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Autor:
Gabriel Pinna Feliciano, Sara Hayama Arimori, Vinicius Watanabe Nakao, Joice Rodrigues Dos Santos, Elizabeth A. L. Martins, Marcelo Porto Bemquerer, Elisabeth Cheng
Publikováno v:
Pharmaceuticals, Vol 15, Iss 10, p 1192 (2022)
Hemophilia A is treated with human plasma coagulation factor VIII (FVIII) replacement therapy and Hemophilia B with coagulation factor IX, which is purified from prothrombin complex concentrate (PCC). In this paper we evaluated the separation of FVII
Externí odkaz:
https://doaj.org/article/7f650b5dd5184a7598fd1ecd5660535c