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Journal Abstract Search

466 related items for PubMed ID: 19209540

  • 41. Diagnosis and management of Wilson's disease: results of a single center experience.
    Medici V, Trevisan CP, D'Incà R, Barollo M, Zancan L, Fagiuoli S, Martines D, Irato P, Sturniolo GC.
    J Clin Gastroenterol; 2006; 40(10):936-41. PubMed ID: 17063115
    [Abstract] [Full Text] [Related]

  • 42. 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]

  • 43. Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case Report.
    Gucev ZS, Pop-Jordanova N, Calovska V, Tasic V, Slavevska N, Laban N, Noli MC, Lepori MB, Loudianos G.
    Prilozi; 2011 Apr; 32(2):307-15. PubMed ID: 22286624
    [Abstract] [Full Text] [Related]

  • 44. Severe hepatic Wilson's disease in preschool-aged children.
    Wilson DC, Phillips MJ, Cox DW, Roberts EA.
    J Pediatr; 2000 Nov; 137(5):719-22. PubMed ID: 11060541
    [Abstract] [Full Text] [Related]

  • 45. Phenotype-genotype correlations in patients with Wilson's disease.
    Ferenci P.
    Ann N Y Acad Sci; 2014 May; 1315():1-5. PubMed ID: 24517292
    [Abstract] [Full Text] [Related]

  • 46. [Wilson disease].
    Shimizu N.
    Nihon Rinsho; 2004 Jan; 62 Suppl():399-403. PubMed ID: 15011394
    [No Abstract] [Full Text] [Related]

  • 47. [Wilson disease in 2003].
    Szalay F.
    Orv Hetil; 2003 Dec 14; 144(50):2451-8. PubMed ID: 15067983
    [Abstract] [Full Text] [Related]

  • 48. Hereditary iron and copper deposition: diagnostics, pathogenesis and therapeutics.
    Aaseth J, Flaten TP, Andersen O.
    Scand J Gastroenterol; 2007 Jun 14; 42(6):673-81. PubMed ID: 17505988
    [Abstract] [Full Text] [Related]

  • 49. Wilson's disease: A 2017 update.
    Poujois A, Woimant F.
    Clin Res Hepatol Gastroenterol; 2018 Dec 14; 42(6):512-520. PubMed ID: 29625923
    [Abstract] [Full Text] [Related]

  • 50. Biological functions of ceruloplasmin and their deficiency caused by mutation in genes regulating copper and iron metabolism.
    Mzhel'skaya TI.
    Bull Exp Biol Med; 2000 Aug 14; 130(8):719-27. PubMed ID: 11177225
    [Abstract] [Full Text] [Related]

  • 51. 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 14; 21(11):1375-7. PubMed ID: 26410678
    [No Abstract] [Full Text] [Related]

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  • 53. [Wilson disease].
    Abonyi M, Folhoffer A, Lakatos PL.
    Orv Hetil; 2004 Oct 17; 145(42):2147-51. PubMed ID: 15566072
    [Abstract] [Full Text] [Related]

  • 54. Wilson disease: pathogenesis and clinical considerations in diagnosis and treatment.
    Rosencrantz R, Schilsky M.
    Semin Liver Dis; 2011 Aug 17; 31(3):245-59. PubMed ID: 21901655
    [Abstract] [Full Text] [Related]

  • 55. A clinical study of Wilson's disease: The experience of a single Egyptian Paediatric Hepatology Unit.
    El-Karaksy H, Fahmy M, El-Raziky MS, El-Hawary M, El-Sayed R, El-Koofy N, El-Mougy F, El-Hennawy A, El-Shabrawi M.
    Arab J Gastroenterol; 2011 Sep 17; 12(3):125-30. PubMed ID: 22055589
    [Abstract] [Full Text] [Related]

  • 56. Wilson's disease: copper unfettered.
    Pfeil SA, Lynn DJ.
    J Clin Gastroenterol; 1999 Jul 17; 29(1):22-31. PubMed ID: 10405226
    [Abstract] [Full Text] [Related]

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  • 59. Wilson disease.
    Harada M.
    Med Electron Microsc; 2002 Jun 17; 35(2):61-6. PubMed ID: 12181646
    [Abstract] [Full Text] [Related]

  • 60. Genetics of Wilson's disease: a clinical perspective.
    Kumar SS, Kurian G, Eapen CE, Roberts EA.
    Indian J Gastroenterol; 2012 Dec 17; 31(6):285-93. PubMed ID: 22941676
    [Abstract] [Full Text] [Related]

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