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Epilepsia|March 15, 2006
Early pattern of epilepsy in the ring chromosome 20 syndromeDorothée Ville, Anna Kaminska, Nadia Bahi-Buisson, et al.
Prenatal Diagnosis|March 16, 2012
Prenatal diagnosis of 'isolated' Dandy-Walker malformation: imaging findings and prenatal counsellingLaurent Guibaud, Anne Larroque, Dorothée Ville, et al.
Epilepsy Research|March 15, 2015
Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disabilityAnne-Lise Poulat, Dorothée Ville, Julitta de Bellescize, et al.
Developmental Medicine and Child Neurology|May 7, 2009
Ring 14 chromosome presenting as early-onset isolated partial epilepsyDorothée Ville, Julitta DE Bellescize, Marie Ange Nguyen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 10, 2013
A proposed diagnostic approach for infantile spasms based on a spectrum of variable aetiologyAnne-Lise Poulat, Gaetan Lesca, Damien Sanlaville, et al.
BMC Medical Genetics|January 10, 2020
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case reportAlice Poisson, Nicolas Chatron, Audrey Labalme, et al.
Epilepsy Research|March 9, 2017
Efficacy of a ketogenic diet in resistant myoclono-astatic epilepsy: A French multicenter retrospective studyElodie Stenger, Mickael Schaeffer, Claude Cances, et al.
Neuropediatrics|June 22, 2019
Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 MutationVincent Zimmern, Florence Riant, Emmanuel Roze, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 19, 2022
CNTNAP1-encephalopathy: Six novel patients surviving the neonatal periodPauline Garel, Gaetan Lesca, Dorothée Ville, et al.
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