A common genetic variation in the 3′untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
Poort SR, Rosendaal FR, Reitsma PH, et al. A common genetic variation in the 3′untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996;88:3698-3703.
Primary thrombophilia in Mexico II. Factor V G1691A (Leiden), prothrombin G20210A and methilenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos
Ruiz Arguellez GJ, Garces Eisele J, Reyes Nunez V, et al. Primary thrombophilia in Mexico II. Factor V G1691A (Leiden), prothrombin G20210A and methilenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos. Am J Hematol 2001;66:28-31.
High risk of cerebralvein thrombosis in carriers of a prothrombingene mutation and in users of oral contraceptives
Martinelli I, Sacchi E, Landi G, et al. High risk of cerebralvein thrombosis in carriers of a prothrombingene mutation and in users of oral contraceptives. N Engl J Med 1998;338:1793-1797.
Increased risk for venous thrombosis in carriers of the prothrombin G->A20210 gene variant
Margaglione M, Brancaccio V, Giuliani N, et al. Increased risk for venous thrombosis in carriers of the prothrombin G->A20210 gene variant. Ann Intern Med 1998;129:89-93.
Prognosis of cerebral vein and dural sinus thrombosis: Results of the International Study on Cerebral Vein and Dural Sinus Thrombosis (ISCVT)
Ferro JM, Canhao P, Stam J, et al. Prognosis of cerebral vein and dural sinus thrombosis: results of the International Study on Cerebral Vein and Dural Sinus Thrombosis (ISCVT). Stroke 2004;35:664-670.
The risk of recurrent venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation
De Stefano V, Martinelli I, Mannucci PM, et al. The risk of recurrent venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation. N Engl J Med 1999;341:801-806.