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Journal Abstract Search

205 related items for PubMed ID: 18489873

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  • 3. Mutations and polymorphisms of the gene of the major human blood protein, serum albumin.
    Minchiotti L, Galliano M, Kragh-Hansen U, Peters T.
    Hum Mutat; 2008 Aug; 29(8):1007-16. PubMed ID: 18459107
    [Abstract] [Full Text] [Related]

  • 4. Additional data on albumin variants in Italy (one new type of slow variant, two new homozygotes for rare variants, four cases of analbuminemia).
    Porta F, Petrini C, Perolini S, Pozzi F, Riboli P, Cannada E, Ignesti C, Pozzoli E, Calabrese M, Fraccaro M.
    Ric Clin Lab; 1980 Aug; 10(1):277-80. PubMed ID: 7466161
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  • 5. [A tricuspid electrophoretic pattern: familial bisalbuminemia with monoclonal immunoglobulin].
    Dubost JJ, Deseubis T, Sauvezie B, Gentou C, Rampon S.
    Pathol Biol (Paris); 1985 Oct; 33(8):837-8. PubMed ID: 3903622
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  • 6. Homozygous bisalbuminemia or homozygous mutant albumin?
    Kulkarni K, Rowe P, Christensen CL, Higgins T.
    Clin Biochem; 2012 Jan; 45(1-2):181-2. PubMed ID: 22040810
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  • 7. In vivo and in vitro binding of fatty acids to genetic variants of human serum albumin.
    Kragh-Hansen U, Nielsen H, Pedersen AO.
    Int J Clin Pharmacol Res; 1995 Jan; 15(2):33-43. PubMed ID: 8593972
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  • 8. Expression of a human serum albumin variant with high affinity for thyroxine.
    Petersen CE, Ha CE, Mandel M, Bhagavan NV.
    Biochem Biophys Res Commun; 1995 Sep 25; 214(3):1121-9. PubMed ID: 7575519
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  • 9. [Point mutations behind familial dysalbuminemic hyperthyroxinemia].
    Nørby S.
    Ugeskr Laeger; 2008 Jun 16; 170(25):2259; author reply 2260. PubMed ID: 18581650
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  • 10. Identification of a human serum albumin species associated with familial dysalbuminemic hyperthyroxinemia.
    Rushbrook JI, Becker E, Schussler GC, Divino CM.
    J Clin Endocrinol Metab; 1995 Feb 16; 80(2):461-7. PubMed ID: 7852505
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  • 12. [Human serum albumin: news about an old acquaintance].
    Kragh-Hansen U.
    Ugeskr Laeger; 2007 Oct 08; 169(41):3467-70. PubMed ID: 17967273
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  • 15. [Familial dysalbuminemic hyperthyroxinemia. A diagnostic pitfall].
    Jensen IW, Stentoft J, Toft E, Faber J.
    Ugeskr Laeger; 1988 Sep 12; 150(37):2178-80. PubMed ID: 3206581
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  • 16. Human serum albumin variants: determination and repartition of allotypes in 24 cases of bisalbuminemia observed in the French population.
    Fine JM, Marneux M, North ML.
    Biomedicine; 1976 Sep 30; 25(8):291-4. PubMed ID: 11852
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  • 20. [Study of a further case of bisalbuminemia in Brittany].
    Le Treut A, Catheline M, Grangaud R.
    C R Seances Soc Biol Fil; 1976 Sep 30; 170(1):168-75. PubMed ID: 134769
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