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Benoit Girard

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2022
Modulation of Hippocampal Network Oscillation by PICK1-Dependent Cell Surface Expression of mGlu3 ReceptorsPola Tuduri, Nathalie Bouquier, Benoit Girard, et al.
Addiction Biology|September 6, 2017
Cafeteria diet induces neuroplastic modifications in the nucleus accumbens mediated by microglia activationMiriam Gutiérrez-Martos, Benoit Girard, Sueli Mendonça-Netto, et al.
Pediatric Neurology|October 2, 2007
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsyJuliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, et al.
Neuron|February 2, 2023
A neural substrate for negative affect dictates female parental behaviorSalvatore Lecca, Mauro Congiu, Léa Royon, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Neurobiology of Disease|February 13, 2018
Seizure progression and inflammatory mediators promote pericytosis and pericyte-microglia clustering at the cerebrovasculatureWendy Klement, Rita Garbelli, Emma Zub, et al.
Nature Neuroscience|June 26, 2026
Conditioned accumbal dopamine transients forecast individual preference for drug versus natural rewards and compulsive behaviorVincent Pascoli, Laurena Python, Agnès Hiver, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Epilepsia|November 11, 2017
Hepatic and hippocampal cytochrome P450 enzyme overexpression during spontaneous recurrent seizuresLeonie Runtz, Benoit Girard, Marion Toussenot, et al.
Epilepsy Research|September 8, 2009
CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancyRima Nabbout, Christel Depienne, Mathilde Chipaux, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2022
Modulation of Hippocampal Network Oscillation by PICK1-Dependent Cell Surface Expression of mGlu3 ReceptorsPola Tuduri, Nathalie Bouquier, Benoit Girard, et al.
Addiction Biology|September 6, 2017
Cafeteria diet induces neuroplastic modifications in the nucleus accumbens mediated by microglia activationMiriam Gutiérrez-Martos, Benoit Girard, Sueli Mendonça-Netto, et al.
Pediatric Neurology|October 2, 2007
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsyJuliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, et al.
Neuron|February 2, 2023
A neural substrate for negative affect dictates female parental behaviorSalvatore Lecca, Mauro Congiu, Léa Royon, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Neurobiology of Disease|February 13, 2018
Seizure progression and inflammatory mediators promote pericytosis and pericyte-microglia clustering at the cerebrovasculatureWendy Klement, Rita Garbelli, Emma Zub, et al.
Nature Neuroscience|June 26, 2026
Conditioned accumbal dopamine transients forecast individual preference for drug versus natural rewards and compulsive behaviorVincent Pascoli, Laurena Python, Agnès Hiver, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Epilepsia|November 11, 2017
Hepatic and hippocampal cytochrome P450 enzyme overexpression during spontaneous recurrent seizuresLeonie Runtz, Benoit Girard, Marion Toussenot, et al.
Epilepsy Research|September 8, 2009
CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancyRima Nabbout, Christel Depienne, Mathilde Chipaux, et al.
Pageof 3