Acute brainstem dysfunction in neonatal hyperammonemia with ornithine transcarbamylase deficiency: A case report
Author:
Funder
National Center for Child Health and Development
Ministry of Health, Labour and Welfare
Publisher
Elsevier BV
Reference18 articles.
1. Comparative folding analyses of unknotted versus trefoil-knotted ornithine transcarbamylases suggest stabilizing effects of protein knots;Sriramoju;Biochem Biophys Res Commun,2018
2. Genotype–phenotype correlations in ornithine transcarbamylase deficiency: a mutation update;Caldovic;J Genet Genomics,2015
3. what urea-lly need to know: case report of severe noncirrhotic hyperammonemic encephalopathy and review of the literature;Upadhyay;Case Report Med,2016
4. Ornithine transcarbamylase deficiency: diagnostic and management challenges in the ICU;Watt;J Intensive Care Soc,2013
5. Amino Acids;Perlman,2018
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