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
Almass, Rawan
30
results:
Search for persons
X
Format
Online (30)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (17)
Sorted by: Relevance
Sorted by: Year
?
1
SHQ1-associated neurodevelopmental disorder: Report of the ..:
AlHargan, Aljouhra
;
AlMuhaizea, Mohammed A.
;
Almass, Rawan
...
Human Genome Variation. 10 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
2
A Novel Homozygous Founder Variant of RTN4IP1 in Two Consan..:
Aldosary, Mazhor
;
Alsagob, Maysoon
;
AlQudairy, Hanan
...
Cells. 11 (2022) 19 - p. 3154 , 2022
Link:
https://doi.org/10.3390/..
?
3
Genetics of ataxia telangiectasia in a highly consanguineou..:
Al‐Muhaizea, Mohammed A.
;
Aldeeb, Hanouf
;
Almass, Rawan
...
Annals of Human Genetics. 86 (2021) 1 - p. 34-44 , 2021
Link:
https://doi.org/10.1111/..
?
4
SLC25A42‐associated mitochondrial encephalomyopathy: Report..:
Aldosary, Mazhor
;
Baselm, Shahad
;
Abdulrahim, Maha
...
JIMD Reports. 60 (2021) 1 - p. 75-87 , 2021
Link:
https://doi.org/10.1002/..
?
5
Bi-allelic variants in HOPS complex subunit VPS41 cause cer..:
Sanderson, Leslie E
;
Lanko, Kristina
;
Alsagob, Maysoon
...
Brain. 144 (2021) 3 - p. 769-780 , 2021
Link:
https://doi.org/10.1093/..
?
6
Hematological findings associated with tubulin‐folding cofa..:
Al‐Bakheet, Albandary
;
Tohary, Mohamed
;
Khan, Sameena
...
Clinical Genetics. 99 (2021) 5 - p. 724-731 , 2021
Link:
https://doi.org/10.1111/..
?
7
Truncating mutations in YIF1B cause a progressive encephalo..:
AlMuhaizea, Mohammed
;
AlMass, Rawan
;
AlHargan, Aljouhra
...
Acta Neuropathologica. 139 (2020) 4 - p. 791-794 , 2020
Link:
https://doi.org/10.1007/..
?
8
Pyrostigmine therapy in a patient with VAMP1-related congen..:
Al-Muhaizea, Mohammad A.
;
AlQuait, Laila
;
AlRasheed, Afnan
...
Neuromuscular Disorders. 30 (2020) 7 - p. 611-615 , 2020
Link:
https://doi.org/10.1016/..
?
9
Further delineation of the phenotypic spectrum ofISCA2 defe..:
Alfadhel, Majid
;
Nashabat, Marwan
;
Alrifai, Muhammad Talal
...
European Journal of Paediatric Neurology. 22 (2018) 1 - p. 46-55 , 2018
Link:
https://doi.org/10.1016/..
?
10
Identification of novel genomic imbalances in Saudi patient..:
Al-Hassnan, Zuhair N.
;
Albawardi, Waad
;
Almutairi, Faten
...
Molecular Cytogenetics. 11 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
11
A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebel..:
Al-Muhaizea, Mohammad A.
;
AlMutairi, Faten
;
Almass, Rawan
...
The Cerebellum. 17 (2017) 3 - p. 276-285 , 2017
Link:
https://doi.org/10.1007/..
?
12
A new association between CDK5RAP2 microcephaly and congeni..:
Alfares, Ahmed
;
Alhufayti, Ibtihal
;
Alsubaie, Lamia
...
Annals of Human Genetics. 82 (2017) 3 - p. 165-170 , 2017
Link:
https://doi.org/10.1111/..
?
13
Molecular and clinical spectra of FBXL4 deficiency:
El-Hattab, Ayman W.
;
Dai, Hongzheng
;
Almannai, Mohammed
...
Human Mutation. 38 (2017) 12 - p. 1649-1659 , 2017
Link:
https://doi.org/10.1002/..
?
14
SHQ1-associated neurodevelopmental disorder: Report of the ..:
AlHargan, Aljouhra
;
AlMuhaizea, Mohammed A
;
AlMass, Rawan
...
https://www.nature.com/articles/s41439-023-00234-z. , 2023
Link:
http://hdl.handle.net/10..
?
15
SHQ1-associated neurodevelopmental disorder: Report of the ..:
AlHargan, Aljouhra
;
AlMuhaizea, Mohammed A
;
Almass, Rawan
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944922/. , 2023
Link:
http://www.ncbi.nlm.nih...
1-15