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Sara Kivity

Showing results (41-50 of 62) with videos related to

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Developmental Medicine and Child Neurology|February 18, 2006
Panayiotopoulos syndrome: a consensus viewColin Ferrie, Roberto Caraballo, Athanasios Covanis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 13, 2014
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblingsAyelet Zerem, Dorit Lev, Lubov Blumkin, et al.
Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.
Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, et al.
Epilepsy Research|November 5, 2016
Mortality in Dravet syndromeMonica S Cooper, Anne Mcintosh, Douglas E Crompton, et al.
American Journal of Human Genetics|August 28, 2010
A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Mark A Corbett, Melanie Bahlo, Lachlan Jolly, et al.
Annals of Neurology|December 26, 2015
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyRichard D Bagnall, Douglas E Crompton, Slavé Petrovski, et al.
Epilepsia|July 31, 2013
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndromeJohn C Mulley, Bree Hodgson, Jacinta M McMahon, et al.
Epilepsia|April 23, 2004
Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex familiesCarla Marini, Ingrid E Scheffer, Kathryn M Crossland, et al.
Neurology|August 27, 2017
Genetic epilepsy with febrile seizures plus: Refining the spectrumYue-Hua Zhang, Rosemary Burgess, Jodie P Malone, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Developmental Medicine and Child Neurology|February 18, 2006
Panayiotopoulos syndrome: a consensus viewColin Ferrie, Roberto Caraballo, Athanasios Covanis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 13, 2014
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblingsAyelet Zerem, Dorit Lev, Lubov Blumkin, et al.
Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.
Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, et al.
Epilepsy Research|November 5, 2016
Mortality in Dravet syndromeMonica S Cooper, Anne Mcintosh, Douglas E Crompton, et al.
American Journal of Human Genetics|August 28, 2010
A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Mark A Corbett, Melanie Bahlo, Lachlan Jolly, et al.
Annals of Neurology|December 26, 2015
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyRichard D Bagnall, Douglas E Crompton, Slavé Petrovski, et al.
Epilepsia|July 31, 2013
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndromeJohn C Mulley, Bree Hodgson, Jacinta M McMahon, et al.
Epilepsia|April 23, 2004
Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex familiesCarla Marini, Ingrid E Scheffer, Kathryn M Crossland, et al.
Neurology|August 27, 2017
Genetic epilepsy with febrile seizures plus: Refining the spectrumYue-Hua Zhang, Rosemary Burgess, Jodie P Malone, et al.
Pageof 7