These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

198 related items for PubMed ID: 12202071

  • 1. 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; 35(3):278-84. PubMed ID: 12202071
    [Abstract] [Full Text] [Related]

  • 2. [Mutation screening and prenatal diagnosis of Wilson's disease by denature high performance liquid chromatography].
    Du J, Gao B, Li L, Li W, Lu G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):527-30. PubMed ID: 18841564
    [Abstract] [Full Text] [Related]

  • 3. 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; 136(Pt 5):1476-87. PubMed ID: 23518715
    [Abstract] [Full Text] [Related]

  • 4. Wilson's disease in two consecutive generations: the detection of three mutated alleles in the ATP7B gene in two Sardinian families.
    Loudianos G, Zappu A, Lepori MB, Incollu S, Dessì V, Mameli E, Garrucciu G, De Virgiliis S, Cao A.
    Dig Liver Dis; 2013 Apr; 45(4):342-5. PubMed ID: 23219664
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease.
    Gu YH, Kodama H, Du SL, Gu QJ, Sun HJ, Ushijima H.
    Clin Genet; 2003 Dec; 64(6):479-84. PubMed ID: 14986826
    [Abstract] [Full Text] [Related]

  • 8. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec; 118(3-4):539. PubMed ID: 16402213
    [No Abstract] [Full Text] [Related]

  • 9. 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 Dec; 25(6):277-82. PubMed ID: 17264425
    [Abstract] [Full Text] [Related]

  • 10. Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease.
    Folhoffer A, Ferenci P, Csak T, Horvath A, Hegedus D, Firneisz G, Osztovits J, Kosa JP, Willheim-Polli C, Szonyi L, Abonyi M, Lakatos PL, Szalay F.
    Eur J Gastroenterol Hepatol; 2007 Feb; 19(2):105-11. PubMed ID: 17272994
    [Abstract] [Full Text] [Related]

  • 11. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec; 118(3-4):544. PubMed ID: 16521291
    [No Abstract] [Full Text] [Related]

  • 12. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec; 118(3-4):544. PubMed ID: 16521292
    [No Abstract] [Full Text] [Related]

  • 13. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec; 118(3-4):544. PubMed ID: 16521293
    [No Abstract] [Full Text] [Related]

  • 14. 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; 70(5):457-62. PubMed ID: 23789284
    [Abstract] [Full Text] [Related]

  • 15. Gene symbol: ATP7B. Disease: Wilson's disease.
    Yang J, Chan P.
    Hum Genet; 2005 Dec; 118(3-4):540. PubMed ID: 16521266
    [No Abstract] [Full Text] [Related]

  • 16. Gene symbol: ATP7B. Disease: Wilson's disease.
    Chan P, Yang J.
    Hum Genet; 2005 Dec; 118(3-4):540. PubMed ID: 16521265
    [No Abstract] [Full Text] [Related]

  • 17. 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; 41(4):409-13. PubMed ID: 10453196
    [Abstract] [Full Text] [Related]

  • 18. 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; 13(3):CS38-40. PubMed ID: 17325640
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. [Genotype and phenotype correlation in Chinese patients with Wilson's Disease].
    Liu XQ, Zhang YF, Liu TT, Gu XF, Hsiao KJ, Bao KR, Yu LH.
    Zhonghua Er Ke Za Zhi; 2003 Jan 23; 41(1):35-8. PubMed ID: 14761325
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.