Copper Metabolism in Normal Adults and in Clinically Normal Relatives of Patients with Wilson's Disease

Overview

Journal J Clin Pathol

Specialty Pathology

Date 1958 Sep 1

PMID 13575563

Citations 6

Authors

F C NEALE

M Fischer-Williams

Affiliations

Soon will be listed here.

Citing Articles

Wilson's Disease-Genetic Puzzles with Diagnostic Implications.

Gromadzka G, Bendykowska M, Przybylkowski A Diagnostics (Basel). 2023; 13(7).

PMID: 37046505 PMC: 10093728. DOI: 10.3390/diagnostics13071287.

Middle-aged heterozygous carriers of Wilson's disease do not present with significant phenotypic deviations related to copper metabolism.

Gromadzka G, Chabik G, Mendel T, Wierzchowska A, Rudnicka M, Czlonkowska A J Genet. 2011; 89(4):463-7.

PMID: 21273697 DOI: 10.1007/s12041-010-0065-3.

A family study of the biochemical defects in Wilson's disease.

Soothill J, Blainey J, NEALE F, Fischer-Williams M, Melnick S J Clin Pathol. 1961; 14(3):264-70.

PMID: 16810973 PMC: 480209. DOI: 10.1136/jcp.14.3.264.

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

Sternlier I, Morell A, BAUER C, Combes B, De Bobes-Sternberg S, Schein-Berg I J Clin Invest. 1961; 40(4):707-15.

PMID: 16695860 PMC: 290777. DOI: 10.1172/JCI104304.

[Advances in the recognition of heterozygous characteristics in hereditary enzymopathies].

LINNEWEH F Klin Wochenschr. 1962; 40:553-8.

PMID: 14465634 DOI: 10.1007/BF01478627.

References

Eden A, GREEN H . Micro-determination of copper in biological material. Biochem J. 1940; 34(8-9):1202-8. PMC: 1265401. DOI: 10.1042/bj0341202. View

Bickel H, NEALE F, Hall G . A clinical and biochemical study of hepatolenticular degeneration (Wilson's disease). Q J Med. 1957; 26(104):527-58. View

UZMAN L, Hood B . The familial nature of the amino-aciduria of Wilson's disease (hepatolenticular degeneration). Am J Med Sci. 1952; 223(4):392-400. DOI: 10.1097/00000441-195204000-00006. View

CARTWRIGHT G, GUBLER C, Wintrobe M . Studies on copper metabolism. XI. Copper and iron metabolism in the nephrotic syndrome. J Clin Invest. 1954; 33(4):685-98. PMC: 1087284. DOI: 10.1172/JCI102939. View

HOLMBERG C, LAURELL C . Oxidase reactions in human plasma caused by coeruloplasmin. Scand J Clin Lab Invest. 1951; 3(2):103-7. DOI: 10.3109/00365515109060581. View