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Journal Abstract Search

279 related items for PubMed ID: 7215719

  • 21. [The reassessment of the diagnostic value of 24-hour urinary copper excretion in children with Wilson's disease].
    Lu Y, Liu XQ, Wang XH, Wang JS.
    Zhonghua Gan Zang Bing Za Zhi; 2010 Jan; 18(1):49-53. PubMed ID: 20128970
    [Abstract] [Full Text] [Related]

  • 22. Copper disposition of the fetus and placenta in a patient with untreated Wilson's disease.
    Oga M, Matsui N, Anai T, Yoshimatsu J, Inoue I, Miyakawa I.
    Am J Obstet Gynecol; 1993 Jul; 169(1):196-8. PubMed ID: 8333453
    [Abstract] [Full Text] [Related]

  • 23. New insights into the pathogenesis of copper toxicosis in Wilson's disease: evidence for copper incorporation and defective canalicular transport of caeruloplasmin.
    Chowrimootoo GF, Ahmed HA, Seymour CA.
    Biochem J; 1996 May 01; 315 ( Pt 3)(Pt 3):851-5. PubMed ID: 8645167
    [Abstract] [Full Text] [Related]

  • 24. Urinary copper excretion after penicillamine in the diagnosis of Wilson's disease in children.
    Gregorio GV, Mieli-Vergani G, Mowat AP.
    J Hepatol; 1993 Nov 01; 19(3):489. PubMed ID: 8151113
    [No Abstract] [Full Text] [Related]

  • 25. The significance of variations in the distribution of copper in liver disease.
    Goldfischer S, Popper H, Sternlieb I.
    Am J Pathol; 1980 Jun 01; 99(3):715-30. PubMed ID: 7386600
    [Abstract] [Full Text] [Related]

  • 26. [Spontaneous and DL-penicillamine-induced renal copper excretion in liver diseases (author's transl)].
    Friedrich K, Henning H.
    Z Gastroenterol; 1979 Mar 01; 17(3):171-6. PubMed ID: 433370
    [Abstract] [Full Text] [Related]

  • 27. A high index of suspicion: the key to an early diagnosis of Wilson's disease in childhood.
    Sánchez-Albisua I, Garde T, Hierro L, Camarena C, Frauca E, de la Vega A, Díaz MC, Larrauri J, Jara P.
    J Pediatr Gastroenterol Nutr; 1999 Feb 01; 28(2):186-90. PubMed ID: 9932853
    [Abstract] [Full Text] [Related]

  • 28. Diagnosis of Wilson's disease: an experience over three decades.
    Gow PJ, Smallwood RA, Angus PW, Smith AL, Wall AJ, Sewell RB.
    Gut; 2000 Mar 01; 46(3):415-9. PubMed ID: 10673307
    [Abstract] [Full Text] [Related]

  • 29. 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 01; 29(2):155-61. PubMed ID: 9646197
    [Abstract] [Full Text] [Related]

  • 30. 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 01; 12(3):125-30. PubMed ID: 22055589
    [Abstract] [Full Text] [Related]

  • 31. Defective biliary copper excretion in Wilson's disease: the role of caeruloplasmin.
    Davis W, Chowrimootoo GF, Seymour CA.
    Eur J Clin Invest; 1996 Oct 01; 26(10):893-901. PubMed ID: 8911863
    [Abstract] [Full Text] [Related]

  • 32. [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 Oct 01; 35(1):11-7. PubMed ID: 9711308
    [Abstract] [Full Text] [Related]

  • 33. Diagnosis of Wilson's disease in children with liver disease. A report of two families.
    Danks DM, Stevens BJ.
    Lancet; 1969 Jan 04; 1(7584):22-5. PubMed ID: 4178768
    [No Abstract] [Full Text] [Related]

  • 34. Treatment of Wilson's disease with zinc: III. Prevention of reaccumulation of hepatic copper.
    Brewer GJ, Hill GM, Dick RD, Nostrant TT, Sams JS, Wells JJ, Prasad AS.
    J Lab Clin Med; 1987 May 04; 109(5):526-31. PubMed ID: 3572199
    [Abstract] [Full Text] [Related]

  • 35. [On hepatolenticular degeneration (Wilson's disease). 3. Hepatic localization of Cu64: scintigraphic and dynamic study before and after treatment with BAL and D-penicillamine].
    D'Addabbo A, Damato VD, Germinario L, Campanella G, Boccuni N.
    Acta Neurol (Napoli); 1971 May 04; 26(4):436-48. PubMed ID: 5132825
    [No Abstract] [Full Text] [Related]

  • 36. [Wilson's disease. A histological review of 7 patients and the value of histological copper positivity in relation to other hepatopathies].
    Blasco A, Domínguez P, Colina F, Castellano G.
    Med Clin (Barc); 1992 Feb 15; 98(6):207-11. PubMed ID: 1373211
    [Abstract] [Full Text] [Related]

  • 37. Relationship between striatal glucose consumption and copper excretion in patients with Wilson's disease treated with D-penicillamine.
    Hefter H, Kuwert T, Herzog H, Arendt G, Stremmel W, Feinendegen LE.
    J Neurol; 1993 Nov 15; 241(1):49-53. PubMed ID: 8138822
    [Abstract] [Full Text] [Related]

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  • 40. Wilson's disease.
    Loudianos G, Gitlin JD.
    Semin Liver Dis; 2000 Nov 15; 20(3):353-64. PubMed ID: 11076401
    [Abstract] [Full Text] [Related]

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