Diagnosis of Wilson's disease

Netherlands Journal of Medicine

Volumn 67, Issue 5, 2009, Pages 195-

  Brewer, G J ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CERULOPLASMIN; COPPER; WILSON DISEASE PROTEIN;

CERULOPLASMIN BLOOD LEVEL; GENE MUTATION; GENETIC ANALYSIS; HUMAN; LETTER; LIVER BIOPSY; QUANTITATIVE ANALYSIS; STAINING; URINALYSIS; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; COPPER; DIAGNOSIS, DIFFERENTIAL; HEPATOLENTICULAR DEGENERATION; HUMANS; LIVER; MOLECULAR BIOLOGY;

EID: 66449124005     PISSN: 03002977     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Kok KF, Hoevenaars B, Waanders E, Drenth JP. Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient. Neth J Med. 2008;66(8):348-350
2. McDonald JA, Snitch P, Painter D, Hensley W, Gallagher ND, McCaughan GW. Striking variability of hepatic copper levels in fulminant hepatic failure. J Gastroenterol Hepatol. 1992;7(4):396-398
3. Brewer GJ. Wilson's disease. In: Fauci AS, Braunward E, Kasper DL, et al. (eds). Harrison's Principles of Internal Medicine. 17 ed. New York: McGraw-Hill Companies Inc, 2008:2449-2452
4. Brewer GJ. Wilson's disease: A clinician's guide to recognition, diagnosis, and management. Boston: Kluwer Academic Publishers, 2001.