Copyright © 2015 Silvia Leoncini et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. An involvement of the immune system has been suggested in Rett syndrome (RTT), a devastating neurodevelopmental disorder related to oxidative stress, and caused by a mutation in the methyl-CpG binding protein 2 gene (MECP2) or, more rarely, cyclin-dependent kinase-like 5 (CDKL5). To date, it is unclear whether both mutations may have an impact on the circulating cytokine patterns. In the present study, cytokines involved in the Th1-, Th2-, and T regulatory (T-reg) response, as well as chemo...
Abstract Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intelle...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
Objectives: Rett syndrome (RTT) is a rare disorder causing severe intellectual and physical disabili...
An involvement of the immune system has been suggested in Rett syndrome (RTT), a devastating neurode...
Copyright © 2014 Anna Maria Papini et al. This is an open access article distributed under the Creat...
Rett syndrome (RTT) is an orphan progressive neurodevelopmental disease affecting almost exclusively...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
Rett syndrome (RTT, MIM 312750) is a rare and orphan progressive neurodevelopmental disorder affecti...
Copyright © 2014 Cinzia Signorini et al.This is an open access article distributed under theCreative...
Background: Mutations in the cyclin-dependent kinase-like 5 gene cause a clinical variant of Rett sy...
Copyright © 2013 Alessio Cortelazzo et al. This is an open access article distributed under the Crea...
Rett syndrome (RTT) is a devastating neurodevelopmental disease, previously included into the autist...
Rett syndrome (RTT) is a devastating genetic disorder that worldwide represents the most common gene...
Mutations in methyl-CpG-binding protein 2 (MECP2) underlie most cases of Rett Syndrome, a neurodevel...
Abstract Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intelle...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
Objectives: Rett syndrome (RTT) is a rare disorder causing severe intellectual and physical disabili...
An involvement of the immune system has been suggested in Rett syndrome (RTT), a devastating neurode...
Copyright © 2014 Anna Maria Papini et al. This is an open access article distributed under the Creat...
Rett syndrome (RTT) is an orphan progressive neurodevelopmental disease affecting almost exclusively...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual dis...
Rett syndrome (RTT, MIM 312750) is a rare and orphan progressive neurodevelopmental disorder affecti...
Copyright © 2014 Cinzia Signorini et al.This is an open access article distributed under theCreative...
Background: Mutations in the cyclin-dependent kinase-like 5 gene cause a clinical variant of Rett sy...
Copyright © 2013 Alessio Cortelazzo et al. This is an open access article distributed under the Crea...
Rett syndrome (RTT) is a devastating neurodevelopmental disease, previously included into the autist...
Rett syndrome (RTT) is a devastating genetic disorder that worldwide represents the most common gene...
Mutations in methyl-CpG-binding protein 2 (MECP2) underlie most cases of Rett Syndrome, a neurodevel...
Abstract Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intelle...
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting...
Objectives: Rett syndrome (RTT) is a rare disorder causing severe intellectual and physical disabili...