Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene

This publication has 26 references indexed in Scilit:

• The Routine Determination of the Endogenous Thrombin Potential, First Results in Different Forms of Hyper- and Hypocoagulability
  Thrombosis and Haemostasis, 1997
• Elevated Levels of Prothrombin Activation Fragment 1+2 in Plasma from Patients with Heterozygous Arg506 to Gin Mutation in the Factor V Gene (APC-Resistance) and/or Inherited Protein S Deficiency
  Thrombosis and Haemostasis, 1996
• Mutation in blood coagulation factor V associated with resistance to activated protein C
  Nature, 1994
• Normalization of markers of coagulation activation with a purified protein C concentrate in adults with homozygous protein C deficiency
  Blood, 1993
• Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.
  Proceedings of the National Academy of Sciences, 1993
• Homozygous protein S deficiency in an infant with purpura fulminans
  The Journal of Pediatrics, 1990
• Hemostatic enzyme generation in the blood of patients with hereditary protein C deficiency
  Blood, 1988
• The pathophysiology of the prethrombotic state in humans: insights gained from studies using markers of hemostatic system activation
  Blood, 1987
• Homozygous Protein C Deficiency Manifested by Massive Venous Thrombosis in the Newborn
  New England Journal of Medicine, 1984
• INHERITED PROTEIN C DEFICIENCY AND COUMARIN-RESPONSIVE CHRONIC RELAPSING PURPURA FULMINANS IN A NEWBORN INFANT
  The Lancet, 1983