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

F Vigevano

Showing results (71-80 of 82) with videos related to

Pageof 9
Sort By:
European Journal of Neurology|November 20, 2010
Childhood refractory focal epilepsy following acute febrile encephalopathyN Specchio, L Fusco, D Claps, et al.
Neurology|December 25, 2003
Experience with immunomodulatory treatments in Rasmussen's encephalitisT Granata, L Fusco, G Gobbi, et al.
Neurology|February 13, 2003
Rasmussen's encephalitis: early characteristics allow diagnosisT Granata, G Gobbi, R Spreafico, et al.
Brain : a Journal of Neurology|May 29, 2000
Dominant partial epilepsies. A clinical, electrophysiological and genetic study of 19 European familiesF Picard, S Baulac, P Kahane, et al.
Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.
Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.
Epilepsia|March 1, 1997
Early-onset benign occipital seizure susceptibility syndromeC D Ferrie, A Beaumanoir, R Guerrini, et al.
Neurology|July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancyP Striano, A Coppola, M Pezzella, et al.
American Journal of Human Genetics|April 28, 2001
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneityM Malacarne, E Gennaro, F Madia, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
European Journal of Neurology|November 20, 2010
Childhood refractory focal epilepsy following acute febrile encephalopathyN Specchio, L Fusco, D Claps, et al.
Neurology|December 25, 2003
Experience with immunomodulatory treatments in Rasmussen's encephalitisT Granata, L Fusco, G Gobbi, et al.
Neurology|February 13, 2003
Rasmussen's encephalitis: early characteristics allow diagnosisT Granata, G Gobbi, R Spreafico, et al.
Brain : a Journal of Neurology|May 29, 2000
Dominant partial epilepsies. A clinical, electrophysiological and genetic study of 19 European familiesF Picard, S Baulac, P Kahane, et al.
Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.
Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.
Epilepsia|March 1, 1997
Early-onset benign occipital seizure susceptibility syndromeC D Ferrie, A Beaumanoir, R Guerrini, et al.
Neurology|July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancyP Striano, A Coppola, M Pezzella, et al.
American Journal of Human Genetics|April 28, 2001
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneityM Malacarne, E Gennaro, F Madia, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
Pageof 9