Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ahmed N. Sahly"'
Autor:
Omar I. Saadah, Babajan Banaganapalli, Naglaa M. Kamal, Ahmed N. Sahly, Hadeel A. Alsufyani, Arif Mohammed, Aftab Ahmad, Khalidah Khalid Nasser, Jumana Y. Al-Aama, Noor Ahmad Shaik, Ramu Elango
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Alström syndrome (AS) is a very rare childhood disorder characterized by cardiomyopathy, progressive hearing loss and blindness. Inherited genetic variants of ALMS1 gene are the known molecular cause of this disease. The objective of thi
Externí odkaz:
https://doaj.org/article/1ca1765bc4174201ac05209968dce87a
Publikováno v:
European Journal of Paediatric Neurology. 44:46-50
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::011de8c84d7efc5b8592126adcfd994f
https://doi.org/10.1016/j.ejpn.2023.04.001
https://doi.org/10.1016/j.ejpn.2023.04.001
Autor:
Ahmed N Sahly, Robyn Whitney, Gregory Costain, Vann Chau, Hiroshi Otsubo, Ayako Ochi, Elizabeth J Donner, Jessie Cunningham, Kevin C Jones, Elysa Widjaja, George M Ibrahim, Puneet Jain
Publikováno v:
Seizure. 107:13-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb72d5f05b85de662953ae714c76cf4c
https://doi.org/10.1016/j.seizure.2023.03.004
https://doi.org/10.1016/j.seizure.2023.03.004
Autor:
Jumana Yousuf Al-Aama, Noor Ahmad Shaik, Babajan Banaganapalli, Mohammed A Salama, Omran Rashidi, Ahmed N Sahly, Mohammed O Mohsen, Harbi A Shawoosh, Hebah Ahmad Shalabi, Mohammad Al Edreesi, Sameer E Alharthi, Jun Wang, Ramu Elango, Omar I Saadah
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176664 (2017)
Celiac disease (CD), a multi-factorial auto-inflammatory disease of the small intestine, is known to occur in both sporadic and familial forms. Together HLA and Non-HLA genes can explain up to 50% of CD's heritability. In order to discover the missin
Externí odkaz:
https://doaj.org/article/131ed546c31e47ea901ac980cfc0d987
Publikováno v:
American journal of medical genetics. Part A. 188(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4f7af9a1434046e21179bc4878b7385
https://pubmed.ncbi.nlm.nih.gov/35920329
https://pubmed.ncbi.nlm.nih.gov/35920329
Publikováno v:
Human Genetics. 139:1575-1578
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed7244f5ea0abf0c99334b67e10e83e
https://doi.org/10.1007/s00439-020-02224-5
https://doi.org/10.1007/s00439-020-02224-5
Autor:
Babajan Banaganapalli, Omran M. Rashidi, Jumana Y. Al-Aama, Omar I. Saadah, Noor Ahmad Shaik, Ramu Elango, Preetha J. Shetty, Ahmed N. Sahly, Naglaa M. Kamal
Publikováno v:
Saudi Journal of Biological Sciences
Saudi Journal of Biological Sciences, Vol 27, Iss 1, Pp 271-278 (2020)
Saudi Journal of Biological Sciences, Vol 27, Iss 1, Pp 271-278 (2020)
Alström syndrome (AS, OMIM ID 203800) is a rare childhood multiorgan disorder, which is widely studied in non-Arab ethnic patients. The clinical and molecular basis of AS and the mode of disease inheritance in consanguineous Arab populations is not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1563e7f2f014a7a6eec0f7d2b4a813e7
https://doi.org/10.1016/j.sjbs.2019.09.006
https://doi.org/10.1016/j.sjbs.2019.09.006
Autor:
Salwa Hindawi, Galila F. Zaher, Ahmed A. Jamjoom, Soheir S. Adam, Maha A. Badawi, Ahmed N. Sahly, Thunayyan M. Almasoudi, Abdulrahman H. Ghoneim
Publikováno v:
Journal of King Abdulaziz University - Medical Sciences. 26:29-36
In the absence of specialized care centers for hemoglobinopathies in Saudi Arabia, there are insufficient data on prevalence of clinical complications in this population. This is a retrospective record review about the clinical complications associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6255d070258b0afc187c064623aa4bce
https://doi.org/10.4197/med.26-1.5
https://doi.org/10.4197/med.26-1.5
Autor:
Abdulhakeem S. Alamri, Ahmed N. Sahly, Ali H Aligiraigri, Noor Ahmad Shaik, Ramu Elango, Babajan Banaganapalli, Thoraia Shinawi, Nabeel S. Bondagji, Khalidah Khalid Nasser, Arif A. Mohammed, Nora Sahly
Publikováno v:
Systems biology in reproductive medicine. 67(3)
Uterine smooth muscular neoplastic growths like benign leiomyomas (UL) and metastatic leiomyosarcomas (ULMS) share similar clinical symptoms, radiological and histological appearances making their clinical distinction a difficult task. Therefore, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d05952034aa66d1315c0dd3ba78dc2e
https://pubmed.ncbi.nlm.nih.gov/33685300
https://pubmed.ncbi.nlm.nih.gov/33685300
Publikováno v:
Autonomic Neuroscience. 237:102907
The underlying pathophysiology of sudden unexpected death in epilepsy (SUDEP) remains unclear. This phenomenon is likely multifactorial, and there is considerable evidence that genetic factors play a role. There are certain genetic causes of epilepsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeebb2aa55aecadae40d94c98f591d62
https://doi.org/10.1016/j.autneu.2021.102907
https://doi.org/10.1016/j.autneu.2021.102907