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Journal Abstract Search

155 related items for PubMed ID: 8820109

  • 21. Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension.
    Hunt SC, Wu LL, Hopkins PN, Stults BM, Kuida H, Ramirez ME, Lalouel JM, Williams RR.
    Arteriosclerosis; 1989; 9(3):335-44. PubMed ID: 2497719
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  • 22. Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia.
    Bredie SJ, van Drongelen J, Kiemeney LA, Demacker PN, Beaty TH, Stalenhoef AF.
    Arterioscler Thromb Vasc Biol; 1997 May; 17(5):834-40. PubMed ID: 9157945
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  • 23. Two newly identified SNPs in the APO AI-CIII intergenic region are strongly associated with familial combined hyperlipidaemia.
    Groenendijk M, Cantor RM, Funke H, Dallinga-Thie GM.
    Eur J Clin Invest; 2001 Oct; 31(10):852-9. PubMed ID: 11737222
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  • 29. Use of DNA polymorphisms of the apolipoprotein genes to study the role of genetic variation in the determination of serum lipid levels.
    Humphries SE, Talmud PJ, Kessling AM.
    Ciba Found Symp; 1987 Oct; 130():128-49. PubMed ID: 2894927
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  • 32. Apolipoproteins C-III and A-V as predictors of very-low-density lipoprotein triglyceride and apolipoprotein B-100 kinetics.
    Chan DC, Watts GF, Nguyen MN, Barrett PH.
    Arterioscler Thromb Vasc Biol; 2006 Mar; 26(3):590-6. PubMed ID: 16410456
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  • 37. Nomogram to diagnose familial combined hyperlipidemia on the basis of results of a 5-year follow-up study.
    Veerkamp MJ, de Graaf J, Hendriks JC, Demacker PN, Stalenhoef AF.
    Circulation; 2004 Jun 22; 109(24):2980-5. PubMed ID: 15184285
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  • 40. Severe hyperlipidemia in apolipoprotein E2 homozygotes due to a combined effect of hyperinsulinemia and an SstI polymorphism.
    Sijbrands EJ, Hoffer MJ, Meinders AE, Havekes LM, Frants RR, Smelt AH, De Knijff P.
    Arterioscler Thromb Vasc Biol; 1999 Nov 22; 19(11):2722-9. PubMed ID: 10559017
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