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Elsayed, Liena E.
79
results:
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Online (79)
Mediatypes
Articles (Online) (28)
Bookchapter (Online) (1)
OpenAccess-fulltext (50)
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?
1
An identical‐by‐descent novel splice‐donor variant inPRUNE1..:
Koko, Mahmoud
;
Yahia, Ashraf
;
Elsayed, Liena E.
...
Annals of Human Genetics. 85 (2021) 5 - p. 186-195 , 2021
Link:
https://doi.org/10.1111/..
?
2
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/..
?
3
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/..
?
4
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/..
?
5
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/..
?
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/..
?
7
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/..
?
8
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
15
PLA2G6-associated late-onset parkinsonism in a Sudanese fam..:
Bakhit, Yousuf
;
Tesson, Christelle
;
Group, Sudanese Parkinson's Disease Study
...
info:eu-repo/semantics/altIdentifier/issn/2328-9503. , 2023
Link:
https://pub.dzne.de/reco..
1-15