Publications by authors named "Aysun Ata"

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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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Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide study.
Sevinc Odabasi Gunes, Merve Sakar, Nursel Muratoglu Sahin, Gulay Karaguzel, Emine Ayca Cimbek, Aysun Ata, Muge Atar

Endocrine· November 2025

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Assessment of hormone measurement methods in girls with premature adrenarche, polycystic ovary syndrome, and non-classical congenital adrenal hyperplasia.
Mert Uçar, Aysun Ata, Burcu Barutçuoğlu, Güneş Ak, Sara Habif

Turk J Pediatr· October 2025

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Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaraş Earthquake.
Gürkan Tarçın, Nurgül Ataş, Mevra Yaşar, Kadriye Cansu Şahin, Gül Trabzon, Aysun Ata

J Clin Res Pediatr Endocrinol· May 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, Aysun Ata

J Clin Res Pediatr Endocrinol· December 2024

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The value of mid-upper arm circumference for malnutrition screening in pediatric celiac disease.
Didem Gülcü Taskin, Aysun Ata

Adv Clin Exp Med· December 2023

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Effect of Continuous Glucose Monitoring Device Assistance on Glycemic Control of 2023 Kahramanmaraş Doublet Earthquake Survivors with Type 1 Diabetes in Adana, Turkey.
Gürkan Tarçın, Semine Özdemir Dilek, Sümeyra Kılıç, Aysun Ata

Turk Arch Pediatr· November 2023

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An unusual manifestation in a pediatric patient with MAFB mutation: Sacroiliitis in multicentric carpotarsal osteolysis syndrome.
Rabia Miray Kisla Ekinci, Ozge Ozalp, Ozlem Anlas, Bahriye Atmis, Aysun Ata

Int J Rheum Dis· October 2023

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The Effect of the SARS-CoV-2 Pandemic on Presentation with Diabetic Ketoacidosis in Children with New Onset Type 1 Diabetes Mellitus.
Arzu Jalilova, Aysun Ata, Günay Demir, Hafize Işıklar, Yasemin Atik Altınok

J Clin Res Pediatr Endocrinol· August 2023

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Effect of metabolic control on cognitive functions in children and adolescents with type 1 diabetes mellitus.
Şeyma Kar, Eren Er, Aysun Ata, İpek İnal-Kaleli, Tuğçe Özcan

J Pediatr Endocrinol Metab· July 2023

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In vivo evaluation of macular microvasculature in childhood malnutrition using optical coherence tomography angiography.
Elif Ceren Yesilkaya, Aynure Sariyeva Aydamirov, Aysun Ata

Photodiagnosis Photodyn Ther· March 2023

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The Screening of Celiac Serology in Pediatric Patients Diagnosed with Type 1 Diabetes Mellitus.
Didem Gülcü Taşkın, Aysun Ata

Turk J Gastroenterol· March 2023

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Electrocardiographic Findings in Children With Growth Hormone Deficiency.
Münevver Yılmaz, Dolunay Gürses, Aysun Ata

Cureus· March 2023

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Association between clinical variations and copy number variations in cases with Turner syndrome.
Ezgi Aksoy, Ozgur Cogulu, Erhan Pariltay, Samim Ozen, Aysun Ata

J Pediatr Endocrinol Metab· September 2022

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The Impact of the CEDD-NET on the Evaluation of Rare Disorders: A Multicenter Scientific Research Platform in the Field of Pediatric Endocrinology.
Samim Özen, Aysun Ata, Feyza Darendeliler

J Clin Res Pediatr Endocrinol· June 2022

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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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Does COVID-19 predispose patients to type 1 diabetes mellitus?
Aysun Ata, Arzu Jalilova, Tarık Kırkgöz, Hafize Işıklar, Günay Demir

Clin Pediatr Endocrinol· November 2021

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A large cohort of disorders of sex development and their genetic characteristics: 6 novel mutations in known genes.
Aysun Ata, Samim Özen, Hüseyin Onay, Selin Uzun, Damla Gökşen

Eur J Med Genet· March 2021

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A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism.
Asude Durmaz, Ayça Aykut, Tahir Atik, Samim Özen, Durdugül Ayyıldız Emecen, Aysun Ata

J Clin Res Pediatr Endocrinol· February 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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Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics.
Ayça Aykut, Samim Özen, Damla Gökşen, Aysun Ata, Hüseyin Onay

Eur J Pediatr· September 2020

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A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature.
Aysun Ata, Samim Özen, Damla Gökşen, Neslihan Edeer Karaca, Güzide Aksu

Case Reports Immunol· September 2020

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