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Practical aspects of extended half-life products for the treatment of haemophilia

Haemophilia A and haemophilia B are congenital X-linked bleeding disorders caused by deficiency of coagulation factor VIII (FVIII) and IX (FIX), respectively. The preferred treatment option for patients with haemophilia is replacement therapy. For patients with severe disease, prophylactic replaceme...

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Foilsithe in:Ther Adv Hematol
Main Authors: Lambert, Thierry, Benson, Gary, Dolan, Gerry, Hermans, Cedric, Jiménez-Yuste, Victor, Ljung, Rolf, Morfini, Massimo, Zupančić-Šalek, Silva, Santagostino, Elena
Formáid: Artigo
Teanga:Inglês
Foilsithe: SAGE Publications 2018
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6130100/
https://ncbi.nlm.nih.gov/pubmed/30210757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2040620718796429
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