-
2
-
-
0030876147
-
Hyperhomocyst (e) inemia is a risk factor for arterial endothelial dysfunction in humans
-
Woo KS, Chook P, Lolin YI, Cheung ASP, Chan LT, Sun YY, et al. Hyperhomocyst (e) inemia is a risk factor for arterial endothelial dysfunction in humans. Circulation 1997; 96: 2542-2544.
-
(1997)
Circulation
, vol.96
, pp. 2542-2544
-
-
Woo, K.S.1
Chook, P.2
Lolin, Y.I.3
Cheung, A.S.P.4
Chan, L.T.5
Sun, Y.Y.6
-
3
-
-
1842331509
-
Plasma homocysteine as a risk factor for vascular disease
-
Graham IM, Daly LE, Refsum HM, Robinson K, Brattstrom LE Ueland PM, et al. Plasma homocysteine as a risk factor for vascular disease. JAMA 1997; 277: 1775-1781.
-
(1997)
JAMA
, vol.277
, pp. 1775-1781
-
-
Graham, I.M.1
Daly, L.E.2
Refsum, H.M.3
Robinson, K.4
Brattstrom, L.E.5
Ueland, P.M.6
-
4
-
-
0000167774
-
Disorders of transsulphuration
-
Scriver C, Beaudet A, Sly W, Valle D (eds.). 8th ed. New York: McGraw Hill Inc
-
Mudd D, Levy HI, Kraus JP. Disorders of transsulphuration. En: Scriver C, Beaudet A, Sly W, Valle D (eds.). The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw Hill Inc.; 2001. p. 2007-2056.
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 2007-2056
-
-
Mudd, D.1
Levy, H.I.2
Kraus, J.P.3
-
7
-
-
0034353203
-
Influence of 699C-T and 1080C-T polymorphisms of the cystathionine B synthase gene on plasma homocysteine levels
-
Aras O, Hanson NQ, Yang F, Tsai MY. Influence of 699C-T and 1080C-T polymorphisms of the cystathionine B synthase gene on plasma homocysteine levels. Clin Genet 2000; 58: 455-459.
-
(2000)
Clin Genet
, vol.58
, pp. 455-459
-
-
Aras, O.1
Hanson, N.Q.2
Yang, F.3
Tsai, M.Y.4
-
8
-
-
0029068922
-
The molecular basis of homocystinuria due to cystathionine b synthase deficiency in Italian families, and report of four novel mutations
-
Sebastio G, Sperandeo MP, Panico M, Francis R, Kraus JP, Andria G. The molecular basis of homocystinuria due to cystathionine b synthase deficiency in Italian families, and report of four novel mutations. Am J Hum Genet 1995; 56: 1324-1333.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1324-1333
-
-
Sebastio, G.1
Sperandeo, M.P.2
Panico, M.3
Francis, R.4
Kraus, J.P.5
Andria, G.6
-
10
-
-
0032521543
-
Homozygous cystathionine b synthase deficiency; combined with factor V leiden or thermolabile methylenetetrahidrofolate reductase in the risk of venous thrombosis
-
Kluijtmans LAJ, Boers GHJ, Verbruggen B, Trijbels FJM, Novàkovà IRO, Blom HJ. Homozygous cystathionine b synthase deficiency; combined with factor V leiden or thermolabile methylenetetrahidrofolate reductase in the risk of venous thrombosis. Blood 1996; 91: 2015-2018.
-
(1996)
Blood
, vol.91
, pp. 2015-2018
-
-
Kluijtmans, L.A.J.1
Boers, G.H.J.2
Verbruggen, B.3
Trijbels, F.J.M.4
Novàkovà, I.R.O.5
Blom, H.J.6
-
11
-
-
0033782733
-
Contribution of the cystathionine b synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia
-
Franchis R, Fermo I, Mazzola G, Sebastio G, Di Minno G, Coppola A, et al. Contribution of the cystathionine b synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia. Thromb Haemost 2000; 84: 576-582.
-
(2000)
Thromb Haemost
, vol.84
, pp. 576-582
-
-
Franchis, R.1
Fermo, I.2
Mazzola, G.3
Sebastio, G.4
Di Minno, G.5
Coppola, A.6
-
12
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahidrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahidrofolate reductase. Nat Genet 1995; 10: 111-113.
-
(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.G.6
-
13
-
-
0025095390
-
Impaired homocysteine metabolism in early-onset cerebral and peripheral occlusive arterial disease
-
Brattstrom L, Israelsson B, Norrving B, Bergqvist D, Thorne J, Hultberg B, et al. Impaired homocysteine metabolism in early-onset cerebral and peripheral occlusive arterial disease. Atherosclerosis 1990; 81: 51-60.
-
(1990)
Atherosclerosis
, vol.81
, pp. 51-60
-
-
Brattstrom, L.1
Israelsson, B.2
Norrving, B.3
Bergqvist, D.4
Thorne, J.5
Hultberg, B.6
-
14
-
-
0021998698
-
Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease
-
Boers GHJ, Smals AGH, Trijbels FJM, Fowler B, Bakkeren JAJM, Schoonderwaldt HC, et al. Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease. N Engl J Med 1985; 313: 709-715.
-
(1985)
N Engl J Med
, vol.313
, pp. 709-715
-
-
Boers, G.H.J.1
Smals, A.G.H.2
Trijbels, F.J.M.3
Fowler, B.4
Bakkeren, J.A.J.M.5
Schoonderwaldt, H.C.6
-
15
-
-
33646037235
-
Diagnóstico y tratamiento del infarto agudo del miocardio
-
Bogotá: Sociedad Colombiana de Cardiología
-
Bohórquez R, Isaza D. Diagnóstico y tratamiento del infarto agudo del miocardio. En: Texto de Cardiología. Bogotá: Sociedad Colombiana de Cardiología; 1999. p. 450-466.
