Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2, Nat Genet, vol.23, pp.185-188, 1999. ,
Rett Syndrome, Child and Adolescent Psychiatric Clinics of North America, vol.16, issue.3, pp.723-743, 2007. ,
DOI : 10.1016/j.chc.2007.03.004
Epilepsy in a representative series of Rett syndrome, Acta Paediatrica, vol.3, issue.14 Suppl, pp.34-39, 2001. ,
DOI : 10.1016/S0387-7604(87)80062-1
Epilepsy in Rett syndrome-The experience of a National Rett Center, Epilepsia, vol.31, issue.7, pp.1252-1258, 2010. ,
DOI : 10.1001/archneur.1971.00480330070006
Predictors of seizure onset in Rett syndrome, The Journal of Pediatrics, vol.149, issue.4, pp.542-547, 2006. ,
DOI : 10.1016/j.jpeds.2006.06.015
Seizures in Rett syndrome: An overview from a one-year calendar study, European Journal of Paediatric Neurology, vol.11, issue.5, pp.310-317, 2007. ,
DOI : 10.1016/j.ejpn.2007.02.008
Treatment of epilepsy in Rett syndrome, European Journal of Paediatric Neurology, vol.11, issue.1, pp.10-16, 2007. ,
DOI : 10.1016/j.ejpn.2006.09.003
Epilepsy and the natural history of Rett syndrome, Neurology, vol.74, issue.11, pp.909-912, 2010. ,
DOI : 10.1212/WNL.0b013e3181d6b852
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype???phenotype associations in Rett syndrome, European Journal of Human Genetics, vol.13, issue.10, pp.1121-1130, 2005. ,
DOI : 10.1093/hmg/ddh142
Epilepsy in Rett syndrome: Clinical and genetic features, Epilepsy & Behavior, vol.19, issue.3, pp.296-300, 2010. ,
DOI : 10.1016/j.yebeh.2010.06.051
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome, Neurology, vol.70, issue.Issue 22, Part 2, pp.2145-2151, 2008. ,
DOI : 10.1212/01.wnl.0000304086.75913.b2
) mutation type is associated with disease severity in Rett syndrome, Journal of Medical Genetics, vol.499, issue.(Suppl 1), pp.152-158, 2014. ,
DOI : 10.1016/j.cell.2012.11.022
URL : http://jmg.bmj.com/content/jmedgenet/51/3/152.full.pdf
Using a large international sample to investigate epilepsy in Rett syndrome, Developmental Medicine & Child Neurology, vol.19, issue.6, pp.553-558, 2013. ,
DOI : 10.1177/088307380401900804
Rett networked database: An integrated clinical and genetic network of rett syndrome databases, Human Mutation, vol.14, issue.2, pp.1031-1036, 2012. ,
DOI : 10.1016/S0387-7604(12)80094-5
URL : https://hal.archives-ouvertes.fr/hal-01668676
Investigating genotype-phenotype relationships in Rett syndrome using an international data set, Neurology, vol.70, issue.11, pp.868-875, 2008. ,
DOI : 10.1212/01.wnl.0000304752.50773.ec
Epilepsy in Rett syndrome: Association between phenotype and genotype, and implications for practice, Seizure, vol.20, issue.8, pp.646-649, 2011. ,
DOI : 10.1016/j.seizure.2011.06.010
Reduced seizure threshold and altered network oscillatory properties in a mouse model of Rett syndrome, Neuroscience, vol.231, pp.195-205, 2013. ,
DOI : 10.1016/j.neuroscience.2012.11.058
Activity-dependent phosphorylation of MECP2 threonine 308 regulates interaction with NcoR, Nature, vol.16, pp.341-345, 2013. ,
DOI : 10.1002/ajmg.a.33184
MeCP2 Binds to 5hmC Enriched within Active Genes and Accessible Chromatin in the Nervous System, Cell, vol.151, issue.7, pp.1417-1430, 2012. ,
DOI : 10.1016/j.cell.2012.11.022
Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses, Nature Neuroscience, vol.5, issue.2, pp.274-283, 2012. ,
DOI : 10.1038/nprot.2009.204
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267879/pdf
Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging, Journal of Neurophysiology, vol.105, issue.4, pp.1768-1784, 2011. ,
DOI : 10.1152/jn.00800.2010
Characterization of seizure-like events recorded in vivo in a mouse model of Rett syndrome, Neural Networks, vol.46, pp.109-115, 2013. ,
DOI : 10.1016/j.neunet.2013.05.002
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor, Nature Neuroscience, vol.7, issue.7, pp.898-902, 2013. ,
DOI : 10.1093/nar/30.5.1139
EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome, Clinical Neurophysiology, vol.121, issue.5, pp.652-657, 2010. ,
DOI : 10.1016/j.clinph.2010.01.003