HEREDITARY COPROPORPHYRIA
- 3 August 1968
- journal article
- Published by Elsevier in The Lancet
- Vol. 292 (7562) , 263-264
- https://doi.org/10.1016/s0140-6736(68)92359-3
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- THE OCCURRENCE AND DETERMINATION OF δ-AMINOLEVULINIC ACID AND PORPHOBILINOGEN IN URINEPublished by Elsevier ,2021
- HEREDITARY COPROPORPHYRIAThe Lancet, 1967
- Hereditary coproporphyria with acute intermittent manifestations.BMJ, 1965
- CONTRAINDICATIONS OF BIOLOGICAL-OXIDATION INHIBITORS IN TREATMENT OF PORPHYRIAThe Lancet, 1965
- CONTRAINDICATIONS OF BIOLOGICAL-OXIDATION INHIBITORS IN THE TREATMENT OF PORPHYRIAThe Lancet, 1965
- Hereditary CoproporphyriaBMJ, 1955
- STUDIES OF COPROPORPHYRIN. III. IDIOPATHIC COPROPORPHYRINURIA; A HITHERTO UNRECOGNIZED FORM CHARACTERIZED BY LACK OF SYMPTOMS IN SPITE OF THE EXCRETION OF LARGE AMOUNTS OF COPROPORPHYRIN 1Journal of Clinical Investigation, 1949
- Simultaneous Excretion of Goproporphyrin I and III in a Case of Chronic PorphyriaExperimental Biology and Medicine, 1936