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Ectopic platelet-delivered factor (F) VIII for the treatment of Hemophilia A: Plasma and platelet FVIII, is it all the same?

Hemophilia A is the most common inherited bleeding diathesis and is due to a deficiency of functional coagulation factor (F) VIII. Most patients have a severe deficiency and require a program of prophylactic plus acute infusions of recombinant FVIII to prevent significant joint and other target orga...

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Detalhes bibliográficos
Main Authors: Greene, Teshell K., Lambert, Michele P., Poncz, Mortimer
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3852407/
https://ncbi.nlm.nih.gov/pubmed/24319630
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4172/2157-7412.S1-001
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