High titers of inhibitors of von Willebrand factor-cleaving metalloproteinase in a fatal case of acute thrombotic thrombocytopenic purpura

This publication has 11 references indexed in Scilit:

• Increased Fragmentation of von Willebrand Factor, Due to Abnormal Cleavage of the Subunit, Parallels Disease Activity in Recurrent Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura and Discloses Predisposition in Families
  Blood, 1999
• Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
  New England Journal of Medicine, 1998
• von Willebrand Factor–Cleaving Protease in Thrombotic Thrombocytopenic Purpura and the Hemolytic–Uremic Syndrome
  New England Journal of Medicine, 1998
• Increased von Willebrand factor binding to platelets in single episode and recurrent types of thrombotic thrombocytopenic purpura
  American Journal of Hematology, 1998
• Late Relapses in Patients Successfully Treated for Thrombotic Thrombocytopenic Purpura
  Annals of Internal Medicine, 1995
• Shear stress enhances the proteolysis of von Willebrand factor in normal plasma
  Blood, 1994
• The high molecular weight form of endothelial cell von Willebrand factor is released by the regulated pathway
  British Journal of Haematology, 1991
• Comparison of Plasma Exchange with Plasma Infusion in the Treatment of Thrombotic Thrombocytopenic Purpura
  New England Journal of Medicine, 1991
• Identification of a cleavage site directing the immunochemical detection of molecular abnormalities in type IIA von Willebrand factor.
  Proceedings of the National Academy of Sciences, 1990
• Brief report: Resistance development to fluoroquinolones in Europe
  The American Journal of Medicine, 1989