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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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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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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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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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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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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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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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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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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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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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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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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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Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A SingleCenter Experience

Turkish Archives of Pediatrics, 2023-05, Vol.58 (3), p.308-313

2023

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Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD

Journal of clinical research in pediatric endocrinology, 2022-06, Vol.14 (2), p.153

2022

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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

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

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

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

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

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

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

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

Adherence to growth hormone therapy: results of a multicenter study

Diagnosis and management of pediatric adrenal insufficiency

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

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

Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A SingleCenter Experience

Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD

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