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Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

The journal of clinical endocrinology and metabolism, 2019-08, Vol.104 (8), p.3049-3067

2019

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Preterm ovarian hyperstimulation syndrome mimicking clitoromegaly

Pediatrics and neonatology, 2023-11, Vol.64 (6), p.690-691

2023

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Early postnatal metabolic profile in neonates with critical CHDs

Cardiology in the young, 2023-03, Vol.33 (3), p.349-353

2023

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Neonatal Problems and Infancy Growth of Term SGA Infants: Does “SGA” Definition Need to Be Re-evaluated?

Frontiers in pediatrics, 2021-11, Vol.9, p.660111-660111

2021

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Early Postnatal Metabolic Profile in Neonates With Different Birth Weight Status: A Pilot Study

Frontiers in pediatrics, 2021-04, Vol.9, p.646860-646860

2021

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CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation

American journal of ophthalmology case reports, 2017-09, Vol.7 (C), p.129-133

2017

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Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

Calcified tissue international, 2022-04, Vol.110 (4), p.441-450

2022

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Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia

Journal of Pediatric Endocrinology and Metabolism, 2021-09, Vol.34 (9), p.1201-1205

2021

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Interdisiplinary and intraobserver reliability of the Greulich-Pyle method among Turkish children

Journal of Pediatric Endocrinology and Metabolism, 2023-12, Vol.36 (12), p.1181-1185

2023

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The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography

International ophthalmology, 2017-08, Vol.37 (4), p.1031-1038

2017

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Challenges in the management of a 7 years old child with thyrotropin-secreting pituitary adenoma and the review of the literature

Hormone research in paediatrics, 2023-10

2023

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Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature

Hormone research in paediatrics, 2023-10, Vol.96 (5), p.527-537

2023

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Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS

Bone (New York, N.Y.), 2015-02, Vol.71, p.53-57

2015

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Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy

Ophthalmic surgery, lasers & imaging retina, 2017-06, Vol.48 (6), p.473-477

2017

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Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis

The journal of clinical endocrinology and metabolism, 2014-01, Vol.99 (1), p.E169-E176

2014

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Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females

Pediatric diabetes, 2017-11, Vol.18 (7), p.607-613

2017

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Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

European journal of pediatrics, 2013-06, Vol.172 (6), p.851-853

2013

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Comparison of two different GnRH analogs' impact on final height in girls with early puberty: Triptorelin acetate vs. leuprolide acetate

Acta endocrinologica (Bucharest, Romania : 2005), 2020-10, Vol.16 (4), p.402-408

2020

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Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females: HALILOGLU et al

Pediatric diabetes, 2017-11, Vol.18 (7), p.607-613

2017

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Novel homozygous inactivating mutation of the calcium-sensing receptor gene ( CASR ) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet

Bone (New York, N.Y.), 2014-07, Vol.64, p.102-107

2014

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Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross‐sectional study

Diabetic medicine, 2019-10, Vol.36 (10), p.1243-1250

2019

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Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex developmentResearch in context

EBioMedicine, 2024-01, Vol.99, p.104941

2024

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Premature Pubarche, Hyperinsulinemia, Hypothyroxinemia and Hyperintensities in Basal Ganglia: All Caused by a Single Congenital Defect

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (1)

2016

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A Rare Presentation of Friedreich's Ataxia in Pediatric Case: Diabetes Mellitus

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2)

2015

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H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2)

2015

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Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

Preterm ovarian hyperstimulation syndrome mimicking clitoromegaly

Early postnatal metabolic profile in neonates with critical CHDs

Neonatal Problems and Infancy Growth of Term SGA Infants: Does “SGA” Definition Need to Be Re-evaluated?

Early Postnatal Metabolic Profile in Neonates With Different Birth Weight Status: A Pilot Study

CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation

Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia

Interdisiplinary and intraobserver reliability of the Greulich-Pyle method among Turkish children

The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography

Challenges in the management of a 7 years old child with thyrotropin-secreting pituitary adenoma and the review of the literature

Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature

Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS

Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy

Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis

Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

Comparison of two different GnRH analogs' impact on final height in girls with early puberty: Triptorelin acetate vs. leuprolide acetate

Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females: HALILOGLU et al

Novel homozygous inactivating mutation of the calcium-sensing receptor gene ( CASR ) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross‐sectional study

Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex developmentResearch in context

Premature Pubarche, Hyperinsulinemia, Hypothyroxinemia and Hyperintensities in Basal Ganglia: All Caused by a Single Congenital Defect

A Rare Presentation of Friedreich's Ataxia in Pediatric Case: Diabetes Mellitus

H Syndrome: A Rare Monogenic Cause of Insulin-Dependent Diabetes Mellitus

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