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Elsayed, Liena, E O
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1

Bi-allelic PRRT2 variants may predispose to Self-limited Fa..:

Koko, Mahmoud ; Elseed, Maha A. ; Mohammed, Inaam N....
European Journal of Human Genetics.  , 2024
Link: https://doi.org/10.1038/..
 
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2

A novel missense variant in the ATPase domain of ATP8A2 and..:

Flannery, Kyle P. ; Safwat, Sylvia ; Matsell, Eli...
Neurogenetics.  , 2024
Link: https://doi.org/10.1007/..
 
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3

PLA2G6‐associated late‐onset parkinsonism in a Sudanese fam..:

Bakhit, Yousuf ; Tesson, Christelle ; Ibrahim, Mohamed O....
Annals of Clinical and Translational Neurology.  10 (2023)  6 - p. 983-989 , 2023
Link: https://doi.org/10.1002/..
 
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4

Machado-Joseph disease in a Sudanese family links East Afri..:

Martins, Sandra ; Yahia, Ashraf ; Costa, Inês P. D....
Human Genetics.  142 (2023)  12 - p. 1747-1754 , 2023
Link: https://doi.org/10.1007/..
 
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5

Intrafamilial and interfamilial heterogeneity of PINK1-asso..:

Bakhit, Yousuf ; Ibrahim, Mohamed O. ; Tesson, Christelle...
Parkinsonism & Related Disorders.  111 (2023)  - p. 105401 , 2023
Link: https://doi.org/10.1016/..
 
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6

Methylation of alpha-synuclein in a Sudanese cohort:

Bakhit, Yousuf ; Schmitt, Ina ; Hamed, Ahlam...
Parkinsonism & Related Disorders.  101 (2022)  - p. 6-8 , 2022
Link: https://doi.org/10.1016/..
 
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7

A novel homozygous mutation in TRAPPC9 gene causing autosom..:

Amin, Mutaz ; Vignal, Cedric ; Eltaraifee, Esraa...
BMC Medical Genomics.  15 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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8

Case Report: A New Family With Pontocerebellar Hypoplasia 1..:

Amin, Mutaz ; Vignal, Cedric ; Hamed, Ahlam A. A....
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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9

Insights into Clinical, Genetic, and Pathological Aspects o..:

Elsayed, Liena E. O. ; Eltazi, Isra Zuhair ; Ahmed, Ammar E..
Frontiers in Molecular Biosciences.  8 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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10

Novel variants causing megalencephalic leukodystrophy in Su..:

Amin, Mutaz ; Vignal, Cedric ; Hamed, Ahlam A. A....
Journal of Human Genetics.  67 (2021)  3 - p. 127-132 , 2021
Link: https://doi.org/10.1038/..
 
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11

Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:

Yahia, Ashraf ; Elsayed, Liena E. O. ; Valter, Remi...
Frontiers in Neurology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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12

Novel Homozygous Missense Mutation in the ARG1 Gene in a La..:

Elsayed, Liena E. O. ; Mohammed, Inaam N. ; Hamed, Ahlam A. A....
Frontiers in Neurology.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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13

Case report of a novel homozygous splice site mutation in P..:

Elsayed, Liena E. O. ; Mohammed, Inaam N. ; Hamed, Ahlam A. A....
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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14

Hereditary spastic paraplegias: identification of a novel S..:

Elsayed, Liena E O ; Mohammed, Inaam N ; Hamed, Ahlam A A...
European Journal of Human Genetics.  25 (2016)  1 - p. 100-110 , 2016
Link: https://doi.org/10.1038/..
 
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15

PLA2G6-associated late-onset parkinsonism in a Sudanese fam..:

Bakhit, Yousuf ; Tesson, Christelle O ; Ibrahim, Mohamed...
Annals of Clinical and Translational Neurology, 2023, 10:6, s. 983-989.  , 2023
Link: http://urn.kb.se/resolve..
 
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