Genetic and phenotypic characterization of complex hereditary spastic paraplegia E Kara, A Tucci, C Manzoni, DS Lynch, M Elpidorou, C Bettencourt, ... Brain 139 (7), 1904-1918, 2016 | 216 | 2016 |
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 189 | 2019 |
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes A Cortese, Y Zhu, AP Rebelo, S Negri, S Courel, L Abreu, CJ Bacon, ... Nature genetics 52 (5), 473-481, 2020 | 120 | 2020 |
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ... Annals of Neurology 86 (2), 225-240, 2019 | 69 | 2019 |
An update on advances in magnetic resonance imaging of multiple system atrophy V Chelban, M Bocchetta, S Hassanein, NA Haridy, H Houlden, JD Rohrer Journal of neurology 266, 1036-1045, 2019 | 60 | 2019 |
Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14 V Chelban, S Wiethoff, BK Fabian‐Jessing, NA Haridy, A Khan, ... Movement Disorders 33 (7), 1119-1129, 2018 | 40 | 2018 |
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia M Wiessner, R Maroofian, MY Ni, A Pedroni, JS Müller, R Stucka, C Beetz, ... Brain 144 (5), 1422-1434, 2021 | 28 | 2021 |
Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination V Chelban, M Alsagob, K Kloth, A Chirita‐Emandi, J Vandrovcova, ... European journal of neurology 27 (2), 334-342, 2020 | 22 | 2020 |
Severe axonal neuropathy is a late manifestation of SPG11 A Manole, V Chelban, NA Haridy, SA Hamed, A Berardo, MM Reilly, ... Journal of neurology 263, 2278-2286, 2016 | 17 | 2016 |
Relationship between Attention Deficit Hyperactivity Disorder and epilepsy: a literature review GK Ahmed, AM Darwish, H Khalifa, NA Haridy The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 58 (1), 52, 2022 | 12 | 2022 |
Sequencing analysis of the SCA6 CAG expansion excludes an influence of repeat interruptions on disease onset S Wiethoff, E O’Connor, NA Haridy, S Nethisinghe, N Wood, P Giunti, ... Journal of Neurology, Neurosurgery & Psychiatry 89 (11), 1226-1227, 2018 | 10 | 2018 |
Effects of transcranial direct current stimulation in pain and opioid consumption after spine surgery R Hamed, EM Khedr, NA Haridy, KO Mohamed, S Elsawy European Journal of Pain 26 (7), 1594-1604, 2022 | 4 | 2022 |
Bridging the gap: associations between gut microbiota and psychiatric disorders GK Ahmed, HKA Ramadan, K Elbeh, NA Haridy Middle East Current Psychiatry 31 (1), 2, 2024 | 3 | 2024 |
Myasthenia gravis with achalasia secondary to thymoma: a case report and literature review NA Haridy, EM Khedr, AM Hasan, AA Maghraby, E Abdelmohsen, ... The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 59 (1), 34, 2023 | 1 | 2023 |
Impact of COVID-19 Pandemic on the Care of People with Epilepsy and Predictors of Epilepsy Worsening: Aswan/Upper Egypt Hospital-based study EM Khedr, NA Haridy, GK Ahmed, MN Othman, AS Elsoghier, ... | | 2024 |
Short-Term Therapeutic Effect of Repetitive Transcranial Magnetic Stimulations of Sleep Disorders in Parkinson’s Disease: A Randomized Clinical Trial (Pilot Study) EM Khedr, GK Ahmed, MA Korayem, SASH Elamary, MM El-kholy, ... Brain Sciences 14 (6), 556, 2024 | | 2024 |
Determining Optimal Cut-Off Value For Ultrasound-Measured Median Nerve Cross-Sectional Area For Diagnosis Of Carpal Tunnel Syndrome In A Sample Of Egyptian Population SSA Abd El Maged, KO Mohamed, HM Farweez, NA Haridy Journal of Current Medical Research and Practice 9 (2), 9-18, 2024 | | 2024 |
Impact of COVID-19 Pandemic on Patients with Tension-Type Headache BM Al Fawal, EM Khedr, NA Haridy, AS Elsoghier, MN Othman, ... Aswan University Medical Journal, 2024 | | 2024 |
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders J Sidpra, S Sudhakar, A Biswas, F Massey, V Turchetti, T Lau, E Cook, ... Brain, awae056, 2024 | | 2024 |
Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders DG Calame, JH Wong, P Panda, DT Nguyen, NCP Leong, R Sangermano, ... medRxiv, 2024 | | 2024 |