Assessment of antioxidant enzymes, total sialic acid, lipid bound sialic acid, vitamins and selected amino acids in children with phenylketonuria
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://www.nature.com/articles/s41390-018-0137-2.pdf
Reference36 articles.
1. Mirás, A. et al. Risk factors for developing mineral bone disease in phenylketonuric patients. Mol. Genet. Metab. 108, 149–154 (2013).
2. Grünert, S. C. et al. Diurnal variation of phenylalanine and tyrosine concentrations in adult patients with phenylketonuria: subcutaneous microdialysis is no adequate tool for the determination of amino acid concentrations. Nutr. J. 12, 60 (2013).
3. Ghaleb A.O. et al. Phenylketonuria in Sohag: a preliminary study. Jordan J. Biol. Sci. 6, 243–245 (2013).
4. Waisbren, S. E. et al. Phenylalanine blood levels and clinical outcomes in phenylketonuria: a systematic literature review and meta-analysis. Mol. Genet. Metab. 92, 63–70 (2007).
5. Anikster, Y. et al. Biallelic mutations in DNAJC12 cause hyperphenylalaninemia, dystonia, and intellectual disability. Am. J. Hum. Genet. 100, 257–266 (2017).
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2. Growth and Nutritional Status of Phenylketonuric Children and Adolescents;BMC Pediatrics;2022-11-17
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