Phenylketonuria Research Today is a free monthly online journal that collates and summarizes the latest research about Phenylketonuria, including details on genetics, causes, symptoms, hereditary disorder.

Volume 4 (2008), Issue 8 (August)

1. Implications of resolving the diagnosis of PKU for parents and children.
   J Pediatr Psychol, 33(8): 855-66. [Abstract] [Full-text]
2. Anabolic function of phenylalanine hydroxylase in Caenorhabditis elegans.
   FASEB J, 22(8): 3046-58. [Abstract] [Full-text]
3. Identification of pharmacological chaperones as potential therapeutic agents to treat phenylketonuria.
   J Clin Invest, 118(8): 2858-67. [Abstract] [Full-text]
4. Maternal phenylketonuria.
   Pediatrics, 122(2): 445-9. [Abstract] [Full-text]
5. Progress toward cell-directed therapy for phenylketonuria.
   Clin Genet, 74(2): 97-104. [Abstract] [Full-text]
6. Does maternal knowledge and parent education affect blood phenylalanine control in phenylketonuria?
   J Hum Nutr Diet, 21(4): 351-8. [Abstract] [Full-text]
7. Clinical genetics of functionally mild non-coding GTP cyclohydrolase 1 (GCH1) polymorphisms modulating pain and cardiovascular risk.
   Mutat Res, 659(3): 195-201. [Abstract] [Full-text]

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