF
HRP0086P1-P749

Age of Onset of Puberty in Yaounde, Which Normative Reference Data?
Direct

Abstract PDF
HRP0086P1-P750

Personalized Health Care: Home POCT Sodium Measurement in Diabetes Insipidus Centralis in a Patient with Impaired Thirst Perception
Direct

Abstract PDF
HRP0086P1-P751

Transcriptional Basis of Idiopathic Central Hypogonadism in Isolated Congenital Cryptorchidism with Defective Mini-Puberty
Direct

Abstract PDF
HRP0086P1-P752

A Novel MKRN3 Frameshift Mutation in a Bulgarian Girl with Central Precocious Puberty
Direct

Abstract PDF
HRP0086P1-P753

The Intra- and Inter-User Reliability of Testicular Volume Estimation - A Simulation Study
Direct

Abstract PDF
HRP0086P1-P754

The Metabolic Negative Effect of Gonadotropin-Releasing Hormone Agonist Therapy in Childhood: Is it Short-Term and Reversible?
Direct

Abstract PDF
HRP0086P1-P755

Gonadotropin-Releasing Hormone Stimulation Test in Girls Younger than 3 Years Old: Does the Stimulated LH Greater Than 5 IU/l Always Mark Central Puberty Precoccious?
Direct

Abstract PDF
HRP0086P1-P756

[beta]-hCG from an Occult Source Causing Peripheral Precocious Puberty: Identification of the Tumour 6 Years After Presentation
Direct

Abstract PDF
HRP0086P1-P757

Silent Corticotroph Adenoma with Adrenocortical Choristoma in an 11-Years Old Boy
Direct

Abstract PDF
HRP0086P2-P758

Clinical Symptoms, Endocrine Dysfunction and Radiologic Findings in Children with Rathke's Cleft Cyst
Direct

Abstract PDF
HRP0086P2-P759

A Case of Central Precocious Puberty in a Patient with Prader-Willi Syndrome
Direct

Abstract PDF
HRP0086P2-P760

Is Amh Level Diagnostic for Premature Telarche, Premature Adrenarche and Central Precocious Puberty?
Direct

Abstract PDF
HRP0086P2-P761

Paediatric Cushing Disease: One Patient's Path to Cure
Direct

Abstract PDF
HRP0086P2-P762

Recovery of Hypothalamic Pituitary Function After Stalk Transection and Panhypopituitarism in an Adolescent
Direct

Abstract PDF
HRP0086P2-P763

A Novel CHD7 Mutation in an Adolescent Presenting with Pubertal and Growth Delay
Direct

Abstract PDF
HRP0086P2-P764

Kallmann Syndrome Due to a Homozygous Missense c.217C>T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene
Direct

Abstract PDF
HRP0086P2-P765

Symptomatic Rathke Cleft Cyst in Pediatric Patients - Clinical Presentations, Surgical Treatment and Postoperative Outcomes - An Analysis of 38 Cases
Direct

Abstract PDF
HRP0086P2-P766

Congenital Craniopharyngioma: Report of Two Cases
Direct

Abstract PDF
HRP0086P2-P767

Congenital Hypopituitarism in a Patient with 18p- Syndrome
Direct

Abstract PDF
HRP0086P2-P768

10 Years Review of Endocrine Diseases in Spanish Patients Diagnosed with Primary Brain Tumors in a Tertiary Hospital
Direct

Abstract PDF
HRP0086P2-P769

Novel Uses of Psychiatric Drugs to Treat Hypothalamic Obesity
Direct

Abstract PDF
HRP0086P2-P770

Postoperative Water and Electrolyte Disorders and Affecting Factors in Children with Intracranial Tumors
Direct

Abstract PDF
HRP0086P2-P771

Compound Heterozygosity for Two Novel POU1F1 Mutations in Siblings with Isolated Childhood Onset Growth Hormone Deficiency (CO-GHD)
Direct

Abstract PDF
HRP0086P2-P772

Brain MRI in Evaluation of Endocrine Diseases of Childhood: Causal and Incidental Lesions
Direct

Abstract PDF
HRP0086P2-P773

Primary Thirst Defect is a Rare But Important Complication Following Surgery for Hypothalamic Hamartoma and Intractable Epilepsy
Direct

Abstract PDF
HRP0086P2-P774

Insulin Sensitivity in Girls with Central Precocious Puberty at Diagnosis and at 6 Months of GnRH Analogue Treatment
Direct

Abstract PDF
HRP0086P2-P775

Effect of Gonadotropin Releasing Hormone Analogues (GnRHa) on Final Height in Girls with Borderline Early Puberty or Normal Physiological Puberty Depend on Bone Age Advancement and Predicted Height
Direct

