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Behavior Genetics|October 24, 2009
Biogenic amines in Rett syndrome: the usual suspectsJean-Christophe Roux, Laurent VillardNeuroscience Letters|October 7, 2008
Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouseJean-Christophe Roux, Emmanuelle Dura, Laurent VillardEpilepsia|September 1, 2022
Mouse models of Kcnq2 dysfunctionLucile Brun, Jean-Charles Viemari, Laurent VillardBrain Research|September 2, 2008
Expression of methyl CpG binding protein 2 (Mecp2) during the postnatal development of the mouse brainstemEmmanuelle Dura, Laurent Villard, Jean-Christophe RouxFaculty Reviews|July 26, 2021
Rett syndrome: think outside the (skull) boxEmilie Borloz, Laurent Villard, Jean-Christophe RouxF1000Research|April 12, 2018
Rett syndrome from bench to bedside: recent advancesYann Ehinger, Valerie Matagne, Laurent Villard, et al.BMC Neuroscience|May 26, 2011
Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brainNicolas Panayotis, Adeline Ghata, Laurent Villard, et al.Journal of Neuroscience Research|December 10, 2009
Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient miceJean-Christophe Roux, Nicolas Panayotis, Emmanuelle Dura, et al.European Journal of Human Genetics : EJHG|March 16, 2002
Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counsellingAnne Moncla, Arlette Kpebe, Chantal Missirian, et al.Pageof 12