-
1
-
-
0029066299
-
A quantitative assessment of plasma homocyst(e)ine as a risk factor for vascular disease: Probable benefits of increasing folic acid intakes
-
Boushey CJ, Beresford SSA, Omenn GS, Motulsky AG. A quantitative assessment of plasma homocyst(e)ine as a risk factor for vascular disease: probable benefits of increasing folic acid intakes. JAMA 1995; 274: 1049-57.
-
(1995)
JAMA
, vol.274
, pp. 1049-1057
-
-
Boushey, C.J.1
Beresford, S.S.A.2
Omenn, G.S.3
Motulsky, A.G.4
-
2
-
-
1842331509
-
The European Concerted Action Project. Plasma homocysteine as a risk factor for vascular disease
-
Graham M. The European Concerted Action Project. Plasma homocysteine as a risk factor for vascular disease. JAMA 1997; 277: 1775-89.
-
(1997)
JAMA
, vol.277
, pp. 1775-1789
-
-
Graham, M.1
-
3
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
-
Kang SS, Wong PWK, Susmano A, Sora J, Norusis M, Ruggie N. Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 1991; 48: 536-45.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 536-545
-
-
Kang, S.S.1
Wong, P.W.K.2
Susmano, A.3
Sora, J.4
Norusis, M.5
Ruggie, N.6
-
4
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews R., Boers GJH, van den Heuvel L., Rosen R. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10: 111-3.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.6
Boers, G.J.H.7
Van Den Heuvel, L.8
Rosen, R.9
-
5
-
-
0027421353
-
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease
-
Kang SS, Passen EL, Ruggie N, Wong PWK, Sora J. Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease. Circulation 1993; 88: 1463-9.
-
(1993)
Circulation
, vol.88
, pp. 1463-1469
-
-
Kang, S.S.1
Passen, E.L.2
Ruggie, N.3
Wong, P.W.K.4
Sora, J.5
-
6
-
-
0028890671
-
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
-
Engbersen AMT, Franken DG, Boers GHJ, Stevens EMB, Trijbels FJM, Blom HJ. Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. Am J Hum Genet 1995; 56: 142-50.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 142-150
-
-
Engbersen, A.M.T.1
Franken, D.G.2
Boers, G.H.J.3
Stevens, E.M.B.4
Trijbels, F.J.M.5
Blom, H.J.6
-
7
-
-
0030610090
-
The Mutation Ala677→Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
-
Arruda VR, von Zuben PM, Chiaparini LC, Annichino-Bizzacchi JM, Costa FF. The Mutation Ala677→Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 1997; 77: 818-21.
-
(1997)
Thromb Haemost
, vol.77
, pp. 818-821
-
-
Arruda, V.R.1
Von Zuben, P.M.2
Chiaparini, L.C.3
Annichino-Bizzacchi, J.M.4
Costa, F.F.5
-
8
-
-
0030897112
-
Genetic polymorphism of 5,10-methylentetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease
-
Morita H, Taguchi J, Kurihara H, Kitaoka M, Kaneda H, Kurihara Y, Maemura K, Shindo T, Minamino T, Ohno M, Yamaoki K, Ogasawara K, Aizawa T, Suzuki S, Yazaki Y. Genetic polymorphism of 5,10-methylentetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease. Circulation 1997; 95: 2032-6.
-
(1997)
Circulation
, vol.95
, pp. 2032-2036
-
-
Morita, H.1
Taguchi, J.2
Kurihara, H.3
Kitaoka, M.4
Kaneda, H.5
Kurihara, Y.6
Maemura, K.7
Shindo, T.8
Minamino, T.9
Ohno, M.10
Yamaoki, K.11
Ogasawara, K.12
Aizawa, T.13
Suzuki, S.14
Yazaki, Y.15
-
9
-
-
0029655724
-
Molecular genetic analysis in mild hyperhomocysteinemia: A common mutation in the methylentetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
-
Kluijtmans LAJ, van den Heuvel LPWJ, Boers GHJ, Frosst P, Stevens EMB, van Oost BA, den Heijer M, Trijbels FJH, Rozen R, Blom H. Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylentetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. Am J Hum Genet 1996; 58: 35-41.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 35-41
-
-
Kluijtmans, L.A.J.1
Van Den Heuvel, L.P.W.J.2
Boers, G.H.J.3
Frosst, P.4
Stevens, E.M.B.5
Van Oost, B.A.6
Den Heijer, M.7
Trijbels, F.J.H.8
Rozen, R.9
Blom, H.10
-
10
-
-
0030057401
-
Distribution in healthy and coronary populations of the methylentetrahydrofolate reductase (MTHFR) C677T mutation
-
Wilcken DEL, Wang XL, Sim AS, McCredie M. Distribution in healthy and coronary populations of the methylentetrahydrofolate reductase (MTHFR) C677T mutation. Arterioscler Thromb Vasc Biol 1996; 16: 878-82.
-
(1996)
Arterioscler Thromb Vasc Biol
, vol.16
, pp. 878-882
-
-
Wilcken, D.E.L.1
Wang, X.L.2
Sim, A.S.3
McCredie, M.4
-
12
-
-
0031049530
-
A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction
-
Brugada R, Marian AJ. A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction. Atherosclerosis 1997; 128: 107-12.
