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Seidahmed, Mohammed Zein
35  Ergebnisse:
Personensuche X
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1

A novel syndrome of lethal familial hyperekplexia associate..:

Seidahmed, Mohammed Zein ; Salih, Mustafa A ; Abdulbasit, Omer B...
BMC Neurology.  12 (2012)  1 - p. , 2012
Link: https://doi.org/10.1186/..
 
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2

Ritscher–Schinzel (cranio‐cerebello‐cardiac, 3C) syndrome: ..:

Seidahmed, Mohammed Zein ; Alkuraya, Fowzan S. ; Shaheed, Meeralebbae...
American Journal of Medical Genetics Part A.  155 (2011)  6 - p. 1393-1397 , 2011
Link: https://doi.org/10.1002/..
 
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3

Variable disease severity in Saudi Arabian and Sudanese fam..:

Di Blasi, Claudia ; Bellafiore, Emanuela ; Salih, Mustafa AM...
BMC Research Notes.  4 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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4

Variable disease severity in Saudi Arabian and Sudanese fam..:

Di Blasi, Claudia ; Bellafiore, Emanuela ; Salih, Mustafa AM...
http://www.biomedcentral.com/1756-0500/4/534.  , 2011
Link: http://www.biomedcentral..
 
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5

Variable disease severity in Saudi Arabian and Sudanese fam..:

Di Blasi Claudia ; Bellafiore Emanuela ; Salih Mustafa AM...
http://www.biomedcentral.com/1756-0500/4/534.  , 2011
Link: https://doi.org/10.1186/..
 
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6

Clinical, genetic, and functional characterization of the g..:

Aboheimed, Ghada I. ; AlRasheed, Maha M. ; Almudimeegh, Sultan...
Journal of Biological Chemistry.  298 (2022)  7 - p. 102018 , 2022
Link: https://doi.org/10.1016/..
 
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7

Hereditary Hyperekplexia in Saudi Arabia:

Aldhilan, Amal ; Alhakeem, Afnan ; Al Hajjaj, Sumayah...
Pediatric Neurology.  134 (2022)  - p. 78-82 , 2022
Link: https://doi.org/10.1016/..
 
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8

GABA transaminase deficiency. Case report and literature re..:

Oshi, Amira ; Alfaifi, Abdullah ; Seidahmed, Mohammed Z....
Clinical Case Reports.  9 (2021)  3 - p. 1295-1298 , 2021
Link: https://doi.org/10.1002/..
 
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9

Recessive mutations in SCYL2 cause a novel syndromic form o..:

Seidahmed, Mohammed Zain ; Al-Kindi, Adila ; Alsaif, Hessa S....
Human Genetics.  139 (2020)  4 - p. 513-519 , 2020
Link: https://doi.org/10.1007/..
 
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10

Ancient founder mutation in RUBCN: a second unrelated famil..:

Seidahmed, Mohammed Z. ; Hamad, Muddathir H. ; AlBakheet, Albandary...
BMC Neurology.  20 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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11

Confirming the involvement of PIEZO2 in the etiology of Mar..:

Seidahmed, Mohammed Zain ; Maddirevula, Sateesh ; Miqdad, Abeer M....
American Journal of Medical Genetics Part A.  185 (2020)  3 - p. 945-948 , 2020
Link: https://doi.org/10.1002/..
 
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12

Autozygome and high throughput confirmation of disease gene..:

Maddirevula, Sateesh ; Alzahrani, Fatema ; Al-Owain, Mohammed...
Genetics in Medicine.  21 (2019)  3 - p. 736-742 , 2019
Link: https://doi.org/10.1038/..
 
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13

The many faces of peroxisomal disorders: Lessons from a lar..:

Alshenaifi, Jumanah ; Ewida, Nour ; Anazi, Shams...
Clinical Genetics.  95 (2018)  2 - p. 310-319 , 2018
Link: https://doi.org/10.1111/..
 
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14

Expanding the phenome and variome of skeletal dysplasia:

Maddirevula, Sateesh ; Alsahli, Saud ; Alhabeeb, Lamees...
Genetics in Medicine.  20 (2018)  12 - p. 1609-1616 , 2018
Link: https://doi.org/10.1038/..
 
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15

The genetic landscape of familial congenital hydrocephalus:

Shaheen, Ranad ; Sebai, Mohammed Adeeb ; Patel, Nisha...
Annals of Neurology.  81 (2017)  6 - p. 890-897 , 2017
Link: https://doi.org/10.1002/..
 
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