Successful adjustment to society by adults with phenylketonuria

Author:

Koch R.,Yusin M.,Fishler K.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference7 articles.

1. Dobson, J. C., Kushida, E., Williamson, M. and Friedman, E. G. Intellectual performance of 36 phenylketonuria patients and their nonaffected siblings.Pediatrics 58 (1976) 53–58

2. Horner, F. A. and Streamer, W. E. Effect of phenylalanine restricted diet on patients with phenylketonuria; clinical observations in three cases.J. Am. Med. Assoc. 161 (1956) 1628

3. Larsson, H. and Alm, P. Frequency of PKU and hyperphenylalaninemia in Sweden: a study in institutions for the mentally retarded as well as in neonates.Clin. Genet. 10 (1976) 313–318

4. Shaw, K., Gutenstein, M., Jacobs, E. E. and Blaskovics, J. C. Biochemical screening and monitoring of patients with phenylketonuria and variant forms of hyperphenylalaninemia. In Bickel, H., Hudson, F. P. and Woolf, L. (eds.)PKU and Other Inborn Errors of Metabolism, Georg Thieme Verlag, Stuttgard, 1971, pp. 163–180

5. Visakorpi, J. and Palo, J. The incidence of PKU in Finland.Acta Pediatr. Scand. 60 (1971) 666–668

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1. Phenylketonuria (PKU);Genes, Brain Function, and Behavior;2019

2. Clinical trial of ‘off diet’ older phenylketonurics with a new phenylalanine-f ree product*;Journal of Intellectual Disability Research;2008-06-28

3. Evaluation of quality of life and description of the sociodemographic state in adolescent and young adult patients with phenylketonuria (PKU);Health and Quality of Life Outcomes;2008

4. Social outcome in treated individuals with inherited metabolic disorders: UK study;Journal of Inherited Metabolic Disease;2005-12

5. Physical Health, Early Childhood;Encyclopedia of Primary Prevention and Health Promotion;2003

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