1762 related articles for article (PubMed ID: 7552582)
1. Wilson's disease: a new gene and an animal model for an old disease.
Cuthbert JA
J Investig Med; 1995 Aug; 43(4):323-36. PubMed ID: 7552582
[TBL] [Abstract][Full Text] [Related]
2. [The onset of psychiatric disorders and Wilson's disease].
Benhamla T; Tirouche YD; Abaoub-Germain A; Theodore F
Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
[TBL] [Abstract][Full Text] [Related]
3. Wilson's disease.
Loudianos G; Gitlin JD
Semin Liver Dis; 2000; 20(3):353-64. PubMed ID: 11076401
[TBL] [Abstract][Full Text] [Related]
4. Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis. A model of Wilson's disease.
Li Y; Togashi Y; Sato S; Emoto T; Kang JH; Takeichi N; Kobayashi H; Kojima Y; Une Y; Uchino J
J Clin Invest; 1991 May; 87(5):1858-61. PubMed ID: 2022751
[TBL] [Abstract][Full Text] [Related]
5. [Wilson's disease].
Kovacević I; Zekan M
Acta Med Croatica; 2003; 57(3):227-35. PubMed ID: 14582469
[TBL] [Abstract][Full Text] [Related]
6. Correction of liver disease following transplantation of normal rat hepatocytes into Long-Evans Cinnamon rats modeling Wilson's disease.
Irani AN; Malhi H; Slehria S; Gorla GR; Volenberg I; Schilsky ML; Gupta S
Mol Ther; 2001 Mar; 3(3):302-9. PubMed ID: 11273771
[TBL] [Abstract][Full Text] [Related]
7. Impaired hepatic copper homeostasis in Long-Evans Cinnamon rats: reduced biliary excretion of copper.
Suzuki M; Aoki T
Pediatr Res; 1994 May; 35(5):598-601. PubMed ID: 8065844
[TBL] [Abstract][Full Text] [Related]
8. Wilson's disease.
Ferenci P
Ital J Gastroenterol Hepatol; 1999; 31(5):416-25. PubMed ID: 10470603
[TBL] [Abstract][Full Text] [Related]
9. 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
[TBL] [Abstract][Full Text] [Related]
10. [Wilson's disease].
Brůha R; Marecek Z; Martásek P; Nevsímalová S; Petrtýl J; Urbánek P; Kalistová H; Pospísilová L
Cas Lek Cesk; 2009; 148(11):544-8. PubMed ID: 20662462
[TBL] [Abstract][Full Text] [Related]
11. Liver transplantation for Wilson's disease.
Sevmis S; Karakayali H; Aliosmanoglu I; Yilmaz U; Ozcay F; Torgay A; Arslan G; Haberal M
Transplant Proc; 2008; 40(1):228-30. PubMed ID: 18261593
[TBL] [Abstract][Full Text] [Related]
12. [Copper level and metallothionein-like Cu-binding protein in cultured skin fibroblasts from patients with Menkes' disease and Wilson's disease].
Sato M; Hayashi A; Ito H; Tojo M; Arima M
No To Shinkei; 1984 Nov; 36(11):1063-8. PubMed ID: 6525319
[TBL] [Abstract][Full Text] [Related]
13. Wilson's disease patients with normal ceruloplasmin levels.
Yüce A; Koçak N; Ozen H; Gürakan F
Turk J Pediatr; 1999; 41(1):99-102. PubMed ID: 10770682
[TBL] [Abstract][Full Text] [Related]
14. The rat homologue of the Wilson's disease gene was partially deleted at the 3' end of its protein-coding region in Long-Evans Cinnamon mutant rats.
Muramatsu Y; Yamada T; Moralejo DH; Cai Y; Xin X; Miwa Y; Izumi K; Matsumoto K
Res Commun Mol Pathol Pharmacol; 1995 Sep; 89(3):421-4. PubMed ID: 8680810
[TBL] [Abstract][Full Text] [Related]
15. Wilson's disease (hepatolenticular degeneration).
Herron BE
Ophthalmic Semin; 1976; 1(1):63-9. PubMed ID: 1023089
[TBL] [Abstract][Full Text] [Related]
16. Abnormal hepatobiliary and circulating lipid metabolism in the Long-Evans Cinnamon rat model of Wilson's disease.
Levy E; Brunet S; Alvarez F; Seidman E; Bouchard G; Escobar E; Martin S
Life Sci; 2007 Mar; 80(16):1472-83. PubMed ID: 17303181
[TBL] [Abstract][Full Text] [Related]
17. 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; 30(3):270-5. PubMed ID: 9759594
[TBL] [Abstract][Full Text] [Related]
18. Significance of copper determination in late onset of Wilson's disease.
Lech T; Hydzik P; Kosowski B
Clin Toxicol (Phila); 2007 Sep; 45(6):688-94. PubMed ID: 17849244
[TBL] [Abstract][Full Text] [Related]
19. Genetic diseases of copper metabolism.
Prohaska JR
Clin Physiol Biochem; 1986; 4(1):87-93. PubMed ID: 3514056
[TBL] [Abstract][Full Text] [Related]
20. Tetrathiomolybdate causes formation of hepatic copper-molybdenum clusters in an animal model of Wilson's disease.
George GN; Pickering IJ; Harris HH; Gailer J; Klein D; Lichtmannegger J; Summer KH
J Am Chem Soc; 2003 Feb; 125(7):1704-5. PubMed ID: 12580588
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]