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Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 geneMarion Delcourt, Florence Riant, Josette Mancini, et al.
Gene|August 12, 2008
Nuclear localization of a novel human syntaxin 1B isoformSandrine Pereira, Annick Massacrier, Patrice Roll, et al.
Plos One|September 24, 2010
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizuresSarah Jamali, Annick Salzmann, Nader Perroud, et al.
Epilepsia|June 29, 2012
Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autismGaetan Lesca, Gabrielle Rudolf, Audrey Labalme, et al.
Frontiers in Cellular Neuroscience|March 22, 2018
In Utero Administration of Drugs Targeting Microglia Improves the Neurodevelopmental Outcome Following Cytomegalovirus Infection of the Rat Fetal BrainRobin Cloarec, Sylvian Bauer, Natacha Teissier, et al.
Epilepsia|December 31, 2013
A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2Sarra Dimassi, Audrey Labalme, Gaetan Lesca, et al.
Plos One|July 30, 2016
Cytomegalovirus Infection of the Rat Developing Brain In Utero Prominently Targets Immune Cells and Promotes Early Microglial ActivationRobin Cloarec, Sylvian Bauer, Hervé Luche, et al.
Brain : a Journal of Neurology|January 10, 2006
Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortexSarah Jamali, Fabrice Bartolomei, Andrée Robaglia-Schlupp, et al.
Neurology|October 19, 2012
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraineRobin Cloarec, Nadine Bruneau, Gabrielle Rudolf, et al.
Epilepsia|August 27, 2010
Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora diseaseGaetan Lesca, Nadia Boutry-Kryza, Bertrand de Toffol, et al.
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