Author:
Groselj Urh,Tansek Mojca Zerjav,Kovac Jernej,Hovnik Tinka,Podkrajsek Katarina Trebusak,Battelino Tadej
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference32 articles.
1. Follow-up study of 16 years neonatal screening for inborn errors of metabolism in West Germany;Mathias;Eur. J. Pediatr.,1986
2. Early detection and follow up of children with phenylketonuria in Slovenia;Battelino;Zdrav. Vestn.,1994
3. Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Scriver,2001
4. Phenylketonuria;Blau;Lancet,2010
5. There is no doubt that the early identification of PKU and prompt and continuous intervention prevents mental retardation in most patients;Blau;Mol. Genet. Metab.,2011
Cited by
35 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