In vivo catecholaminergic metabolism in the medial prefrontal cortex of ENU2 mice: an investigation of the cortical dopamine deficit in phenylketonuria

OBJECTIVE: Phenylketonuria (PKU) is an inherited metabolic disease characterized by plasma hyperphenylalaninemia and several neurological symptoms that can be controlled by rigorous dietetic treatment. The cellular mechanisms underlying impaired brain functions are still unclear. It has been propose...

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Detalles Bibliográficos
Autores principales: Pascucci, Tiziana, Giacovazzo, Giacomo, Andolina, Diego, Conversi, David, Cruciani, Fabio, Cabib, Simona, Puglisi-Allegra, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470696/
https://www.ncbi.nlm.nih.gov/pubmed/22447154
http://dx.doi.org/10.1007/s10545-012-9473-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470696/
https://www.ncbi.nlm.nih.gov/pubmed/22447154
http://dx.doi.org/10.1007/s10545-012-9473-2

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