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Ingrid E Scheffer

Showing results (301-310 of 586) with videos related to

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Epilepsia Open|December 23, 2023
Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort studyRussell Nightscales, Zhibin Chen, Sarah Barnard, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
Developmental Medicine and Child Neurology|December 24, 2019
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizuresIngrid E Scheffer, Katja E Boysen, Amy L Schneider, et al.
Epilepsia|September 24, 2025
Atenolol rescues premature mortality in genetic mouse models of sudden unexpected death in epilepsyMing S Soh, Amanda Hu, Alibek Kuanyshbek, 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|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.
Lancet (London, England)|September 24, 2002
Sodium-channel defects in benign familial neonatal-infantile seizuresSarah E Heron, Kathryn M Crossland, Eva Andermann, et al.
Epilepsia|March 15, 2006
Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaborationLata Vadlamudi, Marianne J Kjeldsen, Linda A Corey, et al.
Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Pageof 59

Showing results (301-310 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia Open|December 23, 2023
Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicenter retrospective cohort studyRussell Nightscales, Zhibin Chen, Sarah Barnard, et al.
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
Developmental Medicine and Child Neurology|December 24, 2019
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizuresIngrid E Scheffer, Katja E Boysen, Amy L Schneider, et al.
Epilepsia|September 24, 2025
Atenolol rescues premature mortality in genetic mouse models of sudden unexpected death in epilepsyMing S Soh, Amanda Hu, Alibek Kuanyshbek, 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|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.
Lancet (London, England)|September 24, 2002
Sodium-channel defects in benign familial neonatal-infantile seizuresSarah E Heron, Kathryn M Crossland, Eva Andermann, et al.
Epilepsia|March 15, 2006
Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaborationLata Vadlamudi, Marianne J Kjeldsen, Linda A Corey, et al.
Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Pageof 59