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 | 71 | 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 |
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 | 5 | 2020 |
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 |
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 | 4 | 2019 |
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 |
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 |
A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity N Fahmy, K Müller, PM Andersen, SL Marklund, M Otto, AC Ludolph, ... Journal of Neurology 270 (3), 1770-1773, 2023 | 2 | 2023 |
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 |