Author:
Charrière Sybil,Maillot Francois,Bouée Stéphane,Douillard Claire,Jacob Christian,Schneider Kim Maren,Theil Julia,Arnoux Jean-Baptiste
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference26 articles.
1. The complete European guidelines on phenylketonuria: diagnosis and treatment;van Wegberg;Orphanet J. Rare Dis.,2017
2. Phenylketonuria;Blau;Lancet,2010
3. Neonatal screening in Europe; the situation in 2004;Loeber;J. Inherit. Metab. Dis.,2007
4. Global prevalence of classic phenylketonuria based on neonatal screening program data: systematic review and meta-analysis;Shoraka;Clin. Exp. Pediatr.,2020
5. Protocole National de Diagnostic et de Soins (PNDS) Nom de la maladie rare - Phénylcétonurie;Haute Autorité de Santé - Filière Maladies Rares G2M,2018
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