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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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Main Authors: Alessio Cortelazzo (Author), Claudio De Felice (Author), Roberto Guerranti (Author), Cinzia Signorini (Author), Silvia Leoncini (Author), Alessandra Pecorelli (Author), Gloria Zollo (Author), Claudia Landi (Author), Giuseppe Valacchi (Author), Lucia Ciccoli (Author), Luca Bini (Author), Joussef Hayek (Author)
Format: Book
Published: Hindawi Limited, 2014-01-01T00:00:00Z.
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