Unraveling the thrombophilia paradox: from hypercoagulability to the prothrombotic state
- 1 February 2010
- journal article
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 8 (2) , 228-233
- https://doi.org/10.1111/j.1538-7836.2009.03702.x
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Past and future of genetic research in thrombosisJournal of Thrombosis and Haemostasis, 2007
- Recurrence Rate After a First Venous Thrombosis in Patients With Familial ThrombophiliaArteriosclerosis, Thrombosis, and Vascular Biology, 2005
- Thrombophilia, Clinical Factors, and Recurrent Venous Thrombotic EventsJAMA, 2005
- Incidence of recurrent venous thromboembolism in relation to clinical and thrombophilic risk factors: prospective cohort studyThe Lancet, 2003
- Laboratory testing for heritable thrombophilia: impact on clinical management of thrombotic diseaseBritish Journal of Haematology, 2000
- Risk of Venous Thromboembolism and Clinical Manifestations in Carriers of Antithrombin, Protein C, Protein S Deficiency, or Activated Protein C ResistanceArteriosclerosis, Thrombosis, and Vascular Biology, 1999
- Thrombotic Risk in Hereditary Antithrombin III, Protein C, or Protein S DeficiencyArteriosclerosis, Thrombosis, and Vascular Biology, 1996
- Mutation in blood coagulation factor V associated with resistance to activated protein CNature, 1994
- Familial protein S deficiency is associated with recurrent thrombosis.Journal of Clinical Investigation, 1984
- Deficiency of protein C in congenital thrombotic disease.Journal of Clinical Investigation, 1981