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Autor:
M. W. F. van Spengler, Ron A. A. Mathôt, Tim Preijers, Frank W.G. Leebeek, Marjon H. Cnossen, K. Fijnvandraat, Karina Meijer, Krista Fischer
Publikováno v:
European Journal of Clinical Pharmacology, 78(2), 237-249. Springer-Verlag
European Journal of Clinical Pharmacology, 78(2), 237-249. Springer Verlag
European journal of clinical pharmacology, 78(2). Springer Verlag
European journal of clinical pharmacology, 78(2), 237-249. Springer Verlag
European Journal of Clinical Pharmacology
European Journal of Clinical Pharmacology, 78(2), 237-249. Springer Verlag
European journal of clinical pharmacology, 78(2). Springer Verlag
European journal of clinical pharmacology, 78(2), 237-249. Springer Verlag
European Journal of Clinical Pharmacology
Purpose Hemophilia B is a bleeding disorder, caused by a factor IX (FIX) deficiency. Recently, FIX concentrates with extended half-life (EHL) have become available. Prophylactic dosing of EHL-FIX concentrates can be optimized by assessment of individ