Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mahasen al Saleh"'
Autor:
H. Al Zahrani, H. Masmali, Abdulmajeed Albanyan, Tarek Owaidah, Randa Alnounou, A. Malik, A. AlJefri, Mahasen al Saleh, Abdulrahman Al-Musa, R. Nasr
Publikováno v:
International Journal of Laboratory Hematology. 37:503-508
Glanzmann thrombasthenia (GT) is a rare inherited platelet disorder that is characterized by spontaneous or postprocedural bleeding. The diagnosis of GT depends on identifying the dysfunction of the platelets.The aim of this study was to compare a wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::affae2a0b63fbfe3c021c8d0b34f93c1
https://doi.org/10.1111/ijlh.12320
https://doi.org/10.1111/ijlh.12320
Autor:
Mahasen al Saleh, Mahmoud Abu Riash, Hala Aba Alkhail, Abdulrahaman Al Musa, Khalid Abu Amero, Tarek Owaidah, Hazzaa Al Zahrani, Ali Alodaib
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 20(6)
Different types of mutations have been reported in patients with hemophilia A. Although about half of all severe factor VIII deficiencies are caused by gene rearrangements (inversions) involving intron 22 in F8, other mutations such as point mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e7e07551183ef31fe4363e75eb3567b
https://pubmed.ncbi.nlm.nih.gov/19448530
https://pubmed.ncbi.nlm.nih.gov/19448530
Autor:
Abdulrahman Al Musa, Tarek Owaidah, Rubina J. Malik, Suleman Al-Sweedan, Sohaib Zulfiqar, Mahasen al Saleh, Rafat Jafri, Nicy Joseph, Hazzaa Alzahrani, Khawar Siddiqui
Publikováno v:
Blood. 124:5064-5064
BACKGROUND The rare coagulation disorders are heritable abnormalities of hemostasis that may present significant difficulties in diagnosis and management to hemophilia center clinicians. The common feature shared by these disorders is that their over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67904794b8b905128c112346c382ccfd
https://doi.org/10.1182/blood.v124.21.5064.5064
https://doi.org/10.1182/blood.v124.21.5064.5064