Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine
- 1 May 1983
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 130 (2) , 231-238
- https://doi.org/10.1016/0009-8981(83)90120-1
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- Hereditary tyrosinemia - fumarylacetoacetase deficiencyPediatric Research, 1979
- Letter to the Editor: Metabolic Studies in TyrosinemiaPediatric Research, 1978
- On the enzymic defects in hereditary tyrosinemia.Proceedings of the National Academy of Sciences, 1977
- Metabolic Studies on Two Patients with Nonhepatic Tyrosinemia Using Deuterated Tyrosine LoadsPediatric Research, 1977
- Gas chromatographic analysis of urinary tyrosine and phenylalanine metabolites in patients with gastrointestinal disordersClinica Chimica Acta; International Journal of Clinical Chemistry, 1971