Hepatolenticular degeneration; Wilson's disease; a report of five cases, with commentary.
作者信息
WARNOCK C G
出版信息
Ulster Med J. 1952 Nov 1;21(2):155-71.
Abstract
摘要
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Hepatolenticular degeneration; Wilson's disease; a report of five cases, with commentary.
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Studies on copper metabolism. XIV. Copper, ceruloplasmin and oxidase activity in sera of normal human subjects, pregnant women, and patients with infection, hepatolenticular degeneration and the nephrotic syndrome.
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本文引用的文献
1
The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration.
Brain. 1948 Dec;71(Pt. 4):410-5. doi: 10.1093/brain/71.4.410.
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Anomalies of pigmentation.
Practitioner. 1952 May;168(1007):453-64.
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Amino-aciduria and copper metabolism in hepatolenticular degeneration.
J Clin Pathol. 1952 Feb;5(1):16-24. doi: 10.1136/jcp.5.1.16.
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The familial nature of the amino-aciduria of Wilson's disease (hepatolenticular degeneration).
Am J Med Sci. 1952 Apr;223(4):392-400. doi: 10.1097/00000441-195204000-00006.
5
The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease).
N Engl J Med. 1951 Dec 13;245(24):917-25. doi: 10.1056/NEJM195112132452401.
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Hepatolenticular degeneration; biochemical observations in children with and without neurological symptoms; hyperamino-aciduria.
Acta Med Scand. 1951;140(5):374-80.
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The effects of B.A.L. in hepatolenticular degeneration.
Brain. 1951 Mar;74(1):10-22. doi: 10.1093/brain/74.1.10.
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Copper excretion in the urine of normal individuals and of patients with hepatolenticular degeneration (Wilson's disease).
Arch Biochem Biophys. 1951 Apr;31(2):262-5. doi: 10.1016/0003-9861(51)90213-5.
9
Paper chromatographic analysis of amino acid excretion in Wilson's disease.
Acta Med Scand. 1950;138(5):344-7. doi: 10.1111/j.0954-6820.1950.tb10132.x.
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