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Federico Vigevano

Showing results (181-190 of 260) with videos related to

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Epilepsy & Behavior : E&B|July 4, 2025
Diagnostic performance of morphometric analysis program in pediatric epilepsy surgeryValentina Di Micco, Mattia Mercier, Camilla Rossi Espagnet, et al.
Life (Basel, Switzerland)|December 24, 2021
Migraine and Its Equivalents: What Do They Share? A Narrative Review on Common Pathophysiological PatternsIlaria Frattale, Claudia Ruscitto, Laura Papetti, et al.
Frontiers in Neurology|August 1, 2022
Interictal Cognitive Performance in Children and Adolescents With Primary Headache: A Narrative ReviewSamuela Tarantino, Martina Proietti Checchi, Laura Papetti, et al.
Brain Sciences|January 21, 2023
Can Presurgical Interhemispheric EEG Connectivity Predict Outcome in Hemispheric Surgery? A Brain Machine Learning ApproachChiara Pepi, Mattia Mercier, Giusy Carfì Pavia, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 1, 2023
Phase-amplitude coupling between low- and high-frequency activities as preoperative biomarker of focal cortical dysplasia subtypesLorenzo Ricci, Eleonora Tamilia, Mattia Mercier, et al.
Epilepsia|May 5, 2017
Reduced steroidogenesis in patients with PCDH19-female limited epilepsyMarina Trivisano, Chiara Lucchi, Cecilia Rustichelli, et al.
Frontiers in Immunology|February 10, 2023
Safety of SARS-CoV2 vaccination and COVID-19 short-term outcome in pediatric acquired demyelinating disorders of central nervous system: A single center experienceGabriele Monte, Laura Papetti, Michela Ada Noris Ferilli, et al.
Epilepsia|September 17, 2024
Unveiling the disease progression in developmental and epileptic encephalopathies: Insights from EEG and neuropsychologyPaolo Surdi, Marina Trivisano, Angela De Dominicis, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
Pageof 26

Showing results (181-190 of 260) with videos related to

Sort By:
Pageof 26
Epilepsy & Behavior : E&B|July 4, 2025
Diagnostic performance of morphometric analysis program in pediatric epilepsy surgeryValentina Di Micco, Mattia Mercier, Camilla Rossi Espagnet, et al.
Life (Basel, Switzerland)|December 24, 2021
Migraine and Its Equivalents: What Do They Share? A Narrative Review on Common Pathophysiological PatternsIlaria Frattale, Claudia Ruscitto, Laura Papetti, et al.
Frontiers in Neurology|August 1, 2022
Interictal Cognitive Performance in Children and Adolescents With Primary Headache: A Narrative ReviewSamuela Tarantino, Martina Proietti Checchi, Laura Papetti, et al.
Brain Sciences|January 21, 2023
Can Presurgical Interhemispheric EEG Connectivity Predict Outcome in Hemispheric Surgery? A Brain Machine Learning ApproachChiara Pepi, Mattia Mercier, Giusy Carfì Pavia, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 1, 2023
Phase-amplitude coupling between low- and high-frequency activities as preoperative biomarker of focal cortical dysplasia subtypesLorenzo Ricci, Eleonora Tamilia, Mattia Mercier, et al.
Epilepsia|May 5, 2017
Reduced steroidogenesis in patients with PCDH19-female limited epilepsyMarina Trivisano, Chiara Lucchi, Cecilia Rustichelli, et al.
Frontiers in Immunology|February 10, 2023
Safety of SARS-CoV2 vaccination and COVID-19 short-term outcome in pediatric acquired demyelinating disorders of central nervous system: A single center experienceGabriele Monte, Laura Papetti, Michela Ada Noris Ferilli, et al.
Epilepsia|September 17, 2024
Unveiling the disease progression in developmental and epileptic encephalopathies: Insights from EEG and neuropsychologyPaolo Surdi, Marina Trivisano, Angela De Dominicis, et al.
Neurogenetics|March 30, 2006
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the MediterraneanNatalia Cannelli, Denise Cassandrini, Enrico Bertini, et al.
Epilepsia|April 13, 2011
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutationsNicola Specchio, Carla Marini, Alessandra Terracciano, et al.
Pageof 26