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Presse Medicale (Paris, France : 1983)|December 27, 2017
Genetics of human epilepsies: Continuing progressPierre SzepetowskiMethods in Molecular Biology (Clifton, N.J.)|October 8, 2017
Magnetofection™ of NMDA Receptor Subunits GluN1 and GluN2A Expression Vectors in Non-Neuronal Host CellsNadine Bruneau, Pierre SzepetowskiCurrent Pharmaceutical Design|June 30, 2011
The role of the urokinase receptor in epilepsy, in disorders of language, cognition, communication and behavior, and in the central nervous systemNadine Bruneau, Pierre SzepetowskiCurrent Opinion in Pharmacology|December 16, 2014
NMDA receptor subunit mutations in neurodevelopmental disordersNail Burnashev, Pierre SzepetowskiEpileptic Disorders : International Epilepsy Journal with Videotape|November 26, 2002
Epilepsy and ionic channelsPatrice Roll, Pierre SzepetowskiEpilepsia|August 18, 2009
From rolandic epilepsy to continuous spike-and-waves during sleep and Landau-Kleffner syndromes: insights into possible genetic factorsGabrielle Rudolf, Maria P Valenti, Edouard Hirsch, et al.Epilepsia|June 13, 2002
Clinical and genetic analysis of a new multigenerational pedigree with GEFS+ (Generalized Epilepsy with Febrile Seizures Plus)Frédérique Gérard, Sandrine Pereira, Andrée Robaglia-Schlupp, et al.Journal of Child Neurology|December 31, 2002
Benign familial infantile seizures: further delineation of the syndromeRoberto Horacio Caraballo, Ricardo Oscar Cersósimo, Hernan Amartino, et al.Epilepsia|August 28, 2018
Transient microstructural brain anomalies and epileptiform discharges in mice defective for epilepsy and language-related NMDA receptor subunit gene Grin2aManal Salmi, Radu Bolbos, Sylvian Bauer, et al.Human Molecular Genetics|September 30, 2010
A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 geneFabienne Schaller, Françoise Watrin, Rachel Sturny, et al.Pageof 5