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C Depienne

Showing results (1-10 of 37) with videos related to

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Revue Neurologique|May 25, 2015
Epilepsy genetics: the ongoing revolutionG Lesca, C Depienne
Revue Neurologique|May 27, 2015
Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still countingS Klebe, G Stevanin, C Depienne
Revue Neurologique|April 9, 2024
Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategiesE Leitão, C Schröder, C Depienne
European Journal of Neurology|February 13, 2013
PRRT2 mutations and paroxysmal disordersA Méneret, C Gaudebout, F Riant, et al.
Neurology|September 15, 2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraineF Riant, A Ducros, C Ploton, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|February 23, 2010
Microsatellite analysis of HSV-1 isolates: from oropharynx reactivation toward lung infection in patients undergoing mechanical ventilationC Deback, C E Luyt, S Lespinats, et al.
The Journal of Biological Chemistry|March 30, 2001
Characterization of the nuclear import pathway for HIV-1 integraseC Depienne, A Mousnier, H Leh, et al.
Experimental Cell Research|October 19, 2000
Cellular distribution and karyophilic properties of matrix, integrase, and Vpr proteins from the human and simian immunodeficiency virusesC Depienne, P Roques, C Créminon, et al.
Revue Neurologique|May 16, 2016
A rare case of SPG11 mutation with multiple sclerosisC Laurencin, L Rascle, F Cotton, et al.
Seizure|February 23, 2010
Unusual consequences of status epilepticus in Dravet syndromeM Chipaux, N Villeneuve, P Sabouraud, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Revue Neurologique|May 25, 2015
Epilepsy genetics: the ongoing revolutionG Lesca, C Depienne
Revue Neurologique|May 27, 2015
Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still countingS Klebe, G Stevanin, C Depienne
Revue Neurologique|April 9, 2024
Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategiesE Leitão, C Schröder, C Depienne
European Journal of Neurology|February 13, 2013
PRRT2 mutations and paroxysmal disordersA Méneret, C Gaudebout, F Riant, et al.
Neurology|September 15, 2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraineF Riant, A Ducros, C Ploton, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|February 23, 2010
Microsatellite analysis of HSV-1 isolates: from oropharynx reactivation toward lung infection in patients undergoing mechanical ventilationC Deback, C E Luyt, S Lespinats, et al.
The Journal of Biological Chemistry|March 30, 2001
Characterization of the nuclear import pathway for HIV-1 integraseC Depienne, A Mousnier, H Leh, et al.
Experimental Cell Research|October 19, 2000
Cellular distribution and karyophilic properties of matrix, integrase, and Vpr proteins from the human and simian immunodeficiency virusesC Depienne, P Roques, C Créminon, et al.
Revue Neurologique|May 16, 2016
A rare case of SPG11 mutation with multiple sclerosisC Laurencin, L Rascle, F Cotton, et al.
Seizure|February 23, 2010
Unusual consequences of status epilepticus in Dravet syndromeM Chipaux, N Villeneuve, P Sabouraud, et al.
Pageof 4