Ali A. Elhassan

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.

Methylation of alpha-synuclein in a Sudanese cohort.

U. Wüllner, I. Schmitt, L. Elsayed, 2022, Parkinsonism & related disorders.