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Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes

Journal of clinical research in pediatric endocrinology, 2021-02, Vol.13 (1), p.72-79

2021

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Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p.Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother

Archives of Endocrinology and Metabolism, 2024-01, Vol.68, p.e210305

2024

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Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs8) Mutation in the BSCL2 Gene: Results From the First-year

Journal of clinical research in pediatric endocrinology, 2023-09, Vol.15 (3), p.329-333

2023

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Clinical and biochemical characteristics and bone mineral density of homozygous, compound heterozygous and heterozygous carriers of three novel IGFALS mutations

European journal of endocrinology, 2017-06, Vol.176 (6), p.657

2017

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The ımportance of art therapy ın the qualıty of lıfe ın hemodıalysıs patıents

Ukraïnsʹkij žurnal nefrologìï ta dìalìzu (Online), 2021-03 (1(69)), p.27-33

2021

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Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.319-328

2020

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Congenital Hyperinsulinism: Diagnosis and Treatment Update

Journal of clinical research in pediatric endocrinology, 2017-12, Vol.9 (Suppl 2), p.69-87

2017

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Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-eastern Region of Turkey

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.295-302

2020

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Congenital Hyperinsulinism and Evolution to Sulfonylurea-responsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation

Journal of clinical research in pediatric endocrinology, 2019-03, Vol.11 (1), p.82-87

2019

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Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report

Journal of clinical research in pediatric endocrinology, 2022-06, Vol.14 (2), p.172-178

2022

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Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

Journal of clinical research in pediatric endocrinology, 2021-03, Vol.13 (1), p.34-43

2021

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The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism

Frontiers in endocrinology (Lausanne), 2019-02, Vol.10, p.111-111

2019

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Continuous Hepatogonodal and Splenogonogal Fusion: A Rare Cause of Bilateral Intra-Abdominal Testis in an 18-Month-Old Boy

European journal of pediatric surgery reports, 2022-01, Vol.10 (1), p.e80-e83

2022

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Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study

Diabetes research and clinical practice, 2016-09, Vol.119, p.32-40

2016

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Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation

Journal of clinical research in pediatric endocrinology, 2019-03, Vol.11 (1), p.82-87

2019

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Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions

Turkish journal of pediatrics, 2018, Vol.60 (5), p.554-561

2018

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Hyperinsulinaemic hypoglycaemia in children and adults

The lancet. Diabetes & endocrinology, 2017-09, Vol.5 (9), p.729-742

2017

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Hypophosphatasia presenting with pyridoxine-responsive seizures, hypercalcemia, and pseudotumor cerebri: case report

Journal of clinical research in pediatric endocrinology, 2012-03, Vol.4 (1), p.34-38

2012

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Ion Transporters, Channelopathies, and Glucose Disorders

International journal of molecular sciences, 2019-05, Vol.20 (10), p.2590

2019

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Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I

Hormone research in paediatrics, 2016-01, Vol.85 (5), p.309-317

2016

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Prepubertal unilateral gynecomastia: report of 2 cases

Journal of clinical research in pediatric endocrinology, 2014-12, Vol.6 (4), p.250-253

2014

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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

The journal of clinical endocrinology and metabolism, 2016-01, Vol.101 (1), p.284-292

2016

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Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

Diabetologia, 2022-02, Vol.65 (2), p.336-342

2022

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Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism

PloS one, 2014-05, Vol.9 (5), p.e98054-e98054

2014

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Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism

Journal of clinical research in pediatric endocrinology, 2012-09, Vol.4 (3), p.121-126

2012

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Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes

Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p.Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother

Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs8) Mutation in the BSCL2 Gene: Results From the First-year

Clinical and biochemical characteristics and bone mineral density of homozygous, compound heterozygous and heterozygous carriers of three novel IGFALS mutations

The ımportance of art therapy ın the qualıty of lıfe ın hemodıalysıs patıents

Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene

Congenital Hyperinsulinism: Diagnosis and Treatment Update

Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-eastern Region of Turkey

Congenital Hyperinsulinism and Evolution to Sulfonylurea-responsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation

Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report

Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism

Continuous Hepatogonodal and Splenogonogal Fusion: A Rare Cause of Bilateral Intra-Abdominal Testis in an 18-Month-Old Boy

Evaluation of therapeutics management patterns and glycemic control of pediatric type 1 diabetes mellitus patients in Turkey: A nationwide cross-sectional study

Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation

Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions

Hyperinsulinaemic hypoglycaemia in children and adults

Hypophosphatasia presenting with pyridoxine-responsive seizures, hypercalcemia, and pseudotumor cerebri: case report

Ion Transporters, Channelopathies, and Glucose Disorders

Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I

Prepubertal unilateral gynecomastia: report of 2 cases

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism

Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism

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