Fetal, Neonatal Endocrinology and Metabolism P2

Clinical Characterstics, Genotype-Phenotype Correlations and Follow Up of Patients with Congenital Hyperinsulinaemic Hypoglycaemia; Single Center Experience from a Southeastern City of Turkey

hrp0089p2-p183 | Fetal, Neonatal Endocrinology and Metabolism P2

Congenital Hyperinsulinism: Management and Outcome in West of Scotland

hrp0089p2-p184 | Fetal, Neonatal Endocrinology and Metabolism P2

20 Cases of Congenital Hyperinsulinism in Ukraine

hrp0089p2-p185 | Fetal, Neonatal Endocrinology and Metabolism P2

Nifedipine Therapy in Hyperinsulinaemic Hypoglycaemia Due to Mutations in the PMM2 Gene Improves Fast Tolerance, Stabilises Blood Glucose Profile, and Enables Rationalisation of Treatments for Glycaemic Control and Hypertension: The First Reported Trial in 3 Patients in a Tertiary Centre

hrp0089p2-p186 | Fetal, Neonatal Endocrinology and Metabolism P2

Potentially Modifiable Predictors of Adverse Neonatal Outcomes in Women with Gestational Diabetes Mellitus (GDM)

hrp0089p2-p187 | Fetal, Neonatal Endocrinology and Metabolism P2

A Boy with Diazoxide Unresponsive Congenital Hyperinsulinism due to a Homozygous ABCC8 Missense Mutation Previously Reported to be Dominant

hrp0089p2-p188 | Fetal, Neonatal Endocrinology and Metabolism P2

Diazoxide Unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation

hrp0089p2-p189 | Fetal, Neonatal Endocrinology and Metabolism P2

Neonatal Hypoglycaemia: Unchanged Risk of Neurodevelopmental Impairment, But Sex-Specific Decreased Fine Motor Function and Increased Internalizing Behaviour at School Age

hrp0089p2-p190 | Fetal, Neonatal Endocrinology and Metabolism P2

Atypical Hepatoblastoma and Wilm’s Tumour in an Infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism

hrp0089p2-p191 | Fetal, Neonatal Endocrinology and Metabolism P2

Association between Rubenstein-Taybi Syndrome and Hyperinsulinaemic Hypoglycaemia

hrp0089p2-p192 | Fetal, Neonatal Endocrinology and Metabolism P2

Hyperinsulinemic Hypoglycemia in Congenital Disorder of Glycosylation Type-1a (CDG-1a)

hrp0089p2-p193 | Fetal, Neonatal Endocrinology and Metabolism P2

A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello Syndrome

hrp0089p2-p194 | Fetal, Neonatal Endocrinology and Metabolism P2

Molecular Defects Identified by Whole Exome Sequencing in a Chinese Boy with Fructose-1,6-Bisphosphatase Deficiency

hrp0089p2-p195 | Fetal, Neonatal Endocrinology and Metabolism P2

The Benefit of Universal Neonatal Screening for Hypoglycemia

hrp0089p2-p196 | Fetal, Neonatal Endocrinology and Metabolism P2

Prematurity of 23 or Less Weeks’ Gestation is a Risk for Transient Late-Onset Hyperglycemia in Neonates

hrp0089p2-p197 | Fetal, Neonatal Endocrinology and Metabolism P2

An unusual cause of neonatal hyperglycemia – case report

hrp0089p2-p198 | Fetal, Neonatal Endocrinology and Metabolism P2

Neonatal Hypocalcemia Due to Maternal Hypovitaminosis D: A Cohort of Children in a Region of Northern Spain

hrp0089p2-p199 | Fetal, Neonatal Endocrinology and Metabolism P2

Evaluation of Vitamin D Status and Its Correlation with Gonadal Function in Children at Mini-puberty

hrp0089p2-p200 | Fetal, Neonatal Endocrinology and Metabolism P2

Systemic Pseudohypoaldosteronism Type 1 Due to 3 Novel Mutations in SCNN1A and SCNN1B Genes; Report of 3 Cases

