A critical evaluation of copper metabolism in Indian Wilson's disease children with special reference to their phenotypes and relatives

Biological Trace Element Research

Volumn 65, Issue 2, 1998, Pages 153-165

  Prasad, Rajendra ^a   Kaur, Gurjit ^b   Walia, B N S ^a  

^a POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH   (India)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

Copper metabolism; Family screening; Hepatic copper; Phenotypes; Wilson's disease

Indexed keywords

CERULOPLASMIN; COPPER; PENICILLAMINE;

ADOLESCENT; ARTICLE; CHILD; CHILDHOOD DISEASE; CONTROLLED STUDY; COPPER METABOLISM; FEMALE; HUMAN; LIVER BIOPSY; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; RELATIVE; WILSON DISEASE;

EID: 0032443733     PISSN: 01634984     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02784267     Document Type: Article

References (26)

1. I. Bremner and J. H. Beattie, Annu. Rev. Nutr. 10, 63 (1990).
2. M. C. Linder and M. Hazegh-Azam, Am. J. Clin. Nutr. 63, 7975 (1996).
3. D. M. Danks, Disorder of copper transport, in The Metabolic Basis of Inherited Disease, 6th ed., C. R. Scriver, A. L. Beaudet, W. S. Sly, and D. Valle, eds., McGraw-Hill, New York, pp. 1411 (1989).
4. Y. Yamaguchi, M. E. Heiny, and J. D. Gittin, Biochem. Biophys. Res. Commun. 197, 271 (1993).
5. P. C. Bull, G. R. Thomas, J. M. Rommens, J. R. Forbes, and D. W. Cox, Nature Genet 5, 327 (1993).
6. I. H. Scheinberg and I. Sternlieb, Wilson's disease, Major Problems in Internal Medicine, in L. H. Smith, ed., W.B. Saunders, Philadelphia, Vol. 23 (1984).
7. F. C. Yarze, P. Martin, S. J. Munoj, and L. S. Friedman, Am. J. Med. 92, 645 (1992).
8. W. Stremmel, K. W. Meyerrose, C. Niederau, C. Hefter, P. Kreuzpainter, and G. Strohmeyer, Ann. Intern. Med. 115, 720 (1991).
9. D. K. Manghani and D. K. Dastur, Ind. J. Gastroenterol. 4, 91 (1985).
10. R. Prasad, G. Kaur, R. Nath, and B. N. S. Walia, Mol. Cell. Biochem. 156, 25 (1996).
11. H. A. Ravin, J. Lab. Clin. Med. 56, 101 (1961).
12. R. Prasad, J. L. Kinsella, and B. Sacktor, Am. J. Physiol. 255, F1183 (1988).
13. P. S. Chen, T. Y. Toribara, and H. Warner, Anal. Chem. 28, 176 (1956).
14. C. J. Gubler, H. Brown, and H. Markowitz, J. Clin. Invest. 32, 405 (1953).
15. D. W. Cox, F. C. Fraser, and A. Sass-Kortsak, Am. J. Hum. genet. 24, 546 (1972).
16. L. E. Mallette and R. Aquaron, Clin. Chim. Acta 132, 245 (1983).
17. R. S. Graul, O. Epstein, S. Sherlock, and P. J. Scheurer, Liver 2, 207 (1982).
18. L. Barrow and M. S. Tanner, Eur. J. Clin. Invest. 18, 555 (1988).
19. J. M. Walshe, Quart. J. Med. New Series 70, 253 (1989).
20. S. Lau and B. Sarkar, Can. J. Biochem. Cell. Biol. 62, 449 (1984).
21. M. J. Czaja, F. R. Weiner, S. J. Schwarzenberg, I. Sternlieb, I. H. Scheinberg, D. H. Vanthiel, et al., J. Clin. Invest. 80, 1200 (1987).
22. E. Azizi, G. Eshel, and M. Aladjem, Eur. J. Pediatr. 148, 548 (1989).
23. M. G. Cogan and F. C. Rector, Acid-base disorders: verification and calculation of acid-base parameters, in The Kidney, 4th ed., B. M. Bremner and F. C. Rector, Jr., eds., W.B. Saunders, Philadelphia, Vol. I, pp. 752 (1991).
24. I. H. Scheinberg and I. Sternlieb, Am. J. Clin. Nutr. 63, 8425 (1996).
25. S. A. Zargar, B. R. Thapa, A. Sahni, and S. Mehta, Indian J. Gastroenterol. 10, 101 (1991).
26. D. Frommer, J. Morris, S. Sherlock, J. Abrams, and S. Newman, Gastroenterology 72, 1331 (1977).