HEPATOLENTICULAR DEGENERATION (WILSON'S DISEASE) A CASE DIAGNOSED BIOCHEMICALLY BEFORE CLINICAL MANIFESTATIONS
- 7 February 1959
- journal article
- Published by Elsevier in The Lancet
- Vol. 273 (7067) , 276-277
- https://doi.org/10.1016/s0140-6736(59)90203-x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- RAPID TEST FOR HEPATOLENTICULAR DEGENERATIONThe Lancet, 1956
- STUDIES ON COPPER METABOLISM. XIV. COPPER, CERULO-PLASMIN AND OXIDASE ACTIVITY IN SERA OF NORMAL HUMAN SUBJECTS, PREGNANT WOMEN, AND PATIENTS WITH INFECTION, HEPATOLENTICULAR DEGENERATION AND THE NEPHROTIC SYNDROME 1Journal of Clinical Investigation, 1955
- Studies on Copper Metabolism. XI. Copper and Iron Metabolism in the Nephrotic Syndrome 1Journal of Clinical Investigation, 1954
- The Amino Acid Content of the Blood and Urine in Wilson's DiseaseJournal of Clinical Investigation, 1954
- Genetic and biochemical aspects of Wilson's diseaseThe American Journal of Medicine, 1953
- Deficiency of Ceruloplasmin in Patients with Hepatolenticular Degeneration (Wilson's Disease)Science, 1952
- Investigations in Serum Copper. I. Nature of Serum Copper and its Relation to the Iron-Binding Protein in Human Serum.Acta Chemica Scandinavica, 1947