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 2 (2006), Issue 11 (November)

1. Primary care physicians' attitudes regarding follow-up care for children with positive newborn screening results.
   Pediatrics, 118(5): 1836-41. [Abstract] [Full-text]
2. Identification and characterization of large deletions in the phenylalanine hydroxylase (PAH) gene by MLPA: evidence for both homologous and non-homologous mechanisms of rearrangement.
   Mol Genet Metab, 89(4): 300-9. [Abstract] [Full-text]
3. Application of an enzyme chip to the microquantification of l-phenylalanine.
   Anal Biochem, 359(1): 72-8. [Abstract] [Full-text]
4. Large neutral amino acids in the treatment of phenylketonuria (PKU).
   J Inherit Metab Dis, 29(6): 732-8. [Abstract] [Full-text]

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