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Genetic Etiology of Idiopathic Hypogonadotropic Hypogonadism

Endocrines, 2022-01, Vol.3 (1), p.1-15

2022

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New-onset diabetes in children during the COVID-19 Pandemic: an assessment of biomarkers and psychosocial risk factors at play in Mississippi

Annals of pediatric endocrinology & metabolism, 2024-08, Vol.29 (4), p.234-241

2024

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Textile dye removal in wastewater by peroxymonosulfate (PMS) activation on a zero-valent iron nanoparticle–modified ultrafiltration catalytic membrane (nZVI@PES)

Environmental science and pollution research international, 2023-09, Vol.30 (41), p.94779-94789

2023

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Gender Identity and Assignment Recommendations in Disorders of Sex Development (DSD) Patients: 20 years’ Experience and Challenges

Journal of clinical research in pediatric endocrinology, 2020-12, Vol.12 (4), p.347-357

2020

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Low serum adiponectin levels in children and adolescents with diabetic retinopathy

The Eurasian journal of medicine, 2011-04, Vol.43 (1), p.18-22

2011

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Etiological Evaluation of Patients Presenting with Isolated Micropenis to an Academic Health Care Center

Indian journal of pediatrics, 2014-08, Vol.81 (8), p.775-779

2014

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Extremely immature infant who developed clitoromegaly during the second month of her postnatal life probably due to frequent whole blood transfusion from an adult male

Pediatrics international, 2003-06, Vol.45 (3), p.347-348

2003

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Chromium levels in healthy and newly diagnosed type 1 diabetic children

Pediatrics international, 2012-12, Vol.54 (6), p.780-785

2012

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A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy

Journal of Pediatric Endocrinology and Metabolism, 2011-03, Vol.24 (1-2), p.105-108

2011

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Denver developmental screening test II for early identification of the infants who will develop major neurological deficit as a sequalea of hypoxic-ischemic encephalopathy

Pediatrics international, 2001-08, Vol.43 (4), p.400-404

2001

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Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism

Journal of clinical research in pediatric endocrinology, 2012-09, Vol.4 (3), p.121-126

2012

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The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient

Clinical endocrinology (Oxford), 2018-08, Vol.89 (2), p.241-242

2018

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Relationship between metabolic control and neurocognitive functions in children diagnosed with type I diabetes mellitus before and after 5 years of age

Turkish journal of pediatrics, 2012-07, Vol.54 (4), p.352-361

2012

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A novel homozygous nonsense NDNF variant in Kallmann syndrome

American journal of medical genetics. Part A, 2023-03, Vol.191 (3), p.831-834

2023

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Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency

The journal of clinical endocrinology and metabolism, 2022-05, Vol.107 (6), p.e2359-e2364

2022

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Modification of polyvinylidene fluoride and polysulfone flat sheet membranes using perovskite nanoparticles for treatment of humic acid in a submerged membrane system

Desalination and water treatment, 2023-07, Vol.297, p.17-25

2023

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DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

Hormone research in paediatrics, 2022-02, Vol.94 (9-10), p.364-368

2022

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Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance

Clinical endocrinology (Oxford), 2018-06, Vol.88 (6), p.799-805

2018

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Clinical and Genetics Approaches to Hypogonadotropic Hypogonadism

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (2)

Topaloglu, Ali Kemal

2015

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Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.496-497

2016

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Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

Journal of clinical research in pediatric endocrinology, 2016-09, Vol.8 (3), p.373-374

2016

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Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

Endocrine, 2015-06, Vol.49 (2), p.479-491

2015

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Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations

Turkish journal of pediatrics, 2017, Vol.59 (4), p.434-441

2017

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Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets

Journal of Pediatric Endocrinology and Metabolism, 2021-05, Vol.34 (5), p.639-648

2021

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Molecular causes of hypogonadotropic hypogonadism

Current opinion in obstetrics & gynecology, 2010-08, Vol.22 (4), p.264-270

2010

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Genetic Etiology of Idiopathic Hypogonadotropic Hypogonadism

New-onset diabetes in children during the COVID-19 Pandemic: an assessment of biomarkers and psychosocial risk factors at play in Mississippi

Textile dye removal in wastewater by peroxymonosulfate (PMS) activation on a zero-valent iron nanoparticle–modified ultrafiltration catalytic membrane (nZVI@PES)

Gender Identity and Assignment Recommendations in Disorders of Sex Development (DSD) Patients: 20 years’ Experience and Challenges

Low serum adiponectin levels in children and adolescents with diabetic retinopathy

Etiological Evaluation of Patients Presenting with Isolated Micropenis to an Academic Health Care Center

Extremely immature infant who developed clitoromegaly during the second month of her postnatal life probably due to frequent whole blood transfusion from an adult male

Chromium levels in healthy and newly diagnosed type 1 diabetic children

A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy

Denver developmental screening test II for early identification of the infants who will develop major neurological deficit as a sequalea of hypoxic-ischemic encephalopathy

Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism

The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient

Relationship between metabolic control and neurocognitive functions in children diagnosed with type I diabetes mellitus before and after 5 years of age

A novel homozygous nonsense NDNF variant in Kallmann syndrome

Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency

Modification of polyvinylidene fluoride and polysulfone flat sheet membranes using perovskite nanoparticles for treatment of humic acid in a submerged membrane system

DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance

Clinical and Genetics Approaches to Hypogonadotropic Hypogonadism

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations

Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets

Molecular causes of hypogonadotropic hypogonadism

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