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Journal Abstract Search

130 related items for PubMed ID: 8345800

  • 1. The response to lovastatin treatment in patients with heterozygous familial hypercholesterolemia is modulated by apolipoprotein E polymorphism.
    Carmena R, Roederer G, Mailloux H, Lussier-Cacan S, Davignon J.
    Metabolism; 1993 Jul; 42(7):895-901. PubMed ID: 8345800
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  • 2. The influence of apolipoprotein E phenotype on the response to lovastatin therapy in patients with heterozygous familial hypercholesterolemia.
    O'Malley JP, Illingworth DR.
    Metabolism; 1990 Feb; 39(2):150-4. PubMed ID: 2299987
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  • 9. Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction.
    Hopkins PN, Wu LL, Schumacher MC, Emi M, Hegele RM, Hunt SC, Lalouel JM, Williams RR.
    Arterioscler Thromb; 1991 Feb; 11(5):1137-46. PubMed ID: 1680391
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  • 11. Apolipoprotein E polymorphism and heterozygous familial hypercholesterolemia. Sex-specific effects.
    Ferrières J, Sing CF, Roy M, Davignon J, Lussier-Cacan S.
    Arterioscler Thromb; 1994 Oct; 14(10):1553-60. PubMed ID: 7918304
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  • 12. Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defects.
    Raal FJ, Pilcher G, Rubinsztein DC, Lingenhel A, Utermann G.
    Atherosclerosis; 1997 Feb 28; 129(1):97-102. PubMed ID: 9069523
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  • 14. Is responsiveness to lovastatin in familial hypercholesterolaemia heterozygotes influenced by the specific mutation in the low-density lipoprotein receptor gene?
    Leren TP, Hjermann I.
    Eur J Clin Invest; 1995 Dec 28; 25(12):967-73. PubMed ID: 8719939
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  • 16. Influence of LDL receptor gene mutation and apo E polymorphism on lipoprotein response to simvastatin treatment among adolescents with heterozygous familial hypercholesterolemia.
    Vohl MC, Szots F, Lelièvre M, Lupien PJ, Bergeron J, Gagné C, Couture P.
    Atherosclerosis; 2002 Feb 28; 160(2):361-8. PubMed ID: 11849659
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  • 17. Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation.
    Ferrières J, Lambert J, Lussier-Cacan S, Davignon J.
    Circulation; 1995 Aug 01; 92(3):290-5. PubMed ID: 7634440
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  • 18. Apolipoprotein E phenotypes in familial hypercholesterolaemia: importance for expression of disease and response to therapy.
    Berglund L, Wiklund O, Eggertsen G, Olofsson SO, Eriksson M, Lindén T, Bondjers G, Angelin B.
    J Intern Med; 1993 Feb 01; 233(2):173-8. PubMed ID: 8433078
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  • 19. Apolipoprotein E polymorphism influences lipid phenotypic expression, but not the low density lipoprotein subfraction distribution in familial combined hyperlipidemia.
    Bredie SJ, Vogelaar JM, Demacker PN, Stalenhoef AF.
    Atherosclerosis; 1996 Oct 25; 126(2):313-24. PubMed ID: 8902157
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