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Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey

The journal of clinical endocrinology and metabolism, 2016-07, Vol.101 (7), p.2759-2767

2016

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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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Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.287-294

2020

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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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Congenital Lipoid Adrenal Hyperplasia: Functional Characterization of Three Novel Mutations in the STAR Gene

The journal of clinical endocrinology and metabolism, 2010-03, Vol.95 (3), p.1301-1308

2010

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Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report

Journal of clinical research in pediatric endocrinology, 2022-03, Vol.14 (1), p.1-9

2022

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Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

Journal of clinical research in pediatric endocrinology, 2021-06, Vol.13 (2), p.180-186

2021

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Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene

Diabetes research and clinical practice, 2023-11, Vol.205, p.110953-110953, Article 110953

2023

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YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress

The Journal of clinical investigation, 2020-12, Vol.130 (12), p.6338-6353

2020

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Short-term results of continuous venovenous haemodiafiltration versus peritoneal dialysis in 40 neonates with inborn errors of metabolism

European journal of pediatrics, 2019-06, Vol.178 (6), p.829-836

2019

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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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Clinical features of generalized lipodystrophy in Turkey: A cohort analysis

Diabetes, obesity & metabolism, 2023-07, Vol.25 (7), p.1950-1963

2023

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Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2021-09, Vol.106 (9), p.e3714-e3724

2021

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Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4359

2020

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The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey

Italian journal of pediatrics, 2022-08, Vol.48 (1), p.1-7, Article 144

2022

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Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.275-280

2020

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A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio

Journal of pediatric endocrinology & metabolism : JPEM, 2020-05, Vol.33 (6), p.735

2020

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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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Investigation of the effect of comorbid psychopathologies on glycemic control in children and adolescents with type 1 diabetes mellitus (eng)

Klinik psikiyatri dergisi, 2022-05, Vol.25 (2), p.148-154

2022

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Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey

Molecular genetics and metabolism reports, 2023-09, Vol.36, p.100979-100979, Article 100979

2023

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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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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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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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Is Isolated Autoantibody Seropositivity a Risk Factor in the Development of Diabetic Nephropathy in Type 1 Diabetic Children?

Turkish journal of nephrology, 2023-07, Vol.32 (3), p.249-254

2023

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Incidence of type 1 diabetes mellitus in Turkish children from the southeastern region of the country: a regional report

Journal of clinical research in pediatric endocrinology, 2013-01, Vol.5 (2), p.98-103

2013

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Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey

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

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants

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

Congenital Lipoid Adrenal Hyperplasia: Functional Characterization of Three Novel Mutations in the STAR Gene

Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene

YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress

Short-term results of continuous venovenous haemodiafiltration versus peritoneal dialysis in 40 neonates with inborn errors of metabolism

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

Clinical features of generalized lipodystrophy in Turkey: A cohort analysis

Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations

The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey

Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism

A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio

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

Investigation of the effect of comorbid psychopathologies on glycemic control in children and adolescents with type 1 diabetes mellitus (eng)

Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey

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

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

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

Is Isolated Autoantibody Seropositivity a Risk Factor in the Development of Diabetic Nephropathy in Type 1 Diabetic Children?

Incidence of type 1 diabetes mellitus in Turkish children from the southeastern region of the country: a regional report

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