C677T MTHFR Mutation and Factor V Leiden Mutation in Patients with TIA/Minor Stroke - An inherited risk factor for coronary artery disease

By Lalouschek W.   Aull S.   Serles W.   Schnider P.   Mannhalter C.   Pabinger-Fasching I.   Deecke L.   Zeiler K.  

Thrombosis Research, Vol. 93, Iss. 2, 1999-01 ,pp. : 61-69

Elsevier

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Homozygous C677T mutation in the MTHFR gene as an independent risk factor for multiple small-artery occlusions

By Choi B.O.   Kim N.K.   Kim S.H.   Kang M.S.   Lee S.   Ahn J.Y.   Kim O.J.   Kim S.   Oh D.  

Thrombosis Research, Vol. 111, Iss. 1, 2003-01 ,pp. : 39-44

Elsevier

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Low Plasma Folate in Combination with the 677 C->T Methylenetetrahydrofolate Reductase Polymorphism Is Associated with Increased Risk of Coronary Artery Disease in Koreans - Result from a cohort of US adults

By Yoo J.-H.   Park S.-C.  

Thrombosis Research, Vol. 97, Iss. 2, 2000-01 ,pp. : 77-84

Elsevier

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Pregnancy and obstetrics. The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C→T mutation

By Hasbargen Uwe  

Human Reproduction, Vol. 15, Iss. 12, 2000-12 ,pp. : 2659-2662

Oxford University Press

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C677T Mutation in the Methylene Tetrahydrofolate Reductase Gene as a Risk Factor for Venous Thrombotic Disease in Austrian Patients

By Seinost G.   Renner W.   Brodmann M.   Winkler M.   Koppel H.   Pilger E.  

Thrombosis Research, Vol. 100, Iss. 5, 2000-12 ,pp. : 405-407

Elsevier

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