Familial and recurrent forms of hemolytic uremic syndrome/thrombotic thrombocytopenic purpura

Contrib Nephrol. 2001:(136):125-39. doi: 10.1159/000060183.
No abstract available

Publication types

  • Review

MeSH terms

  • Complement Factor H / genetics
  • Complement System Proteins / physiology
  • Endothelium, Vascular / pathology
  • Hemolytic-Uremic Syndrome / genetics*
  • Humans
  • Leukocytes / physiology
  • Mutation
  • Purpura, Thrombotic Thrombocytopenic / genetics*
  • Recurrence
  • von Willebrand Factor / metabolism

Substances

  • CFH protein, human
  • von Willebrand Factor
  • Complement Factor H
  • Complement System Proteins