Publications by authors named "Ihsan Turan"

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The First-Year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-Hydroxylase Deficiency and a Higher Detection Rate of Non-Classical Cases.
Tülay Güran, Elif Yürüker, Ahmet Anık, Müge Atar, Emine Çamtosun, İhsan Turan

J Clin Res Pediatr Endocrinol· December 2025

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Corneal parameters in pediatric triple a syndrome patients with alacrima.
Miray Faiz Turan, Ihsan Turan

Ophthalmic Genet· December 2025

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Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2.
Mevra Cay, Ihsan Turan, Bahriye Atmıs, Leman Damla Kotan, Sukriye Tugce Celebi

J Pediatr Endocrinol Metab· December 2025

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Correction to: When it's not juvenile idiopathic arthritis: unmasking monogenic mimickers in children.
Rabia Miray Kisla Ekinci, Sibel Balci, Aybuke Alisan, Fatih Gurbuz, Eda Mengen, Ihsan Turan

Eur J Pediatr· December 2025

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When it's not juvenile idiopathic arthritis: unmasking monogenic mimickers in children monogenic mimickers of chronic arthritis.
Rabia Miray Kisla Ekinci, Sibel Balci, Aybuke Alisan, Fatih Gurbuz, Eda Mengen, Ihsan Turan

Eur J Pediatr· November 2025

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A novel homozygous missense variant in syndromic juvenile-onset diabetes.
Eda Mengen, Deniz Kor, Fatma Derya Bulut, Leman Damla Kotan, İhsan Turan

J Pediatr Endocrinol Metab· September 2025

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Depression, anxiety in adolescents with exogenous obesity and depression, anxiety, caregiver burden, and burnout in their mothers.
Can Celiloğlu, İhsan Turan, Perihan Çam Ray, Semine Özdemir Dilek, Mevra Çay

Front Pediatr· September 2025

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Leptin acutely increases hepatic triglyceride secretion in patients with lipodystrophy.
Marianna Beghini, Matthäus Metz, Clemens Baumgartner, Peter Wolf, Magdalena Bastian, Ihsan Turan

Metabolism· August 2025

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An evaluation of cases of disorders of sex development related to SRD5A2.
Can Celiloglu, Ihsan Turan, Leman Damla Kotan, Ayşe Merve Cimen, Semine Ozdemir Dilek

Endocrine· August 2025

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Evaluation of the Relationship Between Thyroid Hormone Levels and Bisphenol A in Children Aged 6-14 Years.
Pinar Altun Yildirim, Ersin Nazlican, Zeliha Haytoglu, İhsan Turan, Betul Kilincli

Clin Endocrinol (Oxf)· July 2025

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Genotype, Phenotype Characteristics and Long-Term Follow-Up of Patients with Vitamin D-Dependent Rickets Type IA: A Nationwide Multi-Centre Retrospective Cross-Sectional Study.
Atilla Cayir, Huseyin Demirbilek, Ayberk Türkyılmaz, Serap Turan, Abdullah Bereket, Ihsan Turan

Horm Res Paediatr· July 2025

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Optimal timing of repeat thyroid fine-needle aspiration biopsy.
Mevra Cay, Ihsan Turan, Eda Mengen, Ayse Merve Çimen, Şükriye Tuğçe Celebi

J Pediatr Endocrinol Metab· May 2025

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Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.
Fatma Dursun, İhsan Turan, Eda Çelebi Bitkin, Elvan Bayramoğlu, Atilla Çayır

Clin Endocrinol (Oxf)· November 2024

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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.
Zeynep Siklar, Emine Camtosun, Semih Bolu, Melek Yildiz, Aysehan Akinci, Ihsan Turan

Endocrine· September 2024

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Plasma pentraxin-3 levels and its role in childhood obesity-Is it anti-inflammatory? A matched group study.
Merve Uysal, Burak Mete, Ertan Kara, Hakan Demirhindi, Zeliha Haytoglu, İhsan Turan

Clin Endocrinol (Oxf)· July 2024

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mutation in humans with pubertal failure alters GnRH transcript expression.
Hyun-Ju Cho, Fatih Gurbuz, Maria Stamou, Leman Damla Kotan, Stephen Matthew Farmer, Ihsan Turan

Front Endocrinol (Lausanne)· August 2023

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Clinical features of generalized lipodystrophy in Turkey: A cohort analysis.
Ilgin Yildirim Simsir, Beyhan Tuysuz, Mehmet Nuri Ozbek, Seher Tanrikulu, Merve Celik Guler, Ihsan Turan

Diabetes Obes Metab· July 2023

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A novel homozygous nonsense NDNF variant in Kallmann syndrome.
Leman Damla Kotan, Melek Yildiz, Ihsan Turan, Can Celiloglu, Bilgin Yuksel

Am J Med Genet A· March 2023

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The utility of annual growth velocity standard deviation scores and measurements of biochemical parameters in long-term treatment monitoring of children with 21-hydroxylase deficiency.
Semine Ozdemir Dilek, Ihsan Turan, Fatih Gurbuz, Can Celiloglu, Bilgin Yuksel

Hormones (Athens)· September 2022

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DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism.
Ihsan Turan, Korcan Demir, Eda Mengen, Leman Damla Kotan, Fatih Gürbüz

Horm Res Paediatr· April 2022

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PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism.
Bradley A Welch, Hyun-Ju Cho, Seyit Ahmet Ucakturk, Stephen Matthew Farmer, Semra Cetinkaya, Ihsan Turan

J Neuroendocrinol· April 2022

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Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans.
A Kemal Topaloglu, Enver Simsek, Matthew A Kocher, Jamala Mammadova, Ece Bober, Ihsan Turan

Hum Genet· February 2022

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Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey.
Semine Özdemir Dilek, Fatih Gürbüz, İhsan Turan, Can Celiloğlu, Bilgin Yüksel

J Pediatr Endocrinol Metab· October 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.
Leman Damla Kotan, Gaetan Ternier, Aydilek Dagdeviren Cakir, Hamdi Cihan Emeksiz, Ihsan Turan

Genet Med· June 2021

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Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets.
Ihsan Turan, Sevcan Erdem, Leman Damla Kotan, Semine Ozdemir Dilek, Mehmet Tastan

J Pediatr Endocrinol Metab· May 2021

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