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Journal Abstract Search


129 related items for PubMed ID: 15498441

  • 1. [Clinical and biochemical characteristics of familial ligand-defective apo B-100 in a South European population].
    Ejarque I, Real JT, Chaves FJ, Blesa S, González V, Milian E, Ascaso JF, Priego MA, Carmena R.
    Med Clin (Barc); 2004 Oct 09; 123(12):456-9. PubMed ID: 15498441
    [Abstract] [Full Text] [Related]

  • 2. Evaluation of clinical diagnosis criteria of familial ligand defective apoB 100 and lipoprotein phenotype comparison between LDL receptor gene mutations affecting ligand-binding domain and the R3500Q mutation of the apoB gene in patients from a South European population.
    Ejarque I, Real JT, Martinez-Hervas S, Chaves FJ, Blesa S, Garcia-Garcia AB, Millan E, Ascaso JF, Carmena R.
    Transl Res; 2008 Mar 09; 151(3):162-7. PubMed ID: 18279815
    [Abstract] [Full Text] [Related]

  • 3. 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 09; 17(5):826-33. PubMed ID: 9157944
    [Abstract] [Full Text] [Related]

  • 4. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK.
    Dan Med Bull; 2002 Nov 09; 49(4):318-45. PubMed ID: 12553167
    [Abstract] [Full Text] [Related]

  • 5. Differences in the phenotypic characteristics of subjects with familial defective apolipoprotein B-100 and familial hypercholesterolemia.
    Miserez AR, Keller U.
    Arterioscler Thromb Vasc Biol; 1995 Oct 09; 15(10):1719-29. PubMed ID: 7583549
    [Abstract] [Full Text] [Related]

  • 6. Familial defective apolipoprotein B-100.
    Hansen PS.
    Dan Med Bull; 1998 Sep 09; 45(4):370-82. PubMed ID: 9777289
    [Abstract] [Full Text] [Related]

  • 7. [Identification and characterization of the first Spanish familial ligand-defective apolipoprotein B homozygote].
    Ejarque I, Civer M, Francisco Ascaso J, Knecht E, Eugenia Armengod M, Carmen R, Tomás Real J, Francisco Chaves J, Javier Martín De Llano J.
    Med Clin (Barc); 2001 Feb 03; 116(4):138-41. PubMed ID: 11222161
    [Abstract] [Full Text] [Related]

  • 8. Phenotypic heterogeneity associated with defective apolipoprotein B-100 and occurrence of the familial hypercholesterolemia phenotype in the absence of an LDL-receptor defect within a Canadian kindred.
    Davignon J, Dufour R, Roy M, Bétard C, Ma Y, Ouellette S, Boulet L, Lussier-Cacan S.
    Eur J Epidemiol; 1992 May 03; 8 Suppl 1():10-7. PubMed ID: 1505645
    [Abstract] [Full Text] [Related]

  • 9. Influence of LDL receptor gene mutations and the R3500Q mutation of the apoB gene on lipoprotein phenotype of familial hypercholesterolemic patients from a South European population.
    Real JT, Chaves FJ, Ejarque I, García-García AB, Valldecabres C, Ascaso JF, Armengod ME, Carmena R.
    Eur J Hum Genet; 2003 Dec 03; 11(12):959-65. PubMed ID: 14508510
    [Abstract] [Full Text] [Related]

  • 10. [Plasma lipoprotein (a) values in familial defective ligand apo B 100 in a South European population].
    Ejarque I, Leal JT, Ascaso JF, Chaves FJ, Milian E, Priego MA, Carmena R.
    An Med Interna; 2004 Jul 03; 21(7):322-5. PubMed ID: 15347236
    [Abstract] [Full Text] [Related]

  • 11. Compound heterozygous familial hypercholesterolemia and familial defective apolipoprotein B-100 produce exaggerated hypercholesterolemia.
    Tai ES, Koay ES, Chan E, Seng TJ, Loh LM, Sethi SK, Tan CE.
    Clin Chem; 2001 Mar 03; 47(3):438-43. PubMed ID: 11238294
    [Abstract] [Full Text] [Related]

  • 12. Familial defective apolipoprotein B-100 in Slovakia: are differences in prevalence of familial defective apolipoprotein B-100 explained by ethnicity?
    Gasparovic J, Basistová Z, Fábryová L, Wsólová L, Vohnout B, Raslová K, Slovak MED PED FH group.
    Atherosclerosis; 2007 Oct 03; 194(2):e95-107. PubMed ID: 17194460
    [Abstract] [Full Text] [Related]

  • 13. Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patients.
    Ceska R, Vrablík M, Horínek A.
    Physiol Res; 2000 Oct 03; 49 Suppl 1():S125-30. PubMed ID: 10984082
    [Abstract] [Full Text] [Related]

  • 14. Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defects.
    Raal FJ, Pilcher G, Rubinsztein DC, Lingenhel A, Utermann G.
    Atherosclerosis; 1997 Feb 28; 129(1):97-102. PubMed ID: 9069523
    [Abstract] [Full Text] [Related]

  • 15. Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function.
    Myant NB, Gallagher JJ, Knight BL, McCarthy SN, Frostegård J, Nilsson J, Hamsten A, Talmud P, Humphries SE.
    Arterioscler Thromb; 1991 Feb 28; 11(3):691-703. PubMed ID: 1674216
    [Abstract] [Full Text] [Related]

  • 16. Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia.
    Myant NB.
    Atherosclerosis; 1993 Dec 28; 104(1-2):1-18. PubMed ID: 8141833
    [Abstract] [Full Text] [Related]

  • 17. Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100.
    Rubinsztein DC, Raal FJ, Seftel HC, Pilcher G, Coetzee GA, van der Westhuyzen DR.
    Arterioscler Thromb; 1993 Jul 28; 13(7):1076-81. PubMed ID: 8318509
    [Abstract] [Full Text] [Related]

  • 18. Familial defective apolipoprotein B versus familial hypercholesterolemia: an assessment of risk.
    Fouchier SW, Defesche JC, Kastelein JJ, Sijbrands EJ.
    Semin Vasc Med; 2004 Aug 28; 4(3):259-64. PubMed ID: 15630635
    [Abstract] [Full Text] [Related]

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  • 20. 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 28; 11(5):1368-75. PubMed ID: 1911722
    [Abstract] [Full Text] [Related]


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