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pro vyhledávání: '"Abdulrahman Musaad Alhumaid"'
Autor:
Abdulrahman Musaad Alhumaid, Abdulmalek Suliman Aleidi, Abdullelah Saleh Alfakhri, Naif Khalil Alosaimi, Yosra Z Ali, Mohsen Saadi Alzahrani
Publikováno v:
Journal of Applied Hematology, Vol 9, Iss 1, Pp 22-28 (2018)
Introduction: Sickle cell anemia (SCA) is one of the most common genetic diseases worldwide. Patients with SCA present with varied clinical features and complications that may affect many organs in the human body. There are few treatment options for
Externí odkaz:
https://doaj.org/article/09bdbefd069f4056892b6c48b6b1b6e1