| Rev. Gastroenterol. Perú
Vol. 22 Nº 1 2002 |
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BIBLIOGRAFÍA
1. STEINDL, FERENZI P, DIENES HP et al. Wilsons disease in
patients presenting with liver disease: a diagnostic challenge. Gastroenterology 1997;
113:212-218 .
2. FERENCI P. Wilsons disease. Clin Liver Dis l998; 2: 31-49.
3. STERNLIEB I. Wilsons disease. Clin Liver Dis 2000; 4:229-239.
4. DUFOUR J-F, KAPLAN MM. Muddying the water: Wilsons disease
challenges will not soon disappear. Editorial. Gastroenterology 1997; 113:
348-349.
5. SCHILSKY ML, STERNLIEB I. Overcoming obstacles to the diagnosis of
Wilsons disease. Editorial. Gastroenterology 1997; 113: 350-353.
6 . FEENEY DM,BARON JC. Diaschisis.Stroke 1986; 17.817-830.
7. VAN WASSENAER-VAN HALL HN, VAN DER HEUVEL AG , ALGRA A ,et al.
Wilsons disease: findings at MR imaging and CT of the brain with clinical
correlation. Radiology 1996; 198 :531-536.
8. NAZER H , BRISMAR J , AL-KAWI MZ , GUNAZEKARAN TS.
Magnetic
Resonance imaging of the brain in Wilsons disease. Neuroradiology 1993; 35:134-141.
9. THUOMAS KA , AQUILONIUS, BERGSTROM K, WERSTERMARK K. Magnetic
resonance imaging of the brain in Wilsons disease.Neuroradiology 1993;
35: 134-141.
10. GRIMM G, MADL CH, KATZENSCHLAGEN E, et al . Detailed evaluation
of brain dysfunction in patients with Wilsons disease. EEG Clin Neurophysiol
1992; 82: 119-124
11. SEGAWA M, HOSAKA A, MIYAGAWA et al .Hereditary progressive distonia
with marked diurnal fluctuation. Adv Neurol 1976; 14: 235-245.
12. SEGAWA M, NOMURA Y, TANAMA S et al.Hereditary progressive dystonia with marked diurnal
fluctuation: Consideration on its pathophysiology based on the characteristics of
clinical and polysomnographical findings. Adv. Neurol 1998; 50: 367.
13. SCHILSKY ML. Wilsons disease: Genetic basis of copper toxicity and natural
history. Semin Liver Dis 1992; 16: 83-95.
14. ZUCKER SD, GOLLAN JL. Wilsons disease and hepatic copper
toxicosis. En: Zakim D, Boyer TD, editors. Hepatology: a textbook of liver
disease. Filadelfia: WB Saunders,1996 ; 1405 1439.
15. FRYDMAN M, BONNE-TAMIR, FARRER LA et al. Assignment of the gene of
Wilsons disease to chromosome 13: linkage to the esterase D locus. Proc Natl Acad
Sci USA 1985 ; 82 : 1819-1821.
16. CUZA E, MAIER DOBERSBERGER, POLLI C, et al. Screening for
Wilsons disease by serum ceruloplasmin. J Hepatology 1997; 27: 358-362.
17. GU M, COOPER JM, BLUTER P et al. Oxidative-phosphorylation defects
in liver of patients with Wilsons disease. Lancet 2000; 356: 469-470.
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