Incidence of hereditary porphyria cutanea tarda (PCT) in a sample of the Italian population
- 1 August 1992
- journal article
- Published by Springer Nature in Archives of Dermatological Research
- Vol. 284 (4) , 212-214
- https://doi.org/10.1007/bf00375795
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Porphyria cutanea tarda: Erythrocyte Uroporphyrinogen Decarboxylase Activity in 471 Consecutive Patients1Published by S. Karger AG ,1990
- Erythrocyte uropophyrinogen decarboxylase activity in porphyria cutanea tarda: A study of 40 consecutive patientsJournal of Investigative Dermatology, 1989
- Chronische hepatische Porphyrie mit Uroporphyrinogen-Decarboxylase-Defekt in vier GenerationenDeutsche Medizinische Wochenschrift (1946), 1981
- Heredit re und nicht-heredit re Form der chronischen hepatischen Porphyrie: Unterschiedliches Verhalten der Uroporphyrinogen-Decarboxylase in Leber und ErythrozytenJournal of Molecular Medicine, 1980
- Identification of Two Types of Porphyria Cutanea Tarda by Measurement of Erythrocyte Uroporphyrinogen DecarboxylaseClinical Science, 1980
- Familial and sporadic porphyria cutaneaHuman Genetics, 1978
- An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.Journal of Clinical Investigation, 1976
- ERYTHROCYTE METABOLISM. VI. SEPARATION OF ERYTHROCYTE ENZYMES FROM HEMOGLOBIN*Journal of Clinical Investigation, 1962