ADAMTS-13 and Von Willebrand factor in relation to platelet response during plasma exchange in thrombotic thrombocytopenic purpura: a clue for disease mechanism?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-009-0709-7.pdf
Reference13 articles.
1. Lämmle B, Kremer Hovinga JA, Alberio L (2005) Thrombotic thrombocytopenic purpura. J Thromb Haemost 3:1663–1675. doi: 10.1111/j.1538-7836.2005.01425.x
2. Desch KC, Motto DG (2007) Thrombotic thrombocytopenic purpura in humans and mice. Arterioscler Thromb Vasc Biol 27:1901–1908. doi: 10.1161/ATVBAHA.107.145797
3. Gerritsen HE, Turecek PL, Schwarz HP, Lämmle B, Furlan M (1999) Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura. Thromb Haemost 82:1386–1389
4. Loof A, van Vliet HHDM, Kappers-Klunne MC (2001) Low activity of von Willebrand factor-cleaving protease is not restricted to patients suffering from thrombotic thrombocytopenic purpura. Br J Haematol 112:1087–1088. doi: 10.1046/j.1365-2141.2001.02622-5.x
5. Cejka J (1982) Enzyme immunoassay for FVIII-related antigen. Clin Chem 28:1356–1358
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2. ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies;Rambam Maimonides Medical Journal;2014-10-29
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