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124 related items for PubMed ID: 4084360

  • 1. Homozygous familial hypercholesterolemic patients in China.
    Cai HJ, Fan LM, Huang MG, Chen XY, Liu GQ, Chen Q.
    Atherosclerosis; 1985 Nov; 57(2-3):303-12. PubMed ID: 4084360
    [Abstract] [Full Text] [Related]

  • 2. Metabolism of low-density lipoproteins by cultured hepatocytes from normal and homozygous familial hypercholesterolemic subjects.
    Hoeg JM, Edge SB, Demosky SJ, Starzl TE, Triche T, Gregg RE, Brewer HB.
    Biochim Biophys Acta; 1986 May 21; 876(3):646-57. PubMed ID: 3707989
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. The effect of atorvastatin on serum lipids and lipoproteins in patients with homozyous familial hypercholesterolemia undergoing LDL-apheresis therapy.
    Yamamoto A, Harada-Shiba M, Kawaguchi A, Oi K, Kubo H, Sakai S, Mikami Y, Imai T, Ito T, Kato H, Endo M, Sato I, Suzuki Y, Hori H.
    Atherosclerosis; 2000 Nov 27; 153(1):89-98. PubMed ID: 11058703
    [Abstract] [Full Text] [Related]

  • 5. The association of LDL receptor activity, LDL cholesterol level, and clinical course in homozygous familial hypercholesterolemia.
    Sprecher DL, Hoeg JM, Schaefer EJ, Zech LA, Gregg RE, Lakatos E, Brewer HB.
    Metabolism; 1985 Mar 27; 34(3):294-9. PubMed ID: 3856094
    [Abstract] [Full Text] [Related]

  • 6. [Homozygous familial hypercholesterolemia: development and a case illustration].
    Choukri M, Laaroussi N, Taheri H, Chabraoui L.
    Ann Biol Clin (Paris); 2013 Mar 27; 71(1):99-103. PubMed ID: 23396432
    [Abstract] [Full Text] [Related]

  • 7. Lipoprotein Lp(a) in homozygous familial hypercholesterolemia: density profile, particle heterogeneity and apolipoprotein(a) phenotype.
    Guo HC, Chapman MJ, Bruckert E, Farriaux JP, De Gennes JL.
    Atherosclerosis; 1991 Jan 27; 86(1):69-83. PubMed ID: 1829609
    [Abstract] [Full Text] [Related]

  • 8. The longest-lived patient with homozygous familial hypercholesterolemia secondary to a defect in internalization of the LDL receptor.
    Komuro I, Kato H, Nakagawa T, Takahashi K, Mimori A, Takeuchi F, Nishida Y, Miyamoto T.
    Am J Med Sci; 1987 Nov 27; 294(5):341-5. PubMed ID: 3425583
    [Abstract] [Full Text] [Related]

  • 9. A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia.
    Vergopoulos A, Bajari T, Jouma M, Knoblauch H, Aydin A, Bähring S, Mueller-Myhsok B, Dresel A, Joubran R, Luft FC, Schuster H.
    Eur J Hum Genet; 1997 Nov 27; 5(5):315-23. PubMed ID: 9412789
    [Abstract] [Full Text] [Related]

  • 10. FH-Freiburg: a novel missense mutation (C317Y) in growth factor repeat A of the low density lipoprotein receptor gene in a German patient with homozygous familial hypercholesterolemia.
    Nauck MS, Scharnagl H, Nissen H, Schürmann C, Matern D, Nauck MA, Wieland H, März W.
    Atherosclerosis; 2000 Aug 27; 151(2):525-34. PubMed ID: 10924730
    [Abstract] [Full Text] [Related]

  • 11. Siblings with normal LDL receptor activity and severe hypercholesterolemia.
    Harada-Shiba M, Tajima S, Yokoyama S, Miyake Y, Kojima S, Tsushima M, Kawakami M, Yamamoto A.
    Arterioscler Thromb; 1992 Sep 27; 12(9):1071-8. PubMed ID: 1525122
    [Abstract] [Full Text] [Related]

  • 12. Low density lipoprotein receptor mutations in South African homozygous familial hypercholesterolemic patients.
    van der Westhuyzen DR, Coetzee GA, Demasius IP, Harley EH, Gevers W, Baker SG, Seftel HC.
    Arteriosclerosis; 1984 Sep 27; 4(3):238-47. PubMed ID: 6324732
    [Abstract] [Full Text] [Related]

  • 13. Pseudohomozygous type II hyperlipoproteinemia.
    Fujita M, Okamoto S, Shirai K, Saito Y, Yoshida S.
    Dermatologica; 1991 Sep 27; 182(2):94-7. PubMed ID: 2050241
    [Abstract] [Full Text] [Related]

  • 14. Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemia.
    Feussner G, Dobmeyer J, Nissen H, Hansen TS.
    Am J Med Genet; 1996 Oct 16; 65(2):149-54. PubMed ID: 8911609
    [Abstract] [Full Text] [Related]

  • 15. Clinical and biochemical characterisation of patients with autosomal recessive hypercholesterolemia (ARH).
    Fellin R, Zuliani G, Arca M, Pintus P, Pacifico A, Montali A, Corsini A, Maioli M.
    Nutr Metab Cardiovasc Dis; 2003 Oct 16; 13(5):278-86. PubMed ID: 14717060
    [Abstract] [Full Text] [Related]

  • 16. Characterization of hepatic low density lipoprotein binding and cholesterol metabolism in normal and homozygous familial hypercholesterolemic subjects.
    Hoeg JM, Demosky SJ, Schaefer EJ, Starzl TE, Brewer HB.
    J Clin Invest; 1984 Feb 16; 73(2):429-36. PubMed ID: 6321555
    [Abstract] [Full Text] [Related]

  • 17. Effects of ML-236b (compactin) on sterol synthesis and low density lipoprotein receptor activities in fibroblasts of patients with homozygous familial hypercholesterolemia.
    Haba T, Mabuchi H, Yoshimura A, Watanabe A, Wakasugi T, Tatami R, Ueda K, Ueda R, Kametani T, Koizumi J, Miyamoto S, Takeda R, Takeshita H.
    J Clin Invest; 1981 May 16; 67(5):1532-40. PubMed ID: 7229037
    [Abstract] [Full Text] [Related]

  • 18. Accumulation of "small dense" low density lipoproteins (LDL) in a homozygous patients with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor.
    März W, Baumstark MW, Scharnagl H, Ruzicka V, Buxbaum S, Herwig J, Pohl T, Russ A, Schaaf L, Berg A.
    J Clin Invest; 1993 Dec 16; 92(6):2922-33. PubMed ID: 8254047
    [Abstract] [Full Text] [Related]

  • 19. Low density lipoprotein metabolism in cultured fibroblasts from a new group of patients presenting clinically with homozygous familial hypercholesterolemia.
    Coetzee GA, van der Westhuyzen DR, Berger GM, Henderson HE, Gevers W.
    Arteriosclerosis; 1982 Dec 16; 2(4):303-11. PubMed ID: 6287984
    [Abstract] [Full Text] [Related]

  • 20. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
    Wang D, Wu B, Li Y, Heng W, Zhong H, Mu Y, Wang J.
    J Hum Genet; 2001 Dec 16; 46(3):152-4. PubMed ID: 11310584
    [Abstract] [Full Text] [Related]

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