Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals-Reference-Cited by-同舟云学术

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Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals

Published:2015-02-18 Issue: Volume:3 Page:232640981557396
ISSN:2326-4098
Container-title:Journal of Inborn Errors of Metabolism and Screening
language:en
Short-container-title:Journal of Inborn Errors of Metabolism and Screening

Author:

Andrade Roseani¹²,Monteiro Vaneisse¹²,Cruz Cléber²,Silva Carla²,Bastos Adriana²³,Silva Luiz²

Affiliation:

1. Faculty of Nutrition/Institute of Health Sciences/Federal University of Pará, Belém, Pará, Brazil

2. Laboratory of Inborn Errors of Metabolism/Institute of Biological Sciences/ Federal University of Pará, Belém, Pará, Brazil

3. Reference Service for Neonatal Screening of Para/Para State University, Belém, Pará, Brazil

Publisher

FapUNIFESP (SciELO)

Subject

Genetics (clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/2326409815573962

Reference29 articles.

1. Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

2. Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations

3. Effect of high-protein meal plus aspartame ingestion on plasma phenylalanine concentrations in obligate heterozygotes for phenylketonuria

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Functional vitamin B12 deficiency in phenylketonuria patients and healthy controls: An evaluation with combined indicator of vitamin B12 status as a biochemical index;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2020-07

2. Phenylketonuria ( PKU );eLS;2016-11-15

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