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Frontiers in Molecular Biosciences|December 13, 2021
Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive OverviewLiena E O Elsayed, Isra Zuhair Eltazi, Ammar E Ahmed, et al.Saudi Medical Journal|January 25, 2006
Antimony-induced cerebellar ataxiaEltahir Awad G Khalil, Ammar E Ahmed, Ahmed M Musa, et al.BMC Neurology|February 19, 2021
A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case reportAshraf Yahia, Zhefan Stephen Chen, Ammar E Ahmed, et al.Paediatrics and International Child Health|February 7, 2017
Prevalence of epilepsy in 74,949 school children in Khartoum State, SudanInaam N Mohamed, Maha A Elseed, Ahlam A Hamed, et al.Frontiers in Neurology|November 8, 2021
Involvement of <i>ADGRV1</i> Gene in Familial Forms of Genetic Generalized EpilepsyMaha Dahawi, Mohamed S Elmagzoub, Elhami A Ahmed, et al.BMC Medical Genetics|May 10, 2018
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese familyLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.BMC Medical Genomics|November 9, 2022
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disabilityMutaz Amin, Cedric Vignal, Esraa Eltaraifee, et al.Frontiers in Neurology|November 16, 2020
Novel Homozygous Missense Mutation in the <i>ARG1</i> Gene in a Large Sudanese FamilyLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.Frontiers in Genetics|June 20, 2022
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From SudanMutaz Amin, Cedric Vignal, Ahlam A A Hamed, et al.Journal of Human Genetics|September 10, 2021
Novel variants causing megalencephalic leukodystrophy in Sudanese familiesMutaz Amin, Cedric Vignal, Ahlam A A Hamed, et al.Pageof 2