| Selenoprotein N‐related myopathy: a retrospective natural history study to guide clinical trials A Silwal, A Sarkozy, M Scoto, D Ridout, A Schmidt, A Laverty, ... Annals of Clinical and Translational Neurology 7 (11), 2288-2296, 2020 | 20 | 2020 |
| Neuralgic amyotrophy in children F Al‐Ghamdi, PS Ghosh Muscle & nerve 57 (6), 932-936, 2018 | 15 | 2018 |
| Spectrum of nondystrophic skeletal muscle channelopathies in children F Al-Ghamdi, BT Darras, PS Ghosh Pediatric Neurology 70, 26-33, 2017 | 15 | 2017 |
| Spectrum of neuromuscular disorders with HyperCKemia from a tertiary care pediatric neuromuscular center F Al-Ghamdi, BT Darras, PS Ghosh Journal of Child Neurology 33 (6), 389-396, 2018 | 14 | 2018 |
| 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 | 12 | 2021 |
| SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population A Mir, M Almudhry, F Alghamdi, R Albaradie, M Ibrahim, F Aldurayhim, ... Human Genetics 141, 81-99, 2022 | 11 | 2022 |
| Hepatic encephalopathy coexists with acquired chronic hepatocerebral degeneration FZ Huang, X Hou, TQ Zhou, S Chen Neurosciences Journal 20 (3), 277-279, 2015 | 10 | 2015 |
| MYL2-associated congenital fiber-type disproportion and cardiomyopathy with variants in additional neuromuscular disease genes; the dilemma of panel testing M Marttila, W Win, F Al-Ghamdi, HZ Abdel-Hamid, D Lacomis, AH Beggs Molecular Case Studies 5 (4), a004184, 2019 | 7 | 2019 |
| Case report: the genetic diagnosis of Duchenne muscular dystrophy in the Middle East F Alghamdi, A Al-Tawari, H Alrohaif, W Alshuaibi, H Mansour, ... Frontiers in Pediatrics 9, 716424, 2021 | 6 | 2021 |
| Air pollution and performance of the brain MO Aldraihem, F Al-Ghamdi, G Murtaza, S Bashir Arabian Journal of Geosciences 13, 1-10, 2020 | 6 | 2020 |
| Successful treatment of epilepsia partialis continua with perampanel: two pediatric cases A Mir, M Almudhry, F Al‐Ghamdi, S Bashir Epileptic Disorders 23 (2), 385-391, 2021 | 5 | 2021 |
| Comorbidities in Patients with COVID-19 and Their Impact on the Severity of the Disease S Bashir, S Moneeba, A Alghamdi, F Alghamdi, A Niaz, H Anan, I Kaleem Journal of Health and Allied Sciences NU 11 (01), 01-07, 2021 | 4 | 2021 |
| A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19 F Alghamdi, N Alshaikh, AK Bamaga, FA Bashiri, K Hundullah, A Alshehri, ... Neurosciences Journal 25 (3), 230-237, 2020 | 4 | 2020 |
| Gender and hemispheric differences in epilepsy diagnosed by voxel-based morphometry (VBM) method: a pilot cortical thickness study S Bashir, R Baradi, F Al-Ghamdi Acta Informatica Medica 27 (3), 171, 2019 | 4 | 2019 |
| Brain involvement in Charcot–Marie–Tooth disease due to ganglioside-induced differentiation associated-protein 1 mutation F Al-Ghamdi, I Anselm, E Yang, PS Ghosh Neuromuscular Disorders 27 (9), 848-851, 2017 | 3 | 2017 |
| STAC3-related myopathy: A Report of a Cohort of Seven Saudi Arabian Patients M Almomen, F Amer, F Alfaraj, PG Burgon, S Bashir, F Alghamdi Neuropediatrics, 2024 | 1 | 2024 |
| Identifying Clinical and Genetic Characteristics of Spinal Muscular Atrophy Patients and Families in Saudi Arabia A Alghamdi, S AlDossary, WA Alabdulqader, F Amer, M Ali, M Almomen, ... Cureus 15 (10), 2023 | 1 | 2023 |
| Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia AS AlSaman, F Al Ghamdi, AK Bamaga, N AlShaikh, M Al Muqbil, ... Frontiers in Pediatrics 10, 1020059, 2022 | 1 | 2022 |
| Epilepsy in patients with WWOX‐related epileptic encephalopathy (WOREE) syndrome R Al Baradie, A Mir, A Alsaif, M Ali, F Al Ghamdi, S Bashir, Y Howsawi Epileptic Disorders 24 (4), 697-712, 2022 | 1 | 2022 |
| Incidental finding of MEGDEL syndrome based on neuroimaging: case report SA Alshammari, FA Alghamdi, R Alhazmi, S Aldossary Case Reports in Neurology 13 (2), 429-433, 2021 | 1 | 2021 |
