Thrombotic Thrombocytopenic Purpura and Hemolytic-Uremic Syndromes

This publication has 98 references indexed in Scilit:

• Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
  Nature Genetics, 2013
• Origins of theE. coliStrain Causing an Outbreak of Hemolytic–Uremic Syndrome in Germany
  New England Journal of Medicine, 2011
• Escherichia coli-derived von Willebrand factor-A2 domain fluorescence/Förster resonance energy transfer proteins that quantify ADAMTS13 activity
  Analytical Biochemistry, 2011
• Pathophysiology of thrombotic thrombocytopenic purpura
  International Journal of Hematology, 2010
• Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
  New England Journal of Medicine, 2009
• Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura
  Kidney International, 2009
• Two Mechanistic Pathways for Thienopyridine-Associated Thrombotic Thrombocytopenic Purpura: A Report From the SERF-TTP Research Group and the RADAR Project
  Journal of the American College of Cardiology, 2007
• Shear-induced unfolding triggers adhesion of von Willebrand factor fibers
  Proceedings of the National Academy of Sciences, 2007
• Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
  Proceedings of the National Academy of Sciences, 2007
• Pathogenic Escherichia coli
  Nature Reviews Microbiology, 2004