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3. 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]
4. [Wilson's disease. Report of a family with 4 cases of hepatolenticular degeneration]. Bozóti MM; de Oliveira CA; Otto PA Hospital (Rio J); 1970 Apr; 77(4):1200-27. PubMed ID: 5315573 [No Abstract] [Full Text] [Related]
5. 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]
7. Wilson's disease with special reference to ocular manifestations (a case report). Saiduzzafar H; Ansari Z; Kumar M Indian J Ophthalmol; 1978 Jul; 26(2):37-9. PubMed ID: 721242 [No Abstract] [Full Text] [Related]
8. [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]
9. [Hepatic Wilson's disease: clinical presentation and prognosis. Indications for liver transplantation]. Debernardi-Venon W; Balzola FA; Lagget M; Marzano A Minerva Gastroenterol Dietol; 1994 Dec; 40(4):191-5. PubMed ID: 7849147 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Wilson's disease with concomitant beta thalassaemia and factor V deficiency. Giannini E; Fasoli A; Botta F; Testa R Ital J Gastroenterol Hepatol; 1998 Dec; 30(6):633-5. PubMed ID: 10076789 [TBL] [Abstract][Full Text] [Related]
12. [Occurrence of copper metabolism abnormalities in the families of four individuals with newly diagnosed Wilson's disease]. Dastych M Vnitr Lek; 1997 Feb; 43(2):87-90. PubMed ID: 9245074 [TBL] [Abstract][Full Text] [Related]
13. [Wilson's disease or hepatolenticular degeneration]. Podesta HA; Carcia Dadoni LR; Mazzei CM; Diez E; De Prado Isla LH; Macias A Prensa Med Argent; 1968 Mar; 55(1):32-7. PubMed ID: 5746721 [No Abstract] [Full Text] [Related]
14. [Juvenile form of Wilson's disease with mainly hepatic character]. Rasore-Quartino A Minerva Pediatr; 1967 Aug; 19(34):1582-5. PubMed ID: 5610733 [No Abstract] [Full Text] [Related]
16. Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's disease. Anheim M; Chamouard P; Rudolf G; Ellero B; Vercueil L; Goichot B; Marescaux C; Tranchant C Clin Genet; 2010 Sep; 78(3):294-5. PubMed ID: 20695873 [No Abstract] [Full Text] [Related]
17. [Presymptomatic and hepatic forms of Wilson's disease in childhood. Long-term therapy with D-penicillamine]. Kittoe K; Colombo JP Praxis; 1968 Dec; 57(49):1723-9. PubMed ID: 5756864 [No Abstract] [Full Text] [Related]
18. 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]