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Journal Abstract Search

325 related items for PubMed ID: 20708958

  • 1. Genetics of Wilsons disease.
    Behari M, Pardasani V.
    Parkinsonism Relat Disord; 2010 Dec; 16(10):639-44. PubMed ID: 20708958
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  • 2. [Wilson disease: an update].
    Seo JK.
    Korean J Hepatol; 2006 Sep; 12(3):333-63. PubMed ID: 16998287
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  • 3. Neurologic Wilson's disease.
    Lorincz MT.
    Ann N Y Acad Sci; 2010 Jan; 1184():173-87. PubMed ID: 20146697
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  • 4. Currently Clinical Views on Genetics of Wilson's Disease.
    Chen C, Shen B, Xiao JJ, Wu R, Duff Canning SJ, Wang XP.
    Chin Med J (Engl); 2015 Jul 05; 128(13):1826-30. PubMed ID: 26112727
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  • 8. p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease.
    Gromadzka G, Schmidt HH, Genschel J, Bochow B, Rodo M, Tarnacka B, Litwin T, Chabik G, Członkowska A.
    Mov Disord; 2006 Feb 05; 21(2):245-8. PubMed ID: 16211609
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  • 10. [Wilson's disease in paediatric age: diagnosis and treatment. Recent advances].
    Palumbo E.
    Recenti Prog Med; 2008 Nov 05; 99(11):561-4. PubMed ID: 19209540
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  • 13. Late onset fulminant Wilson's disease: a case report and review of the literature.
    Weitzman E, Pappo O, Weiss P, Frydman M, Haviv-Yadid Y, Ben Ari Z.
    World J Gastroenterol; 2014 Dec 14; 20(46):17656-60. PubMed ID: 25516681
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  • 14. Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient.
    Kok KF, Hoevenaars B, Waanders E, Drenth JP.
    Neth J Med; 2008 Sep 14; 66(8):348-50. PubMed ID: 18809983
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  • 16. Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
    de Bie P, van de Sluis B, Burstein E, van de Berghe PV, Muller P, Berger R, Gitlin JD, Wijmenga C, Klomp LW.
    Gastroenterology; 2007 Oct 14; 133(4):1316-26. PubMed ID: 17919502
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  • 17. Screening for mutations in ATP7B gene using conformation-sensitive gel electrophoresis in a family with Wilson's disease.
    Sundaresan S, Eapen CE, Shaji RV, Chandy M, Kurian G, Chandy G.
    Med Sci Monit; 2007 Mar 14; 13(3):CS38-40. PubMed ID: 17325640
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  • 18. ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.
    Santhosh S, Shaji RV, Eapen CE, Jayanthi V, Malathi S, Chandy M, Stanley M, Selvi S, Kurian G, Chandy GM.
    Indian J Gastroenterol; 2006 Mar 14; 25(6):277-82. PubMed ID: 17264425
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  • 19. Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.
    Tomić A, Dobricić V, Novaković I, Svetel M, Pekmezović T, Kresojević N, Potrebić A, Kostić VS.
    Vojnosanit Pregl; 2013 May 14; 70(5):457-62. PubMed ID: 23789284
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