Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Faisal A Al-Allaf"'
Autor:
Khalid F Alhabib, Khalid Al-Rasadi, Turky H Almigbal, Mohammed A Batais, Ibrahim Al-Zakwani, Faisal A Al-Allaf, Khalid Al-Waili, Fahad Zadjali, Mohammad Alghamdi, Fahad Alnouri, Zuhier Awan, Abdulhalim J Kinsara, Ahmed AlQudaimi, Wael Almahmeed, Hani Sabbour, Mahmoud Traina, Bassam Atallah, Mohammed Al-Jarallah, Ahmad AlSarraf, Nasreen AlSayed, Haitham Amin, Hani Altaradi
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0251560 (2021)
Background and aimsFamilial hypercholesterolemia (FH) is a common autosomal dominant disorder that can result in premature atherosclerotic cardiovascular disease (ASCVD). Limited data are available worldwide about the prevalence and management of FH.
Externí odkaz:
https://doaj.org/article/69083c33c4d34aab8bdbcd2889d3ea79
Autor:
Burhan M. Edrees, Mohammad Athar, Zainularifeen Abduljaleel, Faisal A Al-Allaf, Mohiuddin M. Taher, Wajahatullah Khan, Abdellatif Bouazzaoui, Naffaa Al-Harbi, Ramzia Safar, Howaida Al-Edressi, Khawala Alansary, Abulkareem Anazi, Naji Altayeb, Muawia A. Ahmed
Publikováno v:
Genomics Data, Vol 10, Iss C, Pp 127-134 (2016)
A targeted customized sequencing of genes implicated in autosomal recessive polycystic kidney disease (ARPKD) phenotype was performed to identify candidate variants using the Ion torrent PGM next-generation sequencing. The results identified four pot
Externí odkaz:
https://doaj.org/article/81267733890c49ba91161af5642de55b
Autor:
Zainularifeen Abduljaleel, Faisal A Al-Allaf, Wajahatullah Khan, Mohammad Athar, Naiyer Shahzad, Mohiuddin M Taher, Mohamed Elrobh, Mohammed S Alanazi, Waseem El-Huneidi
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e92648 (2014)
Alzheimer's disease is one of the main causes of dementia among elderly individuals and leads to the neurodegeneration of different areas of the brain, resulting in memory impairments and loss of cognitive functions. Recently, a rare variant that is
Externí odkaz:
https://doaj.org/article/9ea755f1c99642bd87c0ddfb0d02915d
Autor:
Abdellatif Bouazzaoui, Neda M. Bogari, Faisal A. Al-Allaf, Samar N. Ekram, Mohammad Athar, Anas Dannoun, Thomas Schubert, Shahzad N. Syed, Abdel-Rahman Youssef, Mashael Alqahtani, Ahmed A.H. Abdellatif
Publikováno v:
Heliyon, Vol 9, Iss 3, Pp e13876- (2023)
Graft versus host disease (GVHD) remains the major cause of morbidity and mortality after allogeneic stem cell transplantation, especially for intestinal GVHD, as steroid resistant GVHD results in high mortality. For this reason, new treatments of GV
Externí odkaz:
https://doaj.org/article/f6fd174e49ba49b0a8a216e18a7f33a0
Autor:
Mohammad Athar, Mawaddah Toonsi, Zainularifeen Abduljaleel, Abdellatif Bouazzaoui, Neda M. Bogari, Anas Dannoun, Faisal A. Al-Allaf
Publikováno v:
Life, Vol 13, Iss 7, p 1542 (2023)
Background: Familial Hypercholesterolemia (FH) is a hereditary condition that causes a rise in blood cholesterol throughout a person’s life. FH can result in myocardial infarction and even sudden death if not treated. FH is thought to be caused mai
Externí odkaz:
https://doaj.org/article/07372f2235cf4103b06a7c00c6c43dd7
Autor:
Neda M. Bogari, Amr A. Amin, Husni H. Rayes, Ahmed Abdelmotelb, Faisal A. Al-Allaf, Anas Dannoun, Hiba S. Al-Amodi, Anas A. Sedayo, Hilal Almalk, Amna Moulana, Rania Balkhair, Fatma Jambi, Fakhriah Madani, Mwafaq Abutalib, Mohiuddin M. Taher, Abdellatif Bouazzaoui, Ashwag Aljohani, Mustafa N. Bogari, Udaya Raja G.K., Ahmed Fawzy, Khalid Khalaf Alharbi, Imran Ali Khan
Publikováno v:
Journal of Infection and Public Health, Vol 13, Iss 1, Pp 27-33 (2020)
Background: Eczema is also known as atopic dermatitis is well-known for the skin disease globally. In Saudi Arabia, exome sequencing studies have not been documented. The purpose of this study was to scrutinize the disease causing mutations in childr
Externí odkaz:
https://doaj.org/article/ffb8dd7690a6478fbe33b25b4360e95a
Autor:
Abdellatif Bouazzaoui, Ahmed A. H. Abdellatif, Faisal A. Al-Allaf, Neda M. Bogari, Saied Al-Dehlawi, Sameer H. Qari
Publikováno v:
Pharmaceutics, Vol 13, Iss 2, p 140 (2021)
The current COVID-19 pandemic, caused by severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2), has raised significant economic, social, and psychological concerns. The rapid spread of the virus, coupled with the absence of vaccines and antivi
Externí odkaz:
https://doaj.org/article/39f87e8ac45e4214a66498843930d2e6
Autor:
G. G. H. A. Shadab, Amani A. Albagenny, Mohammad M. Alkazmi, Neda M. Bogari, Mohammad M. Alkhuzae, Abdulaziz A. Althebyani, Khalid Alquthami, Saeed H. Halawani, Zainularifeen Abduljaleel, Mohammad Athar, Anas Dannoun, Ahmed Elsendiony, Ibrahim S. Ghita, Faisal A. Al-Allaf
Publikováno v:
Clinica Chimica Acta. 519:247-254
Background Thrombophilia is a substantial source of indisposition and mortality in several countries, including Arab populations. Deep venous thrombosis (DVT) with or without pulmonary embolism (PE) is the prevalent clinical manifestation of thrombop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5675838f24ce89c26a56d1d0bb6705d3
https://doi.org/10.1016/j.cca.2021.05.012
https://doi.org/10.1016/j.cca.2021.05.012
Publikováno v:
Bio-Design and Manufacturing
The World Health Organization has declared the rapidly spreading coronavirus to be a global pandemic. The FDA is yet to approve a vaccine for human novel coronavirus. Here, we developed a peptide-based vaccine and used high-throughput screening by mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5065bab94ef03f7fbbc8210e87e27ebd
https://doi.org/10.1007/s42242-020-00114-3
https://doi.org/10.1007/s42242-020-00114-3
Autor:
Zuhier AWAN, Alhanuf BATRAN, Faisal A. AL-ALLAF, Raneem S. ALHARBI, Gehan A. HEJAZY, Bassam JAMALAIL, Majid AL MANSOURI, Abdulhadi I. BIMA, Haifa ALMUKADI, Hussam I. KUTBI, Ahmed EALTAYYAR, Babajan BANAGANAPALLI, Noor A. SHAIK
Publikováno v:
Panminerva medica.
Familial hypercholesterolemia (FH) is a globally underdiagnosed inherited metabolic disorder. Owing to limited published data from Arab world, this study was conducted with the aim of identifying the genetic and molecular basis of FH in highly consan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9c4be0716b42bcb85f63a1e4d9ddc57
https://pubmed.ncbi.nlm.nih.gov/35274909
https://pubmed.ncbi.nlm.nih.gov/35274909