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204 related items for PubMed ID: 13808058

  • 1. Studies on copper metabolism. XXIX. A critical analysis of serum copper and ceruloplasmin concentrations in normal subjects, patients with Wilson's disease and relatives of patients with Wilson's disease.
    CARTWRIGHT GE, MARKOWITZ H, SHIELDS GS, WINTROBE MM.
    Am J Med; 1960 Apr; 28():555-63. PubMed ID: 13808058
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  • 3. Some aspects of the relation of ceruloplasmin to Wilson's disease.
    SCHEINBERG IH, HARRIS RS, MORELL AG, DUBIN D.
    Neurology; 1958 Apr; 8(Suppl 1):44-51. PubMed ID: 13541603
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  • 4. A rapid screening test for deficiency of plasma ceruloplasmin and its value in the diagnosis of Wilson's disease.
    AISEN P, SCHORR JB, MORELL AG, GOLD RZ, SCHEINBERG IH.
    Am J Med; 1960 Apr; 28():550-4. PubMed ID: 13792199
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  • 5. Caeruloplasmin in Wilson's disease.
    ROSENOER VM, FRANGLEN G.
    Lancet; 1959 Dec 26; 2(7113):1163-4. PubMed ID: 14439030
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  • 10. Copper metabolism after living donor liver transplantation for hepatic failure of Wilson's disease from a gene mutated donor.
    Kobayashi S, Ochiai T, Hori S, Suzuki T, Shimizu T, Gunji Y, Shimada H, Yamamoto S, Ogawa A, Kohno Y, Sunaga M, Shimazu M, Tanaka K.
    Hepatogastroenterology; 2001 Dec 26; 48(41):1259-61. PubMed ID: 11677941
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  • 11. [The onset of psychiatric disorders and Wilson's disease].
    Benhamla T, Tirouche YD, Abaoub-Germain A, Theodore F.
    Encephale; 2007 Dec 26; 33(6):924-32. PubMed ID: 18789784
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  • 14. Plasma and erythrocyte copper, zinc, manganese and magnesium concentrations in Wilson's disease.
    Goto I, Kawano Y, Tsuchiya T, Tamagawa Y, Kuroiwa Y.
    Clin Neurol Neurosurg; 1986 Dec 26; 88(3):193-6. PubMed ID: 3780108
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  • 15. Wilson's disease and hepatic transplantation.
    Tang R, Xue Z, Ye Q.
    J Huazhong Univ Sci Technolog Med Sci; 2002 Dec 26; 22(2):142-3. PubMed ID: 12658758
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  • 16. The heterogeneity of caeruloplasmin nd the enzymatic defect in Wilson's disease.
    RICHTERICH R, GAUTIER E, STILLHART H, ROSSI E.
    Helv Paediatr Acta; 1960 Nov 26; 15():424-36. PubMed ID: 13741432
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  • 17. Molecular studies of ceruloplasmin deficiency in Wilson's disease.
    Czaja MJ, Weiner FR, Schwarzenberg SJ, Sternlieb I, Scheinberg IH, Van Thiel DH, LaRusso NF, Giambrone MA, Kirschner R, Koschinsky ML.
    J Clin Invest; 1987 Oct 26; 80(4):1200-4. PubMed ID: 3654978
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  • 18. [Early diagnosis of Wilson's disease in childhood (author's transl)].
    Feist D, Wesch H, Schmid-Rüter E.
    Monatsschr Kinderheilkd (1902); 1978 Jun 26; 126(6):371-4. PubMed ID: 661832
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  • 19. Reduced oxidase activity in the caeruloplasmin of two families with Wilson's disease.
    Gollan JL, Stocks J, Dormandy TL, Sherlock S.
    J Clin Pathol; 1977 Jan 26; 30(1):81-3. PubMed ID: 838874
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  • 20. Serum ceruloplasmin oxidase activity is a sensitive and highly specific diagnostic marker for Wilson's disease.
    Merle U, Eisenbach C, Weiss KH, Tuma S, Stremmel W.
    J Hepatol; 2009 Nov 26; 51(5):925-30. PubMed ID: 19720421
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