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Nourelhoda A. Haridy
Nourelhoda A. Haridy
Lecturer, Department of Neurology and Psychiatry , Faculty of Medicine, ِِAssiut University
Verified email at aun.edu.eg
Title
Cited by
Cited by
Year
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
2282016
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
2242019
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
1402020
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
732019
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
732019
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
462018
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
362021
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
282020
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
192016
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
162022
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
112018
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
82024
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 147 (8), 2775-2790, 2024
72024
The role of infections and inflammation in schizophrenia: review of the evidence
GK Ahmed, HKA Ramadan, K Elbeh, NA Haridy
Middle East Current Psychiatry 31 (1), 9, 2024
72024
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
62022
Relationship between disability and psychiatric outcome in multiple sclerosis patients and its determinants
SS Hassan, ES Darwish, GK Ahmed, SR Azmy, NA Haridy
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery 59 (1), 1-14, 2023
32023
Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum
DG Calame, JH Wong, P Panda, DT Nguyen, NCP Leong, R Sangermano, ...
Genetics in Medicine 27 (1), 101273, 2025
22025
Predictors of long-term health-related quality of life in Guillain-Barre syndrome: A hospital-based study
EM Khedr, DM Mahmoud, GK Ahmed, NA Haridy
Clinical Neurology and Neurosurgery 235, 108026, 2023
22023
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
22023
Long-term outcomes of plasma exchange versus intravenous immunoglobulin for the treatment of Guillain-Barré syndrome: a double-blind, randomized clinical trial
NA Haridy, MM Shehab, EM Khedr
Restorative Neurology and Neuroscience 41 (5-6), 203-217, 2023
22023
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