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pro vyhledávání: '"Mohamd A. Alblihed PhD"'
Autor:
Asmaa M. Zahran MD, Khalid I. Elsayh MD, Khaled Saad MD, Mostafa M. Embaby MD, Mervat A. M. Youssef MD, Yasser F. Abdel-Raheem MD, Shaban M. Sror MD, Shereen M. Galal MD, Helal F. Hetta MD, Mohamed Diab Aboul-Khair MD, Mohamd A. Alblihed PhD, Amira Elhoufey PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Sickle cell disease (SCD) is a genetically inherited hemolytic anemia increasingly appreciated as a chronic inflammatory condition and hypercoagulable state with high thrombotic risk. It is associated with disturbed immune phenotype and function and
Externí odkaz:
https://doaj.org/article/363de7f4fb9543e190dbd3eee057bd4f