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

Aglaia Vignoli

Showing results (81-90 of 129) with videos related to

Pageof 13
Sort By:
Epilepsia|April 21, 2016
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generationStefano Meletti, Andrea Ruggieri, Pietro Avanzini, et al.
Epilepsia|October 9, 2013
Early onset absence epilepsy with onset in the first year of life: a multicenter cohort studyLucio Giordano, Aglaia Vignoli, Raffaella Cusmai, et al.
Epilepsy & Behavior : E&B|August 24, 2010
Epilepsy in Rett syndrome: clinical and genetic featuresMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
Epilepsia|February 4, 2014
Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI studyAnna Elisabetta Vaudano, Andrea Ruggieri, Aglaia Vignoli, et al.
Epilepsy & Behavior : E&B|July 10, 2013
Vagus nerve stimulation in refractory epilepsy: new indications and outcome assessmentCarlo Efisio Marras, Valentina Chiesa, Alessandro De Benedictis, et al.
Neuroradiology|June 18, 2018
Rhinencephalon changes in tuberous sclerosis complexRenzo Manara, Davide Brotto, Samuela Bugin, et al.
BMC Medical Genetics|October 14, 2010
Genetic investigations on 8 patients affected by ring 20 chromosome syndromeDaniela Giardino, Aglaia Vignoli, Lucia Ballarati, et al.
European Journal of Medical Genetics|February 13, 2018
Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2Angela Peron, Aglaia Vignoli, Francesca La Briola, et al.
Annals of Neurology|August 19, 2014
The visual system in eyelid myoclonia with absencesAnna Elisabetta Vaudano, Andrea Ruggieri, Manuela Tondelli, et al.
Neurobiology of Disease|December 1, 2025
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitorsIlaria Musante, Giulia Gorrieri, Serena Tamburro, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Epilepsia|April 21, 2016
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generationStefano Meletti, Andrea Ruggieri, Pietro Avanzini, et al.
Epilepsia|October 9, 2013
Early onset absence epilepsy with onset in the first year of life: a multicenter cohort studyLucio Giordano, Aglaia Vignoli, Raffaella Cusmai, et al.
Epilepsy & Behavior : E&B|August 24, 2010
Epilepsy in Rett syndrome: clinical and genetic featuresMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
Epilepsia|February 4, 2014
Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI studyAnna Elisabetta Vaudano, Andrea Ruggieri, Aglaia Vignoli, et al.
Epilepsy & Behavior : E&B|July 10, 2013
Vagus nerve stimulation in refractory epilepsy: new indications and outcome assessmentCarlo Efisio Marras, Valentina Chiesa, Alessandro De Benedictis, et al.
Neuroradiology|June 18, 2018
Rhinencephalon changes in tuberous sclerosis complexRenzo Manara, Davide Brotto, Samuela Bugin, et al.
BMC Medical Genetics|October 14, 2010
Genetic investigations on 8 patients affected by ring 20 chromosome syndromeDaniela Giardino, Aglaia Vignoli, Lucia Ballarati, et al.
European Journal of Medical Genetics|February 13, 2018
Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2Angela Peron, Aglaia Vignoli, Francesca La Briola, et al.
Annals of Neurology|August 19, 2014
The visual system in eyelid myoclonia with absencesAnna Elisabetta Vaudano, Andrea Ruggieri, Manuela Tondelli, et al.
Neurobiology of Disease|December 1, 2025
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitorsIlaria Musante, Giulia Gorrieri, Serena Tamburro, et al.
Pageof 13