Porphyria cutanea tarda, or the uroporphyrinogen decarboxylase deficiency diseases
- 1 February 1986
- journal article
- review article
- Published by Elsevier in Clinical Biochemistry
- Vol. 19 (1), 3-15
- https://doi.org/10.1016/s0009-9120(86)80064-9
Abstract
No abstract availableThis publication has 78 references indexed in Scilit:
- Hemochromatosis and Red WineActa Medica Scandinavica, 2009
- Lipid peroxidation as a possible cause of TCDD toxicityBiochemical and Biophysical Research Communications, 1983
- Editorial RetrospectiveNew England Journal of Medicine, 1983
- Immunoreactive uroporphyrinogen decarboxylase is unchanged in porphyria caused by TCDD and hexachlorobenzeneBiochemical and Biophysical Research Communications, 1982
- Decreased Hepatic Uroporphyrinogen Decarboxylase Activity in Porphyria Cutanea TardaNew England Journal of Medicine, 1982
- Red-Cell Uroporphyrinogen Decarboxylase Activity in Porphyria Cutanea Tarda and in Other Forms of PorphyriaNew England Journal of Medicine, 1978
- Decreased Activity of Hepatic Uroporphyrinogen Decarboxylase in Sporadic Porphyria Cutanea TardaNew England Journal of Medicine, 1978
- Measurement of urine porphyrins and porphyrinogensBiochemical Medicine, 1976
- The Role of Iron in the Pathogenesis of Porphyria Cutanea TardaJournal of Clinical Investigation, 1972
- STUDIES ON THE CHEMOTHERAPY OF THE HUMAN MALARIAS. VI. THE PHYSIOLOGICAL DISPOSITION, ANTIMALARIAL ACTIVITY, AND TOXICITY OF SEVERAL DERIVATIVES OF 4-AMINOQUINOLINE 12Journal of Clinical Investigation, 1948