Citrullinemia Type 1: Behavioral Improvement with Late Liver Transplantation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-019-02905-8.pdf
Reference7 articles.
1. Bachmann C. Urea cycle disorders. In: Fernandes J, Saudubray J-M, Tada K, editors. Inborn Metabolic Diseases: Diagnosis and Treatment. Berlin, Heidelberg: Springer; 1990. p. 211–28.
2. Häberle J, Boddaert N, Burlina A, et al. Suggested guidelines for the diagnosis and management of urea cycle disorders. Orphanet J Rare Dis. 2012;7:32.
3. Ban K, Sugiyama N, Sugiyama K, et al. A pediatric patient with classical Citrullinemia who underwent living-related partial liver transplantation. Transplantation. 2001;71:1495–7.
4. Campeau PM, Pivalizza PJ, Miller G, Karpen S, Goss J, Lee BH. Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome study. Mol Genet Metab. 2010;100:S84–7.
5. Vara R, Dhawan A, Deheragoda M, et al. Liver transplantation for neonatal-onset citrullinemia. Pediatr Transpl. 2018;22:e13191.
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3. Outcome of Liver Transplantation for Neonatal-onset Citrullinemia Type I;Transplantation;2021-02-22
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