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Journal Abstract Search

382 related items for PubMed ID: 18809983

  • 21.
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  • 22. Neurological manifestations and ATP7B mutations in Wilson's disease.
    Machado AA, Deguti MM, Genschel J, Cançado EL, Bochow B, Schmidt H, Barbosa ER.
    Parkinsonism Relat Disord; 2008; 14(3):246-9. PubMed ID: 17897870
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  • 23. The His1069Gln mutation in the ATP7B gene in Romanian patients with Wilson's disease referred to a tertiary gastroenterology center.
    Iacob R, Iacob S, Nastase A, Vagu C, Ene AM, Constantinescu A, Anghel D, Banica C, Paslaru L, Coriu D, Dima S, Gheorghe C, Ionica E, Gheorghe L.
    J Gastrointestin Liver Dis; 2012 Jun; 21(2):181-5. PubMed ID: 22720308
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  • 24. Gene symbol: ATP7B. Disease: Wilson's Disease.
    Chan P, Yang J.
    Hum Genet; 2005 Dec; 118(3-4):548. PubMed ID: 16521309
    [No Abstract] [Full Text] [Related]

  • 25. Quantification of ATP7B Protein in Dried Blood Spots by Peptide Immuno-SRM as a Potential Screen for Wilson's Disease.
    Jung S, Whiteaker JR, Zhao L, Yoo HW, Paulovich AG, Hahn SH.
    J Proteome Res; 2017 Feb 03; 16(2):862-871. PubMed ID: 27935710
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  • 26. Gene symbol: ATP7B. Disease: Wilson's disease.
    Ray K, Gupta A.
    Hum Genet; 2005 Dec 03; 118(3-4):541. PubMed ID: 16521267
    [No Abstract] [Full Text] [Related]

  • 27. Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease.
    Gromadzka G, Schmidt HH, Genschel J, Bochow B, Rodo M, Tarnacka B, Litwin T, Chabik G, Członkowska A.
    Clin Genet; 2005 Dec 03; 68(6):524-32. PubMed ID: 16283883
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  • 28. Genetics of Wilsons disease.
    Behari M, Pardasani V.
    Parkinsonism Relat Disord; 2010 Dec 03; 16(10):639-44. PubMed ID: 20708958
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  • 30. Molecular analysis and diagnosis in Japanese patients with Wilson's disease.
    Shimizu N, Nakazono H, Takeshita Y, Ikeda C, Fujii H, Watanabe A, Yamaguchi Y, Hemmi H, Shimatake H, Aoki T.
    Pediatr Int; 1999 Aug 03; 41(4):409-13. PubMed ID: 10453196
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  • 33. Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson's Disease Pathogenesis.
    Todorov T, Balakrishnan P, Savov A, Socha P, Schmidt HH.
    PLoS One; 2016 Aug 03; 11(12):e0168372. PubMed ID: 27992490
    [Abstract] [Full Text] [Related]

  • 34. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec 03; 118(3-4):540. PubMed ID: 16521264
    [No Abstract] [Full Text] [Related]

  • 35. Laser ablation inductively coupled plasma mass spectrometry imaging of metals in experimental and clinical Wilson's disease.
    Boaru SG, Merle U, Uerlings R, Zimmermann A, Flechtenmacher C, Willheim C, Eder E, Ferenci P, Stremmel W, Weiskirchen R.
    J Cell Mol Med; 2015 Apr 03; 19(4):806-14. PubMed ID: 25704483
    [Abstract] [Full Text] [Related]

  • 36. [Wilson disease: an update].
    Seo JK.
    Korean J Hepatol; 2006 Sep 03; 12(3):333-63. PubMed ID: 16998287
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