Çoşkun Yarar

Eskişehir Osmangazi Üniversitesi Tıp Fakültesi Hastanesi — Turkey

Medicine · Health Sciences

15h-index984citations149works0.32yr avg
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Research Topics

Cerebral Palsy and Movement Disorders(17), Neonatal and fetal brain pathology(10), Metabolism and Genetic Disorders(9), Epilepsy research and treatment(8), Bacterial Infections and Vaccines(8)

Publications148 total

Vaccination Status of Patients with Spinal Muscular Atrophy: A Multicentre Nationwide SMA-VACC Study
2025Open Access
Rare Diseases Accompanied by Neurological Findings in Childhood
Osmangazi Journal of Medicine·2025
Congenital mirror movements in a family: Outcomes associated with DCC mutations
Journal of Neurogenetics·2025
Pediatristlerin İnme Konusunda Farkındalık, İlgi ve Bilgi Düzeylerinin Değerlendirilmesi
OSMANGAZİ JOURNAL OF MEDICINE·2025Open Access
Canpolat - Pediatrik Multipl Skleroz
2025
A Novel De Novo Exceptional Complex Chromosomal Rearrangement Involving 5 Chromosomes Resulting in Neurodevelopmental Delay and Dysmorphism
Molecular Syndromology·2025· 1 citedOpen Access
A Rare Case of Hereditary Sensory and Autonomic Neuropathy Type 4 in a 3-Year-Old: Clinical and Genetic Findings
Turkiye Klinikleri Journal of Pediatrics·2025Open Access
Evaluation of Quality of Life in Cerebral Palsy Patients: Descriptive Research
Turkiye Klinikleri Journal of Pediatrics·2025Open Access
The relationship between serum phenylalanine levels, genotype, and developmental assessment test results in non-phenylketonuria mild hyperphenylalaninemia patients
European Journal of Pediatrics·2024
A Rare Cause of Fever of Unknown Origin and Pseudotumor Cerebri in Children: Mediterranean Spotted Fever
Çocuk Enfeksiyon Dergisi/Journal of Pediatric Infection·2024Open Access
Çocuklarda Nedeni Bilinmeyen Ateş ve Psödotümör Serebrinin Nadir Nedenlerinden: Akdeniz Benekli Ateşi
Çocuk Enfeksiyon Dergisi/Journal of Pediatric Infection·2024Open Access
Pain in Spinal Muscular Atrophy Type 2 and Type 3 Patients
OSMANGAZİ JOURNAL OF MEDICINE·2024Open Access
The Relationship Between Serum Phenylalanine Levels, Genotype, and Developmental Assessment Test Results in Non-Phenylketonuria Mild Hyperphenylalaninemia Patients
2024Open Access
Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study
Epilepsy Research·2024· 1 cited
Two siblings with Fanconi anemia (FANCQ, ERCC4/XPF) presenting with tumor‐mimicking lesions in the brain and acute neurological deterioration
Pediatric Blood & Cancer·2024Open Access
Differentiation of peripheral and non-peripheral etiologies in children with vertigo/dizziness: The video-head impulse test and suppression head impulse paradigm
International Journal of Pediatric Otorhinolaryngology·2024· 2 cited
Optic neuritis in Turkish children and adolescents: A multicenter retrospective study
Multiple Sclerosis and Related Disorders·2023· 3 cited
Evaluation of MicroRNAs in Pediatric Epilepsy
Turkish Archives of Pediatrics·2023· 6 citedOpen Access
Kumandaş & Canpolat Pediatrik ve Neonatal EEG Atlası
2023Open Access
A Pediatric Case of Reversible Splenial Lesion Syndrome Associated with SARS-CoV-2
Turkiye Klinikleri Journal of Pediatrics·2023Open Access
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Frequent Co-authors

Kürşat Bora Çarman(25), Ayten Yakut(13), Ener Çağrı Dinleyici(9), Ozan Koçak(7), Bilal Yıldız(6), JoEllen M. Sefton(5), Jack W. Berry(5), Didem Arslantaş(5), Çetin Okuyaz(5), Nihal Olgaç Dündar(5), Meltem Dinleyici(4), Kürşad Aydın(4), Hüseyin Per(4), Serdal Güngör(4), Banu Anlar(4), Hasan Tekgül(4), Mustafa Çalık(3), Sedat Işıkay(3), Ömer Kılıç(3), Sevgi Yimenicioğlu(3)