-
1
-
-
0019434645
-
Hypothesis: Iron and the sex difference in heart disease risk
-
Sullivan JL. Hypothesis: iron and the sex difference in heart disease risk. Lancet 1981;i:1293-4.
-
(1981)
Lancet
-
-
Sullivan, J.L.1
-
2
-
-
0026800818
-
High stored iron levels are associated with excess risk of myocardial infarction in eastern Finnish men
-
Salonen JT, Nyyssonen K, Korpela H, et al. High stored iron levels are associated with excess risk of myocardial infarction in eastern Finnish men. Circulation 1992;86:803-11.
-
(1992)
Circulation
, vol.86
, pp. 803-811
-
-
Salonen, J.T.1
Nyyssonen, K.2
Korpela, H.3
-
3
-
-
0033823617
-
Serum ferritin and death from all causes and cardiovascular disease. The NHANES II mortality study
-
Sempos CT, Looker AC, Gillum RF, et al. Serum ferritin and death from all causes and cardiovascular disease. The NHANES II mortality study. Ann Epidemiol 2000;10:441-8.
-
(2000)
Ann Epidemiol
, vol.10
, pp. 441-448
-
-
Sempos, C.T.1
Looker, A.C.2
Gillum, R.F.3
-
4
-
-
0028259016
-
Body iron stores and the risk of coronary heart disease
-
Sempos CT, Looker AC, Gillum RF, et al. Body iron stores and the risk of coronary heart disease. N Engl J Med 1994;330:1119-24.
-
(1994)
N Engl J Med
, vol.330
, pp. 1119-1124
-
-
Sempos, C.T.1
Looker, A.C.2
Gillum, R.F.3
-
5
-
-
0033596677
-
Coronary heart disease and iron status: Meta-analyses of prospective studies
-
Danesh J, Appleby P. Coronary heart disease and iron status: meta-analyses of prospective studies. Circulation 2001;99:852-4.
-
(2001)
Circulation
, vol.99
, pp. 852-854
-
-
Danesh, J.1
Appleby, P.2
-
7
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996;13:399-408.
-
(1996)
Nat Genet
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
-
8
-
-
0005600868
-
A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium
-
Anon. A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium. Gut 1997;41:841-4.
-
(1997)
Gut
, vol.41
, pp. 841-844
-
-
-
9
-
-
0032879932
-
Haemochromatosis mutations in North-East Scotland
-
Miedzybrodzka Z, Loughlin S, Baty D, et al. Haemochromatosis mutations in North-East Scotland. Br J Haematol 1999;106:385-7.
-
(1999)
Br J Haematol
, vol.106
, pp. 385-387
-
-
Miedzybrodzka, Z.1
Loughlin, S.2
Baty, D.3
-
10
-
-
0034609577
-
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic
-
Beutler E, Felitti V, Gelbart T, et al. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Ann Intern Med 2000;133:329-37.
-
(2000)
Ann Intern Med
, vol.133
, pp. 329-337
-
-
Beutler, E.1
Felitti, V.2
Gelbart, T.3
-
11
-
-
0033592395
-
Heterozygosity for a hereditary haemochromatosis gene is associated with cardiovascular death in women
-
Roest M, Van der Schouw YT, de Valk B, et al. Heterozygosity for a hereditary haemochromatosis gene is associated with cardiovascular death in women. Circulation 1999;100:1268-73.
-
(1999)
Circulation
, vol.100
, pp. 1268-1273
-
-
Roest, M.1
Van Der Schouw, Y.T.2
De Valk, B.3
-
12
-
-
0033592398
-
Increased risk of acute myocardial infarction in carriers of the hemochromatosis gene Cys282Tyr mutation: A prospective cohort study in men in eastern Finland
-
Tuomainen TP, Kontula K, Nyyssonen K, et al. Increased risk of acute myocardial infarction in carriers of the hemochromatosis gene Cys282Tyr mutation: a prospective cohort study in men in eastern Finland. Circulation 1999;100:1274-9.
