Suboptimal outcomes in patients with PKU treated early with diet alone: Revisiting the evidence
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference182 articles.
1. Hyperphenylalaninemia: phenylalanine hydroxylase deficiency;Scriver,2001
2. National Institutes of Health Consensus Development Conference Statement. Phenylketonuria (PKU): Screening and Management, October 16–18, 2000;Pediatrics,2001
3. NIH Consensus Development Program http://consensus.nih.gov/.
4. Plasma long-chain polyunsaturated fatty acids and neurodevelopment through the first 12 months of life in phenylketonuria;Agostoni;Dev. Med. Child Neurol.,2003
5. Neuropsychological speed tests and blood phenylalanine levels in patients with phenylketonuria: a meta-analysis;Albrecht;Neurosci. Biobehav. Rev.,2009
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