Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Brain and Language|February 22, 2005
Language in benign childhood epilepsy with centro-temporal spikes abbreviated form: rolandic epilepsy and languageCécile Monjauze, Laurice Tuller, Caroline Hommet, et al.
Epilepsia|October 1, 2014
A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorderGaetano Terrone, Thierry Bienvenu, David Germanaud, et al.
Neuropsychologia|January 8, 2009
Topography of syllable change-detection electrophysiological indices in children and adults with reading disabilitiesCaroline Hommet, Julie Vidal, Sylvie Roux, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Myoclonus dystonia plus syndrome due to a novel 7q21 microdeletionPascale Saugier-Veber, Diane Doummar, Marie-Anne Barthez, et al.
Epilepsia|November 11, 2024
Transition from pediatric to adult care system in patients with complex epilepsies: Necker model for transition evaluated on 70 consecutive patientsRima Nabbout, Agathe Molimard, Giovanna Scorrano, et al.
Epilepsia|April 14, 2007
Epilepsy and language development: the continuous spike-waves during slow sleep syndromeSéverine Debiais, Laurie Tuller, Marie-Anne Barthez, et al.
Developmental Neuropsychology|February 26, 2010
Thalamo-striatal T2-weighted hyperintensities (unidentified bright objects) correlate with cognitive impairments in neurofibromatosis type 1 during childhoodCamille Chabernaud, Dominique Sirinelli, Charlotte Barbier, et al.
Annals of Neurology|March 14, 2002
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findingsDominique Bonneau, Annick Toutain, Annie Laquerrière, et al.
Emerging Infectious Diseases|August 2, 2011
Novel human reovirus isolated from children with acute necrotizing encephalopathyLouise A Ouattara, Francis Barin, Marie Anne Barthez, et al.
Epilepsia|November 26, 2003
Outcome at adulthood of the continuous spike-waves during slow sleep and Landau-Kleffner syndromesJulien Praline, Caroline Hommet, Marie-Anne Barthez, et al.
Pageof 3