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Thomas Sander

Showing results (101-110 of 136) with videos related to

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Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
American Journal of Human Genetics|March 16, 2007
Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and miceNatalia T Leach, Yi Sun, Sebastien Michaud, et al.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsia|July 16, 2015
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsyDennis Lal, Katharina Pernhorst, Karl Martin Klein, et al.
Free Radical Biology & Medicine|February 25, 2017
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsyAlexei P Kudin, Gregor Baron, Gábor Zsurka, et al.
Epilepsy Research|March 1, 2006
Evaluation of CACNA1H in European patients with childhood absence epilepsyBarry Chioza, Kate Everett, Harald Aschauer, et al.
Nature Communications|November 17, 2017
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampusHerbert Schulz, Ann-Kathrin Ruppert, Stefan Herms, et al.
Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Nature Genetics|August 28, 2009
Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsiesKarsten Haug, Maike Warnstedt, Alexi K Alekov, et al.
Pageof 14

Showing results (101-110 of 136) with videos related to

Sort By:
Pageof 14
Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, et al.
American Journal of Human Genetics|March 16, 2007
Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and miceNatalia T Leach, Yi Sun, Sebastien Michaud, et al.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsia|July 16, 2015
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsyDennis Lal, Katharina Pernhorst, Karl Martin Klein, et al.
Free Radical Biology & Medicine|February 25, 2017
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsyAlexei P Kudin, Gregor Baron, Gábor Zsurka, et al.
Epilepsy Research|March 1, 2006
Evaluation of CACNA1H in European patients with childhood absence epilepsyBarry Chioza, Kate Everett, Harald Aschauer, et al.
Nature Communications|November 17, 2017
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampusHerbert Schulz, Ann-Kathrin Ruppert, Stefan Herms, et al.
Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Nature Genetics|August 28, 2009
Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsiesKarsten Haug, Maike Warnstedt, Alexi K Alekov, et al.
Pageof 14