Abstract PDF
HRP0086P2-P776

Central Nervous System Abnormalities on Brain Magnetic Resonance Imaging Among 200 Korean Girls with Central Precocious Puberty
Direct

Abstract PDF
HRP0086P2-P777

Impaired Growth Hormone Secretion Associated with Large Hypothalamic Hamartoma
Direct

Abstract PDF
HRP0086P2-P778

Comparison of Triptorelin Versus Leuprolide in Treatment of Girls with Central Precocious Puberty
Direct

Abstract PDF
HRP0086P2-P779

Central Precocious Puberty in a Female with Gonadal Dysgenesis and Bilateral Gonadoblastoma
Direct

Abstract PDF
HRP0086P2-P780

Precocious Puberty: A Single Academic Center Experience
Direct

Abstract PDF
HRP0086P2-P781

Does Pituitary Volume have the Diagnostic Value on Growth Hormone Deficiency and Prognostic value on the Response to Growth Hormone Therapy?
Direct

Abstract PDF
HRP0086P2-P782

Early Puberty; Diagnosis, Treatment and Prognosis
Direct

Abstract PDF
HRP0086P2-P783

Basal Levels of FSH and LH can be Helpfull in Diagnosis of Puberty Precocious?
Direct

Abstract PDF
HRP0086P2-P784

Body Mass Index and Body Fat Composition are Both Related to Central Precocious Puberty in Chinese Girls
Direct

Abstract PDF
HRP0086P2-P785

Hyperleptinemia in Obese and Non-Obese Children with Early Puberty
Direct

Abstract PDF
HRP0086P2-P786

Association between Congenital Hypopituitarism and Agenesis of the Internal Carotid Artery: A Case Report
Direct

Abstract PDF
HRP0086P2-P787

Giant Macroprolactinoma in a Female Adolescent - Case Report
Direct

Abstract PDF
HRP0086P2-P788

Adenomas Pituitary in Children
Direct

Abstract PDF
HRP0086P2-P789

A Patient with Multiple Endocrine Neoplasia Type 1 Presented with Precocious Puberty
Direct

Abstract PDF
HRP0086P2-P790

Precocious Puberty in a Girl With Prader Willi Syndrome
Direct

Abstract PDF
HRP0086P2-P791

Menstrualcharacteristics and Problems in 9-18 Years Old Turkish School Girls
Direct

Abstract PDF
HRP0086P2-P792

Haplo-insufficiency for LHX4 Alone does not Result in Hypopituitarism
Direct

Abstract PDF
HRP0086P2-P793

A Nursing Perspective: Best Practices for Pubertal Suppression for Individuals with Central Precocious Puberty and Transgender
Direct

Abstract PDF
HRP0086P2-P794

An Unusual Association between Empty Sella and Central Precocious Puberty
Direct

Abstract PDF
HRP0086P2-P795

Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) in Children Born Small for Gestational Age (SGA) - Our Experiences
Direct

Abstract PDF
HRP0086P2-P796

Severe Juvenile Hypertrophy of the Breast with Hypercalcaemia; Mastectomy v's Reduction Surgery
Direct

Abstract PDF
HRP0086P2-P797

Report Two Cases of Dopa-Responsive Dystonia
Direct

Abstract PDF
HRP0086P1-P799

NPR2 Gene Mutations Associated with Acromesomelic Dysplasia Maroteaux Type are Mostly Unique to Families
Direct

Abstract PDF
HRP0086P1-P800

Rare Cases of Ornithine Transcarbamylase Deficiency and Variant Turner Syndrome
Direct

Abstract PDF
HRP0086P1-P801

Prepubertal Ultra-low-dose Estrogen Therapy is Associated with Better Lipid Profile than Conventional Estrogen Replacement for Pubertal Induction in Adolescent Girls with Turner Syndrome - Preliminary results
Direct

Abstract PDF
HRP0086P1-P802

Cognitive Evaluation in Silver Russell Children
Direct

Abstract PDF
HRP0086P1-P803

Body Surface Area Estimation in Girls with Turner Syndrome: Implications for Interpretation of Aortic Sized Index
Direct

Abstract PDF
HRP0086P1-P804

Near-Adult Height in a Large Cohort of Patients with Turner Syndrome and Noonan Syndrome Treated with rhGH: Results from Pfizer International Growth Database
Direct

Abstract PDF
HRP0086P1-P805

Percutaneous Epiphysiodesis Around the Knee Effectively Reduced Predicted Excessive Final Height. Preliminary Results on Final Height, Complications and Satisfaction in a Large Cohort of Dutch Boys and Girls
Direct

