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pro vyhledávání: '"Hafiz Mosa Malhan"'
Autor:
Ahmad Ali Hazzazi, Mohssen Hassen Ageeli, Abdulaziz Mohammed Alfaqih, Abdullah Ali Jaafari, Hafiz Mosa Malhan, Mohammed Mosa Bakkar
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 1, Pp 10-14 (2020)
INTRODUCTION: Sickle cell anemia (SCA) is an autosomal recessive illness caused by the formation of abnormal hemoglobin S. Sickle cell disease has many complications such as vaso-occlusive crisis (VOC), gallstones, stroke, acute chest syndrome (ACS),
Externí odkaz:
https://doaj.org/article/945e2e2add364b7aa27e32554874a1fd
Autor:
Hafiz Mosa Malhan, Mohssen H. Ageeli, Abdullah Ali Jaafari, Mohammed Mosa Bakkar, Abdulaziz Mohammed Alfaqih, Ahmad Ali Hazzazi
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 1, Pp 10-14 (2020)
INTRODUCTION: Sickle cell anemia (SCA) is an autosomal recessive illness caused by the formation of abnormal hemoglobin S. Sickle cell disease has many complications such as vaso-occlusive crisis (VOC), gallstones, stroke, acute chest syndrome (ACS),