0000000000220043

AUTHOR

Lio E

Methionine synthase polymorphism A2756G and its association with thromboembolic disease

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Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase MTHFR A1298C gene polymorphism in subjects affected by thromboembolic disease

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C677T and A1298C polymorphism of the methylentetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis

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Factor V Leiden, Prothrombin G20210A mutations are risk factors for deep vein thrombosis

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Low Fetuin-A plasma levels are associated with the presence of carotid plaques in patients on dialysis.

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Association between angiotensin I - converting enzyme gene insertion/deletion polymorphism and thromboembolic disease.

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Vitamin E and vitamin A plasma levels in patients with Mild Cognitive Impairent (MCI)

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Homocysteine and MTHFR gene polimorphysms in patients with venous tromboembolic disease

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Apo E polymorphism as risk factor for cardiovascular diseases in Sicilian subjects.

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Prevalence and association of the Factor V Leiden and Prothrombin G20210A in healthy subjects and patients with venous tromboembolism

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Effect of MTHFR polymorphism on homocysteine level after methionine loading in thromboembolic patients.

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Mutations in Factor V Leiden (G1691A) and Prothrombin (G2021A) genes are important risk factors for venous thromboembolism

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Apoliprotein E gene polymorphism in subjects affected by cardiovascular disease in Sicilian populations

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Methionine loading test and genetic risk factors in subjects affected by thromboembolic disease

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Hyperhomocysteinemia and methylenetetrahydrofolare reductase 677C→T and 1298A→C mutations in patients with venous thromboembolic disease

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The risk of cardiovascular events is reduced by lowering hyperhomocysteinemia short term B vitamins therapy

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