Abstract PDF
HRP0086P1-P806

Metabolic Health and Safety of GH-Treatment in Silver-Russell Syndrome
Direct

Abstract PDF
HRP0086P1-P807

Auxological Features in Patients with Juvenile Idiopathic Arthritis Treated with Biologic Therapy Preliminary Study Data
Direct

Abstract PDF
HRP0086P1-P808

Identification of 11p14.1-p15.3 Deletion Probably Associated with Short Stature, Macrocephaly and Delayed Closure of the Fontanelles
Direct

Abstract PDF
HRP0086P1-P809

Early Treatment with rhGH in Patients with Prader-Willi Syndrome Results in Improved Height with No Respiratory Adverse Effects
Direct

Abstract PDF
HRP0086P1-P810

Phenotypic Variability in a Family with a New SHOX Gene Mutation
Direct

Abstract PDF
HRP0086P1-P811

Correlations between Prepubertal and Pubertal Estrogen Levels and Final Height Out-Come in Growth Hormone (GH) Treated Boys with Silver Russell syndrome
Direct

Abstract PDF
HRP0086P1-P812

Skeletal Disproportion in Girls with Turner Syndrome
Direct

Abstract PDF
HRP0086P1-P813

Reconsideration of Mid-Parental Height Calculation
Direct

Abstract PDF
HRP0086P1-P814

Changes to Thyroid Function (TF) Following Treatment with Growth Hormone (GH) Therapy in Children with Prader-Willi Syndrome (PWS)
Direct

Abstract PDF
HRP0086P1-P815

6-Year-Old Girl with Mutation in DNMT3A - A New Overgrowth Syndrome
Direct

Abstract PDF
HRP0086P1-P816

A Case of Patient with Rubinstein-Taybi Syndrome Type 2 with Complete Deletion of EP300 Gene and Complex Phenotype
Direct

Abstract PDF
HRP0086P1-P817

Silver-Russell Syndrome with 11p15 Epimutation: Clinical Analysis of Adrenarche, Central Puberty and Body Mass Index in a Cohort of French Children
Direct

Abstract PDF
HRP0086P1-P818

Haploinsufficiency of Short Stature Homeobox Containing Gene: Clinical Signs and Anthropometric Measurements in Children
Direct

Abstract PDF
HRP0086P1-P819

Clinical and Molecular Characterization of a Newly Recognized Overgrowth Syndrome: Interstitial 7q22.1-7q22.3 Microdeletion
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HRP0086P1-P820

International Cooperative Growth Study, NutropinAq® European Registry (iNCGS): Countries Specificities
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Abstract PDF
HRP0086P1-P821

Case Report of 48,xxyy Syndrome Associated to Father's Radioactive Contamination During the Cesium Accident in Goiania - Goias, Brazil
Direct

Abstract PDF
HRP0086P1-P822

Neonatal Haematological Complication in Noonan Syndrome - Future Concerns about Growth Hormone Therapy
Direct

Abstract PDF
HRP0086P1-P823

Effects of a Stressful Environment (SE) on Height, BMI and Menarche
Direct

Abstract PDF
HRP0086P1-P824

Growth Hormone Deficiency in Noonan Syndrome: Does it Influence Clinical Response to GH Therapy?
Direct

Abstract PDF
HRP0086P1-P825

Screening of Birth Length and Parental Height Detects Infants with Poor Catch-Up Growth at Age 2 Years
Direct

Abstract PDF
HRP0086P1-P826

Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic
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HRP0086P1-P827

OSBPL5 Methylation Abnormalities may be Pathogenic in Silver Russell Syndrome Through Genomic Methylation Analysis
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HRP0086P1-P828

A Study of Bone Health Index (BHI) in Girls with Turners Syndrome
Direct

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HRP0086P1-P829

Premature Adrenarche in Silver-Russell Syndrome: A Longitudinal Study
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HRP0086P1-P830

A Rare Case of Deletion in 2q24.1: Clinical Features and Response to Gh Hormone Treatment
Direct

Abstract PDF
HRP0086P1-P831

Serum Levels of IL-6, TNF-a, Omentin-1 are Increased in Girls with Turner Syndrome
Direct

Abstract PDF
HRP0086P1-P832

Effect of Dietetic Management on Weight in Children with Bardet-Biedl Syndrome
Direct

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HRP0086P1-P833

Analysis of Phenotype and HRAS Gene Mutation in a Chinses Girl with Costello Syndrome
Direct

Abstract PDF
HRP0086P2-P834

Auxological Features in Patients with Vernal Keratoconjunctivitis
Direct

Abstract PDF
HRP0086P2-P835

Turner Syndrome: Does GH Treatment Influence Glucose Homeostasis?
Direct

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HRP0086P2-P836

Renal Anomalies in Children with Turner Syndrome: Experience from a Single-Centre
Direct

