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Carla Marini

Showing results (51-60 of 161) with videos related to

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Indian Journal of Pediatrics|June 28, 2020
Dravet Syndrome: A Case SeriesDipti Kapoor, Aakanksha Anand, Suvasini Sharma, et al.
Epilepsia Open|October 30, 2025
Real-world efficacy and safety of cannabidiol in developmental and epileptic encephalopathiesMarco Perulli, Maddalena Bianchetti, Gloria Pantalone, et al.
European Journal of Hospital Pharmacy : Science and Practice|April 12, 2022
A pharmacovigilance study on antiepileptic medications in a paediatric hospital in ItalyNicoletta Monti Guarnieri, Adriana Pompilio, Carla Marini, et al.
Epilepsy & Behavior : E&B|December 11, 2024
Infantile epileptic spasms syndrome: When spasms come out of the blueMarta Conti, Sara Matricardi, Ludovica M Piscitello, et al.
Developmental Medicine and Child Neurology|June 26, 2026
Seizure worsening and sodium channel blockers in HCN1-related epilepsies: A case seriesSilvia Lelli, Lauren E Bleakley, Sally Ackermann, et al.
Translational Psychiatry|January 27, 2024
Multiomic analysis implicates nuclear hormone receptor signalling in clustering epilepsyRebekah de Nys, Clare L van Eyk, Tarin Ritchie, et al.
Epilepsia|September 29, 2009
Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathyDavide Mei, Carla Marini, Francesca Novara, et al.
Brain and Behavior|April 1, 2025
An Italian Survey on the Management of Pediatric Convulsive Status Epilepticus: More Than Just a Pharmacological ChoiceCaterina Zanus, Giulia Cannizzaro, Giacomo Danieli, et al.
Progress in Biophysics and Molecular Biology|July 26, 2021
Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients?Alessandro Porro, Gerardo Abbandonato, Valentina Veronesi, et al.
European Journal of Human Genetics : EJHG|January 27, 2019
Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneityElena Cellini, Annalisa Vetro, Valerio Conti, et al.
Pageof 17

Showing results (51-60 of 161) with videos related to

Sort By:
Pageof 17
Indian Journal of Pediatrics|June 28, 2020
Dravet Syndrome: A Case SeriesDipti Kapoor, Aakanksha Anand, Suvasini Sharma, et al.
Epilepsia Open|October 30, 2025
Real-world efficacy and safety of cannabidiol in developmental and epileptic encephalopathiesMarco Perulli, Maddalena Bianchetti, Gloria Pantalone, et al.
European Journal of Hospital Pharmacy : Science and Practice|April 12, 2022
A pharmacovigilance study on antiepileptic medications in a paediatric hospital in ItalyNicoletta Monti Guarnieri, Adriana Pompilio, Carla Marini, et al.
Epilepsy & Behavior : E&B|December 11, 2024
Infantile epileptic spasms syndrome: When spasms come out of the blueMarta Conti, Sara Matricardi, Ludovica M Piscitello, et al.
Developmental Medicine and Child Neurology|June 26, 2026
Seizure worsening and sodium channel blockers in HCN1-related epilepsies: A case seriesSilvia Lelli, Lauren E Bleakley, Sally Ackermann, et al.
Translational Psychiatry|January 27, 2024
Multiomic analysis implicates nuclear hormone receptor signalling in clustering epilepsyRebekah de Nys, Clare L van Eyk, Tarin Ritchie, et al.
Epilepsia|September 29, 2009
Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathyDavide Mei, Carla Marini, Francesca Novara, et al.
Brain and Behavior|April 1, 2025
An Italian Survey on the Management of Pediatric Convulsive Status Epilepticus: More Than Just a Pharmacological ChoiceCaterina Zanus, Giulia Cannizzaro, Giacomo Danieli, et al.
Progress in Biophysics and Molecular Biology|July 26, 2021
Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients?Alessandro Porro, Gerardo Abbandonato, Valentina Veronesi, et al.
European Journal of Human Genetics : EJHG|January 27, 2019
Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneityElena Cellini, Annalisa Vetro, Valerio Conti, et al.
Pageof 17