Living with phenylketonuria: Perspectives of patients and their families
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-005-4478-8
Reference20 articles.
1. Awiszus D, Unger I (1990) Coping with PKU: results of narrative interviews with parents. Eur J Pediatr 149: S45–51.
2. Fisch RO, Matalon R, Weisberg S, Michals K (1997) Phenylketonuria: current dietary treatment practices in the United States and Canada. J Am Coll Nutr 16: 147–151.
3. Glasgow RE, Anderson RM (1999) In diabetes care, moving from compliance to adherence is not enough. Something entirely different is needed [letter; comment]. Diabetes Care 22: 2090–2092.
4. Koch R, Azen CG, Hurst N, Friedman EG, Fishler K (1987) The effects of diet discontinuation in children with phenylketonuria. Eur J Pediatr 146: A12–16.
5. Koch R, Burton B, Hoganson G, et al (2002) Phenylketonuria in adulthood: a collaborative study. J Inherit Metab Dis 25: 333–346.
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