| Acute cerebellitis or postinfectious cerebellar ataxia? Clinical and imaging features in acute cerebellitis M Yildirim, R Gocmen, B Konuskan, S Parlak, D Yalnizoglu, B Anlar Journal of Child Neurology 35 (6), 380-388, 2020 | 46 | 2020 |
| Retrospective analysis of children with myelin oligodendrocyte glycoprotein antibody-related disorders B Konuskan, M Yildirim, R Gocmen, TD Okur, I Polat, H Kilic, S Saltik, ... Multiple sclerosis and related disorders 26, 1-7, 2018 | 44 | 2018 |
| A retrospective review of children with gallstone: Single-center experience from Central Anatolia S Gökçe, M Yıldırım, D Erdoğan Turk J Gastroenterol 25 (1), 46-53, 2014 | 41 | 2014 |
| Electroencephalographic findings in anti-N-methyl-d-aspartate receptor encephalitis in children: a series of 12 patients M Yildirim, B Konuskan, D Yalnizoglu, H Topaloglu, I Erol, B Anlar Epilepsy & Behavior 78, 118-123, 2018 | 32 | 2018 |
| Clinical presentation of anti-N-methyl-D-aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: a series of 24 cases B Konuskan, M Yildirim, H Topaloglu, I Erol, U Oztoprak, H Tan, ... European Journal of Paediatric Neurology 22 (1), 135-142, 2018 | 23 | 2018 |
| Neurologic involvement in primary immunodeficiency disorders M Yildirim, DC Ayvaz, B Konuskan, R Gocmen, I Tezcan, M Topcu, ... Journal of Child Neurology 33 (5), 320-328, 2018 | 20 | 2018 |
| A sydenham chorea attack associated with COVID-19 infection MF Yüksel, M Yıldırım, Ö Bektaş, S Şahin, S Teber Brain, Behavior, & Immunity-Health 13, 100222, 2021 | 15 | 2021 |
| Levetiracetam monotherapy in children with epilepsy: Experience from a tertiary pediatric neurology center M Yıldırım, Ö Bektaş, ÖA Göktaş, MF Yüksel, S Şahin, ST Teber Epilepsy & Behavior 116, 107745, 2021 | 10 | 2021 |
| Clinical features and outcomes of opsoclonus myoclonus ataxia syndrome M Yıldırım, İ Öncel, Ö Bektaş, G Tanalı, S Şahin, T Kutluk, S Teber, B Anlar European Journal of Paediatric Neurology 41, 19-26, 2022 | 9 | 2022 |
| Therapeutic plasma exchange in clinical pediatric neurology practice: Experience from a tertiary referral hospital M Yıldırım, Ö Bektaş, E Botan, S Şahin, A Gurbanov, S Teber, T Kendirli Clinical Neurology and Neurosurgery 207, 106823, 2021 | 8 | 2021 |
| Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes Ü Yılmaz, K Gücüyener, M Yavuz, İ Öncel, M Canpolat, S Saltık, O Ünver, ... European Journal of Paediatric Neurology 41, 8-18, 2022 | 6 | 2022 |
| Ketogenic diet-responsive drug-resistant epilepsy in a case of asparagine synthetase deficiency with a novel compound heterozygous missense variant M Altıntaş, M Yıldırım, Çİ Uçar, E Köse, Ö Bektaş, S Teber Clinical Neurology and Neurosurgery 230, 107772, 2023 | 5 | 2023 |
| A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene M Yıldırım, Ö Bektaş, E Tunçez, N Yeniay Süt, Y Sayar, Ü Öncül, S Teber Molecular Syndromology 13 (2), 139-145, 2022 | 5 | 2022 |
| Risk of seizure relapse and long-term outcomes after discontinuation of antiseizure medication in children with epilepsy M Yıldırım, Ö Bektaş, AT Kartal, NY Süt, S Teber Epilepsy & Behavior 134, 108779, 2022 | 5 | 2022 |
| Status dystonicus associated with CLN8 disease M Yıldırım, E Köse, AM Keçeli, Ö Balasar, N Şimşek Brain and Development 43 (4), 571-575, 2021 | 5 | 2021 |
| Management of neurological problems in children on home invasive mechanical ventilation Y Sayar, M Yıldırım, S Teber Pediatric pulmonology 59 (8), 2196-2202, 2024 | 4 | 2024 |
| Optic neuritis in Turkish children and adolescents: A multicenter retrospective study MÇ Direk, Ş Besen, İ Öncel, C Günbey, O Özdoğan, LT Orgun, S Sahin, ... Multiple Sclerosis and Related Disorders 81, 105149, 2024 | 4 | 2024 |
| Intracranial calcification associated with 3-methylcrotonyl-CoA carboxylase deficiency S Şahin, M Yıldırım, Ö Bektaş, İ Sürücü Kara, AC Ceylan, S Teber Molecular Syndromology 12 (6), 393-398, 2021 | 4 | 2021 |
| A homozygous mutation in the POMT2 gene in four siblings with limb-girdle muscular dystrophy 2N M Yıldırım, HK Eker, MT Doğan Turkish Archives of Pediatrics 56 (1), 68, 2021 | 4 | 2021 |
| Jeune sendromu (asfiktik torasik displazi): Olgu sunumu Ş Uçar, P Zorlu, G Şahin, M Yıldırım, E Uşak Tüberküloz ve Toraks Dergisi 57 (4), 413-6, 2009 | 4 | 2009 |
