I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Mohammed, Inaam N.
93
results:
Format
Online (93)
Mediatypes
Articles (Online) (72)
Bookchapter (Online) (2)
OpenAccess-fulltext (19)
Sorted by: Relevance
Sorted by: Year
?
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
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/..
?
3
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/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
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/..
?
8
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/..
?
9
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/..
?
10
A Novel Nonsense Mutation in DNAJC6Expands the Phenotype of..:
Elsayed, Liena Elbaghir Omer
;
Drouet, Valérie
;
Usenko, Tatiana
...
Annals of Neurology. 79 (2016) 2 - p. 335-337 , 2016
Link:
https://doi.org/10.1002/..
?
11
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/..
?
12
Research: Prevalence of neural tube defects Khartoum, Sudan..:
Omer, Ilham M.
;
Abdullah, Osman M.
;
Mohammed, Inaam N.
.
BMC Research Notes. 9 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
?
13
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..
?
14
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..
?
15
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..
1-15
