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Epilepsy Research
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February 22, 2011
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
Giorgia Busolin, Sandro Malacrida, Francesca Bisulli, et al.
Human Genetics
|
July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2
Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
Epilepsia
|
October 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology
Simona Balestrini, Ilaria Galli, Maria Luisa Ricci, et al.
Neurology
|
May 11, 2016
Definition and diagnostic criteria of sleep-related hypermotor epilepsy
Paolo Tinuper, Francesca Bisulli, J H Cross, et al.
Epilepsy Research
|
August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsies
Laura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Journal of the Neurological Sciences
|
March 27, 2021
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations
Antonella Riva, Alessandro Orsini, Marcello Scala, et al.
Journal of Neurology
|
June 7, 2025
Effectiveness of perampanel as only concomitant antiseizure medication for highly active epilepsy: insight from a real-world, multicenter retrospective study
Angelo Pascarella, Marilisa Pasquale, Domenico Abelardo, et al.
Epilepsia
|
April 30, 2013
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations
Roberto Michelucci, Elena Pasini, Sandro Malacrida, et al.
Journal of the Neurological Sciences
|
June 26, 2024
Perampanel in post-stroke epilepsy: Clinical practice data from the PERampanel as Only Concomitant antiseizure medication (PEROC) study
Angelo Pascarella, Lucia Manzo, Sara Gasparini, et al.
Epilepsia
|
December 6, 2025
Early neurological symptoms and epilepsy outcomes in individuals with the recurrent GABRG2 p.(Ala106Thr) gain-of-function variant: Structural and phenotypic insights
Sebastian Ortiz, Chiara Bagliani, Susan X N Lin, et al.
Page
of 24
Search research articles
Search
Showing results (201-210 of 236) with videos related to
Sort By:
Page
of 24
Epilepsy Research
|
February 22, 2011
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
Giorgia Busolin, Sandro Malacrida, Francesca Bisulli, et al.
Human Genetics
|
July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2
Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.
Epilepsia
|
October 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology
Simona Balestrini, Ilaria Galli, Maria Luisa Ricci, et al.
Neurology
|
May 11, 2016
Definition and diagnostic criteria of sleep-related hypermotor epilepsy
Paolo Tinuper, Francesca Bisulli, J H Cross, et al.
Epilepsy Research
|
August 26, 2019
An Italian multicentre study of perampanel in progressive myoclonus epilepsies
Laura Canafoglia, Giuseppina Barbella, Edoardo Ferlazzo, et al.
Journal of the Neurological Sciences
|
March 27, 2021
Italian cohort of Lafora disease: Clinical features, disease evolution, and genotype-phenotype correlations
Antonella Riva, Alessandro Orsini, Marcello Scala, et al.
Journal of Neurology
|
June 7, 2025
Effectiveness of perampanel as only concomitant antiseizure medication for highly active epilepsy: insight from a real-world, multicenter retrospective study
Angelo Pascarella, Marilisa Pasquale, Domenico Abelardo, et al.
Epilepsia
|
April 30, 2013
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations
Roberto Michelucci, Elena Pasini, Sandro Malacrida, et al.
Journal of the Neurological Sciences
|
June 26, 2024
Perampanel in post-stroke epilepsy: Clinical practice data from the PERampanel as Only Concomitant antiseizure medication (PEROC) study
Angelo Pascarella, Lucia Manzo, Sara Gasparini, et al.
Epilepsia
|
December 6, 2025
Early neurological symptoms and epilepsy outcomes in individuals with the recurrent GABRG2 p.(Ala106Thr) gain-of-function variant: Structural and phenotypic insights
Sebastian Ortiz, Chiara Bagliani, Susan X N Lin, et al.
Page
of 24