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197 related items for PubMed ID: 11397707

  • 1. Determinants of lipid level variability in French-Canadian children with familial hypercholesterolemia.
    Lambert M, Assouline L, Feoli-Fonseca JC, Brun N, Delvin EE, Lévy E.
    Arterioscler Thromb Vasc Biol; 2001 Jun; 21(6):979-84. PubMed ID: 11397707
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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 27; 96(2 Pt 1):239-46. PubMed ID: 7630677
    [Abstract] [Full Text] [Related]

  • 4. 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 Aug 27; 11(5):1368-75. PubMed ID: 1911722
    [Abstract] [Full Text] [Related]

  • 5. Effect of apolipoprotein E genotype on lipid levels and response to diet in familial hypercholesterolemia.
    Carmena-Ramón R, Real JT, Ascaso JF, Ordovás JM, Carmena R.
    Nutr Metab Cardiovasc Dis; 2000 Feb 27; 10(1):7-13. PubMed ID: 10812582
    [Abstract] [Full Text] [Related]

  • 6. DIAgnosis and Management Of familial hypercholesterolemia in a Nationwide Design (DIAMOND-FH): Prevalence in Switzerland, clinical characteristics and the diagnostic value of clinical scores.
    Miserez AR, Martin FJ, Spirk D.
    Atherosclerosis; 2018 Oct 27; 277():282-288. PubMed ID: 30270060
    [Abstract] [Full Text] [Related]

  • 7. Effects of simvastatin on plasma lipids and apolipoproteins in familial hypercholesterolemic swine.
    Hasler-Rapacz J, Kempen HJ, Princen HM, Kudchodkar BJ, Lacko A, Rapacz J.
    Arterioscler Thromb Vasc Biol; 1996 Jan 27; 16(1):137-43. PubMed ID: 8548414
    [Abstract] [Full Text] [Related]

  • 8. Lipid phenotype and heritage pattern in families with genetic hypercholesterolemia not related to LDLR, APOB, PCSK9, or APOE.
    Jarauta E, Pérez-Ruiz MR, Pérez-Calahorra S, Mateo-Gallego R, Cenarro A, Cofán M, Ros E, Civeira F, Tejedor MT.
    J Clin Lipidol; 2016 Jan 27; 10(6):1397-1405.e2. PubMed ID: 27919357
    [Abstract] [Full Text] [Related]

  • 9. Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia.
    Pimstone SN, Defesche JC, Clee SM, Bakker HD, Hayden MR, Kastelein JJ.
    Arterioscler Thromb Vasc Biol; 1997 May 27; 17(5):826-33. PubMed ID: 9157944
    [Abstract] [Full Text] [Related]

  • 10. Dietary counseling is associated with an improved lipid profile in children with familial hypercholesterolemia.
    Torvik K, Narverud I, Ottestad I, Svilaas A, Gran JM, Retterstøl K, Ellingvåg A, Strøm E, Ose L, Veierød MB, Holven KB.
    Atherosclerosis; 2016 Sep 27; 252():21-27. PubMed ID: 27494447
    [Abstract] [Full Text] [Related]

  • 11. Influence of apolipoprotein E genotypes on plasma lipid and lipoprotein concentrations: results from a segregation analysis in pedigrees with molecularly defined familial hypercholesterolemia.
    Friedlander Y, Leitersdorf E.
    Genet Epidemiol; 1996 Sep 27; 13(2):159-77. PubMed ID: 8722744
    [Abstract] [Full Text] [Related]

  • 12. Interactions of several single nucleotide polymorphisms and high body mass index on serum lipid traits.
    Yin RX, Wu DF, Miao L, Htet Aung LH, Cao XL, Yan TT, Long XJ, Liu WY, Zhang L, Li M.
    Biofactors; 2013 Sep 27; 39(3):315-25. PubMed ID: 23355348
    [Abstract] [Full Text] [Related]

  • 13. Lipid and lipoprotein parameters for detection of familial hypercholesterolemia in childhood. The DECOPIN Project.
    Plana N, Rodríguez-Borjabad C, Ibarretxe D, Ferré R, Feliu A, Caselles A, Masana L, en representación del proyecto DECOPIN.
    Clin Investig Arterioscler; 2018 Sep 27; 30(4):170-178. PubMed ID: 29602595
    [Abstract] [Full Text] [Related]

  • 14. A novel single base deletion in the LDLR gene (211delG): Effect on serum lipid profiles and the influence of other genetic polymorphisms in the ACE, APOE and APOB genes.
    Ward AJ, O'Kane M, Nicholls DP, Young IS, Nevin NC, Graham CA.
    Atherosclerosis; 1996 Feb 27; 120(1-2):83-91. PubMed ID: 8645375
    [Abstract] [Full Text] [Related]

  • 15. Association of an exon 3 mutation (Trp66-->Gly) of the LDL receptor with variable expression of familial hypercholesterolemia in a French Canadian family.
    Levy E, Minnich A, Cacan SL, Thibault L, Giroux LM, Davignon J, Lambert M.
    Biochem Mol Med; 1997 Feb 27; 60(1):59-69. PubMed ID: 9066982
    [Abstract] [Full Text] [Related]

  • 16. [Relationship between gene polymorphism at the apolipoprotein E locus and serum lipid profile in urban children of school age in Beijing].
    Zhu W, Feng N, Wang Y.
    Zhonghua Yu Fang Yi Xue Za Zhi; 2001 Sep 27; 35(5):297-300. PubMed ID: 11769625
    [Abstract] [Full Text] [Related]

  • 17. Reduced apolipoprotein E-rich high-density lipoprotein level at birth is restored to the normal range in patients with familial hypercholesterolemia in the first year of life.
    Nagasaka H, Miida T, Hirano K, Ota A, Yorifuji T, Takatani T, Tsukahara H, Takayanagi M, Hui SP, Kobayashi K, Chiba H.
    J Clin Endocrinol Metab; 2008 Mar 27; 93(3):779-83. PubMed ID: 18182454
    [Abstract] [Full Text] [Related]

  • 18. The molecular basis of familial hypercholesterolemia in the Czech Republic: spectrum of LDLR mutations and genotype-phenotype correlations.
    Tichý L, Freiberger T, Zapletalová P, Soška V, Ravčuková B, Fajkusová L.
    Atherosclerosis; 2012 Aug 27; 223(2):401-8. PubMed ID: 22698793
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. 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 27; 14(10):1553-60. PubMed ID: 7918304
    [Abstract] [Full Text] [Related]

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