Liena E. O. Elsayed

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

Novel Spg57 Variant, Hereditary Spastic Paraplegias, Medicine +10

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 · 26 citations

Mendelian Disorder, Genetic Disorder, Genetics +6

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 · 19 citations · Full text

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 · 18 citations · Full text

Genetics, Genetic Epidemiology, Disease Gene Identification +27

Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family

Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. Hamed et al. · BMC Medical Genetics · 2018 · 13 citations · Full text