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Journal Abstract Search

632 related items for PubMed ID: 26891433

  • 1. [Wilson's disease - a case report].
    Karwowska K, Skrzypek J, Chabik G, Członkowska A, Zaborowska M, Wawrzyniak S.
    Pol Merkur Lekarski; 2016 Jan; 40(235):28-31. PubMed ID: 26891433
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  • 2. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T, Tirouche YD, Abaoub-Germain A, Theodore F.
    Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
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  • 8. [Wilson's disease in paediatric age: diagnosis and treatment. Recent advances].
    Palumbo E.
    Recenti Prog Med; 2008 Nov; 99(11):561-4. PubMed ID: 19209540
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  • 10. New mutations and polymorphisms of the ATP7B gene in sporadic Wilson disease.
    Lu CX, Qing Lin, Huang WQ, Tzeng CM.
    Eur J Med Genet; 2014 Sep; 57(9):498-502. PubMed ID: 24878384
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  • 12. Late-onset Wilson's disease.
    Ferenci P, Członkowska A, Merle U, Ferenc S, Gromadzka G, Yurdaydin C, Vogel W, Bruha R, Schmidt HT, Stremmel W.
    Gastroenterology; 2007 Apr; 132(4):1294-8. PubMed ID: 17433323
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  • 13. Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease.
    Zhang DF, Teng JF.
    Genet Mol Res; 2016 Sep 23; 15(3):. PubMed ID: 27706781
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  • 15. Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence?
    Battisti C, Dotti MT, Loudianos G, Dessì V, Battistini S, Amato T, Rufa A, Federico A.
    Neurol Sci; 2004 Apr 23; 25(1):18-20. PubMed ID: 15060811
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  • 17. 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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  • 20. 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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