Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Athanasios Covanis

Showing results (21-30 of 31) with videos related to

Pageof 4
Sort By:
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsy Research|March 1, 2006
Evaluation of CACNA1H in European patients with childhood absence epilepsyBarry Chioza, Kate Everett, Harald Aschauer, et al.
Epilepsy Research|June 7, 2002
Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14Nichole L Taske, Magali P Williamson, Andrew Makoff, et al.
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.
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|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Epilepsia|April 20, 2007
Autonomic status epilepticus in Panayiotopoulos syndrome and other childhood and adult epilepsies: a consensus viewColin D Ferrie, Roberto Caraballo, Athanasios Covanis, et al.
Epilepsia|February 13, 2003
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Seizure|June 17, 2015
Clinical and genetic analysis of a family with two rare reflex epilepsiesDorothée G A Kasteleijn-Nolst Trenité, Linda Volkers, Eric Strengman, et al.
Brain : a Journal of Neurology|March 19, 2015
CHD2 variants are a risk factor for photosensitivity in epilepsyElizabeth C Galizia, Candace T Myers, Costin Leu, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsy Research|March 1, 2006
Evaluation of CACNA1H in European patients with childhood absence epilepsyBarry Chioza, Kate Everett, Harald Aschauer, et al.
Epilepsy Research|June 7, 2002
Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14Nichole L Taske, Magali P Williamson, Andrew Makoff, et al.
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.
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|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Epilepsia|April 20, 2007
Autonomic status epilepticus in Panayiotopoulos syndrome and other childhood and adult epilepsies: a consensus viewColin D Ferrie, Roberto Caraballo, Athanasios Covanis, et al.
Epilepsia|February 13, 2003
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Seizure|June 17, 2015
Clinical and genetic analysis of a family with two rare reflex epilepsiesDorothée G A Kasteleijn-Nolst Trenité, Linda Volkers, Eric Strengman, et al.
Brain : a Journal of Neurology|March 19, 2015
CHD2 variants are a risk factor for photosensitivity in epilepsyElizabeth C Galizia, Candace T Myers, Costin Leu, et al.
Pageof 4