Liena E. O. Elsayed

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

Thomas Roux, Mathieu Barbier, Mélanie Papin et al. · Genetics in Medicine · 2020 · 49 citations · Full text

Life Sciences, Genetics, Neurology +12

Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan

Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. Hamed et al. · European Journal of Human Genetics · 2016 · 35 citations · Full text

Life Sciences, Genetics, Neurology +7

Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

Edmund Cauley, Ahlam A. Hamed, Inaam N. Mohamed et al. · Neurogenetics · 2019 · 27 citations

Life Sciences, Genetics, Molecular Genetics +10

Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report

Ashraf Yahia, Liena E. O. Elsayed, Arwa Babai et al. · BMC Neurology · 2018 · 20 citations · Full text

Life Sciences, Genetics, Neurology +16

Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy

Maha Dahawi, Mohamed S. Elmagzoub, Elhami A. Ahmed et al. · Frontiers in Neurology · 2021 · 19 citations · Full text

Medicine, Genetics, Molecular Genetics +17