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 3 (2007), Issue 9 (September)

1. Newborn screening in Latin America at the beginning of the 21st century.
   J Inherit Metab Dis, 30(4): 466-81. [Abstract] [Full-text]
2. Effects and clinical significance of tetrahydrobiopterin supplementation in phenylalanine hydroxylase-deficient hyperphenylalaninaemia.
   J Inherit Metab Dis, 30(4): 556-62. [Abstract] [Full-text]
3. Newborn screening: a national public health programme in Brazil.
   J Inherit Metab Dis, 30(4): 615. [Abstract] [Full-text]
4. Phenylalanine blood levels and clinical outcomes in phenylketonuria: A systematic literature review and meta-analysis.
   Mol Genet Metab, 92(1): 63-70. [Abstract] [Full-text]
5. Correction in Female PKU Mice by Repeated Administration of mPAH cDNA Using phiBT1 Integration System.
   Mol Ther, 15(10): 1789-95. [Abstract] [Full-text]
6. Effects of various dietary amino acid preparations for phenylketonuric patients on the metabolic profiles along with postprandial insulin and ghrelin responses.
   Ann Nutr Metab, 51(4): 352-8. [Abstract] [Full-text]

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