Abstract PDF
HRP0086P2-P838

A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in Korean Girl
Direct

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HRP0086P2-P839

Evaluation of Referrals for Short Stature to a Regional Paediatric Centre
Direct

Abstract PDF
HRP0086P2-P840

Testosterone Therapy Improves the First Year Height Velocity in Adolescent Boys with Constitutional Delay of Growth and Puberty
Direct

Abstract PDF
HRP0086P2-P842

Linear Growth in Infants and Children with Atopic Dermatitis
Direct

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HRP0086P2-P843

The Specific Pubertal Height Gain is Higher in Boys as Well as in Children with Lower BMISDS
Direct

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HRP0086P2-P844

Growth Screening in Children Aged Three to Five Years Seen in Community Paediatrics in Dreux District, France: Preliminary Results
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HRP0086P2-P845

The 3M Syndrome: A Cause of Pre- and Post-Natal Severe Growth Retardation
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HRP0086P2-P846

Should We Construct Specific Growth Charts for Ethnic Subgroups?
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HRP0086P2-P847

Late Presenting Girls with Turner Syndrome can Achieve a Normal Final Height
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Abstract PDF
HRP0086P2-P848

Growth of Children Born Preterm During the First 8 Years of Life
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HRP0086P2-P849

Genetic Variability in Patients with Noonan Syndrome in the Republic of Macedonia
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HRP0086P2-P850

An Unusual Cause of Short Stature in a Phenotypic Male with Type I Diabetes Mellitus due to an Unexpected Deletion of the Y Chromosome
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HRP0086P2-P851

An Unusual Case of Growth Hormone Replacement Therapy in a Child with Hereditary Multiple Exostoses and Growth Hormone Deficiency
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HRP0086P2-P852

Assessment of the Medical and Psychological Status of Women with Turner-Syndrome in Young Adulthood
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HRP0086P2-P853

A 3-year-old Boy with Growth Hormone Deficiency and Clinical Features of Ritscher-Schinzel Syndrome
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HRP0086P2-P854

Growth Pattern, Response to GH Treatment and the Effects of Pubertal Spurt on Final Height in Patients Affected by RASopathies
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HRP0086P2-P855

The Usefulness of Magnetic Resonance Imaging of the Heart and Aorta in the Diagnostic Work-up in Girls with Turner Syndrome
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HRP0086P2-P856

A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene
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HRP0086P2-P857

A Case of Familial Silver-Russell Syndrome
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HRP0086P2-P858

Central Precocious Puberty in a Case of SOTOS Syndrome
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HRP0086P2-P859

Hypoglycaemia in Isolated GH Deficiency beyond Infancy
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HRP0086P2-P860

Referral Pattern of Children with Short Stature to a Pediatric Endocrine Clinic in Kuwait
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HRP0086P2-P861

The Effect of Iron Intervention on the Anthropometric Parameters: Pilot Study among Egyptian Preschool Children with Iron Deficiency Anemia
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HRP0086P2-P862

Dopamine Beta-Hydroxylase Deficiency Leading to Growth Hormone Deficiency
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HRP0086P2-P863

Quality of Life in Growth Hormone Treated Children and Adolescents with Growth Hormone Deficiency and Smallness for Gestational Age
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HRP0086P2-P864

Secretion of Somatostatin and Growth Hormone (GH) in Various Forms of Hereditary Pathology
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HRP0086P2-P865

Postnatal Growth and Factors Modifying it in Very Low Birth Weight Preterms (PT) with Bronchopulmonary Dysplasia (BPD)
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HRP0086P2-P866

Endocrine and Metabolic Parameters before Onset of rGH Treatment: Potential Predictive Factors of GH Response in Children Born SGA? Results from Cohort of Nancy
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HRP0086P2-P867

Growth Hormone Treatment in a Child with Trisomy 21 and Turner Mosaicism
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HRP0086P2-P868

Pubertal Development and Final Height in Some Rare Genetic Diseases
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Abstract PDF
HRP0086P2-P869

Growth Hormone Deficiency in a Patient with Ring Chromosome 18
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HRP0086P2-P870

Children with Down's Syndrome Show Quantitative, Phenotypical and Functional Differences of Effector T-Cells Compared to Immunocompetent Controls
Direct

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HRP0086P2-P871

Cardiovascular Anomalies in Turner Syndrome
Direct

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HRP0086P2-P872

Metamemory in Turner Syndrome: A Study Comparing Episodic and Semantic Memory
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HRP0086P2-P873

A XO/XX Girl with Lack of Morphological UTS-Features, Short Stature and Precocious Puberty
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HRP0086P2-P874

Transverse Myelitis in Turner Syndrome
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HRP0086P2-P875

Tricho-Rhino-Phalangeal Syndrome Type I in a Girl with Growth Hormone Deficiency
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HRP0086P2-P876

