Hyperammonaemia as a cause of psychosis in an adolescent
- 27 August 2003
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 162 (11) , 773-775
- https://doi.org/10.1007/s00431-002-1126-2
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- A 6-year-old boy with hyperammonaemia: partial N-acetylglutamate synthase deficiency or portosystemic encephalopathy?European Journal of Pediatrics, 2000
- N‐Acetylglutamate synthetase deficiency: Favourable experience with carbamylglutamateJournal of Inherited Metabolic Disease, 1998
- Partial N-acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamateEuropean Journal of Pediatrics, 1998
- Alternative pathway therapy for urea cycle disordersJournal of Inherited Metabolic Disease, 1998
- Normal N-acetylglutamate concentration measured in liver from a new patient with N-acetylglutamate synthetase deficiency: Physiologic and biochemical implicationsBiochemical Medicine and Metabolic Biology, 1992
- N-Acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxicationEuropean Journal of Pediatrics, 1991
- N‐acetylglutamate synthetase deficiency: Clinical and laboratory observationsJournal of Inherited Metabolic Disease, 1990
- Late-onset form of partial N-acetylglutamate synthetase deficiencyEuropean Journal of Pediatrics, 1990
- N‐acetylglutamate synthetase deficiency, a second patientJournal of Inherited Metabolic Disease, 1987
- HealersNew England Journal of Medicine, 1981