[Congenital coagulopathies: clinical manifestation and molecular mechanism]

Rinsho Ketsueki. 2007 May;48(5):363-70.
[Article in Japanese]
No abstract available

Publication types

  • Review

MeSH terms

  • Blood Coagulation Disorders, Inherited* / blood
  • Blood Coagulation Disorders, Inherited* / diagnosis
  • Blood Coagulation Disorders, Inherited* / genetics
  • Blood Coagulation Disorders, Inherited* / therapy
  • Blood Coagulation Factors / genetics
  • Blood Coagulation Tests
  • Hemophilia A / blood
  • Hemophilia A / diagnosis
  • Hemophilia A / genetics
  • Hemophilia A / therapy
  • Humans
  • Molecular Diagnostic Techniques
  • Mutation
  • Thrombophilia / diagnosis
  • Thrombophilia / genetics
  • Thrombophilia / therapy
  • von Willebrand Diseases / blood
  • von Willebrand Diseases / diagnosis
  • von Willebrand Diseases / genetics
  • von Willebrand Diseases / therapy

Substances

  • Blood Coagulation Factors