Subclinical Inflammatory Status in Rett Syndrome

Inflammation has been advocated as a possible common central mechanism for developmental cognitive impairment. Rett syndrome (RTT) is a devastating neurodevelopmental disorder, mainly caused by de novo loss-of-function mutations in the gene encoding MeCP2. Here, we investigated plasma acute phase re...

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Detalles Bibliográficos
Autores principales: Cortelazzo, Alessio, De Felice, Claudio, Guerranti, Roberto, Signorini, Cinzia, Leoncini, Silvia, Pecorelli, Alessandra, Zollo, Gloria, Landi, Claudia, Valacchi, Giuseppe, Ciccoli, Lucia, Bini, Luca, Hayek, Joussef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913335/
https://www.ncbi.nlm.nih.gov/pubmed/24511209
http://dx.doi.org/10.1155/2014/480980

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913335/
https://www.ncbi.nlm.nih.gov/pubmed/24511209
http://dx.doi.org/10.1155/2014/480980

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