Mustafa A Salih
5PUBLICATIONS
58CO-AUTHORS
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Publications (5)
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|Nov 24, 2025
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.Pritha Bisarad, Yung-Chun Wang, Peter T Skidmore
|Nov 28, 2024
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome.Efil Bayam, Peggy Tilly, Stephan C Collins
|Feb 05, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.Mahmoud Koko, Maha A Elseed, Inaam N Mohammed
|Apr 03, 2023
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations.Ashraf Yahia, Ahlam A A Hamed, Inaam N Mohamed
|Feb 07, 2017
Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan.Inaam N Mohamed, Maha A Elseed, Ahlam A Hamed
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Frequent Collaborators
2 joint publications
Ashraf Yahia
2 joint publications
Mahmoud Koko
2 joint publications
Giovanni Stevanin
2 joint publications
Sateesh Maddirevula
1 joint publications
Abdelgadir H Osman
1 joint publications
Ali A Elhassan
1 joint publications
Mohamed Nimir
1 joint publications
Esraa S A Alfadul
1 joint publications
Muntaser E Ibrahim
1 joint publications
Inaam N Mohammed
