-
1
-
-
1842331509
-
Plasma homocysteine as a risk factor for vascular disease
-
Graham IM, Daly LE, Refsum H, 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.3
Robinson, K.4
Brattstrom, L.E.5
Ueland, P.M.6
-
2
-
-
0032442389
-
Novel risk factors for vascular disease: the homocysteine hypothesis of cardiovascular disease
-
Wilcken DEL Novel risk factors for vascular disease: the homocysteine hypothesis of cardiovascular disease. J Cardiovasc Risk 1998; 5: 217–221.
-
(1998)
J Cardiovasc Risk
, vol.5
, pp. 217-221
-
-
Wilcken, D.E.L.1
-
3
-
-
0032417638
-
Plasma homocysteine and coronary heart disease: systematic review of published epidemiological studies
-
Danesh J, Lewington S. Plasma homocysteine and coronary heart disease: systematic review of published epidemiological studies. J Cardiovasc Risk 1998; 5: 229–232.
-
(1998)
J Cardiovasc Risk
, vol.5
, pp. 229-232
-
-
Danesh, J.1
Lewington, S.2
-
4
-
-
0025944056
-
Risk of fatal coronary heart disease in familial hypercholesterolaemia
-
Simon Broome Register Group. Risk of fatal coronary heart disease in familial hypercholesterolaemia. BMJ 1991; 303: 893–896.
-
(1991)
BMJ
, vol.303
, pp. 893-896
-
-
-
5
-
-
0025745305
-
Detection of the apoB3500 (glutamine for arginine) by gene amplification and cleavage with Mspl.
-
Mansen PS, Rudiger N, Tybaerg-Hansen A, Faergeman O, Gregersen N. Detection of the apoB3500 (glutamine for arginine) by gene amplification and cleavage with Mspl. J Lipid Res 1991; 32: 1229–1233.
-
(1991)
J Lipid Res
, vol.32
, pp. 1229-1233
-
-
Mansen, P.S.1
Rudiger, N.2
Tybaerg-Hansen, A.3
Faergeman, O.4
Gregersen, N.5
-
6
-
-
0029049553
-
A candidate genetic risk factor for vascular disease; a common mutation in methylene tetrahydrofolate 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 methylene tetrahydrofolate reductase. Nature Genet 1995; 10: 111–113.
-
(1995)
Nature 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
-
8
-
-
0001704784
-
Total homocysteine and cardiovascular disease
-
Nygard O, Vollset SE, Refsum H, Brattstrom L, Ueland PM. Total homocysteine and cardiovascular disease. J Intern Med 1999; 246: 425–454.
-
(1999)
J Intern Med
, vol.246
, pp. 425-454
-
-
Nygard, O.1
Vollset, S.E.2
Refsum, H.3
Brattstrom, L.4
Ueland, P.M.5
-
9
-
-
0032497941
-
Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not vascular disease
-
Brattstrom L, Wilcken DEL, Ogrvik J, Brudin L. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not vascular disease. Circulation 1998; 98: 2520–2526.
-
(1998)
Circulation
, vol.98
, pp. 2520-2526
-
-
Brattstrom, L.1
Wilcken, D.E.L.2
Ogrvik, J.3
Brudin, L.4
-
10
-
-
0024546356
-
Development of coronary heart disease in familial hypercholesterolaemia
-
Mabuchi H, Koizumi J, Shimuzu M, Takeda R. Development of coronary heart disease in familial hypercholesterolaemia. Circulation 1989; 79: 225–232.
-
(1989)
Circulation
, vol.79
, pp. 225-232
-
-
Mabuchi, H.1
Koizumi, J.2
Shimuzu, M.3
Takeda, R.4
-
12
-
-
0002282359
-
Homocysteine is not an additional risk factor in familial hyper-cholesterolaemia [abstract]
-
in
-
Defesche JC, Maduro EM, Wittekoek ME, Redeker EJW, Mannens MAMM, Kastelein JJP. Homocysteine is not an additional risk factor in familial hyper-cholesterolaemia [abstract]. in: European Atherosclerosis Society 70th Congress Conference Proceedings; 1998. p. 25.
-
(1998)
European Atherosclerosis Society 70th Congress Conference Proceedings
, pp. 25
-
-
Defesche, J.C.1
Maduro, E.M.2
Wittekoek, M.E.3
Redeker, E.J.W.4
Mannens, M.A.M.M.5
Kastelein, J.J.P.6
-
13
-
-
0031594680
-
The C677T mutation in the methylene-tetra-hydrofolate reductase gene predisposes to hyperhomocysteinemia in children with familial hypercholesterolaemia treated with cholestyramine
-
Tonstad S, Refsum H, Ose L, Ueland P. The C677T mutation in the methylene-tetra-hydrofolate reductase gene predisposes to hyperhomocysteinemia in children with familial hypercholesterolaemia treated with cholestyramine. J Paediatr 1998; 12: 365–368.
-
(1998)
J Paediatr
, vol.12
, pp. 365-368
-
-
Tonstad, S.1
Refsum, H.2
Ose, L.3
Ueland, P.4
-
14
-
-
0029882605
-
The extracranial carotid artery in familial hypercholesterolaemia: relationship of plasma lipids and coronary heart disease
-
Sidhu PS, Naoumova RP, Maher VMG, MacSweeney JE, Neuwirth CKY, Hollyer JS, et al The extracranial carotid artery in familial hypercholesterolaemia: relationship of plasma lipids and coronary heart disease. J Cardiovasc Risk 1996; 3: 61–67.
-
(1996)
J Cardiovasc Risk
, vol.3
, pp. 61-67
-
-
Sidhu, P.S.1
Naoumova, R.P.2
Maher, V.M.G.3
MacSweeney, J.E.4
Neuwirth, C.K.Y.5
Hollyer, J.S.6
-
15
-
-
0030852520
-
Association between plasma homocysteine and parental history of cardiovascular disease in children with familial hypercholesterolaemia
-
Tonstad S, Refsum H, Ueland PM. Association between plasma homocysteine and parental history of cardiovascular disease in children with familial hypercholesterolaemia. Circulation 1997; 96: 1803–1808.
-
(1997)
Circulation
, vol.96
, pp. 1803-1808
-
-
Tonstad, S.1
Refsum, H.2
Ueland, P.M.3
-
16
-
-
0028907712
-
Susceptibility of low-density lipoprotein to oxidation in familial hypercholesterolaemia
-
Raal FJ, Areias AJ, Waisberg R, Von Arb M. Susceptibility of low-density lipoprotein to oxidation in familial hypercholesterolaemia. Atherosclerosis 1995; 115: 9–15.
-
(1995)
Atherosclerosis
, vol.115
, pp. 9-15
-
-
Raal, F.J.1
Areias, A.J.2
Waisberg, R.3
Von Arb, M.4
-
17
-
-
0033135609
-
Low-density lipoprotein cholesterol bulk is the pivotal determinant of atherosclerosis in familial hypercholesterolemia
-
Raal FJ, Pilcher GJ, Waisberg R, Buthelezi EP, Veller MG, Joffe Bl. Low-density lipoprotein cholesterol bulk is the pivotal determinant of atherosclerosis in familial hypercholesterolemia. Am J Cardiol 1999; 83: 1330–1333.
-
(1999)
Am J Cardiol
, vol.83
, pp. 1330-1333
-
-
Raal, F.J.1
Pilcher, G.J.2
Waisberg, R.3
Buthelezi, E.P.4
Veller, M.G.5
Joffe, B.6
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