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Francesca Ragona

Showing results (41-50 of 87) with videos related to

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Epilepsia|May 19, 2023
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetinePaolo Ambrosino, Francesca Ragona, Ilaria Mosca, et al.
Epilepsy Research|May 13, 2014
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patientsTiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Epilepsia|October 24, 2025
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjectsDavide Caputo, Roberta Solazzi, Barbara Castellotti, et al.
Molecular Neurobiology|February 1, 2018
Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP<sub>2</sub>-Dependent K<sup>+</sup> Channel GatingPaolo Ambrosino, Elena Freri, Barbara Castellotti, et al.
Epilepsia Open|December 24, 2024
CLN6-related continuum phenotype caused by aberrant splicingFederica Invernizzi, Barbara Castellotti, Chiara Reale, et al.
Epilepsy & Behavior : E&B|October 18, 2025
Developmental and epileptic encephalopathies: From current care to future perspectives - insights from epilepsy centres in Lombardy, ItalyGiuseppe Didato, Francesca Ragona, Alice Pompili, et al.
Epilepsia|September 18, 2020
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world studyNicola Specchio, Nicola Pietrafusa, Viola Doccini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 26, 2023
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikesMartina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 4, 2026
In search of "what really matters": Insights from a web-based survey on Patient-Centered Outcomes in GLUT1DSCostanza Varesio, Ludovica Pasca, Martina Paola Zanaboni, et al.
Pageof 9

Showing results (41-50 of 87) with videos related to

Sort By:
Pageof 9
Epilepsia|May 19, 2023
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetinePaolo Ambrosino, Francesca Ragona, Ilaria Mosca, et al.
Epilepsy Research|May 13, 2014
Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patientsTiziana Granata, Sara Matricardi, Francesca Ragona, et al.
Epilepsia|October 24, 2025
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjectsDavide Caputo, Roberta Solazzi, Barbara Castellotti, et al.
Molecular Neurobiology|February 1, 2018
Kv7.3 Compound Heterozygous Variants in Early Onset Encephalopathy Reveal Additive Contribution of C-Terminal Residues to PIP<sub>2</sub>-Dependent K<sup>+</sup> Channel GatingPaolo Ambrosino, Elena Freri, Barbara Castellotti, et al.
Epilepsia Open|December 24, 2024
CLN6-related continuum phenotype caused by aberrant splicingFederica Invernizzi, Barbara Castellotti, Chiara Reale, et al.
Epilepsy & Behavior : E&B|October 18, 2025
Developmental and epileptic encephalopathies: From current care to future perspectives - insights from epilepsy centres in Lombardy, ItalyGiuseppe Didato, Francesca Ragona, Alice Pompili, et al.
Epilepsia|September 18, 2020
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world studyNicola Specchio, Nicola Pietrafusa, Viola Doccini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 26, 2023
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikesMartina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 4, 2026
In search of "what really matters": Insights from a web-based survey on Patient-Centered Outcomes in GLUT1DSCostanza Varesio, Ludovica Pasca, Martina Paola Zanaboni, et al.
Pageof 9