83 Hereditary Angioedema and Normal C1-Inhibitor (HAE TYPE III): A Novel Mutation in the Coagulation Factor 12 Gene

Lignende værker

• Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene
  af: Konrad Bork, et al.
  Udgivet: (2020-02-01)
• Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene
  af: Bork, Konrad, et al.
  Udgivet: (2020)
• 165 Early Versus Delayed Treatment of Swelling Attacks with Icatibant, a Bradykinin 2 Receptor Antagonist in Patients With Hereditary Angioedema due to C1-INH Deficiency
  af: Bork, Konrad, et al.
  Udgivet: (2012)
• Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence
  af: Bork, Konrad, et al.
  Udgivet: (2020)
• Complement, coagulation and fibrinolytic parameters in hereditary angioedema (HAE).
  af: Cullmann, W, et al.
  Udgivet: (1982)