BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

361 related articles for article (PubMed ID: 24476933)

  • 21. 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; 25(1):18-20. PubMed ID: 15060811
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Diagnosis of Wilson's disease: a comprehensive review.
    Mak CM; Lam CW
    Crit Rev Clin Lab Sci; 2008; 45(3):263-90. PubMed ID: 18568852
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Wilson's disease in paediatric age: diagnosis and treatment. Recent advances].
    Palumbo E
    Recenti Prog Med; 2008 Nov; 99(11):561-4. PubMed ID: 19209540
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neurologic Wilson's disease.
    Lorincz MT
    Ann N Y Acad Sci; 2010 Jan; 1184():173-87. PubMed ID: 20146697
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Early gestational gene transfer with targeted ATP7B expression in the liver improves phenotype in a murine model of Wilson's disease.
    Roybal JL; Endo M; Radu A; Gray L; Todorow CA; Zoltick PW; Lutsenko S; Flake AW
    Gene Ther; 2012 Nov; 19(11):1085-94. PubMed ID: 22158007
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hypoceruloplasminemia-related movement disorder without Kayser-Fleischer rings is different from Wilson disease and not involved in ATP7B mutation.
    Lirong J; Jianjun J; Hua Z; Guoqiang F; Yuhao Z; Xiaoli P; Xiaomin Z; Yuwen Z; Yu M; Jie C; Jihong D; Yueshi M; Zhenyao M; Chunjiu Z
    Eur J Neurol; 2009 Oct; 16(10):1130-7. PubMed ID: 19572946
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [A novel mutation in ATP7B gene associated with severe neurological impairment in Wilson's disease].
    Elleuch N; Feki I; Turki E; Miladi MI; Boukhris A; Damak M; Mhiri C; Chappuis E; Woimant F
    Rev Neurol (Paris); 2010 May; 166(5):550-2. PubMed ID: 20036408
    [No Abstract]   [Full Text] [Related]  

  • 28. 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; 21(11):1375-7. PubMed ID: 26410678
    [No Abstract]   [Full Text] [Related]  

  • 29. Wilson's Disease.
    Ferenci P
    Clin Gastroenterol Hepatol; 2005 Aug; 3(8):726-33. PubMed ID: 16233999
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Association of ATP7B mutation detection rate with biochemical characteristics in Korean patients with Wilson disease.
    Park HD; Park HK; Chung HS; Lee SY; Kim JW; Ki CS
    Ann Clin Lab Sci; 2010; 40(1):15-9. PubMed ID: 20124325
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 128(13):1826-30. PubMed ID: 26112727
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Population screening for Wilson's disease.
    Hahn SH
    Ann N Y Acad Sci; 2014 May; 1315():64-9. PubMed ID: 24731025
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 11(12):e0168372. PubMed ID: 27992490
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease.
    Gu S; Yang H; Qi Y; Deng X; Zhang L; Guo Y; Huang Q; Li J; Shi X; Song Z; Deng H
    PLoS One; 2013; 8(7):e66526. PubMed ID: 23843956
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Wilson's disease gene and phenotypic diversity.
    Riordan SM; Williams R
    J Hepatol; 2001 Jan; 34(1):165-71. PubMed ID: 11211896
    [No Abstract]   [Full Text] [Related]  

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

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

  • 38. 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; 20(46):17656-60. PubMed ID: 25516681
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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; 56(1):115-20. PubMed ID: 16709660
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.