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Normal binding of plasma von Willebrand factor to platelets in essential thrombocythemia

1999; Wiley; Volume: 61; Issue: 2 Linguagem: Inglês

10.1002/(sici)1096-8652(199906)61

1096-8652

P.J.J. Van Genderen, Henriette Leenknegt,

Renal Diseases and Glomerulopathies

American Journal of HematologyVolume 61, Issue 2 p. 153-154 Letters and CorrespondenceFree Access Normal binding of plasma von Willebrand factor to platelets in essential thrombocythemia Perry J.J. van Genderen, Perry J.J. van Genderen Department of Hematology, University Hospital Dijkzigt, Dr. Molewaterplein 403015, GD Rotterdam, The NetherlandsSearch for more papers by this authorHenriette Leenknegt, Henriette Leenknegt Department of Hematology, University Hospital Dijkzigt, Dr. Molewaterplein 403015, GD Rotterdam, The NetherlandsSearch for more papers by this author Perry J.J. van Genderen, Perry J.J. van Genderen Department of Hematology, University Hospital Dijkzigt, Dr. Molewaterplein 403015, GD Rotterdam, The NetherlandsSearch for more papers by this authorHenriette Leenknegt, Henriette Leenknegt Department of Hematology, University Hospital Dijkzigt, Dr. Molewaterplein 403015, GD Rotterdam, The NetherlandsSearch for more papers by this author First published: 01 June 1999 https://doi.org/10.1002/(SICI)1096-8652(199906)61:2 3.0.CO;2-ZCitations: 4AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL REFERENCES 1Chow, Turner NA, Chintagumpala M, McPherson PD, Nolasco LH, Rice L, Hellums JD, Moake JL. Increased von Willebrand factor binding to platelets in single episode and recurrent types of thrombotic thrombocytopenic purpura. Am J Hematol 1998; 57: 293– 302. Medline 2van Genderen PJJ, Michiels JJ. Erythromelalgia: a pathognomonic microvascular thrombotic complication in essential thrombocythemia and polycythemia vera. Sem Thromb Hemost 1997; 23: 357– 363. 3van Genderen PJJ, Lucas IS, van Strik R, Vuzevski VD, Prins FJ, van Vliet HHDM, Michiels JJ. Erythromelalgia in essential thrombocythemia is characterized by platelet activation adn endothelial cell damage but not by thrombin generation. Thromb Haemost 1996; 76: 333– 338. Medline 4Yosipovitch H, Krause I, Blickstein D. Erythromelalgia in a patient with thrombotic thrombocytopenic purpura. J Am Acad Dermatol 1992; 26: 825– 827. Medline 5Budde U, van Genderen PJJ. Acquired von Willebrand disease in patients with high platelet counts. Sem Thromb Hemost 1997; 23: 425– 431. 6Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, et al. Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic syndrome. N Engl J Med 1998; 339: 1578– 1584. Medline Citing Literature Volume61, Issue2June 1999Pages 153-154 ReferencesRelatedInformation