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December 1, 2000British Journal of Haematology

The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both

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Authors

IMIda MartinelliVascular MedicinePBPaolo BucciarelliVascular MedicineMMMaurizio MargaglioneUniversity of Foggia

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Martinelli et al. (2000) studied this question.

synapsesocial.com/papers/6a70fd2ce71d69abee08fa3ehttps://doi.org/10.1046/j.1365-2141.2000.02502.x
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Venous Thrombotic Risk in Family Members of Unselected Individuals with Factor V Leiden2000 · 79 citations
  2. 2Different Risks of Thrombosis in Four Coagulation Defects Associated With Inherited Thrombophilia: A Study of 150 Families1998 · 448 citations
  3. 3Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.1993 · 1,986 citations
  4. 4Incidence of Venous Thromboembolism in Families with Inherited Thrombophilia1999 · 323 citations
  5. 5The 20210 A Allele of the Prothrombin Gene Is a Common Risk Factor among Swedish Outpatients with Verified Deep Venous Thrombosis1997 · 250 citations