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 5 (2009), Issue 6 (June)

1. Purification and use of glycomacropeptide for nutritional management of phenylketonuria.
   J Food Sci, 74(4): E199-206. [Abstract] [Full-text]
2. Dietary management practices in phenylketonuria across European centres.
   Clin Nutr, 28(3): 231-6. [Abstract] [Full-text]
3. Newborn screening for genetic disorders.
   Pediatr Clin North Am, 56(3): 505-13, Table of Contents. [Abstract] [Full-text]
4. Genotype-predicted tetrahydrobiopterin (BH4)-responsiveness and molecular genetics in Croatian patients with phenylalanine hydroxylase (PAH) deficiency.
   Mol Genet Metab, 97(3): 165-71. [Abstract] [Full-text]
5. Evaluation of the birthweight values of newborns presenting at the Mother-Child Health and Family Planning Center in Yenibosna, Istanbul, Turkey.
   Nurs Health Sci, 11(2): 174-9. [Abstract] [Full-text]
6. A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin.
   J Hum Genet, 54(6): 335-9. [Abstract] [Full-text]

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