S. Taha

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

G. Stevanin, A. Bakhiet, M. Ibrahim, 2023, European journal of human genetics : EJHG.

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

A. Brice, G. Stevanin, M. Salih, 2018, BMC Neurology.

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

G. Stevanin, Z. Chen, H. Chan, 2021, BMC Neurology.

Neonatal hypocalcemia and its relation to vitamin D and calcium supplementation

O. Zaki, A. Elsary, Alkassem A. Elgameel, 2018, Saudi medical journal.