Project Epi Peg-Premeb. Clinical Situation of a Person Born SGA Followed from Birth Cohort. GLOBAL Causes and Clinical Situation of Partial Birth Cohort and 12 Months
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HRP0086P2-P877

Pituitary Gigantism and Central Precocious Puberty Presenting with Prognathism in a Pediatric Patient
Direct

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HRP0086P2-P878

The Monitoring of Endocrine Functions in Children with Rare Genetic Syndromes
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HRP0086P2-P879

SHORT Syndrome and rhGH Treatment - Is It Useful?
Direct

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HRP0086P2-P880

Late Diagnosis of Mixed Gonadal Dysgenesis - Clinical and Psychological Implications
Direct

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HRP0086P2-P881

The Structure of Genetically Determined Types of Short Stature in Uzbekistan According to Retrospective Analysis
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HRP0086P2-P882

Evaluation of Growth Pattern in Prader-Willi Syndrome
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HRP0086P2-P883

Prader-Willi Syndrome - Different Patients, Different Attitude
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HRP0086P1-P884

Clinicopathological Characteristics of Papillary Thyroid Cancer in Children With Emphasis on the Pubertal Status and Association With BRAFV600E Mutation
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HRP0086P1-P885

Elevation of Serum Fibroblast Growth Factor 21 in Congenital Hypothyroidism
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HRP0086P1-P886

Evaluation of Epicardial AdiposeTissue Thickness in Children Detected Subclinical Hypothyroidism
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HRP0086P1-P887

EEG Alterations are Common in Hashimoto's Thyroiditis
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HRP0086P1-P888

[ldquo]Semi-Hot[rdquo] Thyroid Nodules Associated with GNAS Mutations in Three Adolescents
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HRP0086P1-P889

Evaluation of Body Composition via Bioelectrical Impedance Analysis in Children with Subclinical Hypothyroidism and Effect of LT4 Treatment; Follow-up Results
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Abstract PDF
HRP0086P1-P890

The Molecular Causes of Congenital Hypothyroidism: The Scottish experience
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HRP0086P1-P891

Newborn Screening Program for Congenital Hypothyroidism: Eighteen Years of Experience in Buenos Aires Province, Argentina
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HRP0086P1-P892

Transient TSH Elevation in Infants Referred on Newborn Screening - Features, Prevalence and Trends
Direct

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HRP0086P1-P893

Resolution of Hepatic Hemangiomas and Consumptive Hypothyroidism in an Infant Treated with Propranolol and Levothyroxine
Direct

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HRP0086P1-P894

Comprehensive Analysis of Seven Toll-Like Receptor Genes Including 15 Single-Nucleotide Polymorphisms with Autoimmune Thyroid Disease in Korean Children
Direct

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HRP0086P1-P895

Thyroid Cancer is the Most Frequent Secondary Solid Tumour Following Allogeneic Stem Cell Transplantation in Childhood - A Single Centre Experience
Direct

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HRP0086P1-P896

Iodide Transport Defect: Identification of a Novel Mutation in the Carboxy-terminus of the Sodium/iodide Symporter in a Pediatric Patient with Congenital Hypothyroidism
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HRP0086P1-P897

Congenital Hypothyroidism: The Use of a TSH Cut-off Limit of 6mU/L and the ESPE Criteria for LT4 Treatment Leads to the Diagnosis of Mild but mostly Permanent Forms of Hypothyroidism
Direct

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HRP0086P1-P898

Do Different Initial Doses of L-T4 within the Range of 10-15 mcg/kg/day Influence Neurodevelopment during the First Two Years of Life in Children with Congenital Hypothyroidism?
Direct

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HRP0086P1-P899

Clinical and Histopathologic Features and Follow-up of Paediatric Patients with Papillary Thyroid Cancer: A 10 Years Experience
Direct

Abstract PDF
HRP0086P1-P900

Meta-analysis of Children with Multiple Endocrine Neoplasia (MEN) Type 2A from 1995-2014: Impact of RET Mutation Screening on Age at Thyroidectomy and Frequency of Metastatic Disease
Direct

Abstract PDF
HRP0086P1-P901

Screening of Congenital Hypothyroidism in Low Birth Weight and Very Low Birth Weight Neonates: A Systematic Review
Direct

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HRP0086P1-P902

Identification of Zinc Transporter ZnT8 in Thyroid Tissues from Children and Adolescents with Thyroid Nodular Hyperplasia
Direct

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HRP0086P1-P903

HABP2 as Genetic Susceptibility Factor for Familial Differentiated Thyroid Carcinoma
Direct

