Predicting the phenylalanine blood concentration from urine analyses. An approach to noninvasive monitoring of patients with phenylketonuria
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-005-0160-4
Reference24 articles.
1. Badugu R, Lakowicz JR, Geddes CD (2004) Ophthalmic glucose monitoring using disposable contact lenses. A review. J Fluoresc 14: 617–633.
2. Baum F (1985) Korrelierte biochemische und psychologische Studien an geistig retardierten Patienten mit Phenylketonurie. Med. thesis, University of Göttingen.
3. Becker K, Harenz J, Kalle N, Hommel G, Behbehani AW (1985) Comparative column chromatographic estimations of phenylalanine in plasma, whole blood, native and paper-dried capillary blood of healthy children and adults, and patients with hyperphenylalaninaemia. J Inherit Metab Dis 8: 119–122.
4. Bekhof J, van Rijn M, Sauer PJJ, Ten Vergert EM, Reijngoud D-J, van Spronsen FJ (2005) Plasma phenylalanine in patients with phenylketonuria self-managing their diet. Arch Dis Child 90: 163–164.
5. Berry HK, Umbarger B, Livingston B (1963) Excretion of phenylalanine by normal children and by patients with phenylketonuria. J Pediatr 63: 954–960.
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