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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: SAGE Publications 2018
Fag:
Review
Online adgang: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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