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HRP0086P1-P904

Cardiac Size and Function in Children with Subclinical Hypothyroidism
Direct

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HRP0086P1-P905

Association of CTLA4, PADI4 and FTO Polymorphisms with Autoimmune Thyroid Diseases in Male Children
Direct

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HRP0086P1-P906

Thyroid Cancers in Korean Pediatric Populations with Thyroid Nodules
Direct

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HRP0086P1-P907

Dysregulation of the Immune System in Children with Graves Disease - the Role of NK and NKT-Like Cells
Direct

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HRP0086P1-P908

Thyroid Function Anomalies in Children with Down Syndrome: Early TSH Alteration can Predict Future Hypothyroidism Development?
Direct

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HRP0086P1-P909

Identification of a [ldquo]Cryptic[rdquo] De Novo Deletion in NKX2.1 in the Brain-Lung-Thyroid Syndrome using Genomic SNP Arrays
Direct

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HRP0086P1-P910

Partial Thyroxine Binding Globulin Deficiency in Test Tube Babies: Cases Report and Literatures Review
Direct

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HRP0086P1-P911

Hyperthyroidism after Bone Marrow Transplantation: A Report of Two Cases
Direct

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HRP0086P1-P912

A Case of a Young Girl with High Risk RET Mutation Successfully Diagnosed as Medullary Thyroid Carcinoma in Very Early Stage
Direct

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HRP0086P1-P913

Nerve Conduction Studies in Children with Subclinical Hypothyroidism
Direct

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HRP0086P1-P914

Van Wyk Grumbach Syndrome with Kocher Smeglaine Debre Syndrome: Case Report of a Rare Association
Direct

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HRP0086P1-P915

Macro TSH- a Rare Cause of High Levels of TSH
Direct

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HRP0086P1-P916

Papillary Thyroid Carcinoma in a Mother and Child Evolving after the Manifestation of Grave's Disease
Direct

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HRP0086P1-P917

Hypercholesterolemia in Two Siblings with THRB Mutation
Direct

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HRP0086P1-P918

Thyroid Autoimmunity and Vitamin D Status in Euthyroid Girls with Hashimoto's Thyroiditis
Direct

Abstract PDF
HRP0086P1-P919

Etiology and Severity of Congenital Hypothyroid Children Detected through Neonatal Screening: A Cut-off based Analysis
Direct

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HRP0086P1-P920

Lowering of the TSH cut-off Limit Substantially Alters Universally Accepted Key Features of Congenital Hypothyroidism. Reconsideration of the Use of FT4 levels for Diagnosis and Treatment
Direct

Abstract PDF
HRP0086P1-P921

Differentiated Thyroid Cancer: Onset and Outcome in a Pediatric Population with and without Risk Factors
Direct

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HRP0086P1-P922

Evaluation of the Usefulness of Serum Cytokines IL-1[beta] and sFasL Measurements in the Diagnosis of Autoimmune Hypothyroidism and Hyperthyroidism in Children
Direct

Abstract PDF
HRP0086P1-P923

Small Thyroid Volume on Ultrasound in Infants with Transient TSH Elevation Following Referral by Newborn Screening
Direct

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HRP0086P1-P924

In Children with Autoimmune Thyroid Diseases the Association with Down syndrome can Modify the Clustering of Extra-Thyroidal Autoimmune Disorders
Direct

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HRP0086P1-P925

L-selenomethionine Supplementation in Children and Adolescents with Autoimmune Thyroiditis: Preliminary Results of a Randomized Double-blinded Placebo-controlled Clinical Trial
Direct

Abstract PDF
HRP0086P1-P926

Minimally Invasive Video-Assisted Thyroid Surgery in Children: A Single Center Ten-Years Experience
Direct

Abstract PDF
HRP0086P1-P927

Prevalence of Congenital Hypothyroidism and Thyroid Function Follow-Up of Children with Tsh Cutoff between 5 and 10 mIU/l in Neonatal Screening
Direct

Abstract PDF
HRP0086P1-P928

Preliminary Results: Body Composition of Adolescent Patients with Congenital Hypothyroidism and Correlation with Laboratory Parameters
Direct

Abstract PDF
HRP0086P1-P929

Neonatal Thyrotoxicosis and Craniosynostosis Associated with Maternal Graves' Disease and High Dose maternal Thyroxine Therapy for Papillary Carcinoma
Direct

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HRP0086P1-P930

Seasonality of Month of Birth in Children and Adolescents with Hashimoto Thyroiditis
Direct

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HRP0086P1-P931

Radioiodine Therapy for Graves' Disease - the Experience of a Portuguese Single Centre
Direct

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HRP0086P2-P932

Multinodular Goiter and Differentiated Thyroid Cancer in Pediatrics
Direct

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HRP0086P2-P933

Clinical Case of Acute Liver Injury in Pediatric Patient with Autoimmune Hyperthyroidism
Direct

