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24. Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13). Plaimauer B, Zimmermann K, Völkel D, Antoine G, Kerschbaumer R, Jenab P, Furlan M, Gerritsen H, Lämmle B, Schwarz HP, Scheiflinger F. Blood; 2002 Nov 15; 100(10):3626-32. PubMed ID: 12393399 [Abstract] [Full Text] [Related]
25. [Thrombotic Thrombocytopenic Purpura --Pathophysiology and Assays of ADAMTS13 Activity]. Kato S, Fujimura Y. Rinsho Byori; 2015 Oct 15; 63(10):1228-36. PubMed ID: 26897861 [Abstract] [Full Text] [Related]
26. Deficiency of von Willebrand factor-cleaving protease in familial and acquired thrombotic thrombocytopenic purpura. Furlan M, Lämmle B. Baillieres Clin Haematol; 1998 Jun 15; 11(2):509-14. PubMed ID: 10097823 [Abstract] [Full Text] [Related]
34. 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 (TTP). Gerritsen HE, Turecek PL, Schwarz HP, Lämmle B, Furlan M. Thromb Haemost; 1999 Nov 01; 82(5):1386-9. PubMed ID: 10595623 [Abstract] [Full Text] [Related]
36. ADAMTS 13 genotype and vWF protease activity in an Italian family with TTP. Bestetti G, Stellari A, Lattuada A, Corbellino M, Parravicini C, Calzarossa C, Cenzuales S, Moroni M, Galli M, Rossi E. Thromb Haemost; 2003 Nov 01; 90(5):955-6. PubMed ID: 14597993 [No Abstract] [Full Text] [Related]