Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia

International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS)

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Factor V Leiden (FV R506Q) in Families with Inherited Antithrombin Deficiency

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Binding of high affinity heparin to antithrombin III. Stopped flow kinetic studies of the binding interaction.

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Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT)

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Hereditary Deficiency of Protein C or Protein S Confers Increased Risk of Arterial Thromboembolic Events at a Young Age

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