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Silvana Franceschetti

Showing results (141-150 of 178) with videos related to

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Epilepsia|December 5, 2012
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutationsLaura Canafoglia, Elena Gennaro, Giuseppe Capovilla, et al.
Journal of Neurology|December 6, 2018
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotypeLorenzo Nanetti, Elisa Sarto, Anna Castaldo, 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.
Neurology|September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factorsLaura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Epilepsia|June 15, 2007
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutationEleonora Colosimo, Antonio Gambardella, Massimo Mantegazza, et al.
Epilepsia|March 11, 2015
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsyLaura Mumoli, Patrizia Tarantino, Roberto Michelucci, 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.
Neuropsychological Rehabilitation|March 11, 2017
Evidence of altered pressure pain thresholds in persons with disorders of consciousness as measured by the Nociception Coma Scale-Italian versionDavide Sattin, Caroline Schnakers, Marco Pagani, et al.
Epilepsia Open|February 9, 2024
Myoclonus: Differential diagnosis and current managementAntonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, et al.
Neurology|January 4, 2014
Progressive myoclonic epilepsies: definitive and still undetermined causesSilvana Franceschetti, Roberto Michelucci, Laura Canafoglia, et al.
Pageof 18

Showing results (141-150 of 178) with videos related to

Sort By:
Pageof 18
Epilepsia|December 5, 2012
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutationsLaura Canafoglia, Elena Gennaro, Giuseppe Capovilla, et al.
Journal of Neurology|December 6, 2018
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotypeLorenzo Nanetti, Elisa Sarto, Anna Castaldo, 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.
Neurology|September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factorsLaura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Epilepsia|June 15, 2007
Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutationEleonora Colosimo, Antonio Gambardella, Massimo Mantegazza, et al.
Epilepsia|March 11, 2015
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsyLaura Mumoli, Patrizia Tarantino, Roberto Michelucci, 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.
Neuropsychological Rehabilitation|March 11, 2017
Evidence of altered pressure pain thresholds in persons with disorders of consciousness as measured by the Nociception Coma Scale-Italian versionDavide Sattin, Caroline Schnakers, Marco Pagani, et al.
Epilepsia Open|February 9, 2024
Myoclonus: Differential diagnosis and current managementAntonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, et al.
Neurology|January 4, 2014
Progressive myoclonic epilepsies: definitive and still undetermined causesSilvana Franceschetti, Roberto Michelucci, Laura Canafoglia, et al.
Pageof 18