PB2642: EVALUATION OF INNOVATIVE LABORATORY TESTS TO PREDICT A THROMBOTIC PHENOTYPE IN A FAMILY WITH DYSFIBRINOGENEMIA AND A NOVEL FGG MUTATION.

Lignende værker

• A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype
  af: Nuo Xu, et al.
  Udgivet: (2024-01-01)
• PB2642: EVALUATION OF INNOVATIVE LABORATORY TESTS TO PREDICT A THROMBOTIC PHENOTYPE IN A FAMILY WITH DYSFIBRINOGENEMIA AND A NOVEL FGG MUTATION.
  af: Amaury Monard, et al.
  Udgivet: (2023-08-01)
• Pseudohomozygous dysfibrinogenemia
  af: Rachel C. Peck, et al.
  Udgivet: (2021-08-01)
• Intrinsic activated thrombin generation for treatment efficacy and monitoring of octocog alfa and emicizumab in severe hemophilia A
  af: Emma H. Urlings, et al.
  Udgivet: (2026-05-01)
• Fibrinogen Deficiency with Thrombotic Manifestations
  af: Alvaro Tamayo-Velasco, et al.
  Udgivet: (2022-06-01)