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Samuel F Berkovic

Showing results (151-160 of 464) with videos related to

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Genome Research|September 3, 2017
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretationJoshua Traynelis, Michael Silk, Quanli Wang, et al.
Annals of Neurology|May 4, 2019
Epilepsy in families: Age at onset is a familial trait, independent of syndromeColin A Ellis, Leonid Churilov, Michael P Epstein, et al.
Epilepsy & Behavior : E&B|March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsyAmanda G Wood, Michael M Saling, Marco Fedi, et al.
Plos One|January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhoodKenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.
Epigenomics|June 6, 2019
Evidence for type-specific DNA methylation patterns in epilepsy: a discordant monozygotic twin approachNamitha Mohandas, Yuk Jing Loke, Stephanie Hopkins, et al.
Neurology Research International|July 26, 2011
The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile SeizuresJohn C Mulley, Xenia Iona, Bree Hodgson, et al.
The Lancet. Neurology|May 8, 2010
Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective studyAnne M McIntosh, Jacinta McMahon, Leanne M Dibbens, et al.
Neurology|August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy casesRichard D Bagnall, Douglas E Crompton, Carina Cutmore, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsyAlexander G Bassuk, Eileen Geraghty, Shu Wu, et al.
Epilepsia|May 1, 2014
Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutationLaura Canafoglia, Michela Morbin, Vidmer Scaioli, et al.
Pageof 47

Showing results (151-160 of 464) with videos related to

Sort By:
Pageof 47
Genome Research|September 3, 2017
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretationJoshua Traynelis, Michael Silk, Quanli Wang, et al.
Annals of Neurology|May 4, 2019
Epilepsy in families: Age at onset is a familial trait, independent of syndromeColin A Ellis, Leonid Churilov, Michael P Epstein, et al.
Epilepsy & Behavior : E&B|March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsyAmanda G Wood, Michael M Saling, Marco Fedi, et al.
Plos One|January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhoodKenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.
Epigenomics|June 6, 2019
Evidence for type-specific DNA methylation patterns in epilepsy: a discordant monozygotic twin approachNamitha Mohandas, Yuk Jing Loke, Stephanie Hopkins, et al.
Neurology Research International|July 26, 2011
The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile SeizuresJohn C Mulley, Xenia Iona, Bree Hodgson, et al.
The Lancet. Neurology|May 8, 2010
Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective studyAnne M McIntosh, Jacinta McMahon, Leanne M Dibbens, et al.
Neurology|August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy casesRichard D Bagnall, Douglas E Crompton, Carina Cutmore, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsyAlexander G Bassuk, Eileen Geraghty, Shu Wu, et al.
Epilepsia|May 1, 2014
Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutationLaura Canafoglia, Michela Morbin, Vidmer Scaioli, et al.
Pageof 47