MTHFR 677C>T (rsRS1801133) variant is associated with hyperhomocysteinemia but not with clinical severity in patients with peripheral arterial disease (original) (raw)

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Compound heterozygosity for the C677T and A1298C mutations of the MTHFR gene in a case of hyperhomocysteinemia with recurrent deep thrombosis at young age

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Common Methylenetetrahydrofolate Reductase Gene Mutation Leads to Hyperhomocysteinemia but Not to Vascular Disease

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The graded effect of hyperhomocysteinemia on the severity and extent of coronary atherosclerosis

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Hyperhomocysteinemia and C677T Polymorphism of Methylenetetrahydrofolate Reductase Gene in Patients with Cardiovascular Disease

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The screening power of methylenetetrahydrofolate reductase C677T polymorphism versus plasma homocysteine concentration in patients with stenosis of the internal carotid artery

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The risk of venous and arterial thrombosis in hyperhomocysteinaemia is low and mainly depends on concomitant thrombophilic defects

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The 677 C/T MTHFR Polymorphism is Associated with Essential Hypertension, Coronary Artery Disease, and Higher Homocysteine Levels

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Association of Methylenetetrahydrofolate Reductase C677T Polymorphism with Hyperhomocysteinemia and Deep Vein Thrombosis in the Iranian Population

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Hyperhomocysteinemia Is Associated With an Increased Risk of Cardiovascular Disease, Especially in Non Insulin-Dependent Diabetes Mellitus : A Population-Based Study

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Homocysteinemia and Methylentetrahydrofolate Reductase Gene Mutation as a Risk Factor for Blood Vessel Disease

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Association of MTHFR 677C>T genetic polymorphism with hyperhomocysteinemia in type 2 diabetes patients

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An MTHFR variant, homocysteine, and cardiovascular comorbidity in renal disease

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Plasma homocysteine level and 677C-->T mutation on the MTHFR gene in patients with venous thromboembolism

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Homocysteine levels are associated with the severity of peripheral arterial disease in Type 2 diabetic patients

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Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

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Single Nucleotide Polymorphisms in Homocysteine Metabolism Pathway Genes: Association of CHDH A119C and MTHFR C677T With Hyperhomocysteinemia

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