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Journal Abstract Search

509 related items for PubMed ID: 9781014

  • 1. Concentrations of the atherogenic Lp(a) are elevated in FH.
    Lingenhel A, Kraft HG, Kotze M, Peeters AV, Kronenberg F, Kruse R, Utermann G.
    Eur J Hum Genet; 1998 Jan; 6(1):50-60. PubMed ID: 9781014
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  • 2. Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.
    van der Hoek YY, Lingenhel A, Kraft HG, Defesche JC, Kastelein JJ, Utermann G.
    J Clin Invest; 1997 May 01; 99(9):2269-73. PubMed ID: 9151801
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  • 3. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK.
    Dan Med Bull; 2002 Nov 01; 49(4):318-45. PubMed ID: 12553167
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  • 4. Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664----leu mutation in the LDL receptor gene.
    Soutar AK, McCarthy SN, Seed M, Knight BL.
    J Clin Invest; 1991 Aug 01; 88(2):483-92. PubMed ID: 1830890
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  • 5. [Familial hypercholesterolemia and plasma Lp(a) levels: 2 cardiovascular risk factors].
    Real JT, Romero G, Priego MA, Chaves FJ, Ascaso JF, Carmena R.
    An Med Interna; 1999 Feb 01; 16(2):69-72. PubMed ID: 10192997
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  • 6. Lipoprotein(a) in homozygous familial hypercholesterolemia.
    Kraft HG, Lingenhel A, Raal FJ, Hohenegger M, Utermann G.
    Arterioscler Thromb Vasc Biol; 2000 Feb 01; 20(2):522-8. PubMed ID: 10669652
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  • 7. Low density lipoprotein receptor (LDLR) gene mutations in Canadian subjects with familial hypercholesterolemia, but not of French descent.
    Wang J, Huff E, Janecka L, Hegele RA.
    Hum Mutat; 2001 Oct 01; 18(4):359. PubMed ID: 11668627
    [Abstract] [Full Text] [Related]

  • 8. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB).
    Azian M, Hapizah MN, Khalid BA, Khalid Y, Rosli A, Jamal R.
    Malays J Pathol; 2006 Jun 01; 28(1):7-15. PubMed ID: 17694954
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  • 9. 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 Jun 01; 46(3):152-4. PubMed ID: 11310584
    [Abstract] [Full Text] [Related]

  • 10. Segregation analysis of plasma lipoprotein(a) levels in pedigrees with molecularly defined familial hypercholesterolemia.
    Friedlander Y, Leitersdorf E.
    Genet Epidemiol; 1995 Jun 01; 12(2):129-43. PubMed ID: 7607414
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  • 11. Plasma Lp(a) values in familial hypercholesterolemia and its relation to coronary heart disease.
    Real JT, Ascaso JF, Chaves FJ, Tenés S, Priego MA, Puig O, Armengod ME, Carmena R.
    Nutr Metab Cardiovasc Dis; 1999 Feb 01; 9(1):41-4. PubMed ID: 10726108
    [Abstract] [Full Text] [Related]

  • 12. Familial defective apolipoprotein B-100.
    Hansen PS.
    Dan Med Bull; 1998 Sep 01; 45(4):370-82. PubMed ID: 9777289
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  • 17. [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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  • 18. Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece.
    Diakou M, Miltiadous G, Xenophontos SL, Manoli P, Cariolou MA, Elisaf M.
    Eur J Intern Med; 2011 Oct 25; 22(5):e55-9. PubMed ID: 21925044
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  • 19. Lipoprotein(a) plasma concentrations, apolipoprotein (a) polymorphism and family history of coronary heart disease in patients with essential hypertension.
    Gazzaruso C, Buscaglia P, Garzaniti A, Bonetti G, Savino S, Mariotti S, Jucci A, Finardi G, Geroldi D.
    J Cardiovasc Risk; 1996 Apr 25; 3(2):191-7. PubMed ID: 8836862
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