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
Gleeson, Ghada
21
results:
Search for persons
X
Format
Online (21)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (8)
Sorted by: Relevance
Sorted by: Year
?
1
Efficiency and Resource Allocation in Government Hospitals ..:
Alshehri, Abdulrahman
;
Balkhi, Bander
;
Gleeson, Ghada
.
Healthcare. 11 (2023) 18 - p. 2513 , 2023
Link:
https://doi.org/10.3390/..
?
2
Efficiency and Resource Allocation in Government Hospitals ..:
Abdulrahman Alshehri
;
Bander Balkhi
;
Ghada Gleeson
.
https://www.mdpi.com/2227-9032/11/18/2513. , 2023
Link:
https://doi.org/10.3390/..
?
3
Non-manifesting AHI1 truncations indicate localized loss-of..:
Elsayed, Solaf M.
;
Phillips, Jennifer B.
;
Heller, Raoul
...
Human Molecular Genetics. 24 (2015) 9 - p. 2594-2603 , 2015
Link:
https://doi.org/10.1093/..
?
4
El‐Hattab‐Alkuraya syndrome caused by biallelic WDR45B path..:
Almannai, Mohammed
;
Marafi, Dana
;
Abdel‐Salam, Ghada M. H.
...
Clinical Genetics. 101 (2022) 5-6 - p. 530-540 , 2022
Link:
https://doi.org/10.1111/..
?
5
Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvat..:
Ghosh, Shereen G.
;
Lee, Sangmoon
;
Fabunan, Rudy
...
Genetics in Medicine. 23 (2021) 3 - p. 524-533 , 2021
Link:
https://doi.org/10.1038/..
?
6
Biallelic FRA10AC1 variants cause a neurodevelopmental diso..:
von Elsner, Leonie
;
Chai, Guoliang
;
Schneeberger, Pauline E
...
Brain. 145 (2021) 4 - p. 1551-1563 , 2021
Link:
https://doi.org/10.1093/..
?
7
A founder mutation in PEX12 among Egyptian patients in pero..:
Zaki, Maha S.
;
Issa, Mahmoud Y.
;
Thomas, Manal M.
...
Neurological Sciences. 42 (2020) 7 - p. 2737-2745 , 2020
Link:
https://doi.org/10.1007/..
?
8
PYCR2 Mutations cause a lethal syndrome of microcephaly and..:
Zaki, Maha S.
;
Bhat, Gifty
;
Sultan, Tipu
...
Annals of Neurology. 80 (2016) 1 - p. 59-70 , 2016
Link:
https://doi.org/10.1002/..
?
9
Extending the mutation spectrum for Galloway–Mowat syndrome..:
Rosti, Rasim O.
;
Dikoglu, Esra
;
Zaki, Maha S.
...
American Journal of Medical Genetics Part A. 170 (2016) 4 - p. 992-998 , 2016
Link:
https://doi.org/10.1002/..
?
10
Exome Sequencing Links Corticospinal Motor Neuron Disease t..:
Novarino, Gaia
;
Fenstermaker, Ali G.
;
Zaki, Maha S.
...
Science. 343 (2014) 6170 - p. 506-511 , 2014
Link:
http://www.jstor.org/sta..
?
11
A homozygous IER3IP1 mutation causes microcephaly with simp..:
Abdel‐Salam, Ghada M.H.
;
Schaffer, Ashleigh E.
;
Zaki, Maha S.
...
American Journal of Medical Genetics Part A. 158A (2012) 11 - p. 2788-2796 , 2012
Link:
https://doi.org/10.1002/..
?
12
New recessive syndrome of microcephaly, cerebellar hypoplas..:
Zaki, Maha S.
;
Salam, Ghada M. H. Abdel
;
Saleem, Sahar N.
...
American Journal of Medical Genetics Part A. 155 (2011) 12 - p. 3035-3041 , 2011
Link:
https://doi.org/10.1002/..
?
13
Identification of a novel recessive RELN mutation using a h..:
Zaki, Maha
;
Shehab, Marwa
;
El‐Aleem, Alice Abd
...
American Journal of Medical Genetics Part A. 143A (2007) 9 - p. 939-944 , 2007
Link:
https://doi.org/10.1002/..
?
14
AHI1 gene mutations cause specific forms of Joubert syndrom..:
Valente, Enza Maria
;
Brancati, Francesco
;
Silhavy, Jennifer L.
...
Annals of Neurology. 59 (2006) 3 - p. 527-534 , 2006
Link:
https://doi.org/10.1002/..
?
15
Exome sequencing links corticospinal motor neuron disease t..:
Novarino, Gaia
;
Fenstermaker, Ali
;
Zaki, Maha
...
info:eu-repo/semantics/altIdentifier/doi/10.1126/science.1247363. , 2014
Link:
https://research-explore..
1-15