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Angelo Labate

Showing results (161-170 of 216) with videos related to

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Epilepsia|March 11, 2015
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsyLaura Mumoli, Patrizia Tarantino, Roberto Michelucci, et al.
Frontiers in Neurology|August 29, 2022
Perampanel and childhood absence epilepsy: A real life experienceFrancesca Felicia Operto, Alessandro Orsini, Gianpiero Sica, et al.
Epilepsia|January 22, 2005
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsyAntonio Gambardella, Umberto Aguglia, Rosanna Chifari, et al.
International Journal of Neural Systems|July 22, 2016
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive DementiaFrancesco Carlo Morabito, Maurizio Campolo, Nadia Mammone, et al.
Epilepsia Open|February 9, 2024
Myoclonus: Differential diagnosis and current managementAntonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, et al.
Neurobiology of Disease|June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityMattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, et al.
Frontiers in Molecular Neuroscience|August 22, 2018
A Loss-of-Function <i>HCN4</i> Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal ExcitabilityGiulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, et al.
Journal of Neurology|November 16, 2007
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian familiesPasquale Striano, Antonio Gambardella, Antonietta Coppola, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Epilepsia|August 16, 2003
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plusGrazia Annesi, Antonio Gambardella, Sara Carrideo, et al.
Pageof 22

Showing results (161-170 of 216) with videos related to

Sort By:
Pageof 22
Epilepsia|March 11, 2015
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsyLaura Mumoli, Patrizia Tarantino, Roberto Michelucci, et al.
Frontiers in Neurology|August 29, 2022
Perampanel and childhood absence epilepsy: A real life experienceFrancesca Felicia Operto, Alessandro Orsini, Gianpiero Sica, et al.
Epilepsia|January 22, 2005
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsyAntonio Gambardella, Umberto Aguglia, Rosanna Chifari, et al.
International Journal of Neural Systems|July 22, 2016
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive DementiaFrancesco Carlo Morabito, Maurizio Campolo, Nadia Mammone, et al.
Epilepsia Open|February 9, 2024
Myoclonus: Differential diagnosis and current managementAntonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, et al.
Neurobiology of Disease|June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityMattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, et al.
Frontiers in Molecular Neuroscience|August 22, 2018
A Loss-of-Function <i>HCN4</i> Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal ExcitabilityGiulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, et al.
Journal of Neurology|November 16, 2007
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian familiesPasquale Striano, Antonio Gambardella, Antonietta Coppola, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Epilepsia|August 16, 2003
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plusGrazia Annesi, Antonio Gambardella, Sara Carrideo, et al.
Pageof 22