-
(1999)
Texto De Cardiología
, pp. 450-466
-
-
Bohórquez, R.1
Isaza, D.2
-
16
-
-
0027198477
-
Disordered methionine/homocysteine metabolism in premature vascular disease
-
Dudman NPB, Wilcken D, Wang J, Lynch JF, Macey D, Lundberg P. Disordered methionine/homocysteine metabolism in premature vascular disease. Arterioscler Thromb 1993; 13: 1253-1260.
-
(1993)
Arterioscler Thromb
, vol.13
, pp. 1253-1260
-
-
Dudman, N.P.B.1
Wilcken, D.2
Wang, J.3
Lynch, J.F.4
Macey, D.5
Lundberg, P.6
-
17
-
-
0029035643
-
Rapid, fully automated measurement of plasma homocyst (e) ine with the Abbott IMx analyzer
-
Shipchandler MT, Moore EG. Rapid, fully automated measurement of plasma homocyst (e) ine with the Abbott IMx analyzer. Clin Chem 1995; 41: 991-994.
-
(1995)
Clin Chem
, vol.41
, pp. 991-994
-
-
Shipchandler, M.T.1
Moore, E.G.2
-
18
-
-
0037269292
-
Cystathionine B-synthase polymorphisms and hyperhomocysteinemia: An association study
-
Lievers KJA, Kluijtmans LAJ, Heil SG, Boers GHJ, Verhoef P, Heijer M, et al. Cystathionine B-synthase polymorphisms and hyperhomocysteinemia: an association study. Eur J Hum Genet 2003; 11: 23-29.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 23-29
-
-
Lievers, K.J.A.1
Kluijtmans, L.A.J.2
Heil, S.G.3
Boers, G.H.J.4
Verhoef, P.5
Heijer, M.6
-
19
-
-
0343503018
-
High prevalence of the thermolabile methylenetetrahidrofolate reductase variant in Mexico: A country with a very high prevalence of neural tube defect
-
Mutchinick OM, López MA, Luna L, Waxman J, Babinsky VE. High prevalence of the thermolabile methylenetetrahidrofolate reductase variant in Mexico: A country with a very high prevalence of neural tube defect. Mol Genet Metab 1999; 68: 461-467.
-
(1999)
Mol Genet Metab
, vol.68
, pp. 461-467
-
-
Mutchinick, O.M.1
López, M.A.2
Luna, L.3
Waxman, J.4
Babinsky, V.E.5
-
20
-
-
12344309062
-
Homocysteine and stroke: Evidence on a causal link from Mendelian randomisation
-
Casas JP, Bautista LE, Smeeth L, Sharma P, Hingorani AD. Homocysteine and stroke: evidence on a causal link from Mendelian randomisation. Lancet 2005; 365: 224-231.
-
(2005)
Lancet
, vol.365
, pp. 224-231
-
-
Casas, J.P.1
Bautista, L.E.2
Smeeth, L.3
Sharma, P.4
Hingorani, A.D.5
-
21
-
-
33646043359
-
Concentración plasmática de homocisteína en ayunas
-
Córdoba A., Arbeláez L, Castañeda S. Concentración plasmática de homocisteína en ayunas. Acta Med Colomb 2002; 27: 196-197.
-
(2002)
Acta Med Colomb
, vol.27
, pp. 196-197
-
-
Córdoba, A.1
Arbeláez, L.2
Castañeda, S.3
-
22
-
-
0030035427
-
The effect of a subnormal vitamin B-6 status on homocysteine metabolism
-
Ubbink JB, Van der Merwe A, Delpot R, Allen RH, Stabler SP, Riezier R. The effect of a subnormal vitamin B-6 status on homocysteine metabolism. J Clin Invest 1996; 98: 177-184.
-
(1996)
J Clin Invest
, vol.98
, pp. 177-184
-
-
Ubbink, J.B.1
Van der Merwe, A.2
Delpot, R.3
Allen, R.H.4
Stabler, S.P.5
Riezier, R.6
-
23
-
-
33646041206
-
High prevalence of CBS p.T191M mutation in homocystinuric patients from Colombia
-
Bermúdez M, Frank N, Bernal J, Urreizti R, Briceño I, Merinero B, et al. High prevalence of CBS p.T191M mutation in homocystinuric patients from Colombia. Hum Mutat 2006; 27: 296-303.
-
(2006)
Hum Mutat
, vol.27
, pp. 296-303
-
-
Bermúdez, M.1
Frank, N.2
Bernal, J.3
Urreizti, R.4
Briceño, I.5
Merinero, B.6
-
24
-
-
2342485635
-
Methylenetetrahidrofolate reductase gene C677T and A1298 C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease
-
Kolling K, Ndrepepa G, Werner K. Methylenetetrahidrofolate reductase gene C677T and A1298 C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease. Am J Cardiol 2004; 93: 1201-1205.
-
(2004)
Am J Cardiol
, vol.93
, pp. 1201-1205
-
-
Kolling, K.1
Ndrepepa, G.2
Werner, K.3
-
25
-
-
0032042477
-
Frequency of factor V (FV) Leiden and C677T methylenetetrahidrofolate reductase (MTHFR) mutations in Colombians
-
Camacho O, Giusti B, Restrepo CM, Abbate R, Pepe G. Frequency of factor V (FV) Leiden and C677T methylenetetrahidrofolate reductase (MTHFR) mutations in Colombians. Thromb Haemost 1998; 79: 883-884.
-
(1998)
Thromb Haemost
, vol.79
, pp. 883-884
-
-
Camacho, O.1
Giusti, B.2
Restrepo, C.M.3
Abbate, R.4
Pepe, G.5
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