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785 related items for PubMed ID: 9245074

  • 1. [Occurrence of copper metabolism abnormalities in the families of four individuals with newly diagnosed Wilson's disease].
    Dastych M.
    Vnitr Lek; 1997 Feb; 43(2):87-90. PubMed ID: 9245074
    [Abstract] [Full Text] [Related]

  • 2. Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected members.
    Merli M, Patriarca M, Loudianos G, Valente C, Riggio O, De Felice G, Petrucci F, Caroli S, Attili AF.
    Ital J Gastroenterol Hepatol; 1998 Jun; 30(3):270-5. PubMed ID: 9759594
    [Abstract] [Full Text] [Related]

  • 3. A critical evaluation of copper metabolism in Indian Wilson's disease children with special reference to their phenotypes and relatives.
    Prasad R, Kaur G, Walia BN.
    Biol Trace Elem Res; 1998 Nov; 65(2):153-65. PubMed ID: 9881519
    [Abstract] [Full Text] [Related]

  • 4. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T, Tirouche YD, Abaoub-Germain A, Theodore F.
    Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
    [Abstract] [Full Text] [Related]

  • 5. Syndromic variability of Wilson's disease in children. Clinical study of 44 cases.
    Giacchino R, Marazzi MG, Barabino A, Fasce L, Ciravegna B, Famularo L, Boni L, Callea F.
    Ital J Gastroenterol Hepatol; 1997 Apr; 29(2):155-61. PubMed ID: 9646197
    [Abstract] [Full Text] [Related]

  • 6. Wilson's disease: a diagnosis made in two individuals greater than 40 years of age.
    Bellary SV, Van Thiel DH.
    J Okla State Med Assoc; 1993 Sep; 86(9):441-4. PubMed ID: 8229372
    [Abstract] [Full Text] [Related]

  • 7. [Wilson's disease--a factor in the differential diagnosis in hepatopathies].
    Dastych M, Jezek P, Snelerová M.
    Vnitr Lek; 1989 Jul; 35(7):695-700. PubMed ID: 2800377
    [Abstract] [Full Text] [Related]

  • 8. Diagnosis of Wilson's disease presenting as fulminant hepatic failure.
    McCullough AJ, Fleming CR, Thistle JL, Baldus WP, Ludwig J, McCall JT, Dickson ER.
    Gastroenterology; 1983 Jan; 84(1):161-7. PubMed ID: 6847842
    [Abstract] [Full Text] [Related]

  • 9. Wilson's disease patients with normal ceruloplasmin levels.
    Yüce A, Koçak N, Ozen H, Gürakan F.
    Turk J Pediatr; 1999 Jan; 41(1):99-102. PubMed ID: 10770682
    [Abstract] [Full Text] [Related]

  • 10. Liver transplantation for Wilson's disease.
    Sevmis S, Karakayali H, Aliosmanoglu I, Yilmaz U, Ozcay F, Torgay A, Arslan G, Haberal M.
    Transplant Proc; 2008 Jan; 40(1):228-30. PubMed ID: 18261593
    [Abstract] [Full Text] [Related]

  • 11. Wilson's disease.
    Ferenci P.
    Ital J Gastroenterol Hepatol; 1999 Jan; 31(5):416-25. PubMed ID: 10470603
    [Abstract] [Full Text] [Related]

  • 12. Aspects of cuprogenic disorder in Wilson's Disease in India.
    Dastur DK, Manghani DK.
    Clin Exp Neurol; 1979 Jan; 16():1-8. PubMed ID: 550935
    [Abstract] [Full Text] [Related]

  • 13. [Wilson's disease ("hepatic form") in a region endemic for schistosomiasis mansoni: clinical presentation of 25 patients].
    Galizzi-Filho J, Andrade Mde O, Cota Mde M, Penna FJ, Figueiredo-Filho PP, Valadares CA, Machado-Silva R, Barquete J, de Oliveira JP, de Almeida JA.
    Arq Gastroenterol; 1998 Jan; 35(1):11-7. PubMed ID: 9711308
    [Abstract] [Full Text] [Related]

  • 14. Not Wilson's disease: a review of misdiagnosed cases.
    Walshe JM, Yealland M.
    QJM; 1995 Jan; 88(1):55-9. PubMed ID: 7894989
    [Abstract] [Full Text] [Related]

  • 15. Protean manifestations of Wilson's disease: a review of seven Saudi patients.
    Bahemuka M, Karrar ZA, Mofleh IA, Bahakim H, Hafeez MA.
    Trop Geogr Med; 1988 Apr; 40(2):131-8. PubMed ID: 3407002
    [Abstract] [Full Text] [Related]

  • 16. Failure of simple biochemical indexes to reliably differentiate fulminant Wilson's disease from other causes of fulminant liver failure.
    Sallie R, Katsiyiannakis L, Baldwin D, Davies S, O'Grady J, Mowat A, Mieli-Vergani G, Williams R.
    Hepatology; 1992 Nov; 16(5):1206-11. PubMed ID: 1427659
    [Abstract] [Full Text] [Related]

  • 17. [Copper level and metallothionein-like Cu-binding protein in cultured skin fibroblasts from patients with Menkes' disease and Wilson's disease].
    Sato M, Hayashi A, Ito H, Tojo M, Arima M.
    No To Shinkei; 1984 Nov; 36(11):1063-8. PubMed ID: 6525319
    [Abstract] [Full Text] [Related]

  • 18. [Wilson's disease].
    Kovacević I, Zekan M.
    Acta Med Croatica; 2003 Nov; 57(3):227-35. PubMed ID: 14582469
    [Abstract] [Full Text] [Related]

  • 19. Diagnosis and characterization of presymptomatic patients with Wilson's disease and the use of molecular genetics to aid in the diagnosis.
    Yuzbasiyan-Gurkan V, Johnson V, Brewer GJ.
    J Lab Clin Med; 1991 Nov; 118(5):458-65. PubMed ID: 1940586
    [Abstract] [Full Text] [Related]

  • 20. [Familial Wilson's disease: copper induced hemolysis, hypersplenism and hyperpigmentation as the main symptoms].
    Steiner P, Frey P, Lupi GA, Kistler HJ.
    Schweiz Med Wochenschr; 1975 Jul 05; 105(27):872-9. PubMed ID: 1215885
    [Abstract] [Full Text] [Related]

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