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Growth and relationship of phenotypic characteristics with gonadal pathology and tumour risk in patients with 45, X/46, XY mosaicism

Clinical endocrinology (Oxford), 2021-06, Vol.94 (6), p.973-979

2021

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A novel 3′ untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non‐autoimmune insulin‐dependent diabetes mellitus syndrome

Pediatric diabetes, 2019-06, Vol.20 (4), p.474-481

2019

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Effect of obesity and NAFLD on leukocyte telomere length and hTERT gene MNS16A VNTR variant

Scientific reports, 2024-10, Vol.14 (1), p.25055-9, Article 25055

2024

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Pelvic and breast ultrasound abnormalities and associated metabolic disturbances in girls with premature pubarche due to adrenarche

Clinical endocrinology (Oxford), 2022-03, Vol.96 (3), p.339-345

2022

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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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Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty

European journal of pediatrics, 2018-11, Vol.177 (11), p.1593-1601

2018

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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 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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Growth references for Turkish children aged 6 to 18 years

Acta Paediatrica, 2006-12, Vol.95 (12), p.1635-1641

2006

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Joubert syndrome with multiple pituitary hormone deficiency

BMJ case reports, 2019-04, Vol.12 (4), p.e229016

2019

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Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.2061-2070

2022

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Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families

European journal of medical genetics, 2017-03, Vol.60 (3), p.163-168

2017

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Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children

Journal of clinical research in pediatric endocrinology, 2015-12, Vol.7 (4), p.280-293

2015

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A Rare Cause of Adrenal Insufficiency – Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature

Hormone research in paediatrics, 2020-06, Vol.92 (6), p.395-403

2020

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Measurement of serum vitamin B12-related metabolites in newborns: implications for new cutoff values to detect B12 deficiency

The journal of maternal-fetal & neonatal medicine, 2021-04, Vol.34 (8), p.1260-1268

2021

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Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene

The Journal of steroid biochemistry and molecular biology, 2018-07, Vol.181, p.88-97

2018

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Body proportions in patients with Turner syndrome on growth hormone treatment

Turkish journal of medical sciences, 2023-01, Vol.53 (2), p.518-525

2023

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Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

European journal of medical genetics, 2022-12, Vol.65 (12), p.104654-104654, Article 104654

2022

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The relationship between infancy growth rate and the onset of puberty in both genders

Pediatric research, 2017-12, Vol.82 (6), p.940-946

2017

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Adherence to growth hormone therapy: results of a multicenter study

Endocrine practice, 2014-01, Vol.20 (1), p.46-51

2014

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Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

American journal of human genetics, 2013-01, Vol.92 (1), p.131-136

2013

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SPIOMET4HEALTH—efficacy, tolerability and safety of lifestyle intervention plus a fixed dose combination of spironolactone, pioglitazone and metformin (SPIOMET) for adolescent girls and young women with polycystic ovary syndrome: study protocol for a multicentre, randomised, double-blind, placebo-controlled, four-arm, parallel-group, phase II clinical trial

Trials, 2023-09, Vol.24 (1), p.589-589, Article 589

2023

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Diagnosis and management of pediatric adrenal insufficiency

World journal of pediatrics : WJP, 2016-08, Vol.12 (3), p.261-274

2016

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Evaluation of Children with Secondary Osteoporosis: A Single-center Experience

Medical journal of Bakirköy, 2023-03, Vol.19 (1), p.51-56

2023

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Determination of insulin resistance and its relationship with hyperandrogenemia,anti-Müllerian hormone, inhibin A, inhibin B, and insulin-like peptide-3 levels in adolescent girls with polycystic ovary syndrome

TURKISH JOURNAL OF MEDICAL SCIENCES, 2019-08, Vol.49 (4), p.1117-1125

2019

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Growth and relationship of phenotypic characteristics with gonadal pathology and tumour risk in patients with 45, X/46, XY mosaicism

A novel 3′ untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non‐autoimmune insulin‐dependent diabetes mellitus syndrome

Effect of obesity and NAFLD on leukocyte telomere length and hTERT gene MNS16A VNTR variant

Pelvic and breast ultrasound abnormalities and associated metabolic disturbances in girls with premature pubarche due to adrenarche

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

Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty

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

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

Growth references for Turkish children aged 6 to 18 years

Joubert syndrome with multiple pituitary hormone deficiency

Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome

Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children

A Rare Cause of Adrenal Insufficiency – Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature

Measurement of serum vitamin B12-related metabolites in newborns: implications for new cutoff values to detect B12 deficiency

Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene

Body proportions in patients with Turner syndrome on growth hormone treatment

Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

The relationship between infancy growth rate and the onset of puberty in both genders

Adherence to growth hormone therapy: results of a multicenter study

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Diagnosis and management of pediatric adrenal insufficiency

Evaluation of Children with Secondary Osteoporosis: A Single-center Experience

Determination of insulin resistance and its relationship with hyperandrogenemia,anti-Müllerian hormone, inhibin A, inhibin B, and insulin-like peptide-3 levels in adolescent girls with polycystic ovary syndrome

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