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Volumn 56, Issue 226, 1996, Pages 65-71

A prospective cardiovascular population study used in genetic epidemiology. The Copenhagen City Heart Study

Author keywords

angiotensin converting enzyme gene polymorphism; glucose; high density lipoprotein; ischemic heart disease; lipoprotein lipase; mutation; stroke; triglycerides

Indexed keywords

DIPEPTIDYL CARBOXYPEPTIDASE; LIPOPROTEIN LIPASE;

EID: 0030340911     PISSN: 0085591X     EISSN: None     Source Type: Journal    
DOI: 10.1080/00365519609168300     Document Type: Article
Times cited : (10)

References (10)
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  • 2
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    • Collins, R.1    Peto, R.2    MacMahon, S.3    Hebert, P.4    Fiebach, N.H.5    Eberlein, K.A.6
  • 5
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    • The Copenhagen City Heart Study. Østerbroundersøgelsen. A book of tables with data from the first examination (1976-78) and a five year follow-up (1981-83)
    • The Copenhagen City Heart Study Group
    • Appleyard M, Hansen AT, Jensen G, Schnohr P, Nyboe J. The Copenhagen City Heart Study. Østerbroundersøgelsen. A book of tables with data from the first examination (1976-78) and a five year follow-up (1981-83). The Copenhagen City Heart Study Group. Scand J Soc Med 1989;Suppl 41:1-160.
    • (1989) Scand J Soc Med , Issue.41 SUPPL. , pp. 1-160
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  • 6
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    • 188 → Glu mutation in the lipoprotein lipase gene: Screening among 1000 heart patients and 5400 persons from the general population (The Copenhagen City Heart Study)
    • 188 → Glu mutation in the lipoprotein lipase gene: screening among 1000 heart patients and 5400 persons from the general population (The Copenhagen City Heart Study). Atherosclerosis 1994:109:205.
    • (1994) Atherosclerosis , vol.109 , pp. 205
    • Nordestgaard, B.G.1    Reeler, S.2    Steffensen, R.3    Tybjærg-Hansen, A.4
  • 7
    • 0001033625 scopus 로고
    • Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome
    • Scriver C, Beaudet A, Sly W, Valle D, eds. New York: McGraw-Hill Inc.
    • Brunzell J. Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. In: Scriver C, Beaudet A, Sly W, Valle D, eds. The metabolic and molecular bases of inherited disease, 7th ed. New York: McGraw-Hill Inc. 1995:1913-32.
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    • Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction
    • Cambien F, Poirier O, Lecerf L, Evans A, Cambou JP, Arveiler D, et al. Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature 1992;359: 641-4.
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    • Cambien, F.1    Poirier, O.2    Lecerf, L.3    Evans, A.4    Cambou, J.P.5    Arveiler, D.6
  • 9
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    • A prospective evaluation of an angiotensin-converting-enzyme gene polymorphism and the risk of ischemic heart disease
    • Lindpaintner K, Pfeffer MA, Kreutz R, Stampfer MJ, Grodstein F, LaMotte F, et al A prospective evaluation of an angiotensin-converting-enzyme gene polymorphism and the risk of ischemic heart disease. New Engl J Med 1995;332:706-11.
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  • 10
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    • The angiotensin-converting-enzyme gene polymorphism fails to predict coronary heart disease in a case-cohort study of 7300 individuals
    • Agerholm-Larsen B, Nordestgaard BG, Steffensen R, Sørensen TLA, The Copenhagen City Heart Study Group, Tybjærg-Hansen A. The angiotensin-converting-enzyme gene polymorphism fails to predict coronary heart disease in a case-cohort study of 7300 individuals. Circulation 1995;92, Suppl. 1:1 800.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.