RECENT ADVANCES IN THE IDENTIFICATION OF ENZYME DEFICIENCIES IN THE PORPHYRIAS
- 1 June 1983
- journal article
- review article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 108 (6) , 729-734
- https://doi.org/10.1111/j.1365-2133.1983.tb01088.x
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Neurologic Manifestations of Acute PorphyriaSeminars in Liver Disease, 1982
- New type of acute porphyria with porphobilinogen synthase (δ-aminolevulinic acid dehydratase) defect in the homozygous stateClinical Biochemistry, 1982
- The inherited enzymatic defect in porphyria variegataHuman Genetics, 1981
- Characterization of the Porphobilinogen Deaminase Deficiency in Acute Intermittent PorphyriaJournal of Clinical Investigation, 1981
- HEPATOERYTHROPOIETIC PORPHYRIA: A NEW UROPORPHYRINOGEN DECARBOXYLASE DEFECT OR HOMOZYGOUS PORPHYRIA CUTANEA TARDA?The Lancet, 1981
- Identification of Two Types of Porphyria Cutanea Tarda by Measurement of Erythrocyte Uroporphyrinogen DecarboxylaseClinical Science, 1980
- Biosynthesis of the pigments of life: formation of the macrocycleNature, 1980
- The Enzymatic Defect in Variegate PorphyriaNew England Journal of Medicine, 1980
- Decreased Activity of Hepatic Uroporphyrinogen Decarboxylase in Sporadic Porphyria Cutanea TardaNew England Journal of Medicine, 1978
- Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.Journal of Clinical Investigation, 1975