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Hypogonadism: Is It Always Hypogonadotropic in an Adolescent With a Cleft Palate? A Surprising Case of Klinefelter Syndrome

The Cleft palate-craniofacial journal, 2021-06, Vol.58 (6), p.787-790

2021

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Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2

Journal of clinical research in pediatric endocrinology, 2021-06, Vol.13 (2), p.232-238

2021

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Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

Journal of clinical research in pediatric endocrinology, 2024-09, Vol.16 (3), p.288-296

2024

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The association between vitamin B12, folate, homocysteine levels, and carotid intima-media thickness in children with obesity: a cross-sectional study

Journal of Pediatric Endocrinology and Metabolism, 2022-08, Vol.35 (8), p.1051-1058

2022

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Is Waist-height Ratio Associated with Thyroid Antibody Levels in Children with Obesity?

Journal of clinical research in pediatric endocrinology, 2021-06, Vol.13 (2), p.152-159

2021

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The Relationship Between Obesity, Depressive Symptoms and Sleep Duration in Children and Adolescents

Acta medica Alanya, 2021-04, Vol.5 (1), p.42-47

2021

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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Genetics in medicine, 2021-06, Vol.23 (6), p.1008-1016

2021

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Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

Journal of clinical research in pediatric endocrinology, 2019-06, Vol.11 (2), p.164-172

2019

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Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Journal of clinical research in pediatric endocrinology, 2021-09, Vol.13 (3), p.308-319

2021

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Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

Journal of clinical research in pediatric endocrinology, 2018-06, Vol.10 (2), p.168-174

2018

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Lipid accumulation product is a predictor of nonalcoholic fatty liver disease in childhood obesity

Korean journal of pediatrics, 2019-12, Vol.62 (12), p.450-455

2019

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Vitamin D Deficiency and Hashimoto's Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

Journal of clinical research in pediatric endocrinology, 2015-06, Vol.7 (2), p.128-133

2015

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Evaluation of Adenovirus-36 (Ad-36) antibody seropositivity and adipokine levels in obese children

Microbial pathogenesis, 2017-07, Vol.108, p.27-31

2017

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Management of Rapidly Progressive Precocious Puberty in a Patient with Mosaic Turner Syndrome

Acta endocrinologica (Bucharest, Romania : 2005), 2021-01, Vol.17 (1), p.101-105

2021

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A Case of Sotos Syndrome Caused by a Novel Variant in the NSD1 Gene: A Proposed Rationale to Treat Accompanying Precocious Puberty

Acta endocrinologica (Bucharest, Romania : 2005), 2020-04, Vol.16 (2), p.245-249

Ozcabi, B

2020

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Evaluation of Thyroid Nodules in Children and Adolescents: Multicenter Study in Turkey

Güncel pediatri, 2021-12, Vol.19 (3), p.354-362

2021

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (3), p.242-248

2015

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Effective sociodemographic and clinical factors in weight loss in childhood obesity

Turk Pediatri Arsivi, 2018-09, Vol.53 (3), p.169-176

2018

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Associations of Respiratory Distress Syndrome Severity and Other Factors With Transient Hypothyroxinemia of Prematurity

Curēus (Palo Alto, CA), 2021-08

2021

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Primary adrenal insufficiency caused by a novel mutation in DAX1 gene

Journal of clinical research in pediatric endocrinology, 2013-01, Vol.5 (1), p.55-57

2013

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A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment

Journal of clinical research in pediatric endocrinology, 2023-10

2023

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Severe adrenal insufficiency in six neonates with normal newborn screening for CAH

Clinical endocrinology (Oxford), 2024-08, Vol.101 (2), p.108-113

2024

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Factors Affecting Metabolic Bone Disease of Prematurity: Is Hypothyroxinemia Included?

Şişli Etfal Hastanesi tıp bülteni, 2022-01, Vol.56 (1), p.84-90

2022

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Evaluation of clinical, endocrine and metabolic findings in obese children with and without hepatosteatosis

Journal of Pediatric Endocrinology and Metabolism, 2021-09, Vol.34 (9), p.1081-1087

2021

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On dört yaşında akut lenfoblastik lösemili hastada düzelmeyen taşikardi

Turk Pediatri Arsivi, 2013-06, Vol.48 (2), p.176-178

2013

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Hypogonadism: Is It Always Hypogonadotropic in an Adolescent With a Cleft Palate? A Surprising Case of Klinefelter Syndrome

Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

The association between vitamin B12, folate, homocysteine levels, and carotid intima-media thickness in children with obesity: a cross-sectional study

Is Waist-height Ratio Associated with Thyroid Antibody Levels in Children with Obesity?

The Relationship Between Obesity, Depressive Symptoms and Sleep Duration in Children and Adolescents

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

Lipid accumulation product is a predictor of nonalcoholic fatty liver disease in childhood obesity

Vitamin D Deficiency and Hashimoto's Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

Evaluation of Adenovirus-36 (Ad-36) antibody seropositivity and adipokine levels in obese children

Management of Rapidly Progressive Precocious Puberty in a Patient with Mosaic Turner Syndrome

A Case of Sotos Syndrome Caused by a Novel Variant in the NSD1 Gene: A Proposed Rationale to Treat Accompanying Precocious Puberty

Evaluation of Thyroid Nodules in Children and Adolescents: Multicenter Study in Turkey

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

Effective sociodemographic and clinical factors in weight loss in childhood obesity

Associations of Respiratory Distress Syndrome Severity and Other Factors With Transient Hypothyroxinemia of Prematurity

Primary adrenal insufficiency caused by a novel mutation in DAX1 gene

A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment

Severe adrenal insufficiency in six neonates with normal newborn screening for CAH

Factors Affecting Metabolic Bone Disease of Prematurity: Is Hypothyroxinemia Included?

Evaluation of clinical, endocrine and metabolic findings in obese children with and without hepatosteatosis

On dört yaşında akut lenfoblastik lösemili hastada düzelmeyen taşikardi

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