Publications by authors named "Hasan Onal"

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Atypical pediatric presentation of hyperparathyroidism: gene mutation and parathyroid carcinoma.
Emel Hatun Aytaç Kaplan, Mehmet Çakmak, M Banu Yilmaz Özgüven, Şeyma Tuna Şentürk, Hasan Önal

J Pediatr Endocrinol Metab· December 2025

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Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase Deficiency.
Zehra Yavas Abali, Melek Yildiz, Saygin Abali, Ariorad Moniri, Firdevs Bas, Hasan Onal

J Clin Endocrinol Metab· December 2025

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Clinical characteristics, surgical and endocrinological outcomes of sellar and parasellar masses in pediatric patients: a single-center experience.
Zümrüt Kocabey Sütçü, Emel Hatun Aytaç Kaplan, Buruç Erkan, Hasan Önal

Pituitary· September 2025

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A Rare Case of Monogenic Obesity Due to a Novel Variant in the Gene: Challenges in Follow-up and Treatment.
Bahar Özcabı, Asude Durmaz, Ayça Aykut, Hasan Önal, Samim Özen

J Clin Res Pediatr Endocrinol· August 2025

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Pediatric hypoparathyroidism: etiological and clinical evaluation in a tertiary center.
Zümrüt Kocabey Sütçü, Emel Hatun Aytaç Kaplan, Hasan Önal

Endocrine· March 2025

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Developmental outcomes of children with biotinidase deficiency and the psychological state of their parents.
Seda Bozduman Çelebi, Berhan Akdağ, Hatice Cimbar, Canan Dağ, Fatma Topal

Eur J Pediatr· March 2025

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A novel graphene oxide-based fluorescence method for detection of urine glycosaminoglycans.
Ceren Bakır Kösoğlu, Süreyya Dede, Emine Karakuş, Ali Erdoğmuş, Bahadır Keskin

Biotechnol Appl Biochem· June 2024

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Evaluation of cardiac autonomic dysfunctions in children with type 1 diabetes mellitus.
Davut Gözüküçük, Berkut A İleri, Serra Karaca Başkan, Ece Öztarhan, Dilek Güller

BMC Pediatr· April 2024

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Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes.
Cansu Altuntaş, Tugce Aksu Uzunhan, Biray Ertürk, Mey Talip Petmezci, Nafiye Emel Çakar

Clin Neurol Neurosurg· January 2024

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Ambulatory blood pressure monitorisation in children with recombinant growth hormone treatment.
Emel Hatun Aytaç Kaplan, Zümrüt Kocabey Sütçü, Eren Soyaltın, Hasan Onal

J Pediatr Endocrinol Metab· January 2024

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Investigation of (Epi)genetic causes in syndromic short children born small for gestational age.
Beyhan Tüysüz, Büşra Kasap, Dilek Uludağ Alkaya, Zeynep Alp Ünkar, Pınar Köseoğlu

Eur J Med Genet· November 2023

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A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy.
Cansu Altuntaş, Tugce Aksu Uzunhan, Biray Ertürk, Mey Talip Petmezci, Nafiye Emel Çakar

Clin Neurol Neurosurg· June 2023

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Can we predict risk for cardiac involvement in paediatric inflammatory multi-system syndrome?
Nurhayat Yakut, Ibrahim Cansaran Tanidir, Kahraman Yakut, Sezgin Sahin, Arda Kilinc, Hasan Onal

Cardiol Young· December 2022

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Angiotensin (1-7) peptide replacement therapy with plasma transfusion in COVID-19.
Hasan Onal, Nurcan Ucuncu Ergun, Bengu Arslan, Seyma Topuz, Seda Yilmaz Semerci

Transfus Apher Sci· August 2022

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Clinical, biochemical and genotypical characteristics in biotinidase deficiency.
Abdurrahman Akgun, Askin Sen, Hasan Onal

J Pediatr Endocrinol Metab· November 2021

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The frequency of and factors affecting functional gastrointestinal disorders in infants that presented to tertiary care hospitals.
Omer Faruk Beser, Fugen Cullu Cokugras, Guzide Dogan, Ozlem Akgun, Murat Elevli, Hasan Onal

Eur J Pediatr· August 2021

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Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency.
Melek Yildiz, Emregul Isik, Zehra Yavas Abali, Mehmet Keskin, Mehmet Nuri Ozbek, Hasan Onal

J Clin Endocrinol Metab· August 2021

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Treatment of COVID-19 patients with quercetin: a prospective, single center, randomized, controlled trial.
Hasan Önal, Bengü Arslan, Nurcan Üçüncü Ergun, Şeyma Topuz, Seda Yilmaz Semerci

Turk J Biol· August 2021

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Possible genotype-phenotype correlations in Niemann-Pick type C patients and miglustat treatment.
Nafiye Emel Çakar, Hasan Önal

Ideggyogy Sz· March 2021

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The factors relevant to partial remission in children with type 1 diabetes mellitus after measles vaccination: A retrospective study.
Gonca Bektaş, Hasan Önal, Erdal Adal

J Med Virol· December 2020

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Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations.
Huseyin Demirbilek, Atilla Cayir, Sarah E Flanagan, Ruken Yıldırım, Yılmaz Kor, Hasan Onal

J Clin Endocrinol Metab· December 2020

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Novel variants in Turkish patients with glycogen storage disease.
Nafiye Emel Çakar, Alper Gezdirici, Hanım Şeyma Topuz, Hasan Önal

Pediatr Int· October 2020

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Children with Hashimoto’s Thyroiditis Have Increased Intestinal Permeability: Results of a Pilot Study.
Banu Küçükemre Aydın, Melek Yıldız, Abdurrahman Akgün, Neval Topal, Erdal Adal

J Clin Res Pediatr Endocrinol· September 2020

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A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.
Işık Odaman-Al, Alper Gezdirici, Melek Yıldız, Gizem Ersoy, Gönül Aydoğan

Turk J Pediatr· July 2020

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A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome.
Işık Odaman-Al, Alper Gezdirici, Melek Yıldız, Gizem Ersoy, Gönül Aydoğan

Turk J Pediatr· July 2020

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