Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Nasser A, Elhawary"'
Autor:
Enas Omran, Abdullah R. Alzahrani, Samar F. Ezzat, Ghada Ellithy, Marwa Tarek, Eman Khairy, Mohamed M. Ghit, Ahmed Elgeushy, Tahani Mohamed Ibrahim Al-Hazani, Ibrahim Abdel Aziz Ibrahim, Alaa Hisham Falemban, Ghazi A. Bamagous, Nasser A. Elhawary, Mariusz Jaremko, Essa M. Saied, Doaa I. Mohamed
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Rheumatoid arthritis (RA) is a debilitating autoimmune condition characterized by chronic synovitis, joint damage, and inflammation, leading to impaired joint functionality. Existing RA treatments, although effective to some extent, are not without s
Externí odkaz:
https://doaj.org/article/60b13c4e21f64d3aa5905a512716317a
Autor:
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, Zohor A. Azher, Alaa H. Falemban, Wefaq M. Madani, Wafaa Alosaimi, Ghydda Alghamdi, Ikhlas A. Sindi
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-15 (2023)
Abstract This review discusses the discovery, epidemiology, pathophysiology, genetic etiology, molecular diagnosis, and medication-based management of fragile X syndrome (FXS). It also highlights the syndrome’s variable expressivity and common como
Externí odkaz:
https://doaj.org/article/3c0b8312931542ca91a8be99b5e1acde
Autor:
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, Ezzeldin N. Elhawary, Nagwa Gaboon, Mohammed Dandini, Abdulelah Madkhali, Wafaa Alosaimi, Abdulmajeed Alzahrani, Fawzia Aljohani, Ehab M. Melibary, Osama A. Kensara
Publikováno v:
Human Genomics, Vol 16, Iss 1, Pp 1-17 (2022)
Abstract This review discusses the epidemiology, pathophysiology, genetic etiology, and management of phenylketonuria (PKU). PKU, an autosomal recessive disease, is an inborn error of phenylalanine (Phe) metabolism caused by pathogenic variants in th
Externí odkaz:
https://doaj.org/article/4583e2e4e7bb46e0adcd2247e7f26fe4
Autor:
Nasser A. Elhawary, Essam H. Jiffri, Samira Jambi, Ahmad H. Mufti, Anas Dannoun, Hassan Kordi, Asim Khogeer, Osama H. Jiffri, Abdelrahman N. Elhawary, Mohammed T. Tayeb
Publikováno v:
Human Genomics, Vol 12, Iss 1, Pp 1-11 (2018)
Abstract Background In individuals with Duchenne muscular dystrophy (DMD), exon skipping treatment to restore a wild-type phenotype or correct the frame shift of the mRNA transcript of the dystrophin (DMD) gene are mutation-specific. To explore the m
Externí odkaz:
https://doaj.org/article/a0ad8400a7a945fd9970a2e02136f578
Autor:
Nasser A Elhawary, Samar N Ekram, Iman S Abumansour, Zohor A Azher, Imad A AlJahdali, Najiah M Alyamani, Hind M Naffadi, Ikhlas A Sindi, Abdulaziz Baazeem, Anmar M Nassir, Ahmad H Mufti
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96a481d1426442e705975aff83332729
https://doi.org/10.7759/cureus.36293
https://doi.org/10.7759/cureus.36293
Autor:
Hind Naffadi, Ahmed O. Babalghith, Samar N. Ekram, Nasser A. Elhawary, Ezzeldin N. Elhawary, Munaifah Alenezi, Mohammed T. Tayeb, Ahmad H. Mufti, Ikhlas A. Sindi
Publikováno v:
International Journal of General Medicine. 14:1311-1323
Ikhlas A Sindi,1 Ahmed O Babalghith,2 Mohammed T Tayeb,2 Ahmad H Mufti,2 Hind Naffadi,3 Samar N Ekram,2,4 Ezzeldin N Elhawary,5,6 Munaifah Alenezi,2 Nasser A Elhawary2,7 1Department of Biotechnology, Faculty of Science, King Abdulaziz University, Jed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b5d7b7d436f28c30a29a870f39a52cf
https://doi.org/10.2147/ijgm.s294802
https://doi.org/10.2147/ijgm.s294802
Autor:
Ahmad H Mufti, Imad A AlJahdali, Nasser A Elhawary, Samar N Ekram, Iman Abumansour, Ikhlas A Sindi, Hind Naffadi, Ezzeldin N Elhawary, Najiah M Alyamani, Ghydda Alghamdi, Wafaa Alosaimi, Ghufran Rawas, Amaal Alharbi, Mohammed T Tayeb
Publikováno v:
International Journal of General Medicine.
Ahmad H Mufti, 1 Imad A AlJahdali, 2 Nasser A Elhawary, 1 Samar N Ekram, 1 Iman Abumansour, 1 Ikhlas A Sindi, 3 Hind Naffadi, 4 Ezzeldin N Elhawary, 5 Najiah M Alyamani, 6 Ghydda Alghamdi, 1 Wafaa Alosaimi, 7 Ghufran Rawas, 8 Amaal Alharbi, 9 Mohamme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1988d062ae9d9e442565e038a84c232f
https://www.dovepress.com/variations-in-tap1-and-psmb9-genes-involved-in-antigen-processing-and--peer-reviewed-fulltext-article-IJGM
https://www.dovepress.com/variations-in-tap1-and-psmb9-genes-involved-in-antigen-processing-and--peer-reviewed-fulltext-article-IJGM
Autor:
Ahmad H, Mufti, Imad A, AlJahdali, Nasser A, Elhawary, Samar N, Ekram, Iman, Abumansour, Ikhlas A, Sindi, Hind, Naffadi, Ezzeldin N, Elhawary, Najiah M, Alyamani, Ghydda, Alghamdi, Wafaa, Alosaimi, Ghufran, Rawas, Amaal, Alharbi, Mohammed T, Tayeb
Publikováno v:
International Journal of General Medicine
Background The antigen processing 1 (TAP1) and proteasome 20S subunit beta 9 (PSMB9) genes are associated with strong susceptibility to many autoimmune diseases. Here, we explored whether TAP1/PSMB9 genetic variants, individually or combined, affecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7b6601a3dde10811f3cab21533d5c79
https://pubmed.ncbi.nlm.nih.gov/34984025
https://pubmed.ncbi.nlm.nih.gov/34984025
Autor:
Arwa H. Arab, Nasser A. Elhawary
Publikováno v:
Neuropsychiatric Disease and Treatment. 15:3569-3581
Purpose Several interacting genes or single nucleotide polymorphisms (SNPs) are vulnerable to the risk of autism spectrum disorder (ASD). Here we explored associations between SNPs in the methylenetetrahydrofolate reductase (MTHFR) gene or combined g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::129fbd4fff315cc61b36f3d5f6130ef2
https://doi.org/10.2147/ndt.s230348
https://doi.org/10.2147/ndt.s230348
Autor:
Ikhlas A, Sindi, Ahmed O, Babalghith, Mohammed T, Tayeb, Ahmad H, Mufti, Hind, Naffadi, Samar N, Ekram, Ezzeldin N, Elhawary, Munaifah, Alenezi, Nasser A, Elhawary
Publikováno v:
International Journal of General Medicine
Purpose Colorectal carcinoma (CRC) represents a considerable public health burden in Saudi Arabia. Several candidate genes and genetic variants have been associated with morbidity and mortality among patients with CRC. We explored whether allelic var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66cfafeee98270f0ad7723a854510b11
https://pubmed.ncbi.nlm.nih.gov/33883929
https://pubmed.ncbi.nlm.nih.gov/33883929