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Journal Abstract Search

92 related items for PubMed ID: 7607414

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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; 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; 16(2):69-72. PubMed ID: 10192997
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  • 7. 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; 9(1):41-4. PubMed ID: 10726108
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  • 8. Lipoprotein(a) levels in familial hypercholesterolemia: an important predictor of cardiovascular disease independent of the type of LDL receptor mutation.
    Alonso R, Andres E, Mata N, Fuentes-Jiménez F, Badimón L, López-Miranda J, Padró T, Muñiz O, Díaz-Díaz JL, Mauri M, Ordovás JM, Mata P, SAFEHEART Investigators.
    J Am Coll Cardiol; 2014 May 20; 63(19):1982-9. PubMed ID: 24632281
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  • 9. Lipoprotein(a) in homozygous familial hypercholesterolemia.
    Kraft HG, Lingenhel A, Raal FJ, Hohenegger M, Utermann G.
    Arterioscler Thromb Vasc Biol; 2000 Feb 20; 20(2):522-8. PubMed ID: 10669652
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  • 11. [Lipoprotein(a) in heterozygote familial hypercholesterolemia].
    Ochoa Sosa CA, Zamora González J, González Hermosillo JA, Ize Lema I, Cardoso Saldaña G, Posadas Romero C.
    Arch Inst Cardiol Mex; 1994 Feb 20; 64(6):549-55. PubMed ID: 7726691
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  • 12. Influence of lipoprotein (a) levels and isoforms on fibrinolytic activity--study in families with high lipoprotein (a) levels.
    Falcó C, Estellés A, Dalmau J, España F, Aznar J.
    Thromb Haemost; 1998 Apr 20; 79(4):818-23. PubMed ID: 9580386
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  • 13. 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 Apr 20; 46(3):152-4. PubMed ID: 11310584
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  • 14. Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and Canada.
    Defesche JC, van de Ree MA, Kastelein JJ, van Diermen DE, Janssens NW, van Doormaal JJ, Hayden MR.
    Clin Genet; 1992 Dec 20; 42(6):273-80. PubMed ID: 1493640
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  • 15. [Relationship between lipoprotein A, apolipoprotein A and their isoforms in parents and children].
    Ferrer Lorente B, Dalmau Serra J, Falcó Couchoud C, Estellés Cortés A, España Furió F, Aznar Lucea J.
    An Esp Pediatr; 1998 Jun 20; 48(6):587-92. PubMed ID: 9662841
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  • 16. 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 20; 16(1):129-36. PubMed ID: 8548413
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  • 17. HDL cholesterol levels in patients with molecularly defined familial hypercholesterolemia.
    Miltiadous G, Cariolou MA, Elisaf M.
    Ann Clin Lab Sci; 2002 Jan 20; 32(1):50-4. PubMed ID: 11848618
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  • 18. 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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  • 19. 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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  • 20. A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia.
    Hopkins PN, Wu LL, Stephenson SH, Xin Y, Katsumata H, Nobe Y, Nakajima T, Hirayama T, Emi M, Williams RR.
    J Hum Genet; 1999 Jun 01; 44(6):364-7. PubMed ID: 10570905
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