| Change in presurgical diagnostic imaging evaluation affects subsequent pediatric epilepsy surgery outcome L Rubinger, C Chan, F D'Arco, R Moineddin, O Muthaffar, JT Rutka, ... Epilepsia 57 (1), 32-40, 2016 | 42 | 2016 |
| Rasmussen encephalitis: an update KC Cay-Martinez, RA Hickman, GM McKhann II, FA Provenzano, ... Seminars in neurology 40 (02), 201-210, 2020 | 41 | 2020 |
| Public awareness and attitudes toward epilepsy in Saudi Arabia is improving OY Muthaffar, MM Jan Neurosciences Journal 19 (2), 124-126, 2014 | 32 | 2014 |
| Reoperation after failed resective epilepsy surgery in children O Muthaffar, K Puka, L Rubinger, C Go, OC Snead, JT Rutka, E Widjaja Journal of Neurosurgery: Pediatrics 20 (2), 134-140, 2017 | 28 | 2017 |
| Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly MI Naseer, AA Abdulkareem, OY Muthaffar, S Sogaty, H Alkhatabi, ... Frontiers in pediatrics 8, 627122, 2021 | 22 | 2021 |
| Rasmussen encephalitis: response to early immunotherapy in a case of immune-mediated encephalitis Z Liba, O Muthaffar, J Tang, B Minassian, W Halliday, H Branson, ... Neuroimmunology & Neuroinflammation 2 (2), e69, 2015 | 17 | 2015 |
| Consensus statement on the management of duchenne muscular dystrophy in Saudi Arabia during the coronavirus disease 2019 pandemic AK Bamaga, F Alghamdi, N Alshaikh, W Altwaijri, FA Bashiri, K Hundallah, ... Frontiers in pediatrics 9, 629549, 2021 | 14 | 2021 |
| A cross-sectional study to evaluate the quality of life of caregivers for children with cerebral palsy AA Aman, B Baharoon, HJ Idrees, AM Taj, BA Alzahrani, OY Muthaffar Pharmacophore 12 (5-2021), 69-75, 2021 | 9 | 2021 |
| Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases Q Zaman, MA Khan, K Sahar, G Rehman, H Khan, M Rehman, ... Genes 14 (2), 328, 2023 | 7 | 2023 |
| Acute hemiplegia as a rare presentation of infantile Guillain-Barre syndrome OY Muthaffar, AA Mahmoud, AS Al-Saman Saudi Med J 35 (8), 861-864, 2014 | 7 | 2014 |
| Report of Hermansky–Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes Q Zaman, Sadeeda, M Anas, G Rehman, Q Khan, A Iftikhar, M Ahmad, ... Genes 14 (1), 145, 2023 | 6 | 2023 |
| Treating epilepsy with options other than antiepileptic medications OY Muthaffar Neurosciences Journal 25 (4), 253-261, 2020 | 6 | 2020 |
| The efficacy of non-fasting ketogenic diet protocol in the management of intractable epilepsy in pediatric patients: a single center study from Saudi Arabia H Alameen Ali, O Muthaffar, N AlKarim, H Kayyali, A Elmardenly, A Tamim, ... Journal of International Medical Research 50 (3), 03000605221081714, 2022 | 5 | 2022 |
| Valproic acid for children below 2 years of age with epilepsy OY Muthaffar, SM Almahmudi, MO Alrabghi, MMB Mahfouz, NS Alfawaz Neurosciences Journal 26 (4), 357-365, 2021 | 5 | 2021 |
| Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy MI Naseer, AA Abdulkareem, M Rasool, H Algahtani, OY Muthaffar, ... Frontiers in Pediatrics 10, 919996, 2022 | 4 | 2022 |
| Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi … MI Naseer, PN Pushparaj, AA Abdulkareem, OY Muthaffar Frontiers in Pediatrics 9, 829251, 2022 | 4 | 2022 |
| The utility of whole exome sequencing in diagnosing pediatric neurological disorders OY Muthaffar Balkan Journal of Medical Genetics 23 (2), 17-24, 2020 | 4 | 2020 |
| Pretreatment with troxerutin protects/improves neurological deficits in a mouse model of traumatic brain injury AAK Malik, W Ahmad, F Younas, H Badshah, S Alharazy, SU Rehman, ... Heliyon 9 (7), 2023 | 3 | 2023 |
| Evaluation of Health Science Students’ Health Fatalism and Perception Towards Patients With Epilepsy: A Cross-Sectional Global Study AS Alyazidi, OY Muthaffar, FA Alotibi, A Almubarak, L Tamai, ... Cureus 14 (10), 2022 | 3 | 2022 |
| Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease MI Naseer, AA Abdulkareem, PN Pushparaj, S Saharti, OY Muthaffar Frontiers in Pediatrics 10, 862722, 2022 | 3 | 2022 |
