Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ahmed Tarawah"'
Autor:
Tarek Owaidah MD, Salwa Bakr MD, Nouf Al-Numair PhD, Hala AbaAlkhail PhD, Hazzaa Alzahrani MD, Mahasen Saleh MD, Haitham Khogeer MD, Ahmed Tarawah MD, Hadeel Akkad MD, Faisal Al-Allaf PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 29 (2023)
Establishing a national screening program for hemophilia patients is highly encouraged by the World Health Organization and the World Federation of Hemophilia. Hence, this study aimed to analyze the variant spectrum of F8 and F9 genes in Arab hemophi
Externí odkaz:
https://doaj.org/article/a915efd2ecf849689c48cc1393e88a04
Autor:
Tarek, Owaidah, Abdulakareem, Almomen, Ahmed, Tarawah, Ashraf, Warsi, Fawaz, Alkasim, Hazzaa, Alzahrani, Mahassen, Saleh, Ohoud, Kashari, Wasil, Jastaniah
Publikováno v:
Am J Blood Res
Introduction: Emicizumab is a bispecific monoclonal antibody with the ability to bridge FIXa and FX, mimic FVIII, and restore normal hemostasis in patients with hemophilia A. Moreover, substantial evidence has shown that emicizumab-treated patients d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67c12a3b081b79f1a3b66599d05d6e99
https://pubmed.ncbi.nlm.nih.gov/35873100
https://pubmed.ncbi.nlm.nih.gov/35873100
Autor:
Esraa Abu-Douleh, Tarek Owaidah, Nouf S. Al-Numair, Ahmed Tarawah, Mahasen Saleh, Lina Elbaik, Faiqa Imtiaz, Hazzaa Alzahrani, Khushnooda Ramzan
Publikováno v:
Blood Coagulation & Fibrinolysis. 30:224-232
Coagulation factor V plays a significant role in the blood coagulation cascade as part of the prothrombinase complex. Factor V deficiency (FVD) is a rare autosomal recessive bleeding disorder with a variable phenotypic expression which varies from be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9558f3c528f6f77c832c8a9a7842c8a
https://doi.org/10.1097/mbc.0000000000000828
https://doi.org/10.1097/mbc.0000000000000828
Autor:
Batoul Baz, Dorota Monies, Thamer A Alamoudi, Ahmed Tarawah, Nouf S Al-Numair, Mahasen Saleh, Nada Al Tassan, Hala AbaAlkhail, M. Abouelhoda, Randa AlNounou, Hazza Alzahrani, Abdulrahman Al-Musa, Rahaf Altahan, Amjad Jabaan, Basma Al Abdulaziz, Tarek Owaidah
Publikováno v:
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-7 (2019)
NPJ Genomic Medicine
NPJ Genomic Medicine
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder. Around 490 mutations in ITGA2B and ITGB3 genes were reported. We aimed to use targeted next-generation sequencing (NGS) to identify variants in patients with GT. We screen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0ca044888b0a091b31dba2f34499d67
http://link.springer.com/article/10.1038/s41525-019-0079-6
http://link.springer.com/article/10.1038/s41525-019-0079-6
Autor:
Mahmoud Abu-Riash, Tarek Owaidah, Ali Al-Omari, Hazzaa Alzahrani, Abdulkareem Al Momen, Mahasen Saleh, Fahad Alothman, Fawaz Alkasim, Abdulrahman Al-Musa, Said Y Mohamed, Khawar Siddiqui, Randa Al Nouno, Mansor Ahmed, Ahmed Tarawah, Fatima Al Batniji, Saud Abu-Herbish
Publikováno v:
Medicine. 96:e5456
Hemophilia A and B are X-linked diseases that predominantly affect male patients. Patients can develop coagulation factor inhibitors, which exponentially increases the treatment cost. However, the prevalence of factor VIII and IX inhibitors in Saudi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb0f6860e40275bc90a5e97ab205fce
https://doi.org/10.1097/md.0000000000005456
https://doi.org/10.1097/md.0000000000005456