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Gleeson, Ghada
27  Ergebnisse:
Personensuche X
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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/..
 
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2

Efficiency and Resource Allocation in Government Hospitals ..:

Alshehri, Abdulrahman ; Balkhi, Bander ; Gleeson, Ghada.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531133/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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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/..
 
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7

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/..
 
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8

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/..
 
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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/..
 
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10

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/..
 
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11

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..
 
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12

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/..
 
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13

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/..
 
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14

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/..
 
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15

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/..
 
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