Phenylketonuria in Iranian population: a study in institutions for mentally retarded in Isfahan

Author:

Vallian Sadeq,Barahimi Elham,Moeini Hasan

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology

Reference28 articles.

1. Phenylketonuria: old disease, new approach to treatment;Levy;Proc. Natl. Acad. Sci. U.S.A.,1999

2. C.R. Scriver, S. Kaufman, The hyperphenylalaninemia, in: C.R. Scriver, S. Kaufman, E. Eisensmith, S.L.C. Woo, B. Vogelstein, B. Childs, The Metabolic and Molecular Bases of Inherited Disease, 8th ed., McGraw Hill, NY, 2001,Chapter 27.

3. Neonatal neurological assessment of offspring in maternal phenylketonuria;Matalon;J. Inherit. Metab. Dis.,1998

4. Neurological outcome in adult patients with early-treated phenylketonuria;Pietz;Eur. J. Pediatr.,1998

5. Neurological deterioration in adult phenylketonuria;Villasana;J. Inherit. Metab. Dis.,1989

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