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Journal Abstract Search


205 related items for PubMed ID: 870369

  • 21. A prospective clinical trial of D-penicillamine in the treatment of primary biliary cirrhosis.
    Bodenheimer HC, Schaffner F, Sternlieb I, Klion FM, Vernace S, Pezzullo J.
    Hepatology; 1985; 5(6):1139-42. PubMed ID: 3905561
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  • 22. The interactions of penicillamine with copper in vivo and the effect on hepatic metallothionein levels and copper/zinc distribution: the implications for Wilson's disease and arthritis therapy.
    McQuaid A, Lamand M, Mason J.
    J Lab Clin Med; 1992 Jun; 119(6):744-50. PubMed ID: 1593220
    [Abstract] [Full Text] [Related]

  • 23. [Wilson's disease: physiopathology, therapeutic approach and case report].
    Gallo V, Riva P, Sidoli L, Bisbocci D.
    Minerva Gastroenterol Dietol; 1994 Dec; 40(4):197-201. PubMed ID: 7849148
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  • 24. Time course of histological progression in primary biliary cirrhosis.
    Locke GR, Therneau TM, Ludwig J, Dickson ER, Lindor KD.
    Hepatology; 1996 Jan; 23(1):52-6. PubMed ID: 8550048
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  • 26. Primary biliary cirrhosis: critical evaluation and treatment policies.
    Sherlock S.
    Scand J Gastroenterol Suppl; 1982 Jan; 77():63-74. PubMed ID: 6750830
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  • 27. Usefulness of penicillamine-stimulated urinary copper excretion in the diagnosis of adult Wilson's disease.
    Foruny JR, Boixeda D, López-Sanroman A, Vázquez-Sequeiros E, Villafruela M, Vázquez-Romero M, Rodríguez-Gandía M, de Argila CM, Camarero C, Milicua JM.
    Scand J Gastroenterol; 2008 Jan; 43(5):597-603. PubMed ID: 18415754
    [Abstract] [Full Text] [Related]

  • 28. [Abnormal hepatic copper accumulation and its significance in LEC rats developing spontaneous hepatitis and hepatoma].
    Li Y.
    Hokkaido Igaku Zasshi; 1991 Sep; 66(5):658-64. PubMed ID: 1959841
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  • 30. Long-term ursodeoxycholic acid delays histological progression in primary biliary cirrhosis.
    Angulo P, Batts KP, Therneau TM, Jorgensen RA, Dickson ER, Lindor KD.
    Hepatology; 1999 Mar; 29(3):644-7. PubMed ID: 10051462
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  • 32. Effect of D-penicillamine on liver fibrosis and inflammation in Wilson disease.
    Kazemi K, Geramizadeh B, Nikeghbalian S, Salahi H, Bahador A, Reza Nejatollahi SM, Dehghani SM, Dehghani M, Kakaei F, Malek-Hosseini SA.
    Exp Clin Transplant; 2008 Dec; 6(4):261-3. PubMed ID: 19338486
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  • 36. Wilson disease in children: analysis of 57 cases.
    Manolaki N, Nikolopoulou G, Daikos GL, Panagiotakaki E, Tzetis M, Roma E, Kanavakis E, Syriopoulou VP.
    J Pediatr Gastroenterol Nutr; 2009 Jan; 48(1):72-7. PubMed ID: 19172127
    [Abstract] [Full Text] [Related]

  • 37. 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
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  • 38. Hepatic copper accumulation in patients with primary biliary cirrhosis.
    Takeshima H, Yagi A, Yano M, Sakamoto N, Kato S, Kuriki J, Arao M, Takikawa T, Hayashi H.
    Nagoya J Med Sci; 1993 Mar; 55(1-4):115-23. PubMed ID: 8247100
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  • 39. Cryoglobulins in primary biliary cirrhosis: prevalence and modulation by immunosuppressive therapy.
    Taal BG, Schalm SW.
    Z Gastroenterol; 1985 May; 23(5):228-34. PubMed ID: 3909671
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