Pathophysiological analysis of thrombosis and hemorrhage from the von Willebrand factor and ADAMTS13 axis
Author:
Affiliation:
1. 奈良県立医科大学血液内科・輸血部
Publisher
Japanese Society on Thrombosis and Hemostasis
Link
https://www.jstage.jst.go.jp/article/jjsth/35/4/35_2024_JJTH_35_4_489-496/_pdf
Reference37 articles.
1. 1) Matsumoto M, Miyakawa Y, Kokame K, et al.: Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) in Japan 2023. Int J Hematol 118: 529–546, 2023. doi: 10.1007/s12185-023-03657-0.
2. 2) Federici AB, Canciani MT, Forza I, et al.: Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand disease—single center comparison of four different assays. Thromb Haemost 84: 1127–1128, 2000.
3. 3) Vincentelli A, Susen S, Le Tourneau T, et al.: Acquired von Willebrand syndrome in aortic stenosis. N Engl J Med 349: 343–349, 2003. doi: 10.1056/NEJMoa022831.
4. 4) Ruggeri ZM: Von Willebrand factor, platelets and endothelial cell interactions. J Thromb Haemost 1: 1335–1342, 2003. doi: 10.1046/j.1538-7836.2003.00260.x.
5. 5) Moake JL: Thrombotic microangiopathies. N Engl J Med 347: 589–600, 2002. doi: 10.1056/NEJMra020528.
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