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
325 related items for PubMed ID: 20708958
1. Genetics of Wilsons disease. Behari M, Pardasani V. Parkinsonism Relat Disord; 2010 Dec; 16(10):639-44. PubMed ID: 20708958 [Abstract] [Full Text] [Related]
2. [Wilson disease: an update]. Seo JK. Korean J Hepatol; 2006 Sep; 12(3):333-63. PubMed ID: 16998287 [Abstract] [Full Text] [Related]
3. Neurologic Wilson's disease. Lorincz MT. Ann N Y Acad Sci; 2010 Jan; 1184():173-87. PubMed ID: 20146697 [Abstract] [Full Text] [Related]
4. 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 [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. Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient. Kok KF, Hoevenaars B, Waanders E, Drenth JP. Neth J Med; 2008 Sep 14; 66(8):348-50. PubMed ID: 18809983 [Abstract] [Full Text] [Related]
16. Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. de Bie P, van de Sluis B, Burstein E, van de Berghe PV, Muller P, Berger R, Gitlin JD, Wijmenga C, Klomp LW. Gastroenterology; 2007 Oct 14; 133(4):1316-26. PubMed ID: 17919502 [Abstract] [Full Text] [Related]
17. 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]
18. 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 Mar 14; 25(6):277-82. PubMed ID: 17264425 [Abstract] [Full Text] [Related]
19. 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 14; 70(5):457-62. PubMed ID: 23789284 [Abstract] [Full Text] [Related]