Shaimaa Taha

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

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

Ashraf Yahia, Ahlam A. Hamed, Inaam N. Mohamed et al. · European Journal of Human Genetics · 2023 · 13 citations · Full text

Life Sciences, Genetics, Neurology +17

A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

Ashraf Yahia, Zhefan Stephen Chen, Ammar Ahmed et al. · BMC Neurology · 2021 · 12 citations · Full text

Life Sciences, Genetics, Neurology +17

MDS-Related Anemia Is Associated with Impaired Quality of Life but Improvement Is Not Always Achieved by Increased Hemoglobin Level

Yael Haring, Noa Goldschmidt, Shaimaa Taha et al. · Journal of Clinical Medicine · 2023 · 10 citations · Full text

Medicine, Hematology, Internal Medicine +17