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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 studyAngelo Pascarella, Marilisa Pasquale, Domenico Abelardo, 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.
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) studyAngelo Pascarella, Lucia Manzo, Sara Gasparini, et al.
Frontiers in Molecular Neuroscience|April 23, 2024
Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disordersMichele Iacomino, Nadia Houerbi, Sara Fortuna, et al.
Epilepsia|March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medicationsStefan Wolking, Claudia Moreau, Anne T Nies, et al.
Epilepsia|December 13, 2023
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencingAntonietta Coppola, S Krithika, Michele Iacomino, et al.
Epilepsia Open|August 24, 2019
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsyKatri Silvennoinen, Nikola de Lange, Sara Zagaglia, et al.
Orphanet Journal of Rare Diseases|September 28, 2018
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional studyGuja Astrea, Alessandro Romano, Corrado Angelini, et al.
Neurology|June 3, 2021
Clinical and Genetic Features in Patients With Reflex Bathing EpilepsyAndrea Accogli, Gert Wiegand, Marcello Scala, et al.
Epilepsia|February 6, 2019
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsyHerbert Schulz, Ann-Kathrin Ruppert, Federico Zara, et al.
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