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Patrizia Riguzzi

Showing results (21-30 of 33) with videos related to

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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 5, 2015
BRAF V600E mutation in neocortical posterior temporal epileptogenic gangliogliomasMatteo Martinoni, Gianluca Marucci, Dario de Biase, et al.
Epilepsia|July 2, 2022
Risk of hospitalization and death for COVID-19 in persons with epilepsy over a 20-month period: The EpiLink Bologna cohort, ItalyLorenzo Muccioli, Corrado Zenesini, Lisa Taruffi, et al.
Neurology|September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factorsLaura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Epilepsy Research|May 30, 2008
Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate lociRoberto Michelucci, Eva Scudellaro, Stefania Testoni, et al.
Epilepsia|April 28, 2023
IRF2BPL as a novel causative gene for progressive myoclonus epilepsyElena Gardella, Roberto Michelucci, Hanne M Christensen, et al.
European Journal of Neurology|January 31, 2025
Causes of hospitalization and mortality in persons with epilepsy: The EpiLink Bologna cohort, ItalyLorenzo Muccioli, Corrado Zenesini, Laura Licchetta, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Neurology. Genetics|November 17, 2021
Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved CasesLaura Canafoglia, Silvana Franceschetti, Antonio Gambardella, et al.
Epilepsy Research|August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsiesLaura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Epilepsia|April 30, 2013
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutationsRoberto Michelucci, Elena Pasini, Sandro Malacrida, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 5, 2015
BRAF V600E mutation in neocortical posterior temporal epileptogenic gangliogliomasMatteo Martinoni, Gianluca Marucci, Dario de Biase, et al.
Epilepsia|July 2, 2022
Risk of hospitalization and death for COVID-19 in persons with epilepsy over a 20-month period: The EpiLink Bologna cohort, ItalyLorenzo Muccioli, Corrado Zenesini, Lisa Taruffi, et al.
Neurology|September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factorsLaura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Epilepsy Research|May 30, 2008
Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate lociRoberto Michelucci, Eva Scudellaro, Stefania Testoni, et al.
Epilepsia|April 28, 2023
IRF2BPL as a novel causative gene for progressive myoclonus epilepsyElena Gardella, Roberto Michelucci, Hanne M Christensen, et al.
European Journal of Neurology|January 31, 2025
Causes of hospitalization and mortality in persons with epilepsy: The EpiLink Bologna cohort, ItalyLorenzo Muccioli, Corrado Zenesini, Laura Licchetta, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Neurology. Genetics|November 17, 2021
Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved CasesLaura Canafoglia, Silvana Franceschetti, Antonio Gambardella, et al.
Epilepsy Research|August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsiesLaura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Epilepsia|April 30, 2013
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutationsRoberto Michelucci, Elena Pasini, Sandro Malacrida, et al.
Pageof 4