Search research articles
Contact Us
Filters
Showing results (81-90 of 132) with videos related to
Page
of 14
Sort By:
Epilepsia
|
April 8, 2015
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1
Guido Rubboli, Pierangelo Veggiotti, Antonella Pini, et al.
Epilepsia
|
February 13, 2008
Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy
Nicola Specchio, Giovanni Boero, Roberto Michelucci, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
May 5, 2015
BRAF V600E mutation in neocortical posterior temporal epileptogenic gangliogliomas
Matteo Martinoni, Gianluca Marucci, Dario de Biase, et al.
Epilepsia
|
July 5, 2025
Tumor-related epilepsy in glioma: A multidisciplinary overview
Roberto Michelucci, Giada Pauletto, Antonio Silvani, et al.
Epilepsy & Behavior : E&B
|
August 28, 2025
The 9th annual Lafora science symposium: a rare epilepsy community makes progress towards clinical readiness
Meredith I Williams, Katherine J Donohue, Pascual Sanz, et al.
Expert Review of Neurotherapeutics
|
January 17, 2020
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy
Marcello Scala, Amedeo Bianchi, Francesca Bisulli, 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, Italy
Lorenzo Muccioli, Corrado Zenesini, Lisa Taruffi, et al.
Epilepsy Research
|
November 5, 2024
Parameter analysis in stereoelectroencephalography-guided radiofrequency thermocoagulation: A common basis for objective comparison between protocols
Luca Zanuttini, Federico Mason, Lorenzo Ferri, et al.
Epilepsia
|
December 5, 2012
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations
Laura Canafoglia, Elena Gennaro, Giuseppe Capovilla, et al.
Neurology
|
September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factors
Laura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Page
of 14
Search research articles
Search
Showing results (81-90 of 132) with videos related to
Sort By:
Page
of 14
Epilepsia
|
April 8, 2015
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1
Guido Rubboli, Pierangelo Veggiotti, Antonella Pini, et al.
Epilepsia
|
February 13, 2008
Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy
Nicola Specchio, Giovanni Boero, Roberto Michelucci, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
May 5, 2015
BRAF V600E mutation in neocortical posterior temporal epileptogenic gangliogliomas
Matteo Martinoni, Gianluca Marucci, Dario de Biase, et al.
Epilepsia
|
July 5, 2025
Tumor-related epilepsy in glioma: A multidisciplinary overview
Roberto Michelucci, Giada Pauletto, Antonio Silvani, et al.
Epilepsy & Behavior : E&B
|
August 28, 2025
The 9th annual Lafora science symposium: a rare epilepsy community makes progress towards clinical readiness
Meredith I Williams, Katherine J Donohue, Pascual Sanz, et al.
Expert Review of Neurotherapeutics
|
January 17, 2020
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy
Marcello Scala, Amedeo Bianchi, Francesca Bisulli, 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, Italy
Lorenzo Muccioli, Corrado Zenesini, Lisa Taruffi, et al.
Epilepsy Research
|
November 5, 2024
Parameter analysis in stereoelectroencephalography-guided radiofrequency thermocoagulation: A common basis for objective comparison between protocols
Luca Zanuttini, Federico Mason, Lorenzo Ferri, et al.
Epilepsia
|
December 5, 2012
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations
Laura Canafoglia, Elena Gennaro, Giuseppe Capovilla, et al.
Neurology
|
September 22, 2017
Variable course of Unverricht-Lundborg disease: Early prognostic factors
Laura Canafoglia, Edoardo Ferlazzo, Roberto Michelucci, et al.
Page
of 14