Restoration of nitrogen homeostasis in a man with ornithine transcarbamylase deficiency
- 1 October 1993
- journal article
- case report
- Published by Elsevier in Metabolism
- Vol. 42 (10) , 1336-1339
- https://doi.org/10.1016/0026-0495(93)90135-b
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (HD 26358, RR-00052)
- U.S. Food and Drug Administration (FD-R-000198)
This publication has 17 references indexed in Scilit:
- Phenylacetylglutamine May Replace Urea as a Vehicle for Waste Nitrogen ExcretionPediatric Research, 1991
- Late-onset ornithine transcarbamylase deficiency in male patientsThe Journal of Pediatrics, 1990
- Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase LocusNew England Journal of Medicine, 1990
- Allopurinol-Induced OrotidinuriaNew England Journal of Medicine, 1990
- Late onset ornithine carbamoyl transferase deficiency in males.Archives of Disease in Childhood, 1988
- Ornithine Transcarbamylase Deficiency — A Cause of Bizarre Behavior in a ManNew England Journal of Medicine, 1986
- Natural History of Symptomatic Partial Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1986
- Risk of serious illness in heterozygotes for ornithine transcarbamylase deficencyThe Journal of Pediatrics, 1986
- Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.Journal of Clinical Investigation, 1984
- STUDIES IN THE SYNTHESIS OF HIPPURIC ACID IN THE ANIMAL ORGANISMPublished by Elsevier ,1914