| Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness A Töpf, K Johnson, A Bates, L Phillips, KR Chao, EM England, ... Genetics in medicine 22 (9), 1478-1488, 2020 | 70 | 2020 |
| Egyptian experience in increasing utilization of reperfusion therapies in acute ischemic stroke MF Zakaria, H Aref, A Abd ElNasser, N Fahmy, MA Tork, MM Fouad, ... International Journal of Stroke 13 (5), 525-529, 2018 | 35 | 2018 |
| Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients RM El Sherif, NA Fahmy, I Nonaka, MA Etribi Acta Myologica 26 (3), 147, 2007 | 16 | 2007 |
| Assessment of diagnostic potential of some circulating microRNAs in amyotrophic lateral sclerosis patients, an Egyptian study R Soliman, NO Mousa, HR Rashed, RR Moustafa, N Hamdi, A Osman, ... Clinical Neurology and Neurosurgery 208, 106883, 2021 | 13 | 2021 |
| ACE gene in Egyptian ischemic stroke patients MA Mostafa, LM El-Nabiel, NA Fahmy, H Aref, E Shreef, F Abd El-Tawab, ... Journal of Stroke and Cerebrovascular Diseases 25 (9), 2167-2171, 2016 | 11 | 2016 |
| Arabic adaptation and validation of the revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R): Egyptian study HR Rashed, MA Tork, R Soliman, R Serag, N Fahmy Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22 (3-4), 220-222, 2021 | 10 | 2021 |
| Circulating MicroRNAs in Duchenne muscular dystrophy NO Mousa, A Abdellatif, N Fahmy, S Zada, H El-Fawal, A Osman Clinical neurology and neurosurgery 189, 105634, 2020 | 8 | 2020 |
| Global longitudinal strain detects subtle left ventricular systolic dysfunction in Duchenne muscular dystrophy patients and carriers M Shehta, MM Rayan, NA Fahmy, A Onsy, I Bastawy The Egyptian Heart Journal 73, 1-8, 2021 | 7 | 2021 |
| Whole-body muscle MRI characteristics of LAMA2-related congenital muscular dystrophy children: an emerging pattern HM Sakr, N Fahmy, NS Elsayed, H Abdulhady, TA El-Sobky, AM Saadawy, ... Neuromuscular Disorders 31 (9), 814-823, 2021 | 6 | 2021 |
| The clinical characteristics of patients with pre-existing leukoaraiosis compared to those without leukoaraiosis in acute ischemic stroke S Farag, FF Kenawy, HM Shokri, M Zakaria, H Aref, N Fahmi, N Khayat, ... Journal of Stroke and Cerebrovascular Diseases 30 (9), 105956, 2021 | 6 | 2021 |
| Neurofibromatosis type 1 and multiple sclerosis: genetically related diseases SM Elsayed, N Fahmy, R Gamal, M Wafik, D Zamzam, M Fahmy, ... Egyptian Journal of Medical Human Genetics 18 (3), 295-298, 2017 | 6 | 2017 |
| Ambulatory Duchenne muscular dystrophy children: Cross-sectional correlation between function, quantitative muscle ultrasound and MRI H Abdulhady, HM Sakr, NS Elsayed, TA El-Sobky, N Fahmy, AM Saadawy, ... Acta Myologica 41 (1), 1, 2022 | 5 | 2022 |
| Egyptian adaptation and validation of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-EG) R Soliman, HR Rashed, RR Moustafa, N Hamdi, MS Swelam, A Osman, ... Neurological Sciences 44 (6), 1871-1880, 2023 | 4 | 2023 |
| Vitamin D receptor gene polymorphism in patients with osteomalacic myopathy in Egypt HM Shokri, KO Mohamed, NA Fahmy, AO Mostafa, A Ghareeb Neurological Sciences 42, 1031-1037, 2021 | 4 | 2021 |
| Predictive value of haptoglobin genotype as a risk of cerebral vasospasm after aneurysmal subarachnoid hemorrhage AM Ateia, A Elbassiouny, SH El-Nabi, NA Fahmy, MH Ibrahim, ... Clinical Neurology and Neurosurgery 199, 106296, 2020 | 4 | 2020 |
| Borderzone infarction and small vessel disease in a sample of egyptian stroke patients: differences and similarities NM El Nahas, HM Aref, TK Alloush, NA Fahmy, KA Ahmed, ... Neurology India 69 (3), 670-675, 2021 | 3 | 2021 |
| Prediction of outcome in patients with Guillain Barre syndrome—An Egyptian study T Alloush, NA Fahmy, MM Fouad, HO Albaroudy, M Hamdy, HH Salem Neuroscience and Medicine 10 (3), 232-246, 2019 | 3 | 2019 |
| Site and degree of intracranial arterial stenosis in acute stroke patients with metabolic syndrome among a sample of Egyptian patients. TK Aloush, NA Fahmy, DA Elaidy, RS Abdel-Baki Egyptian Journal of Neurology, Psychiatry & Neurosurgery 53 (2), 2016 | 3 | 2016 |
| MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13. 2 genes with disease phenotype in Egyptian patients HA Hassan, NA Fahmy, NM El-Bagoury, NR Eissa, WE Sharaf-Eldin, ... Egyptian Journal of Medical Human Genetics 23 (1), 156, 2022 | 2 | 2022 |
| Cognitive and neurobehavioral patterns in a sample of Egyptian patients genetically diagnosed with Duchenne muscular dystrophy MM Sayed, NA Fahmy, MMM El Habiby, NSE Elsayed, SMKM El Bukhari, ... Middle East Current Psychiatry 29 (1), 76, 2022 | 2 | 2022 |
hany arefProfessor of neurology, Ain shams universityVerified email at med.asu.edu.eg
