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Renzo Guerrini

Showing results (361-370 of 611) with videos related to

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Brain : a Journal of Neurology|April 21, 2010
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsRichard J Leventer, Anna Jansen, Daniela T Pilz, 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.
European Journal of Neurology|May 20, 2025
High Prevalence of GALC Gene Variants in Adults With Neurodegenerative ConditionsFederica Feo, Luciana Tramacere, Silvia Ramat, et al.
Human Molecular Genetics|October 13, 2025
Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortexAntonio Falace, Léa Corbières, Lucas Silvagnoli, et al.
Epilepsia|March 27, 2026
A phase 3, randomized clinical trial of soticlestat as adjunctive therapy for Lennox-Gastaut syndromeRenzo Guerrini, Eric D Marsh, Wei-Ping Liao, et al.
Plos One|September 8, 2020
Patterns and predictors of language representation and the influence of epilepsy surgery on language reorganization in children and young adults with focal lesional epilepsyCarmen Barba, Domenico Montanaro, Laura Grisotto, et al.
Epilepsia|January 15, 2025
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathyCathrine E Gjerulfsen, Madeleine J Oudin, Francesca Furia, et al.
Epilepsia|June 15, 2007
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalitiesCarla Marini, Davide Mei, Teresa Temudo, et al.
Human Molecular Genetics|October 4, 2017
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndromeCaterina Garone, Aaron R D'Souza, Cristina Dallabona, et al.
Human Mutation|November 20, 2016
Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different GenesElena Parrini, Carla Marini, Davide Mei, et al.
Pageof 62

Showing results (361-370 of 611) with videos related to

Sort By:
Pageof 62
Brain : a Journal of Neurology|April 21, 2010
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsRichard J Leventer, Anna Jansen, Daniela T Pilz, 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.
European Journal of Neurology|May 20, 2025
High Prevalence of GALC Gene Variants in Adults With Neurodegenerative ConditionsFederica Feo, Luciana Tramacere, Silvia Ramat, et al.
Human Molecular Genetics|October 13, 2025
Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortexAntonio Falace, Léa Corbières, Lucas Silvagnoli, et al.
Epilepsia|March 27, 2026
A phase 3, randomized clinical trial of soticlestat as adjunctive therapy for Lennox-Gastaut syndromeRenzo Guerrini, Eric D Marsh, Wei-Ping Liao, et al.
Plos One|September 8, 2020
Patterns and predictors of language representation and the influence of epilepsy surgery on language reorganization in children and young adults with focal lesional epilepsyCarmen Barba, Domenico Montanaro, Laura Grisotto, et al.
Epilepsia|January 15, 2025
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathyCathrine E Gjerulfsen, Madeleine J Oudin, Francesca Furia, et al.
Epilepsia|June 15, 2007
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalitiesCarla Marini, Davide Mei, Teresa Temudo, et al.
Human Molecular Genetics|October 4, 2017
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndromeCaterina Garone, Aaron R D'Souza, Cristina Dallabona, et al.
Human Mutation|November 20, 2016
Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different GenesElena Parrini, Carla Marini, Davide Mei, et al.
Pageof 62