-
(1999)
Circulation
, vol.100
, pp. 1274-1279
-
-
Tuomainen, T.P.1
Kontula, K.2
Nyyssonen, K.3
-
13
-
-
0035864617
-
A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: The atherosclerosis risk in communities (ARIC) study
-
Rasmussen ML, Folsom AR, Catellier DJ, et al. A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the atherosclerosis risk in communities (ARIC) study. Atherosclerosis 2001;154:739-46.
-
(2001)
Atherosclerosis
, vol.154
, pp. 739-746
-
-
Rasmussen, M.L.1
Folsom, A.R.2
Catellier, D.J.3
-
14
-
-
0034089969
-
Haemochromatosis gene mutations and risk of coronary artery disease
-
Battiloro E, Ombres D, Pascale E, et al. Haemochromatosis gene mutations and risk of coronary artery disease. Eur J Hum Genet 2000;8:389-92.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 389-392
-
-
Battiloro, E.1
Ombres, D.2
Pascale, E.3
-
15
-
-
0035009328
-
Association studies between hameochromatosis gene mutations and the risk of cardiovascular diseases
-
Hetet G, Elbaz A, Gariepy J, et al. Association studies between hameochromatosis gene mutations and the risk of cardiovascular diseases. Eur J Clin Invest 2001;31:382-8.
-
(2001)
Eur J Clin Invest
, vol.31
, pp. 382-388
-
-
Hetet, G.1
Elbaz, A.2
Gariepy, J.3
-
16
-
-
0031720168
-
Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease
-
Franco RF, Zago MA, Trip MD, et al. Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease. Br J Haematol 1998;102:1172-5.
-
(1998)
Br J Haematol
, vol.102
, pp. 1172-1175
-
-
Franco, R.F.1
Zago, M.A.2
Trip, M.D.3
-
17
-
-
0034863686
-
Genetic hemochromatosis, a Celtic disease: Is it now time for population screening?
-
Byrnes V, Ryan E, Barrett S, et al. Genetic hemochromatosis, a Celtic disease: is it now time for population screening? Genet Test 2001;5:127-30.
-
(2001)
Genet Test
, vol.5
, pp. 127-130
-
-
Byrnes, V.1
Ryan, E.2
Barrett, S.3
-
18
-
-
0029934416
-
Sex differences in myocardial infarction and coronary deaths in the Scottish MONICA population of Glasgow 1985-1991: Presentation, diagnosis, treatment, and 28-day case fatality of 2991 events in men and 1551 events in women
-
Tunstall-Pedoe H, Morrison C, Woodward M, et al. Sex differences in myocardial infarction and coronary deaths in the Scottish MONICA population of Glasgow 1985-1991: presentation, diagnosis, treatment, and 28-day case fatality of 2991 events in men and 1551 events in women. Circulation 1996;93:1981-92.
-
(1996)
Circulation
, vol.93
, pp. 1981-1992
-
-
Tunstall-Pedoe, H.1
Morrison, C.2
Woodward, M.3
-
20
-
-
0034510324
-
Detection of an unusual combination of mutations in the HFE gene for hemochromatosis
-
Thorstensen K, Asberg A, Kvitland M, et al. Detection of an unusual combination of mutations in the HFE gene for hemochromatosis. Genet Test 2000;4:371-6.
-
(2000)
Genet Test
, vol.4
, pp. 371-376
-
-
Thorstensen, K.1
Asberg, A.2
Kvitland, M.3
-
21
-
-
37049251476
-
Mendelian proportions in a mixed population
-
Hardy GH. Mendelian proportions in a mixed population. Science 1908;28:41-50.
-
(1908)
Science
, vol.28
, pp. 41-50
-
-
Hardy, G.H.1
-
24
-
-
6844258231
-
Relation of HFE gene mutations, high iron stores and early onset coronary artery disease
-
Nassar BA, Zayed EM, Title LM, et al. Relation of HFE gene mutations, high iron stores and early onset coronary artery disease. Can J Cardiol 1998;14:215-20.
-
(1998)
Can J Cardiol
, vol.14
, pp. 215-220
-
-
Nassar, B.A.1
Zayed, E.M.2
Title, L.M.3
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