Tyrosine monitoring in children with early and continuously treated phenylketonuria: results of an international practice survey
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-010-9211-6
Reference18 articles.
1. Antshel KM, Waisbren SE (2003) Timing is everything: executive functions in children exposed to elevated levels of phenylalanine. Neuropsychology 17:458–468
2. Arnold GL, Vladutiu CJ, Orlowski CC, Blakely EM, DeLuca J (2004) Prevalence of stimulant use for attentional dysfunction in children with phenylketonuria. J Inherit Metab Dis 27:137–143
3. Australian Society for Inborn Errors of Metabolism (2005) The PKU handbook. Human Genetic Society of Australia, Alexandra
4. Burgard P (2000) Development of intelligence in early treated phenylketonuria. Eur J Ped 159(Suppl 2):74–79
5. Chace DH, Sherwin JE, Hillman SL, Lorey F, Cunningham GC (1998) Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens. Clin Chem 44:2405–2409
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1. Comparison of Tandem Mass Spectrometry and the Fluorometric Method—Parallel Phenylalanine Measurement on a Large Fresh Sample Series and Implications for Newborn Screening for Phenylketonuria;International Journal of Molecular Sciences;2023-01-27
2. Maternal phenylketonuria: newborn outcomes in women treated and not treated before pregnancy;PROG NUTR;2021
3. Tyrosine metabolism in health and disease: slow-release amino acids therapy improves tyrosine homeostasis in phenylketonuria;Journal of Pediatric Endocrinology and Metabolism;2020-11-19
4. The significant role of educational status in PKU patients: the beneficial effect of psychological support in depression;International Journal of Adolescent Medicine and Health;2019-03-19
5. The complete European guidelines on phenylketonuria: diagnosis and treatment;Orphanet Journal of Rare Diseases;2017-10-12
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