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Francesco Fortunato

Showing results (111-120 of 120) with videos related to

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Epilepsy & Behavior : E&B|November 27, 2025
Epilepsy beyond seizures: embracing a holistic perspective. Proceedings of the 2nd meeting (Episicily) of the epilepsy study group of the Italian Society of neurologyAngelo Labate, Eleonora Palma, Vincenzo Belcastro, et al.
JAMA Neurology|February 9, 2026
Comparative Effectiveness of Brivaracetam, Cenobamate, Lacosamide, and Perampanel in Focal EpilepsyEmanuele Cerulli Irelli, Roberta Roberti, Maria Sole Borioni, et al.
Epilepsia|February 27, 2024
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy studyRebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy studyRebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA studyHuantao Wen, Bin Wan, Taha Gholipour, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Epilepsia|June 3, 2022
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional dataSeymour M Lopez, Leon M Aksman, Neil P Oxtoby, et al.
Medrxiv : the Preprint Server for Health Sciences|July 2, 2026
Global Socioeconomic Context and Brain Ageing in Epilepsy: an ENIGMA-Epilepsy studyHeath R Pardoe, Orrin Devinsky, Jemima Robson Bbiomed, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Pageof 12

Showing results (111-120 of 120) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 120 results.
Epilepsy & Behavior : E&B|November 27, 2025
Epilepsy beyond seizures: embracing a holistic perspective. Proceedings of the 2nd meeting (Episicily) of the epilepsy study group of the Italian Society of neurologyAngelo Labate, Eleonora Palma, Vincenzo Belcastro, et al.
JAMA Neurology|February 9, 2026
Comparative Effectiveness of Brivaracetam, Cenobamate, Lacosamide, and Perampanel in Focal EpilepsyEmanuele Cerulli Irelli, Roberta Roberti, Maria Sole Borioni, et al.
Epilepsia|February 27, 2024
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy studyRebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy studyRebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Sex-related structural alterations across common epilepsies: a worldwide ENIGMA studyHuantao Wen, Bin Wan, Taha Gholipour, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Epilepsia|June 3, 2022
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional dataSeymour M Lopez, Leon M Aksman, Neil P Oxtoby, et al.
Medrxiv : the Preprint Server for Health Sciences|July 2, 2026
Global Socioeconomic Context and Brain Ageing in Epilepsy: an ENIGMA-Epilepsy studyHeath R Pardoe, Orrin Devinsky, Jemima Robson Bbiomed, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Pageof 12