SummarM.Current strategies for the management of neonatal urea cycle disorders. J Pediatr. 2001;138(1 suppl):S30-S39.
2.
QuinonezSCThoeneJG.Citrullinemia type I. In: AdamMPArdingerHHPagonRA, et al, eds. GeneReviews®. Seattle, WA: University of Washington; 1993. https://www.ncbi.nlm.nih.gov/books/NBK1458/. Accessed April 17, 2020.
3.
BraissantO.Current concepts in the pathogenesis of urea cycle disorders. Mol Genet Metab. 2010;100(suppl 1):S3-S12.
4.
IyerHSenMPrasadCRuparCALindsayRM.Coma, hyperammonemia, metabolic acidosis, and mutation: lessons learned in the acute management of late onset urea cycle disorders. Hemodial Int. 2012;16:95-100.
5.
Ah MewNSimpsonKLGropmanALLanpherBCChapmanKASummarML.Urea cycle disorders overview. In: AdamMPArdingerHHPagonRA, et al eds. GeneReviews®. Seattle, WA: University of Washington; 1993. https://www.ncbi.nlm.nih.gov/books/NBK1217/. Accessed April 17, 2020.
6.
VaraRDhawanADeheragodaM, et al. Liver transplantation for neonatal-onset citrullinemia. Pediatr Transplant. 2018;22:e13191.
7.
WasimMAwanFRKhanHNTawabAIqbalMAyeshaH.Aminoacidopathies: prevalence, etiology, screening, and treatment options. Biochem Genet. 2018;56:7-21.