Factor XIII combined with recombinant factor VIIa: a new means of treating severe hemophilia A
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2010.04171.x/fullpdf
Reference27 articles.
1. What is all that thrombin for?;Mann;J Thromb Haemost,2003
2. Thrombin generation and bleeding in haemophilia A;Brummel-Ziedins;Haemophilia,2009
3. Influence of fibrin network conformation and fibrin fiber diameter on fibrinolysis speed: dynamic and structural approaches by confocal microscopy;Collet;Arterioscler Thromb Vasc Biol,2000
4. Discordant fibrin formation in hemophilia;Brummel-Ziedins;J Thromb Haemost,2009
5. Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: the CANAL cohort study;Gouw;Blood,2007
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1. Mechanistic rationale for factor XIII cotreatment in haemophilia;Haemophilia;2019-10-02
2. Platelet rescue by macrophage depletion in obese ADAMTS-13-deficient mice at risk of thrombotic thrombocytopenic purpura;Journal of Thrombosis and Haemostasis;2017-11-28
3. Factor XIII cotreatment with hemostatic agents in hemophilia A increases fibrin α-chain crosslinking;Journal of Thrombosis and Haemostasis;2017-11-20
4. Temporal changes in clot lysis and clot stability following tranexamic acid in cardiac surgery;Blood Coagulation & Fibrinolysis;2017-06
5. Tissue factor-dependent coagulation activation by heme: A thromboelastometry study;PLOS ONE;2017-04-24
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