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Francesca Bisulli

Showing results (221-230 of 236) with videos related to

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Frontiers in Neurology|June 7, 2021
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut SyndromeLuigi Francesco Iannone, Gabriele Arena, Domenica Battaglia, et al.
Epilepsia|August 22, 2025
Standard complete blood count to predict long-term outcomes in febrile infection-related epilepsy syndrome (FIRES): A multicenter studyMartin Guillemaud, Aurélie Hanin, James J Riviello, et al.
Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Epilepsia|July 28, 2025
Trends in epilepsy surgery in Italy before and after the COVID-19 pandemic: A nationwide studyGiuseppe Didato, Federico Vigevano, Laura Tassi, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Epilepsia|March 15, 2025
Effectiveness and safety of adjunctive cenobamate in people with focal-onset epilepsy: Interim results after 24-week observational period from the BLESS studySimona Lattanzi, Fedele Dono, Giuseppe d'Orsi, et al.
Epilepsia Open|June 1, 2026
On-site exposure to clinical epilepsy practice for experimental scientists engaged in epilepsy research: A pilot study by the ILAE commission on neurobiologyMarco de Curtis, Giulia Battaglia, Gustavo Aguado-Carrillo, et al.
Neurology|June 26, 2025
Phenotypic Spectrum in Individuals With Pathogenic <i>GABRG2</i> Loss- and Gain-of-Function VariantsAlessandra Rossi, Susan X N Lin, Nathan L Absalom, et al.
Neurology|October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.
Epilepsia|January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies, Costin Leu, Carolien G F de Kovel, et al.
Pageof 24

Showing results (221-230 of 236) with videos related to

Sort By:
Pageof 24
Frontiers in Neurology|June 7, 2021
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut SyndromeLuigi Francesco Iannone, Gabriele Arena, Domenica Battaglia, et al.
Epilepsia|August 22, 2025
Standard complete blood count to predict long-term outcomes in febrile infection-related epilepsy syndrome (FIRES): A multicenter studyMartin Guillemaud, Aurélie Hanin, James J Riviello, et al.
Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Epilepsia|July 28, 2025
Trends in epilepsy surgery in Italy before and after the COVID-19 pandemic: A nationwide studyGiuseppe Didato, Federico Vigevano, Laura Tassi, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Epilepsia|March 15, 2025
Effectiveness and safety of adjunctive cenobamate in people with focal-onset epilepsy: Interim results after 24-week observational period from the BLESS studySimona Lattanzi, Fedele Dono, Giuseppe d'Orsi, et al.
Epilepsia Open|June 1, 2026
On-site exposure to clinical epilepsy practice for experimental scientists engaged in epilepsy research: A pilot study by the ILAE commission on neurobiologyMarco de Curtis, Giulia Battaglia, Gustavo Aguado-Carrillo, et al.
Neurology|June 26, 2025
Phenotypic Spectrum in Individuals With Pathogenic <i>GABRG2</i> Loss- and Gain-of-Function VariantsAlessandra Rossi, Susan X N Lin, Nathan L Absalom, et al.
Neurology|October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of <i>KCNH5</i>Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.
Epilepsia|January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies, Costin Leu, Carolien G F de Kovel, et al.
Pageof 24