The truth of treating patients with phenylketonuria after childhood: The need for a new guideline
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-008-0918-6
Reference76 articles.
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2. Bekhof J, van Spronsen FJ, Crone MR, van Rijn M, Oudshoorn CG, Verkerk PH (2003) Influence of knowledge of the disease on metabolic control in phenylketonuria. Eur J Pediatr 162: 440–442
3. Bekhof J, van Rijn M, Sauer PJ, Ten Vergert EM, Reijngoud DJ, van Spronsen FJ (2005) Plasma phenylalanine in patients with phenylketonuria self-managing the diet. Arch Dis Child 90: 163–164. doi: 10.1136/adc.2003.040451
4. Bosch AM, Tybout W, van Spronsen FJ, de Valk HW, Wijburg FA, Grootenhuis MA (2007) The course of life and quality of life of early and continuously treated Dutch patients with phenylketonuria. J Inherit Metab Dis 30: 29–34. doi: 10.1007/s10545-006-0433-6
5. Brown AS, Fernhoff PM, Waisbren SE, et al (2002) Barriers to successful dietary control among pregnant women with phenylketonuria. Genet Med 4: 84–89. doi: 10.1097/00125817-200203000-00006
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