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Edoardo Canale

Showing results (1-10 of 6) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|May 24, 2025
Co-occurrence of childhood absence epilepsy and self-limited focal epilepsy interictal discharges: Differences from childhood absence epilepsy aloneGiulia Barbagallo, Giulia Nobile, Maria Grazia Calevo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 16, 2024
Subclinical rhythmic EEG discharge of adults (SREDA) in pediatric population: A case series with systematic review of the literatureLuca Bosisio, Maria Margherita Mancardi, Silvia Boeri, et al.
Genes|April 28, 2023
Exome Analysis Reveals Novel Missense and Deletion Variants in the <i>CC2D2A</i> Gene as Causative of Joubert SyndromeRute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 26, 2020
Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 EncephalopathyMatteo Lenge, Carla Marini, Edoardo Canale, et al.
Neuropediatrics|October 6, 2023
Electroclinical Features of Epilepsy in Kleefstra SyndromeThea Giacomini, Ramona Cordani, Irene Bagnasco, et al.
Multiple Sclerosis and Related Disorders|February 5, 2026
First demyelinating attack in children: A twelve year single center cohortAlessandro Santagostino Barbone, Thea Giacomini, Silvia Casabona, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Epileptic Disorders : International Epilepsy Journal with Videotape|May 24, 2025
Co-occurrence of childhood absence epilepsy and self-limited focal epilepsy interictal discharges: Differences from childhood absence epilepsy aloneGiulia Barbagallo, Giulia Nobile, Maria Grazia Calevo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 16, 2024
Subclinical rhythmic EEG discharge of adults (SREDA) in pediatric population: A case series with systematic review of the literatureLuca Bosisio, Maria Margherita Mancardi, Silvia Boeri, et al.
Genes|April 28, 2023
Exome Analysis Reveals Novel Missense and Deletion Variants in the <i>CC2D2A</i> Gene as Causative of Joubert SyndromeRute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 26, 2020
Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 EncephalopathyMatteo Lenge, Carla Marini, Edoardo Canale, et al.
Neuropediatrics|October 6, 2023
Electroclinical Features of Epilepsy in Kleefstra SyndromeThea Giacomini, Ramona Cordani, Irene Bagnasco, et al.
Multiple Sclerosis and Related Disorders|February 5, 2026
First demyelinating attack in children: A twelve year single center cohortAlessandro Santagostino Barbone, Thea Giacomini, Silvia Casabona, et al.
Pageof 1