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Journal Abstract Search

1024 related items for PubMed ID: 8879444

  • 1. 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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  • 4. 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
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  • 6. 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 27; 21(6):979-84. PubMed ID: 11397707
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  • 7. Presence and type of low density lipoprotein receptor (LDLR) mutation influences the lipid profile and response to lipid-lowering therapy in Brazilian patients with heterozygous familial hypercholesterolemia.
    Santos PC, Morgan AC, Jannes CE, Turolla L, Krieger JE, Santos RD, Pereira AC.
    Atherosclerosis; 2014 Mar 27; 233(1):206-10. PubMed ID: 24529145
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  • 8. Neonatal diagnosis of familial hypercholesterolemia in newborns born to a parent with a molecularly defined heterozygous familial hypercholesterolemia.
    Vuorio AF, Turtola H, Kontula K.
    Arterioscler Thromb Vasc Biol; 1997 Nov 27; 17(11):3332-7. PubMed ID: 9409330
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  • 9. 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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  • 11. 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
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  • 12. Genetics and kinetics of familial hypercholesterolemia, with the special focus on FH-(Marburg) p.W556R.
    Soufi M, Kurt B, Schweer H, Sattler AM, Klaus G, Zschocke J, Schaefer JR.
    Atheroscler Suppl; 2009 Dec 29; 10(5):5-11. PubMed ID: 20129366
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  • 13. Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment.
    Vuorio AF, Ojala JP, Sarna S, Turtola H, Tikkanen MJ, Kontula K.
    J Intern Med; 1995 Jan 29; 237(1):43-8. PubMed ID: 7830029
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  • 14. [Identification of a novel mutation at the point of low density lipoprotein receptor gene from a subject with familial hypercholesterolemia].
    Liu YR, Tao QM, Chen JZ, Tao M, Guo XG, Shang YP, Zhu JH, Zhang FR, Zheng LR, Wang XX.
    Sheng Li Xue Bao; 2004 Oct 25; 56(5):566-72. PubMed ID: 15497035
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  • 16. 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 Oct 25; 46(3):152-4. PubMed ID: 11310584
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  • 18. Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia.
    Ajmal M, Ahmed W, Sadeque A, Ali SH, Bokhari SH, Ahmed N, Qamar R.
    Mol Biol Rep; 2010 Dec 25; 37(8):3869-75. PubMed ID: 20217239
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