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pro vyhledávání: '"Mubarak Alshraim"'
Autor:
Hassan A Hamali, Orwa G Elhussein, Abdulmoneim Jamil, Sadaqat Hussain, Mubarak Alshraim, Abdulrahman Alshehri
Publikováno v:
Journal of Applied Hematology, Vol 6, Iss 3, Pp 115-118 (2015)
Introduction: Sickle cell disease (SCD) is an inherited genetic disorder characterized by various complications, including thrombosis. Increased levels of circulating microvesicles (MVs) and tissue factor (TF)- bearing MVs have been reported in SCD.
Externí odkaz:
https://doaj.org/article/948afa754d36443c8f096fcedf0e4cce
