Brain dysfunction in phenylketonuria: Is phenylalanine toxicity the only possible cause?
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-008-0946-2
Reference58 articles.
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2. Antoshechkin AG, Chentsova TV, Tatur VY, Naritsin DB, Railian GP (1991) Content of phenylalanine, tyrosine and their metabolites in CSF in phenylketonuria. J Inherit Metab Dis 14: 749–754. doi: 10.1007/BF01799945 .
3. Bauman ML, Kemper TL (1982) Morphologic and histoanatomic observations of the brain in untreated human phenylketonuria. Acta Neuropathol 58: 55–63. doi: 10.1007/BF00692698 .
4. Bonafé L, Blau N, Burlina AP, et al (2001) Treatable neurotransmitter deficiency in mild phenylketonuria. Neurology 57: 908–911.
5. Burlina AB, Bonafé L, Ferrari V, et al (2000) Measurement of neurotransmitter metabolites in the cerebrospinal fluid of phenylketonuric patients under dietary treatment. J Inherit Metab Dis 2000; 23: 313–316. doi: 10.1023/A:1005694122277 .
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