Cognitive functioning in mild hyperphenylalaninemia

BACKGROUND: Hyperphenylalaninemia is a hereditary metabolic disorder that causes elevated blood phenylalanine (Phe). Hyperphenylalaninemias are classified as Phenylketonuria PKU (Phe > 6 mg/dL) or mild hyperphenylalaninemia (mHPA) (Phe 2–6 mg/dL). This study examines the cognitive functioning of...

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Detalles Bibliográficos
Autores principales: de la Parra, Alicia, García, María Ignacia, Waisbren, Susan E., Cornejo, Verónica, Raimann, Erna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471391/
https://www.ncbi.nlm.nih.gov/pubmed/28649547
http://dx.doi.org/10.1016/j.ymgmr.2015.10.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471391/
https://www.ncbi.nlm.nih.gov/pubmed/28649547
http://dx.doi.org/10.1016/j.ymgmr.2015.10.009

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