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Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

Journal of pediatric endocrinology & metabolism : JPEM, 2020-04, Vol.33 (4), p.557

2020

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Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

Journal of clinical research in pediatric endocrinology, 2018-12, Vol.10 (4), p.336-342

2018

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Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

Journal of clinical research in pediatric endocrinology, 2021-12, Vol.13 (4), p.433-438

2021

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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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A rare cause of hypertension in childhood: Answers

Pediatric nephrology (Berlin, West), 2020, Vol.35 (1), p.79-82

2020

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GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey

Clinical endocrinology (Oxford), 2016-09, Vol.85 (3), p.393-399

2016

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Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: a multicenter study

Journal of clinical research in pediatric endocrinology, 2013-01, Vol.5 (1), p.20-26

2013

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Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty

The journal of clinical endocrinology and metabolism, 2021-07, Vol.106 (7), p.e2557-e2566

2021

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Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children

Hormone research in paediatrics, 2015-01, Vol.83 (4), p.282-287

2015

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Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus

Pediatric diabetes, 2015-08, Vol.16 (5), p.361-366

2015

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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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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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Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus: Detemir vs. glargine in children

Pediatric diabetes, 2015-08, Vol.16 (5), p.361-366

2015

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Molecular Diagnosis of Monogenic Diabetes and Their Clinical/Laboratory Features in Turkish Children

Journal of clinical research in pediatric endocrinology, 2021-11, Vol.13 (4), p.433-438

2021

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Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty

Journal of pediatric endocrinology & metabolism : JPEM, 2018-02, Vol.31 (2), p.175

2018

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Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Journal of clinical research in pediatric endocrinology, 2020-06, Vol.12 (2), p.150-159

2020

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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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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 (2), p.14

2016

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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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Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

American journal of medical genetics. Part A, 2016-04, Vol.170A (4), p.942-948

2016

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The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

Journal of clinical research in pediatric endocrinology, 2016-09, Vol.8 (3), p.305-312

2016

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Growth without Growth Hormone Syndrome in a Patient with Craniopharyngioma

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1)

2015

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Follow-up of Two Cases of Medulloblastoma with/without Growth Hormone Therapy

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1)

2015

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A rare cause of hypertension in childhood: Questions

Pediatric nephrology (Berlin, West), 2020, Vol.35 (1), p.77-78

2020

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A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B

Bone (New York, N.Y.), 2022-04, Vol.157, p.116344-116344, Article 116344

2022

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Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

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

A rare cause of hypertension in childhood: Answers

GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey

Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: a multicenter study

Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty

Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children

Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

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

Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus: Detemir vs. glargine in children

Molecular Diagnosis of Monogenic Diabetes and Their Clinical/Laboratory Features in Turkish Children

Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Preterm ovarian hyperstimulation syndrome mimicking clitoromegaly

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

Early postnatal metabolic profile in neonates with critical CHDs

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

Growth without Growth Hormone Syndrome in a Patient with Craniopharyngioma

Follow-up of Two Cases of Medulloblastoma with/without Growth Hormone Therapy

A rare cause of hypertension in childhood: Questions

A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B

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