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Elseed, Maha A.
60
results:
Search for persons
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Format
Online (60)
Mediatypes
Articles (Online) (23)
OpenAccess-fulltext (37)
Sorted by: Relevance
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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/..
?
2
Functional abilities, respiratory and cardiac function in a..:
Schiava, Marianela
;
Lofra, Robert Muni
;
Bourke, John P.
...
European Journal of Neurology. 31 (2024) 6 - p. , 2024
Link:
https://doi.org/10.1111/..
?
3
Disease-associated comorbidities, medication records and an..:
Schiava, Marianela
;
Lofra, Robert Muni
;
Bourke, John P.
...
Neuromuscular Disorders. 41 (2024) - p. 8-19 , 2024
Link:
https://doi.org/10.1016/..
?
4
266th ENMC International Workshop: Remote delivery of clini..:
Alfano, Lindsay N.
;
James, Meredith K.
;
Ramdharry, Gita M.
...
Neuromuscular Disorders. 33 (2023) 4 - p. 339-348 , 2023
Link:
https://doi.org/10.1016/..
?
5
Clinical phenotyping and genetic diagnosis of a large cohor..:
Yahia, Ashraf
;
Hamed, Ahlam A. A.
;
Mohamed, Inaam N.
...
European Journal of Human Genetics. , 2023
Link:
https://doi.org/10.1038/..
?
6
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/..
?
7
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/..
?
8
Genetic diagnosis in Sudanese and Tunisian families with sy..:
Yahia, Ashraf
;
Ayed, Ikhlas Ben
;
Hamed, Ahlam A.
...
Annals of Human Genetics. 86 (2022) 4 - p. 181-194 , 2022
Link:
https://doi.org/10.1111/..
?
9
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/..
?
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
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/..
?
13
A children's epilepsy diagnosis aid: Development and early ..:
Mohamed, Inaam N.
;
Mohamed, Ruwa A.F.
;
Hamed, Ahlam
..
Epilepsy & Behavior. 121 (2021) - p. 108062 , 2021
Link:
https://doi.org/10.1016/..
?
14
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/..
?
15
Intelligence quotient (IQ) among children with epilepsy: Na..:
Mohamed, Inaam N.
;
Osman, Abdelgadir H.
;
Mohamed, Somia
...
Epilepsy & Behavior. 103 (2020) - p. 106813 , 2020
Link:
https://doi.org/10.1016/..
1-15