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HRP0086P2-P934

Thyroid Function in Children Affected By Congenital Hypothyroidism (CH) with Eutopic Thyroid After Discontinuation of Treatment with Levothyroxine
Direct

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HRP0086P2-P935

Hyperthyroidism in an Infant of a Mother with Autoimmune Hypothyroidism with Positive TSH Receptor Antibodies
Direct

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HRP0086P2-P936

Thyroid Cancer Presentation in Children is Different than in Young Adults
Direct

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HRP0086P2-P937

Starting Treatment in Congenital Hypothyroidism with Normal FT4 Levels and Thyroid Gland in situ Detected at Neonatal Screening
Direct

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HRP0086P2-P938

Distal Monosomy 10q Presented as Congenital Hypothyroidism
Direct

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HRP0086P2-P939

Five-Year Prospective Evaluation of Thyroid Function Test Evolution in Children with Hashimoto's Thyroiditis Presenting with Either Euthyroidism or Subclinical Hypothyroidism
Direct

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HRP0086P2-P940

An Unusual Case of Impaired Renal Function and Thrombocytopenia
Direct

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HRP0086P2-P941

Celiac Disease in Children and Adolescents with Hashimoto Thyroiditis
Direct

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HRP0086P2-P942

Euthyroid Hashimoto Thyroiditis in Children: Evolution Over Time
Direct

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HRP0086P2-P943

Thyrotoxic Periodic Paralysis, an Under-Recognized Condition
Direct

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HRP0086P2-P944

Age at Diagnosis and Mental Development in Children with Congenital Hypothyroidism in the Absence of Newborn Screening Programme
Direct

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HRP0086P2-P945

Vitamin D Levels in Children with Hashimoto's Thyroiditis: Before and after I-Thyroxine Therapy
Direct

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HRP0086P2-P946

The Aim of This Study was to Recognize Difference between Transient Congenital Hypothyroidism (TCH) from Permanent Congenital Hypothyroidism by Determining Clinical Characteristics, Laboratory Tests and Imaging Studies
Direct

Abstract PDF
HRP0086P2-P947

Delayed Diagnosis of a TSH-Adenoma due to Coexisting Autoimmune Thyroid Disease
Direct

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HRP0086P2-P948

Kocher-Debre-Semelaigne Syndrome: Hypothyroidism with Muscle Pseudohypertrophy
Direct

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HRP0086P2-P949

Thyroid Function in Obese Children and Its Correlations with Chosen Atherogenic Risk Factors
Direct

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HRP0086P2-P950

The Evolution of Thyroid Function after Hashimoto's Thyroiditis Presentation is Different in Initially Euthyroid Girls with or without Turner Syndrome
Direct

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HRP0086P2-P951

Hashimoto's Thyroiditis in Childhood: An 8 Year Experience
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HRP0086P2-P952

Congenital Malformations, Dysmorphic Syndromes and Neurodevelopmental Problems in Children with Congenital Hypothyroidism
Direct

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HRP0086P2-P953

Clinical Value of Thyroid-Stimulating Immunoglobulin in Paediatric Autoimmune Thyroid Diseases
Direct

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HRP0086P2-P954

Hearing, Language and Communication Abilities in Children with Congenital Hypothyroidism
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HRP0086P2-P955

Lack of Catch Up Growth in Severe Hashimoto Thyroiditis (HT) in Young Children
Direct

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HRP0086P2-P956

Perinatal Factors Associated with Neonatal Thyroid Stimulating Hormone in Normal Newborns
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HRP0086P2-P957

TBG Excess as a Cause of Hyperthyroxinemia and High T3 Detected Incidentally or Through Neonatal Screening Test
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HRP0086P2-P958

Beta Thallassemia: The Relation between Ferritin and Hypothyroisdism and the Suppressing Effect of Ferritin on Autoimmune Disorders (a Hypothesis)
Direct

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HRP0086P2-P959

Thyroid Hormones and Risk Factors in Obese and Overweight Children
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HRP0086P2-P960

FNA: A Gold Standard in the Diagnosis of Thyroid Nodules in Children after Chemotherapy
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HRP0086P2-P961

Profound Growth Failure in Peripubertal Adolescents Presenting with Severe Acquired Autoimmune Hypothyroidism: A Case Series
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HRP0086P2-P962

Two Patients with Resistance to Thyroid Hormones
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HRP0086P2-P963

The Influence of Etiology and Treatment Factors on Intellectual Outcome in Congenital Hypothyroidism
Direct

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HRP0086P2-P964

An Unusual Complication of Graves' Disease
Direct

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HRP0086P2-P965

An Unusual form of Precocious Puberty: Van Wyk and Grumbach Syndrome
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HRP0086P2-P966

