I agree that this site is using cookies. You can find further informations here.
X
Alowain, Mohammed Abdulaziz
94  results:
Search for persons X
?
1

Tectocerebellar dysraphia with occipital encephalocele: a p..:

Nicolas-Jilwan, Manal ; Al-Ahmari, Ahmed Nasser ; Alowain, Mohammed Abdulaziz..
Child's Nervous System.  35 (2019)  7 - p. 1257-1261 , 2019
Link: https://doi.org/10.1007/..
 
?
2

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/..
 
?
3

Novel homozygous DEAF1 variant suspected in causing white m..:

Faqeih, Eissa A. ; Al‐Owain, Mohammed ; Colak, Dilek...
American Journal of Medical Genetics Part A.  164 (2014)  6 - p. 1565-1570 , 2014
Link: https://doi.org/10.1002/..
 
?
4

Clinical and biochemical features associated with BCS1L mut..:

Al‐Owain, Mohammed ; Colak, Dilek ; Albakheet, Albandary...
Journal of Inherited Metabolic Disease.  36 (2012)  5 - p. 813-820 , 2012
Link: https://doi.org/10.1007/..
 
?
5

Emergency management of critically ill adult patients with ..:

Sulaiman, Raashda A. ; Alali, Abdulaziz ; Hosaini, Sulaiman...
The American Journal of Emergency Medicine.  55 (2022)  - p. 138-142 , 2022
Link: https://doi.org/10.1016/..
 
?
6

Phenotypical spectrum of cerebellar ataxia associated with ..:

Kaya, Namik ; Aldhalaan, Hesham ; Al-Younes, Banan...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  156 (2011)  7 - p. 826-834 , 2011
Link: https://doi.org/10.1002/..
 
?
7

Lessons Learned from Large-Scale, First-Tier Clinical Exome..:

Monies, Dorota ; Abouelhoda, Mohammed ; Assoum, Mirna...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817532/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
?
8

Identification of the TTC26 Splice Variant in a Novel Compl..:

Alfadhel, Majid ; Umair, Muhammad ; Almuzzaini, Bader...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215951/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
?
9

Knowledge, Attitude, and Practice of Organ Donation Among t..:

Almutairi, Ahmed H ; Alhassan, SultanA ; Alrajeh, SaudA...
Cureus.  , 2024
Link: https://doi.org/10.7759/..
 
?
10

Clinical and Molecular Spectrum of Autosomal Recessive CA8‐..:

Kaiyrzhanov, Rauan ; Ortigoza‐Escobar, Juan Darío ; Stringer, Brett W....
Movement Disorders.  39 (2024)  6 - p. 983-995 , 2024
Link: https://doi.org/10.1002/..
 
?
11

Clinical and molecular features of four families with CLDN1..:

Qudair, Ahmad ; Hussein, Maged ; Alowain, Mohammed...
European Journal of Medical Genetics.  66 (2023)  12 - p. 104886 , 2023
Link: https://doi.org/10.1016/..
 
?
12

Novel biallelic variants expand the phenotype of NAA20‐rela..:

D'Onofrio, Gianluca ; Cuccurullo, Claudia ; Larsen, Silje Kathrine...
Clinical Genetics.  104 (2023)  3 - p. 371-376 , 2023
Link: https://doi.org/10.1111/..
 
?
13

ZNFX1 Deficiency in a Child with Interstitial Pneumonitis a..:

Al-Saud, Bandar ; Al-Mogarri, Ibrahim ; Alajlan, Huda...
Journal of Clinical Immunology.  43 (2023)  7 - p. 1529-1532 , 2023
Link: https://doi.org/10.1007/..
 
?
14

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/..
 
?
15

Genetic basis of pulmonary arterial hypertension: a prospec..:

Aldalaan, Abdullah M. ; Ramzan, Khushnooda ; Saleemi, Sarfraz A....
Pulmonary Circulation.  11 (2021)  3 - p. 1-8 , 2021
Link: https://doi.org/10.1177/..
 
1-15