The use of intermediate purity factor VIII concentrate BPL 8Y as prophylaxis and treatment in congenital thrombotic thrombocytopenic purpura
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2006.06264.x/fullpdf
Reference12 articles.
1. von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura
2. Mutation analysis and clinical implications of von Willebrand factor–cleaving protease deficiency
3. Purification of human von Willebrand factor–cleaving protease and its identification as a new member of the metalloproteinase family
4. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
5. Recovery and Half-Life of von Willebrand Factor-Cleaving Protease after Plasma Therapy in Patients with Thrombotic Thrombocytopenic Purpura
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