Biochemical diagnosis of the porphyrias
- 30 June 1985
- journal article
- Published by Elsevier in Clinics in Dermatology
- Vol. 3 (2) , 24-40
- https://doi.org/10.1016/0738-081x(85)90033-1
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- CARBAMAZEPINE-INDUCED NON-HEREDITARY ACUTE PORPHYRIAThe Lancet, 1983
- Screening for latent acute intermittent porphyria: the value of measuring both leucocyte delta-aminolaevulinic acid synthase and erythrocyte uroporphyrinogen-1-synthase activities.Journal of Medical Genetics, 1982
- Analysis and separation of natural and synthetic mixtures of uroporphyrins by high-pressure liquid chromatographyBiochemical Journal, 1982
- High-performance liquid chromatography of porphyrin estersAnalytical Biochemistry, 1981
- Urinary Coproporphyrin isomers in Rotor’s syndrome: A study in eight familiesHepatology, 1981
- Altered coproporphyrin-isomer excretion in patients with the Dubin-Johnson syndromeInternational Journal of Biochemistry, 1980
- Rotor's syndromeThe American Journal of Medicine, 1976
- Abnormal Excretion of the Isomers of Urinary Coproporphyrin by Patients with Dubin—Johnson Syndrome in IsraelClinical Science, 1971
- Excretion of δ-aminolevulinic acid in hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- Separation of the coproporphyrin isomers I and III by thin layer chromatographyJournal of Chromatography A, 1963