Tyrosinemia type 1 in pediatric nephrology: Not always straightforward
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference12 articles.
1. Long-Term Outcomes and Practical Considerations in the Pharmacological Management of Tyrosinemia Type 1;Van Ginkel;Paediatr Drugs,2019
2. Inborn Errors of Metabolism with Hepatopathy: Metabolism Defects of Galactose, Fructose, and Tyrosine;Demirbas;Pediatr Clin North Am,2018
3. Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations;Chinsky;Genet Med,2017
4. Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs;De Jesús;Mol Genet Metab,2014
5. Recommendations for the management of tyrosinaemia type 1;de Laet;Orphanet J Rare Dis,2013
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical Spectrum of Hereditary Tyrosinemia Type 1 in a Cohort of Pakistani Children;Clinical Medicine Insights: Pediatrics;2024-01
2. Diagnostic tardif de la tyrosinémie héréditaire de type I, le cas de deux faux jumeaux;Revue Francophone des Laboratoires;2022-09
3. Influence of nitisinone and its metabolites on l-tyrosine metabolism in a model system;Chemosphere;2022-01
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