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Thomas Sander

Showing results (111-120 of 136) with videos related to

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Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Epilepsy Research|July 30, 2015
Investigation of GRIN2A in common epilepsy phenotypesDennis Lal, Sandra Steinbrücker, Julian Schubert, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsia|January 9, 2013
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsyRikke S Møller, Yvonne G Weber, Laura L Klitten, et al.
Nature Genetics|March 4, 2003
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsiesKarsten Haug, Maike Warnstedt, Alexi K Alekov, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Plos One|August 28, 2018
Rare gene deletions in genetic generalized and Rolandic epilepsiesKamel Jabbari, Dheeraj R Bobbili, Dennis Lal, et al.
Nature Genetics|August 28, 2009
CLCN2 variants in idiopathic generalized epilepsyAiling Kleefuss-Lie, Waltraut Friedl, Sven Cichon, et al.
Pageof 14

Showing results (111-120 of 136) with videos related to

Sort By:
Pageof 14
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Epilepsy Research|July 30, 2015
Investigation of GRIN2A in common epilepsy phenotypesDennis Lal, Sandra Steinbrücker, Julian Schubert, et al.
Epilepsia|January 29, 2013
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsyDennis Lal, Holger Trucks, Rikke S Møller, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsia|January 9, 2013
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsyRikke S Møller, Yvonne G Weber, Laura L Klitten, et al.
Nature Genetics|March 4, 2003
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsiesKarsten Haug, Maike Warnstedt, Alexi K Alekov, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Plos One|August 28, 2018
Rare gene deletions in genetic generalized and Rolandic epilepsiesKamel Jabbari, Dheeraj R Bobbili, Dennis Lal, et al.
Nature Genetics|August 28, 2009
CLCN2 variants in idiopathic generalized epilepsyAiling Kleefuss-Lie, Waltraut Friedl, Sven Cichon, et al.
Pageof 14