0000000000166458

AUTHOR

Mingoia G

Stato di metilazione del promotore 2 del gene PTHrP in pazienti affetti da mieloma multiplo

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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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Changes in serum fetuin-A and inflammatory markers levels in end stage renal disease (ESRD): effect of a single session haemodialysis.

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

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Nuove tecniche: Imaging pesato in diffusione: descrizione della tecnica e principali applicazioni cliniche.

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