Tyrosinemia with aminolevulinicdehydratase deficiency
Authors:
- Joel M. LamonJLJoel M. Lamon
- Bruce C. FrykholmBFBruce C. Frykholm
- Donald P. TschudyDTDonald P. Tschudy
- 1 February 1978
- journal article
- other
- Published by Elsevier in The Journal of Pediatrics
- Vol. 92 (2) , 346
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Tyrosinemia with acute intermittent porphyria: Aminolevulinic acid dehydratase deficiency related to elevated urinary aminolevulinic acid levelsThe Journal of Pediatrics, 1977
- Acute Intermittent Porphyria: Clinical and Selected Research AspectsAnnals of Internal Medicine, 1975
- A Red Cell Enzyme Method for the Diagnosis of Acute Intermittent PorphyriaBlood, 1974
- Improved Method for Measurement of delta-Aminolevulinic Acid Dehydratase Activity of Human ErythrocytesClinical Chemistry, 1971
- Hereditary tyrosinemia and abnormal pyrrolemetabolismThe Journal of Pediatrics, 1970
- Excretion of δ-aminolevulinic acid in hereditary tyrosinemiaClinica Chimica Acta, 1969