Clinical Features of Newborn with Congenital Hypothyroidism Diagnosed by Neonatal Screening: Single Center Experience
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HRP0086P2-P967

Postoperative Complications of Thyroidectomy in Children with Nodular Goiter
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HRP0086P2-P968

Peculiarities of Course and Therapy of Basedow-Graves' Disease in Children in Different Age Groups
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HRP0086P2-P969

An Unusual Presentation of Hashimoto Thyroiditis (HT) and Precocious Puberty: The Van Wyk-Grumbach Syndrome
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HRP0086P2-P970

Rare Case of Severe Hyperthyroidism due to Grave's Disease in a Female Toddler
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HRP0086P2-P971

Youngest Known Case of Autoimmune Thyroiditis Causing Hyperthyroidism in a Down's Syndrome Toddler
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HRP0086P2-P972

Thyroid Hormones in Obese Children
Direct

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HRP0086P2-P973

A Case of Neonatal Graves in a Premature Infant with Negative Thyroid Stimulating Immunoglobulins (TSI)
Direct

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HRP0086P2-P974

Severe Growth Retardation and Hypothyroidism due to Hashimoto's Thyroidits
Direct

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HRP0086P2-P975

Beta Thallassemia: the Relation between Ferritin and Hypothyroisdism and the Suppressing Effect of Ferritin on Autoimmune Disorders (a Hypothesis)
Direct

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HRP0086P2-P976

Severe Hyponatremia and Repeated Intestinal Resections for Intestinal Dysmotility Mimicking Congenital Aganglionic Megacolon due to Delay in the Diagnosis of Congenital Hypothyroidism
Direct

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HRP0086P2-P977

Very Early Onset of Autoimmune Thyroiditis in a Toddler with Multi-organ Involvement
Direct

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HRP0086P2-P978

A Case of the Thyroid Gland Dystopia in the Root of the Tongue
Direct

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HRP0086P2-P979

Conversion of Hypothyroidism to Hyperthyroidism in A Child with Down's Syndrome
Direct

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HRP0086P2-P980

Transient Congenital Hypothyroidism: About Six Cases
Direct

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HRP0086LBP1

46,XY DSD due to Isolated AMH Deficiency Resulting in Persistent Mullerian Duct Syndrome (PMDS) as a Consequence of a Single-Base Deletion in a SF1-Response Element of the AMH promoter
Direct

Abstract PDF
HRP0086LBP2

Sexual Outcomes in Brazilian Patients with 46,XY DSD
Direct

Abstract PDF
HRP0086LBP3

The Growth Hormone - Insulin Like Growth Factor I (IGF-1) System in Early Non-Alcoholic Fatty Liver Disease: From an Animal Model to a Children's Cohort
Direct

Abstract PDF
HRP0086LBP4

Sirolimus Precipitating Diabetes in a Patient with Congenital Hyperinsulinism due to Autosomal Dominant ABCC8 Mutation
Direct

Abstract PDF
HRP0086LBP5

Development of Skeletal Microarchitecture and Biomechanics Over 2 Years Following 6 Month Intragastric Balloon Insertion in Obese Adolescents
Direct

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HRP0086LBP6

Children with Brain Tumors have Enhanced Visceral Adiposity Compared to Non-Cancer Controls: A Preliminary Analysis from the Canadian Study of Determinants of Endometabolic Health in Children Study
Direct

Abstract PDF
HRP0086LBP7

Loss of Functional Osteoprotegerin: More than a Skeletal Problem
Direct

Abstract PDF
HRP0086LBP8

Impact of Weight Loss after Bariatric Surgery on Gonadic Function in Severely Obese Female Adolescents
Direct

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HRP0086LBP9

Osteoprotegerin and Insulin Resistance in Childhood Obesity: A New Interplay?
Direct

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HRP0086LBP10

Molecular Analysis of AR, SRD5A2, NR5A1 and HSD17B3 Genes in a Brazilian 46,XY DSD Cohort
Direct

Abstract PDF
HRP0086LBP11

Long-Term Safety and Effectiveness of Growth Hormone Treatment in Pediatric Patients with Growth Hormone Deficiency: Interim Results of LG Growth Study
Direct

Abstract PDF
HRP0086LBP12

An Analysis of Symptoms and Signs of Adrenal Insufficiency in Children with CAH Admitted to Hospital in Australia
Direct

Abstract PDF
HRP0086LBP13

Hyperprolactinemia in Children and Adolescents: A Review of Patients Presenting to a Tertiary Center in Australia
Direct

Abstract PDF

ESPE Abstracts

55th Annual ESPE (ESPE 2016)

EPosters

BiosciAbstracts