Cognitive outcome in urea cycle disorders
- 1 April 2004
- journal article
- review article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 81, 58-62
- https://doi.org/10.1016/j.ymgme.2003.11.016
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Ornithine transcarbamylase deficiency presenting with strokelike episodesThe Journal of Pediatrics, 1993
- Prospective treatment of urea cycle disordersThe Journal of Pediatrics, 1991
- Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase LocusNew England Journal of Medicine, 1990
- Behavior management of feeding disturbances in urea cycle and organic acid disordersThe Journal of Pediatrics, 1987
- Ornithine transcarbamylase deficiency: Neuropathologic changes acquired in uteroThe Journal of Pediatrics, 1986
- Anorexia and altered serotonin metabolism in a patient with argininosuccinic aciduriaThe Journal of Pediatrics, 1986
- Risk of serious illness in heterozygotes for ornithine transcarbamylase deficencyThe Journal of Pediatrics, 1986
- Neurologic Outcome in Children with Inborn Errors of Urea SynthesisNew England Journal of Medicine, 1984
- Treatment of Inborn Errors of Urea SynthesisNew England Journal of Medicine, 1982
- Cerebral Dysfunction in Asymptomatic Carriers of Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1980