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Volumn 2, Issue 3, 2002, Pages 5-7

Environmental modulation of atherosclerosis end points in familial hypercholesterolemia

Author keywords

[No Author keywords available]

Indexed keywords

LIVER TRIACYLGLYCEROL LIPASE; LOW DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN RECEPTOR;

EID: 0036514388     PISSN: 15675688     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1567-5688(01)00013-7     Document Type: Article
Times cited : (21)

References (11)
  • 2
    • 0031728287 scopus 로고    scopus 로고
    • Prevention of coronary heart disease in clinical practice: Recommendations of the Second Joint Task Force of European and other Societies on Coronary Prevention
    • Wood D., De Backer G., Faergeman O., Graham I., Mancia G., Pyorala K. Prevention of coronary heart disease in clinical practice: recommendations of the Second Joint Task Force of European and other Societies on Coronary Prevention. Atherosclerosis. 140:1998;199-270.
    • (1998) Atherosclerosis , vol.140 , pp. 199-270
    • Wood, D.1    De Backer, G.2    Faergeman, O.3    Graham, I.4    Mancia, G.5    Pyorala, K.6
  • 3
    • 0030823635 scopus 로고    scopus 로고
    • Candidate genes, small effects, and the prediction of atherosclerosis
    • Hegele R.A. Candidate genes, small effects, and the prediction of atherosclerosis. Crit. Rev. Clin. Lab. Sci. 34:1997;343-367.
    • (1997) Crit. Rev. Clin. Lab. Sci. , vol.34 , pp. 343-367
    • Hegele, R.A.1
  • 5
    • 84944284065 scopus 로고
    • Evidence that men with familial hypercholesterolemia can avoid early coronary death. An analysis of 77 gene carriers in four Utah pedigrees
    • Williams R.R., Hasstedt S.J., Wilson D.E., et al. Evidence that men with familial hypercholesterolemia can avoid early coronary death. An analysis of 77 gene carriers in four Utah pedigrees. J. Am. Med. Assoc. 255:1986;219-224.
    • (1986) J. Am. Med. Assoc. , vol.255 , pp. 219-224
    • Williams, R.R.1    Hasstedt, S.J.2    Wilson, D.E.3
  • 6
    • 0024496082 scopus 로고
    • Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia
    • Hegele R.A., Emi M., Wu L.L., Hopkins P.N., Williams R.R., Lalouel J.M. Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia. Am. J. Cardiol. 63:1989;109-112.
    • (1989) Am. J. Cardiol. , vol.63 , pp. 109-112
    • Hegele, R.A.1    Emi, M.2    Wu, L.L.3    Hopkins, P.N.4    Williams, R.R.5    Lalouel, J.M.6
  • 7
    • 0031838215 scopus 로고    scopus 로고
    • Phenotypic variation in heterozygous familial hypercholesterolemia: A comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or Canada
    • Pimstone S.N., Sun X.M., du Souich C., Frohlich J.J., Hayden M.R., Soutar A.K. Phenotypic variation in heterozygous familial hypercholesterolemia: a comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or Canada. Arterioscler. Thromb. Vasc. Biol. 18:1998;309-315.
    • (1998) Arterioscler. Thromb. Vasc. Biol. , vol.18 , pp. 309-315
    • Pimstone, S.N.1    Sun, X.M.2    Du Souich, C.3    Frohlich, J.J.4    Hayden, M.R.5    Soutar, A.K.6
  • 9
    • 0028157828 scopus 로고
    • Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia
    • Ng D.S., Leiter L.A., Vezina C., Connelly P.W., Hegele R.A. Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia. J. Clin. Invest. 93:1994;223-229.
    • (1994) J. Clin. Invest. , vol.93 , pp. 223-229
    • Ng, D.S.1    Leiter, L.A.2    Vezina, C.3    Connelly, P.W.4    Hegele, R.A.5
  • 10
    • 0033027001 scopus 로고    scopus 로고
    • The hepatic nuclear factor-1alpha G319S variant is associated with early-onset type 2 diabetes in Canadian Oji-Cree
    • Hegele R.A., Cao H., Harris S.B., Hanley A.J., Zinman B. The hepatic nuclear factor-1alpha G319S variant is associated with early-onset type 2 diabetes in Canadian Oji-Cree. J. Clin. Endocrinol. Metab. 84:1999;1077-1082.
    • (1999) J. Clin. Endocrinol. Metab. , vol.84 , pp. 1077-1082
    • Hegele, R.A.1    Cao, H.2    Harris, S.B.3    Hanley, A.J.4    Zinman, B.5
  • 11
    • 0034059075 scopus 로고    scopus 로고
    • Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
    • Cao H., Hegele R.A. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy. Hum. Mol. Genet. 9:2000;109-112.
    • (2000) Hum. Mol. Genet. , vol.9 , pp. 109-112
    • Cao, H.1    Hegele, R.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.