-
(1997)
Atherosclerosis
, vol.128
, pp. 107-112
-
-
Brugada, R.1
Marian, A.J.2
-
13
-
-
76549154241
-
Transluminal treatment of arteriosclerotic obstruction: Description of a new technique and a preliminary report of its application
-
Dotter CT, Judkins MP. Transluminal treatment of arteriosclerotic obstruction: description of a new technique and a preliminary report of its application. Circulation 1964; 30: 654-70.
-
(1964)
Circulation
, vol.30
, pp. 654-670
-
-
Dotter, C.T.1
Judkins, M.P.2
-
14
-
-
0028950718
-
Local lesion-related factors and restenosis after coronary angioplasty
-
De Groote P, Bauters C, Mc Fadden E, Lablanche JM, Leroy F, Bertrand ME. Local lesion-related factors and restenosis after coronary angioplasty. Circulation 1995; 91: 968-72.
-
(1995)
Circulation
, vol.91
, pp. 968-972
-
-
De Groote, P.1
Bauters, C.2
Mc Fadden, E.3
Lablanche, J.M.4
Leroy, F.5
Bertrand, M.E.6
-
16
-
-
0028298802
-
Myocardial infarction and coronary deaths in the World Health Organization MONICA Project
-
Tunstall-Pedoe H, Kuulasmaa K, Amouyel P, Arveiler D, Rajakangas AM, Pajak A. Myocardial infarction and coronary deaths in the World Health Organization MONICA Project. Circulation 1994; 90: 583-612.
-
(1994)
Circulation
, vol.90
, pp. 583-612
-
-
Tunstall-Pedoe, H.1
Kuulasmaa, K.2
Amouyel, P.3
Arveiler, D.4
Rajakangas, A.M.5
Pajak, A.6
-
17
-
-
0026651085
-
Wine, alcohol, platelets, and the French paradox for coronary artery disease
-
Renaud S, De Lorgeril M. Wine, alcohol, platelets, and the French paradox for coronary artery disease. Lancet 1992; 339: 1523-6.
-
(1992)
Lancet
, vol.339
, pp. 1523-1526
-
-
Renaud, S.1
De Lorgeril, M.2
-
18
-
-
2642705332
-
The VITA project: Risk of venous thromboembolism and C677T mutation of the MTHFR gene
-
(abstract).
-
Missiaglia E, Tosetto A, Rodeghiero F. The VITA project: risk of venous thromboembolism and C677T mutation of the MTHFR gene (abstract). Thromb Haemost 1997; (suppl.): 393.
-
(1997)
Thromb Haemost
, Issue.SUPPL.
, pp. 393
-
-
Missiaglia, E.1
Tosetto, A.2
Rodeghiero, F.3
-
19
-
-
0001059635
-
Prevalence of factor V 1691 C to a and methylentetrahydrofolate reductase 677C to T mutated genes in patients with venous thrombosis
-
(abstract).
-
De Stefano V, Chiusolo P, Paciaroni K, Casarelli I, Serra FG, Bizzi B, Leone G. Prevalence of factor V 1691 C to A and methylentetrahydrofolate reductase 677C to T mutated genes in patients with venous thrombosis (abstract). Thromb Haemost 1997; (suppl): 569.
-
Thromb Haemost
, vol.1997
, Issue.SUPPL.
, pp. 569
-
-
De Stefano, V.1
Chiusolo, P.2
Paciaroni, K.3
Casarelli, I.4
Serra, F.G.5
Bizzi, B.6
Leone, G.7
-
20
-
-
0030743692
-
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia
-
Grandone E, Margaglione M, Calaizzo D, Cappucci G, Paladini D, Martinelli P, Montanaro S, Pavone G, Di Minno G. Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997; 77: 1052-4.
-
(1997)
Thromb Haemost
, vol.77
, pp. 1052-1054
-
-
Grandone, E.1
Margaglione, M.2
Calaizzo, D.3
Cappucci, G.4
Paladini, D.5
Martinelli, P.6
Montanaro, S.7
Pavone, G.8
Di Minno, G.9
-
22
-
-
0030027668
-
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase and plasma homocysteine concentrations
-
Jacques P, Bostom A, Williams R. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase and plasma homocysteine concentrations. Circulation 1996; 93: 7-9.
-
(1996)
Circulation
, vol.93
, pp. 7-9
-
-
Jacques, P.1
Bostom, A.2
Williams, R.3
-
23
-
-
0005775025
-
The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African Americans
-
Mc Andrew P, Brandt JT, Pearl DK, Prior TW. The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African Americans. Thromb Res 1996; 83: 195-8.
-
(1996)
Thromb Res
, vol.83
, pp. 195-198
-
-
Mc Andrew, P.1
Brandt, J.T.2
Pearl, D.K.3
Prior, T.W.4
-
24
-
-
0031066138
-
Is the common 677 C → T mutation in the 5-10 methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis
-
Van der Put NMJ, Eskes AC, Blom HJ. Is the common 677 C → T mutation in the 5-10 methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis. Q J Med 1997; 90: 111-5.
-
(1997)
Q J Med
, vol.90
, pp. 111-115
-
-
Van Der Put, N.M.J.1
Eskes, A.C.2
Blom, H.J.3
-
25
-
-
0028803474
-
A genetic defect in 5-10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, Kirke PN, burke H, Molloy AM, Weir DG, Shields DC, Scott JM. A genetic defect in 5-10 methylenetetrahydrofolate reductase in neural tube defects. Q J Med 1995; 88: 763-6.
-
(1995)
Q J Med
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
Kirke, P.N.4
Burke, H.5
Molloy, A.M.6
Weir, D.G.7
Shields, D.C.8
Scott, J.M.9
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