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Elseed, Maha A.
24
results:
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?
1
Clinical phenotyping and genetic diagnosis of a large cohor..:
Yahia, Ashraf
;
Hamed, Ahlam, a A
;
Mohamed, Inaam, N
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-023-01344-6. , 2023
Link:
https://hal.sorbonne-uni..
?
2
Methylation of alpha-synuclein in a Sudanese cohort ; Parki..:
BAKHIT, Yousuf
;
SCHMITT, Ina
;
HAMED, Ahlam
...
1353-8020. , 2022
Link:
https://oskar-bordeaux.f..
?
3
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:
Yahia, Ashraf
;
Elsayed, Liena, E O
;
Valter, Remi
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2021.720201. , 2021
Link:
https://hal.sorbonne-uni..
?
4
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:
Yahia, Ashraf
;
Elsayed, Liena
;
Valter, Remi
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2021.720201. , 2021
Link:
https://hal.sorbonne-uni..
?
5
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:
Yahia, Ashraf
;
Elsayed, Liena, E O
;
Valter, Remi
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2021.720201. , 2021
Link:
https://hal.sorbonne-uni..
?
6
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor De..:
Yahia, Ashraf
;
Elsayed, Liena, E O
;
Valter, Remi
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2021.720201. , 2021
Link:
https://hal.sorbonne-uni..
?
7
Novel Homozygous Missense Mutation in the ARG1 Gene in a La..:
Elsayed, Liena
;
Mohammed, Inaam
;
Hamed, Ahlam
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.569996. , 2020
Link:
https://hal.sorbonne-uni..
?
8
Novel Homozygous Missense Mutation in the ARG1 Gene in a La..:
Elsayed, Liena, E O
;
Mohammed, Inaam, N
;
Hamed, Ahlam, a A
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.569996. , 2020
Link:
https://hal.sorbonne-uni..
?
9
Novel Homozygous Missense Mutation in the ARG1 Gene in a La..:
Elsayed, Liena, E O
;
Mohammed, Inaam, N
;
Hamed, Ahlam, a A
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.569996. , 2020
Link:
https://hal.sorbonne-uni..
?
10
Novel Homozygous Missense Mutation in the ARG1 Gene in a La..:
Elsayed, Liena, E O
;
Mohammed, Inaam, N
;
Hamed, Ahlam, a A
...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.569996. , 2020
Link:
https://hal.sorbonne-uni..
?
11
Case report of a novel homozygous splice site mutation in P..:
Elsayed, Liena, E O
;
Mohammed, Inaam, N
;
Hamed, Ahlam A. A
...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12881-018-0592-y. , 2018
Link:
https://hal.sorbonne-uni..
?
12
Case report of a novel homozygous splice site mutation in P..:
Elsayed, Liena, E O
;
Mohammed, Inaam, N
;
Hamed, Ahlam A. A
...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12881-018-0592-y. , 2018
Link:
https://hal.sorbonne-uni..
?
13
Case report of a novel homozygous splice site mutation in P..:
Elsayed, Liena
;
Mohammed, Inaam
;
Hamed, Ahlam A. A
...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12881-018-0592-y. , 2018
Link:
https://hal.sorbonne-uni..
?
14
Case report of a novel homozygous splice site mutation in P..:
Elsayed, Liena, E O
;
Mohammed, Inaam, N
;
Hamed, Ahlam A. A
...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12881-018-0592-y. , 2018
Link:
https://hal.sorbonne-uni..
?
15
A novel homozygous mutation in TRAPPC9 gene causing autosom..:
Mutaz Amin
;
Cedric Vignal
;
Esraa Eltaraifee
...
https://doi.org/10.1186/s12920-022-01354-1. , 2022
Link:
https://doi.org/10.1186/..
1-15
