Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/8904_2015_508
Reference36 articles.
1. Bartholomé K, Lutz P, Bickel H (1975) Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia. Pediatr Res 9:899–903. doi: 10.1203/00006450-197512000-00006
2. Berkemeyer S, Remer T (2006) Anthropometrics provide a better estimate of urinary organic acid anion excretion than a dietary mineral intake-based estimate in children, adolescents and adults. J Nutr 136:1203–1208
3. Bertram D, Rind H, Gladtke E (1970) Die Elimination von para-Aminohippursäure beim Kind. Z Kinderheilk 108:208–220. doi: 10.1007/BF00447033
4. Blau N, Yue W, Perez B (2015) PAHvdb. http://www.biopku.org/pah/ . Assessed 30 Mar 2015
5. Chalmers RA, Watts RWE (1974) Quantitative studies on the urinary excretion of unconjugated aromatic acids in phenylketonuria. Clin Chim Acta 55:281–294. doi: 10.1016/0009-8981(74)90002-3
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