PKU—What is daily practice in various centres in Europe?
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-008-0966-y
Reference9 articles.
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2. Burgard P, Bremer HJ, Bührdel P, et al (1999) Rationale for the German recommendations for phenylalanine level control in phenylketonuria. Eur J Pediat 158: 46–54. doi: 10.1007/s004310051008 .
3. Camfield CS, Joseph M, Hurley T, Campbell K, Sanderson S, Camfield PR (2004) Optimal management of phenylketonuria: a centralized expert team is more successful than a decentralized model of care. J Pediatr 145: 53–57. doi: 10.1016/j.jpeds.2004.04.029 .
4. Hanley WB, Feigenbaum A, Clarke JT, Schoonheyt W, Austin V (1993) Vitamin B12 deficiency in adolescents and young adults with phenylketonuria. Lancet 342: 997. doi: 10.1016/0140-6736(93)92047-W .
5. MRC (1993a) Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria. BMJ 306: 115–119.
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