Publications by authors named "Ferda Evin"

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Detection of copy number variations by chromosomal microarray analysis in disorders of sex development of unexplained molecular etiology and association with clinical findings.
Murat Çağlar Karataş, Ferda Evin, Tahir Atik, Aysun Ata, Eren Er

Endocrine· December 2025

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Basal and Bolus Insulin Distribution According to Treatment Modality: Data from SWEET Diabetes Registry.
Ferda Evin, Sascha R Tittel, Barbara Piccini, Roque Cardona-Hernandez, Dick Mul

Pediatr Diabetes· April 2025

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Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and their Genotype-phenotype Correlation.
Samim Özen, Damla Gökşen, Ferda Evin, Esra Işık, Hüseyin Onay

J Clin Res Pediatr Endocrinol· December 2024

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"Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment".
Ferda Evin, Tarık Kırkgöz, Tahir Atik, Güneş Ak, Timur Köse

J Diabetes Complications· November 2024

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Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta.
Ferda Evin, Tahir Atik, Huseyin Onay, Damla Goksen, Sukran Darcan

J Pediatr Endocrinol Metab· August 2024

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Evaluation of Digit Ratios in Youth With Polycystic Ovary Syndrome.
Ferda Evin, İlkay Ayrancı

Cureus· August 2024

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A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype-phenotype correlations.
Ferda Evin, Derya Aydın, Ertürk Levent, Samim Özen, Şükran Darcan

J Pediatr Endocrinol Metab· December 2023

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Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene.
Damla Goksen, Ferda Evin, Esra Isik, Samim Ozen, Tahir Atik

Diabetes Res Clin Pract· November 2023

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ABCC8-related maturity-onset diabetes of the young: switching from insulin to sulphonylurea therapy: how long do we need for a good metabolic control?
Ferda Evin, Esra Işık, Hüseyin Onay, Samim Özen, Şükran Darcan

J Pediatr Endocrinol Metab· June 2023

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Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition.
Uğur Cem Yilmaz, Ferda Evin, Huseyin Onay, Samim Ozen, Sukran Darcan

J Pediatr Endocrinol Metab· January 2023

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The Value of Telemedicine for the Follow-up of Patients with New Onset Type 1 Diabetes Mellitus During COVID-19 Pandemic in Turkey: A Report of Eight Cases.
Ferda Evin, Eren Er, Aysun Ata, Arzu Jalilova, Günay Demir

J Clin Res Pediatr Endocrinol· November 2021

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Treatment and long-term follow-up of patients diagnosed with type 1 diabetes mellitus before age 5.
Aysun Ata, Eren Er, Ferda Evin, Hafize Işıklar, Nushaba Abdullayev

J Pediatr Endocrinol Metab· February 2021

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Glycated hemoglobin variability and microvascular complications in patients with type 1 diabetes mellitus.
Eren Er, Aysun Ata, Ferda Evin, Yasemin Atik Altınok, Günay Demir

J Pediatr Endocrinol Metab· December 2020

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