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Aglaia Vignoli

Showing results (101-110 of 129) with videos related to

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Frontiers in Neurology|January 11, 2020
Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal SpikesAnna Elisabetta Vaudano, Pietro Avanzini, Gaetano Cantalupo, et al.
International Journal of Molecular Sciences|January 27, 2024
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter StudyBenedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, et al.
Frontiers in Neurology|July 2, 2024
24-h continuous non-invasive multiparameter home monitoring of vitals in patients with Rett syndrome by an innovative wearable technology: evidence of an overlooked chronic fatigue statusSilvia Leoncini, Lidia Boasiako, Sofia Di Lucia, et al.
Journal of Neurosurgery. Pediatrics|April 11, 2025
Epilepsy surgery outcomes in children with tuberous sclerosis complex: a systematic review and meta-analysisAndrew T Hale, Cody Savage, Dagoberto Estevez-Ordonez, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 11, 2026
Transition from adolescence to adulthood: Dedicated health services for young people with epilepsy in ItalyIlaria Viganò, Ilaria Venezia, Maurizio Bonati, et al.
Epilepsia|February 16, 2011
Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 casesRuta Mameniskiene, Thomas Bast, Carla Bentes, et al.
Epilepsia Open|June 21, 2025
Is highly purified cannabidiol a treatment opportunity for drug-resistant epilepsy in subjects with typical Rett syndrome and CDKL5 deficiency disorder?Aglaia Vignoli, Giulia Prato, Enrico Alfei, et al.
Epilepsy Research|May 7, 2011
A clinical and genetic study of 33 new cases with early-onset absence epilepsyLucio Giordano, Aglaia Vignoli, Patrizia Accorsi, et al.
Human Mutation|March 15, 2012
Rett networked database: an integrated clinical and genetic network of Rett syndrome databasesElisa Grillo, Laurent Villard, Angus Clarke, et al.
Epilepsia|July 20, 2007
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsyFerdinanda Annesi, Antonio Gambardella, Roberto Michelucci, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
Frontiers in Neurology|January 11, 2020
Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal SpikesAnna Elisabetta Vaudano, Pietro Avanzini, Gaetano Cantalupo, et al.
International Journal of Molecular Sciences|January 27, 2024
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter StudyBenedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, et al.
Frontiers in Neurology|July 2, 2024
24-h continuous non-invasive multiparameter home monitoring of vitals in patients with Rett syndrome by an innovative wearable technology: evidence of an overlooked chronic fatigue statusSilvia Leoncini, Lidia Boasiako, Sofia Di Lucia, et al.
Journal of Neurosurgery. Pediatrics|April 11, 2025
Epilepsy surgery outcomes in children with tuberous sclerosis complex: a systematic review and meta-analysisAndrew T Hale, Cody Savage, Dagoberto Estevez-Ordonez, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|April 11, 2026
Transition from adolescence to adulthood: Dedicated health services for young people with epilepsy in ItalyIlaria Viganò, Ilaria Venezia, Maurizio Bonati, et al.
Epilepsia|February 16, 2011
Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 casesRuta Mameniskiene, Thomas Bast, Carla Bentes, et al.
Epilepsia Open|June 21, 2025
Is highly purified cannabidiol a treatment opportunity for drug-resistant epilepsy in subjects with typical Rett syndrome and CDKL5 deficiency disorder?Aglaia Vignoli, Giulia Prato, Enrico Alfei, et al.
Epilepsy Research|May 7, 2011
A clinical and genetic study of 33 new cases with early-onset absence epilepsyLucio Giordano, Aglaia Vignoli, Patrizia Accorsi, et al.
Human Mutation|March 15, 2012
Rett networked database: an integrated clinical and genetic network of Rett syndrome databasesElisa Grillo, Laurent Villard, Angus Clarke, et al.
Epilepsia|July 20, 2007
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsyFerdinanda Annesi, Antonio Gambardella, Roberto Michelucci, et al.
Pageof 13