Clumsiness, confusion, coma, and valproate
- 1 April 1999
- journal article
- case report
- Published by Elsevier in The Lancet
- Vol. 353 (9162) , 1408
- https://doi.org/10.1016/s0140-6736(99)01433-6
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Identification of ‘private’ mutations in patients with ornithine transcarbamylase deficiencyJournal of Inherited Metabolic Disease, 1997
- Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonemia during initiation of valproate therapyNeurology, 1992
- Structure of the Human Ornithine Transcarbamylase Gene1The Journal of Biochemistry, 1988
- VALPROATE TOXICITY AND ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCYThe Lancet, 1986