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Andrew Escayg

Showing results (21-30 of 60) with videos related to

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Case Reports in Genetics|November 10, 2018
Epileptic Encephalopathy and Cerebellar Atrophy Resulting from Compound Heterozygous <i>CACNA2D2</i> VariantsKameryn M Butler, Philip J Holt, Sarah S Milla, et al.
Experimental Neurology|April 5, 2017
Early-life febrile seizures worsen adult phenotypes in Scn1a mutantsStacey B B Dutton, Karoni Dutt, Ligia A Papale, et al.
Headache|July 27, 2006
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4Michael von Brevern, Nga Ta, Anupama Shankar, et al.
Novartis Foundation Symposium|January 5, 2002
Mutations of voltage-gated sodium channels in movement disorders and epilepsyMiriam H Meisler, Jennifer A Kearney, Leslie K Sprunger, et al.
Scientific Reports|January 11, 2018
Selective targeting of Scn8a prevents seizure development in a mouse model of mesial temporal lobe epilepsyJennifer C Wong, Christopher D Makinson, Tyra Lamar, et al.
Brain : a Journal of Neurology|July 3, 2018
De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsyKameryn M Butler, Olivia A Moody, Elisabeth Schuler, et al.
Neurobiology of Disease|August 29, 2012
Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibilityStacey B Dutton, Christopher D Makinson, Ligia A Papale, et al.
Psychopharmacology|March 16, 2013
Effects of an epilepsy-causing mutation in the SCN1A sodium channel gene on cocaine-induced seizure susceptibility in miceRyan H Purcell, Ligia A Papale, Christopher D Makinson, et al.
Epilepsia|January 15, 2013
Altered sleep regulation in a mouse model of SCN1A-derived genetic epilepsy with febrile seizures plus (GEFS+)Ligia A Papale, Christopher D Makinson, J Christopher Ehlen, et al.
Epilepsy Research|November 23, 2016
De novo and inherited SCN8A epilepsy mutations detected by gene panel analysisKameryn M Butler, Cristina da Silva, Yuval Shafir, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

Sort By:
Pageof 6
Case Reports in Genetics|November 10, 2018
Epileptic Encephalopathy and Cerebellar Atrophy Resulting from Compound Heterozygous <i>CACNA2D2</i> VariantsKameryn M Butler, Philip J Holt, Sarah S Milla, et al.
Experimental Neurology|April 5, 2017
Early-life febrile seizures worsen adult phenotypes in Scn1a mutantsStacey B B Dutton, Karoni Dutt, Ligia A Papale, et al.
Headache|July 27, 2006
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4Michael von Brevern, Nga Ta, Anupama Shankar, et al.
Novartis Foundation Symposium|January 5, 2002
Mutations of voltage-gated sodium channels in movement disorders and epilepsyMiriam H Meisler, Jennifer A Kearney, Leslie K Sprunger, et al.
Scientific Reports|January 11, 2018
Selective targeting of Scn8a prevents seizure development in a mouse model of mesial temporal lobe epilepsyJennifer C Wong, Christopher D Makinson, Tyra Lamar, et al.
Brain : a Journal of Neurology|July 3, 2018
De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsyKameryn M Butler, Olivia A Moody, Elisabeth Schuler, et al.
Neurobiology of Disease|August 29, 2012
Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibilityStacey B Dutton, Christopher D Makinson, Ligia A Papale, et al.
Psychopharmacology|March 16, 2013
Effects of an epilepsy-causing mutation in the SCN1A sodium channel gene on cocaine-induced seizure susceptibility in miceRyan H Purcell, Ligia A Papale, Christopher D Makinson, et al.
Epilepsia|January 15, 2013
Altered sleep regulation in a mouse model of SCN1A-derived genetic epilepsy with febrile seizures plus (GEFS+)Ligia A Papale, Christopher D Makinson, J Christopher Ehlen, et al.
Epilepsy Research|November 23, 2016
De novo and inherited SCN8A epilepsy mutations detected by gene panel analysisKameryn M Butler, Cristina da Silva, Yuval Shafir, et al.
Pageof 6