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Journal Abstract Search

395 related items for PubMed ID: 4791768

  • 1.
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  • 2. [Radioactive copper in the diagnosis of Wilson's disease].
    Czlonkowska A, Wehr H, Galewicz A, Harmak E, Rodo M, Wald I.
    Pol Tyg Lek; 1973 May 23; 28(17):597-9. PubMed ID: 4712325
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  • 4. Evolution of the hepatic lesion in Wilson's disease (hepatolenticular degeneration).
    Sternlieb I.
    Prog Liver Dis; 1972 May 23; 4():511-25. PubMed ID: 4569009
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  • 8. Detection of the heterozygote of Wilson's disease.
    O'Reilly S, Weber P, Pollycove M, Shipley L.
    J Nucl Med; 1969 Mar 23; 10(3):143-4. PubMed ID: 5785018
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  • 9. Determination of liver enzymes, serum ceruloplasmin and urine copper in parents of children with Wilson's disease.
    Haghighat M, Dehghani SM, Imanieh MH, Gholami S.
    Saudi Med J; 2008 Jul 23; 29(7):1056-7. PubMed ID: 18626543
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  • 10. The urinary excretion of radiocopper in presymptomatic and symptomatic Wilson's disease, heterozygotes and controls: its significance in diagnosis and management.
    Gibbs K, Hanka R, Walshe JM.
    Q J Med; 1978 Jul 23; 47(187):349-64. PubMed ID: 715173
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  • 11. Screening asymptomatic family members for Wilson's disease.
    Lindahl JA, Sharp HL.
    Minn Med; 1982 Aug 23; 65(8):473-5. PubMed ID: 6752690
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  • 12. [Features of the course and disorders of copper and ceruloplasmin metabolism in hepatolenticular degeneration].
    Davidenkova EF, Neĭfakh SA, Butomo IV, Mashkov BA, Lapchenkov VI.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1967 Aug 23; 67(7):982-90. PubMed ID: 5598796
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  • 13. Introduction. Symposium on copper metabolism and Wilson's disease.
    Goldstein NP, Owen CA.
    Mayo Clin Proc; 1974 Jun 23; 49(6):363-7. PubMed ID: 4599351
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  • 15. 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 23; 65(2):153-65. PubMed ID: 9881519
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  • 16. 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 23; 30(3):270-5. PubMed ID: 9759594
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  • 18. [Wilson's disease--a factor in the differential diagnosis in hepatopathies].
    Dastych M, Jezek P, Snelerová M.
    Vnitr Lek; 1989 Jul 23; 35(7):695-700. PubMed ID: 2800377
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  • 20. Penicillamine-induced normalization of clinical signs, and liver morphology and histochemistry in a case of Wilson's disease.
    Falkmer S, Samuelson G, Sjölin S.
    Pediatrics; 1970 Feb 23; 45(2):260-8. PubMed ID: 5413388
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