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

382 related items for PubMed ID: 18809983

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. Novel mutations of the ATP7B gene in Han Chinese families with pre-symptomatic Wilson's disease.
    Yuan ZF, Wu W, Yu YL, Shen J, Mao SS, Gao F, Xia ZZ.
    World J Pediatr; 2015 Aug 15; 11(3):255-60. PubMed ID: 26253413
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 25(1):18-20. PubMed ID: 15060811
    [Abstract] [Full Text] [Related]

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

  • 6. 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 15; 21(2):245-8. PubMed ID: 16211609
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Wilson's disease - a case report].
    Karwowska K, Skrzypek J, Chabik G, Członkowska A, Zaborowska M, Wawrzyniak S.
    Pol Merkur Lekarski; 2016 Jan 15; 40(235):28-31. PubMed ID: 26891433
    [Abstract] [Full Text] [Related]

  • 11. Timely diagnosis of Wilson's disease using whole exome sequencing.
    Rodríguez-Quiroga SA, Rosales J, Arakaki T, Cordoba M, González-Morón D, Medina N, Garretto NS, Kauffman MA.
    Parkinsonism Relat Disord; 2015 Nov 15; 21(11):1375-7. PubMed ID: 26410678
    [No Abstract] [Full Text] [Related]

  • 12. 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 15; 70(5):457-62. PubMed ID: 23789284
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Mutation analysis of the ATP7B gene in a new group of Wilson's disease patients: contribution to diagnosis.
    Lepori MB, Zappu A, Incollu S, Dessì V, Mameli E, Demelia L, Nurchi AM, Gheorghe L, Maggiore G, Sciveres M, Leuzzi V, Indolfi G, Bonafé L, Casali C, Angeli P, Barone P, Cao A, Loudianos G.
    Mol Cell Probes; 2012 Aug 14; 26(4):147-50. PubMed ID: 22484412
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Apolipoprotein E gene (APOE) genotype in Wilson's disease: impact on clinical presentation.
    Litwin T, Gromadzka G, Członkowska A.
    Parkinsonism Relat Disord; 2012 May 14; 18(4):367-9. PubMed ID: 22221592
    [Abstract] [Full Text] [Related]

  • 18. Modifying factors and phenotypic diversity in Wilson's disease.
    Lutsenko S.
    Ann N Y Acad Sci; 2014 May 14; 1315():56-63. PubMed ID: 24702697
    [Abstract] [Full Text] [Related]

  • 19. 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 14; 45(4):342-5. PubMed ID: 23219664
    [Abstract] [Full Text] [Related]

  • 20. Gene symbol: ATP7B. Disease: Wilson's disease.
    Margarit E.
    Hum Genet; 2005 Dec 14; 118(3-4):544-5. PubMed ID: 16521294
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.