Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: Diagnostic failure of protein loading and allopurinol challenge tests
- 31 August 1994
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 125 (2) , 249-251
- https://doi.org/10.1016/s0022-3476(94)70205-5
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea SynthesisNew England Journal of Medicine, 1984
- Carrier detection in ornithine transcarbamylase deficiencyThe Journal of Pediatrics, 1978
- Effects of pH on the kinetics of human liver ornithine-carbamyl phosphate transferaseBiochemistry, 1968