Liena Elsayed
5PUBLICATIONS
20CO-AUTHORS
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Publications (5)
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|Feb 05, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.Mahmoud Koko, Maha A Elseed, Inaam N Mohammed
|Nov 13, 2023
Machado-Joseph disease in a Sudanese family links East Africa to Portuguese families and allows reestimation of ancestral age of the Machado lineage.Sandra Martins, Ashraf Yahia, Inês P D Costa
|Feb 19, 2021
A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report.Ashraf Yahia, Zhefan Stephen Chen, Ammar E Ahmed
|Oct 25, 2018
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 Elsayed, Arwa Babai
|May 10, 2018
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 A Hamed
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Frequent Collaborators
2 joint publications
Ashraf Yahia
2 joint publications
Mahmoud Koko
1 joint publications
Sandra Martins
1 joint publications
Inês P D Costa
1 joint publications
Rayan Abubaker
1 joint publications
Marc Corral-Juan
1 joint publications
Antoni Matilla-Dueñas
1 joint publications
Alexis Brice
1 joint publications
Alexandra Durr
1 joint publications
Laura P W Ranum
