Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Amal Kentab"'
Autor:
Fahad A. Bashiri, Rawan AlSheikh, Muddathir H. Hamad, Hamad Alsheikh, Rana Abdullah Alsheikh, Amal Kentab, Najd AlTheeb, Malak Alghamdi
Publikováno v:
Children, Vol 10, Iss 8, p 1334 (2023)
Background: Despite the high consanguinity rates, data on genetic epilepsy in Saudi Arabia is limited. The objective of the current study was to characterize genetic mutations associated with epilepsy in pediatric patients and describe their phenotyp
Externí odkaz:
https://doaj.org/article/680062900ff24d18a657b938f924b3be
Autor:
Hanin Alsini, Abdulaziz Alghamdi, Shatha Alshafi, Khalid Hundallah, Sameer Almehmadi, Daad Alsowat, Suad Al-Yamani, Hanin Almuzaini, Ali Alwadie, Ali Al-Otaibi, Lamyaa Jad, Asma Almadhi, Fahad Bashiri, Amal Kentab, Muddathir H Hamad, Duaa Baarmah, Mohammed Alrifaie, Mohammed Almuqbel, Raidah Al Baradie, Ali Mir, Mohammed Jan, Osama Muthaffar, Mohammed Aljabri, Elsayed Ali, Mohammed Saeed, Abeer Matar, Brahim Tabarki
Publikováno v:
Seizure. 107:146-154
Autor:
Amal Kentab
Publikováno v:
Journal of Pediatric Epilepsy. 11:117-124
Gamma-aminobutyric acid transaminase (GABA-T) deficiency is a rare, autosomal recessive disorder caused by mutations in the 4-aminobutyrate aminotransferase (ABAT) gene, which encodes an enzyme involved in GABA catabolism. It is characterized by seve
Autor:
Amal Kentab
Publikováno v:
Journal of Neurology & Stroke. 11:122-125
A case of a 4-year-old boy who developed acute disseminated encephalomyelitis (ADEM) and optic neuritis (ON) following Mycoplasma pneumoniae infection is reported. His symptoms, including excessive sleepiness, frontal headache, bilateral vision impai
Autor:
Fahad A. Bashiri, Rawan AlSheikh, Rana AlSheikh, Hamad AlSheikh, Muddathir H. Hamad, Amal Kentab, Najd AlTheeb, Malak AlGhamdi
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
Genome Biology
To understand the contribution of Mendelian mutations to the burden of undiagnosed diseases that are suspected to be genetic in origin, we developed a next-generation sequencing-based multiplexing assay that encompasses the ~3000 known Mendelian gene
Autor:
Salih, M. A. M., Abdel-Gader, A. -G M., Al-Jarallah, A. A., Amal Kentab, Gadelrab, M. O., Alorainy, I. A., Hassan, H. H., Zahraa, J. N.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::657a20c58efc1e80a600ce169621543d
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645231658&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645231658&partnerID=MN8TOARS
Autor:
Salih, M. A. M., Abdel-Gader, A. -G M., Al-Jarallah, A. A., Amal Kentab, Alorainy, I. A., Hassan, H. H., Al-Nasser, M. N.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8f7611b696719b135ef9f7c2c2773d09
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645215276&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645215276&partnerID=MN8TOARS
Autor:
Salih, M. A. M., Murshid, W. R., Zahraa, J. N., Abdel-Gader, A. -G M., Al-Jarallah, A. A., Amal Kentab, Alorainy, I. A., Hassan, H. H., Tjan, G. T.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3cf80b2985d6b71bf685baddba1eb5e1
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645242537&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645242537&partnerID=MN8TOARS
Autor:
Salih, M. A. M., Murshid, W. R., Al-Salman, M. M., Abdel-Gader, A. -G M., Al-Jarallah, A. A., Alorainy, I. A., Hassan, H. H., Amal Kentab, Maldergem, L., Othman, S. A., El-Desouki, M. I., Elgamal, E. A.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::07cc19b23e04370cb19bc26998a33797
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645214045&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645214045&partnerID=MN8TOARS