Attention-deficit hyperactivity disorder in Brazilian patients with phenylketonuria-Reference-Cited by-同舟云学术

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Attention-deficit hyperactivity disorder in Brazilian patients with phenylketonuria

Published:2018-07-06 Issue:4 Volume:120 Page:893-899
ISSN:0300-9009
Container-title:Acta Neurologica Belgica
language:en
Short-container-title:Acta Neurol Belg

Author:

da Silva Fernanda Gabriel Santos,e Vairo Filippo Pinto,de Souza Carolina Fischinger Moura,Schwartz Ida Vanessa Doederlein

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s13760-018-0972-2.pdf

Reference38 articles.

1. Blau N, van Spronsen FJ, Levy HL (2010) Phenylketonuria. Lancet 376:1417–1427. https://doi.org/10.1016/S0140-6736(10)60961-0

2. van Wegberg AMJ, MacDonald A, Ahring K et al (2017) The complete European guidelines on phenylketonuria: diagnosis and treatment. Orphanet J Rare Dis 12:162. https://doi.org/10.1186/s13023-017-0685-2

3. van Spronsen FJ, van Wegberg AM, Ahring K et al (2017) Key European guidelines for the diagnosis and management of patients with phenylketonuria. Lancet Diabetes Endocrinol 8587:1–14. https://doi.org/10.1016/S2213-8587(16)30320-5

4. Vockley J, Andersson HC, Antshel KM et al (2014) Phenylalanine hydroxylase deficiency: diagnosis and management guideline. Genet Med 16:188–200. https://doi.org/10.1038/gim.2013.157

5. Ney DM, Stroup BM, Clayton MK et al (2016) Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial. Am J Clin Nutr 104:334–345. https://doi.org/10.3945/ajcn.116.135293

Cited by 3 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. Neuropsychiatric Function Improvement in Pediatric Patients with Phenylketonuria;The Journal of Pediatrics;2023-09

2. Neuropsychological and quality of life outcomes in PKU patients: expert recommendations of assessment tools in Brazil;Arquivos de Neuro-Psiquiatria;2023-06-19

3. Burden of phenylketonuria in Latin American patients: a systematic review and meta-analysis of observational studies;Orphanet Journal of Rare Diseases;2022-07-30

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