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Journal Abstract Search

180 related items for PubMed ID: 10777157

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  • 2. A novel ATP7B gene mutation in a liver failure patient with normal ceruloplasmin and low serum alkaline phosphatase.
    Chen L, Li X, Zheng Z, Lu X, Lin M, Pan C, Liu J.
    Gene; 2014 Mar 15; 538(1):204-6. PubMed ID: 24476933
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  • 5. Copper metabolism after living donor liver transplantation for hepatic failure of Wilson's disease from a gene mutated donor.
    Kobayashi S, Ochiai T, Hori S, Suzuki T, Shimizu T, Gunji Y, Shimada H, Yamamoto S, Ogawa A, Kohno Y, Sunaga M, Shimazu M, Tanaka K.
    Hepatogastroenterology; 2001 Mar 15; 48(41):1259-61. PubMed ID: 11677941
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  • 6. Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study.
    Merle U, Schaefer M, Ferenci P, Stremmel W.
    Gut; 2007 Jan 15; 56(1):115-20. PubMed ID: 16709660
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  • 7. New novel mutation of the ATP7B gene in a family with Wilson disease.
    Lee JY, Kim YH, Kim TW, Oh SY, Kim DS, Shin BS.
    J Neurol Sci; 2012 Feb 15; 313(1-2):129-31. PubMed ID: 22075048
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  • 9. High frequency of the c.3207C>A (p.H1069Q) mutation in ATP7B gene of Lithuanian patients with hepatic presentation of Wilson's disease.
    Kucinskas L, Jeroch J, Vitkauskiene A, Sakalauskas R, Petrenkiene V, Kucinskas V, Naginiene R, Schmidt H, Kupcinskas L.
    World J Gastroenterol; 2008 Oct 14; 14(38):5876-9. PubMed ID: 18855987
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  • 10. A genetic study of Wilson's disease in the United Kingdom.
    Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O.
    Brain; 2013 May 14; 136(Pt 5):1476-87. PubMed ID: 23518715
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  • 14. 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 14; 21(2):245-8. PubMed ID: 16211609
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  • 15. Rapid identification of Wilson's disease carriers by denaturing high-performance liquid chromatography.
    Weirich G, Cabras AD, Serra S, Coni PP, Nurchi AM, Faa G, Höfler H.
    Prev Med; 2002 Sep 14; 35(3):278-84. PubMed ID: 12202071
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  • 16. 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 14; 19(4):806-14. PubMed ID: 25704483
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  • 17. Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.
    Shah AB, Chernov I, Zhang HT, Ross BM, Das K, Lutsenko S, Parano E, Pavone L, Evgrafov O, Ivanova-Smolenskaya IA, Annerén G, Westermark K, Urrutia FH, Penchaszadeh GK, Sternlieb I, Scheinberg IH, Gilliam TC, Petrukhin K.
    Am J Hum Genet; 1997 Aug 14; 61(2):317-28. PubMed ID: 9311736
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  • 18. Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration.
    Zong YN, Kong XD.
    Genet Mol Res; 2015 Dec 29; 14(4):18764-70. PubMed ID: 26782526
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  • 19. Severe hepatic Wilson's disease in preschool-aged children.
    Wilson DC, Phillips MJ, Cox DW, Roberts EA.
    J Pediatr; 2000 Nov 29; 137(5):719-22. PubMed ID: 11060541
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