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Journal Abstract Search

285 related items for PubMed ID: 7634440

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  • 3. Elevated lipoprotein(a), hypertension and renal insufficiency as predictors of coronary artery disease in patients with genetically confirmed heterozygous familial hypercholesterolemia.
    Chan DC, Pang J, Hooper AJ, Burnett JR, Bell DA, Bates TR, van Bockxmeer FM, Watts GF.
    Int J Cardiol; 2015 Dec 15; 201():633-8. PubMed ID: 26340131
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  • 4. Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect.
    Carmena R, Lussier-Cacan S, Roy M, Minnich A, Lingenhel A, Kronenberg F, Davignon J.
    Arterioscler Thromb Vasc Biol; 1996 Jan 15; 16(1):129-36. PubMed ID: 8548413
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  • 6. The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia.
    Heath KE, Gudnason V, Humphries SE, Seed M.
    Atherosclerosis; 1999 Mar 15; 143(1):41-54. PubMed ID: 10208479
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  • 7. Metabolic factors clustering, lipoprotein cholesterol, apolipoprotein B, lipoprotein (a) and apolipoprotein E phenotypes in premature coronary artery disease in French Canadians.
    Weber M, McNicoll S, Marcil M, Connelly P, Lussier-Cacan S, Davignon J, Latour Y, Genest J.
    Can J Cardiol; 1997 Mar 15; 13(3):253-60. PubMed ID: 9117913
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  • 8. 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 Mar 15; 11(5):1137-46. PubMed ID: 1680391
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  • 10. Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrations.
    Torres AL, Moorjani S, Vohl MC, Gagné C, Lamarche B, Brun LD, Lupien PJ, Després JP.
    Atherosclerosis; 1996 Sep 27; 126(1):163-71. PubMed ID: 8879444
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  • 11. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK.
    Dan Med Bull; 2002 Nov 27; 49(4):318-45. PubMed ID: 12553167
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  • 12. Relationships of abdominal obesity and hyperinsulinemia to angiographically assessed coronary artery disease in men with known mutations in the LDL receptor gene.
    Gaudet D, Vohl MC, Perron P, Tremblay G, Gagné C, Lesiège D, Bergeron J, Moorjani S, Després JP.
    Circulation; 1998 Mar 10; 97(9):871-7. PubMed ID: 9521335
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  • 13. Serum low density lipoprotein cholesterol level and cholesterol absorption efficiency are influenced by apolipoprotein B and E polymorphism and by the FH-Helsinki mutation of the low density lipoprotein receptor gene in familial hypercholesterolemia.
    Gylling H, Aalto-Setälä K, Kontula K, Miettinen TA.
    Arterioscler Thromb; 1991 Mar 10; 11(5):1368-75. PubMed ID: 1911722
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  • 14. Genetic and environmental factors affecting the incidence of coronary artery disease in heterozygous familial hypercholesterolemia.
    Hill JS, Hayden MR, Frohlich J, Pritchard PH.
    Arterioscler Thromb; 1991 Mar 10; 11(2):290-7. PubMed ID: 1998646
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  • 15. Comparison of the effect of two low-density lipoprotein receptor class mutations on coronary heart disease among French-Canadian patients heterozygous for familial hypercholesterolaemia.
    Vohl MC, Gaudet D, Moorjani S, Tremblay G, Perron P, Gagné C, Lesiège D, Bergeron J, Lupien PJ, Després JP.
    Eur J Clin Invest; 1997 May 10; 27(5):366-73. PubMed ID: 9179542
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  • 16. 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 10; 14(10):1553-60. PubMed ID: 7918304
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  • 17. Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.
    Assouline L, Levy E, Feoli-Fonseca JC, Godbout C, Lambert M.
    Pediatrics; 1995 Aug 10; 96(2 Pt 1):239-46. PubMed ID: 7630677
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  • 18. Achilles tendon xanthomas are associated with the presence and burden of subclinical coronary atherosclerosis in heterozygous familial hypercholesterolemia: A pilot study.
    Mangili LC, Miname MH, Silva PRS, Bittencourt MS, Rocha VZ, Mangili OC, Salgado Filho W, Chacra AP, Jannes CE, Pereira AC, Santos RD.
    Atherosclerosis; 2017 Aug 10; 263():393-397. PubMed ID: 28499609
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  • 19. Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study.
    Vuorio AF, Turtola H, Piilahti KM, Repo P, Kanninen T, Kontula K.
    Arterioscler Thromb Vasc Biol; 1997 Nov 10; 17(11):3127-38. PubMed ID: 9409302
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  • 20. Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype.
    Bertolini S, Cantafora A, Averna M, Cortese C, Motti C, Martini S, Pes G, Postiglione A, Stefanutti C, Blotta I, Pisciotta L, Rolleri M, Langheim S, Ghisellini M, Rabbone I, Calandra S.
    Arterioscler Thromb Vasc Biol; 2000 Sep 10; 20(9):E41-52. PubMed ID: 10978268
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