Clinical and electrophysiological findings in patients with phenylketonuria and epilepsy: Reflex features
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Neurology (clinical),Neurology
Reference21 articles.
1. Phenylalanine hydroxylase deficiency;Mitchell;Genet Med,2011
2. Phenylketonuria;Blau;Lancet,2010
3. Phenylketonuria: an inborn error of phenylalanine metabolism;Williams;Clin Biochem Rev,2008
4. Epilepsy in phenylketonuria: a complex dependence on serum phenylalanine levels;Martynyuk;Epilepsia,2007
5. Adult care in phenylketonuria and hyperphenylalaninaemia: the relevance of neurological abnormalities;Brenton;Eur J Pediatr,2000
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