hrp0089p2-p201 | Fetal, Neonatal Endocrinology and Metabolism P2

Postnatal Growth of Infants with Neonatal Diabetes: Insulin Pump (CSII) Versus Multiple Daily Injection (MDI) Therapy

hrp0089p2-p202 | Fetal, Neonatal Endocrinology and Metabolism P2

Serum Vaspin Concentration in Full-term, Appropriate-for-Gestational-Age Newborns: Effect of Early-Onset Infections

hrp0089p2-p203 | Fetal, Neonatal Endocrinology and Metabolism P2

First Three Years of The Congenital Adrenal Hyperplasia Neonatal Screening Program of the State of Parana, Southern Brazil

hrp0089p2-p204 | Fetal, Neonatal Endocrinology and Metabolism P2

Assessment of the Stretched Penile Length in Sri Lankan Newborns

hrp0089p2-p205 | Fetal, Neonatal Endocrinology and Metabolism P2

Auxological Catch Up Growth and Evaluation of Spontaneous Motility in the Term Newborn Small for Gestational Age Employing the Prechtl Assessment of General Movements

ESPE Abstracts

57th Annual ESPE (ESPE 2018)

Poster Presentations

Clinical characteristics of Congenital Hyperinsulinism Caused by Dominant KCNJ11/ABCC8 Mutations

Clinical Characterstics, Genotype-Phenotype Correlations and Follow Up of Patients with Congenital Hyperinsulinaemic Hypoglycaemia; Single Center Experience from a Southeastern City of Turkey

Congenital Hyperinsulinism: Management and Outcome in West of Scotland

20 Cases of Congenital Hyperinsulinism in Ukraine

Nifedipine Therapy in Hyperinsulinaemic Hypoglycaemia Due to Mutations in the PMM2 Gene Improves Fast Tolerance, Stabilises Blood Glucose Profile, and Enables Rationalisation of Treatments for Glycaemic Control and Hypertension: The First Reported Trial in 3 Patients in a Tertiary Centre

Potentially Modifiable Predictors of Adverse Neonatal Outcomes in Women with Gestational Diabetes Mellitus (GDM)

A Boy with Diazoxide Unresponsive Congenital Hyperinsulinism due to a Homozygous ABCC8 Missense Mutation Previously Reported to be Dominant

Diazoxide Unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation

Neonatal Hypoglycaemia: Unchanged Risk of Neurodevelopmental Impairment, But Sex-Specific Decreased Fine Motor Function and Increased Internalizing Behaviour at School Age

Atypical Hepatoblastoma and Wilm’s Tumour in an Infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism

Association between Rubenstein-Taybi Syndrome and Hyperinsulinaemic Hypoglycaemia

Hyperinsulinemic Hypoglycemia in Congenital Disorder of Glycosylation Type-1a (CDG-1a)

A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello Syndrome

Molecular Defects Identified by Whole Exome Sequencing in a Chinese Boy with Fructose-1,6-Bisphosphatase Deficiency

The Benefit of Universal Neonatal Screening for Hypoglycemia

Prematurity of 23 or Less Weeks’ Gestation is a Risk for Transient Late-Onset Hyperglycemia in Neonates

An unusual cause of neonatal hyperglycemia – case report

Neonatal Hypocalcemia Due to Maternal Hypovitaminosis D: A Cohort of Children in a Region of Northern Spain

Evaluation of Vitamin D Status and Its Correlation with Gonadal Function in Children at Mini-puberty

Systemic Pseudohypoaldosteronism Type 1 Due to 3 Novel Mutations in SCNN1A and SCNN1B Genes; Report of 3 Cases

Postnatal Growth of Infants with Neonatal Diabetes: Insulin Pump (CSII) Versus Multiple Daily Injection (MDI) Therapy

Serum Vaspin Concentration in Full-term, Appropriate-for-Gestational-Age Newborns: Effect of Early-Onset Infections

First Three Years of The Congenital Adrenal Hyperplasia Neonatal Screening Program of the State of Parana, Southern Brazil

Assessment of the Stretched Penile Length in Sri Lankan Newborns

Auxological Catch Up Growth and Evaluation of Spontaneous Motility in the Term Newborn Small for Gestational Age Employing the Prechtl Assessment of General Movements

BiosciAbstracts