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296 related items for PubMed ID: 17934856

  • 1. Serum copper, ceruloplasmin and 24-h urine copper evaluations in celiac patients.
    Ince AT, Kayadibi H, Soylu A, Ovunç O, Gültepe M, Toros AB, Yaşar B, Kendir T, Abut E.
    Dig Dis Sci; 2008 Jun; 53(6):1564-72. PubMed ID: 17934856
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  • 2. 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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  • 3. Urinary copper excretion before and after oral intake of d-penicillamine in parents of patients with Wilson's disease.
    Vieira J, Oliveira PV, Juliano Y, Warde KR, Deguti MM, Barbosa ER, Carrilho FJ, Cancado EL.
    Dig Liver Dis; 2012 Apr; 44(4):323-7. PubMed ID: 22169274
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  • 4. Wilson's disease patients with normal ceruloplasmin levels.
    Yüce A, Koçak N, Ozen H, Gürakan F.
    Turk J Pediatr; 1999 Apr; 41(1):99-102. PubMed ID: 10770682
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  • 6. Contribution to the data on copper concentration in blood and urine in patients with Wilson's disease and in normal subjects.
    Lech T, Sadlik JK.
    Biol Trace Elem Res; 2007 Jul; 118(1):16-20. PubMed ID: 17848726
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  • 8. 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 Jul; 48(41):1259-61. PubMed ID: 11677941
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  • 9. The treatment of Wilson's disease with zinc. IV. Efficacy monitoring using urine and plasma copper.
    Brewer GJ, Hill G, Prasad A, Dick R.
    Proc Soc Exp Biol Med; 1987 Apr; 184(4):446-55. PubMed ID: 3562454
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  • 10. Is low serum tocopherol in Wilson's disease a significant symptom?
    Sinha S, Christopher R, Arunodaya GR, Prashanth LK, Gopinath G, Swamy HS, Taly AB.
    J Neurol Sci; 2005 Feb 15; 228(2):121-3. PubMed ID: 15694191
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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 15; 33(6):924-32. PubMed ID: 18789784
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  • 12. 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 15; 51(5):925-30. PubMed ID: 19720421
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  • 13. 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 15; 16(5):1206-11. PubMed ID: 1427659
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  • 14. Wilson's disease and hepatic transplantation.
    Tang R, Xue Z, Ye Q.
    J Huazhong Univ Sci Technolog Med Sci; 2002 Nov 15; 22(2):142-3. PubMed ID: 12658758
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  • 15. [Early diagnosis of Wilson's disease in childhood (author's transl)].
    Feist D, Wesch H, Schmid-Rüter E.
    Monatsschr Kinderheilkd (1902); 1978 Jun 15; 126(6):371-4. PubMed ID: 661832
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  • 18. Significance of copper determination in late onset of Wilson's disease.
    Lech T, Hydzik P, Kosowski B.
    Clin Toxicol (Phila); 2007 Sep 15; 45(6):688-94. PubMed ID: 17849244
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  • 19. Copper and zinc in the serum, urine, and hair of patients with Wilson's disease treated with penicillamine and zinc.
    Dastych M, Procházková D, Pokorný A, Zdrazil L.
    Biol Trace Elem Res; 2010 Mar 15; 133(3):265-9. PubMed ID: 19562272
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  • 20. Urinary 24-hour copper excretion at the time of diagnosis in children with Wilson's disease.
    Aksu AÜ, Sarı S, Gürkan ÖE, Dalgıç B.
    Acta Gastroenterol Belg; 2018 Mar 15; 81(3):410-414. PubMed ID: 30350530
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