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Neuroscience Letters|March 22, 2008
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsyGiorgia Bovo, Erica Diani, Francesca Bisulli, et al.
Frontiers in Physiology|January 10, 2022
STXBP1 Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEGSimon J Houtman, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Seizure|October 12, 2022
Brivaracetam add-on treatment in pediatric patients with severe drug-resistant epilepsy: Italian real-world evidenceAngelo Russo, Jacopo Pruccoli, Carlo Alberto Cesaroni, et al.
Epilepsia Open|September 9, 2022
Effectiveness of perampanel as the only add-on: Retrospective, multicenter, observational real-life study on epilepsy patientsSara Gasparini, Edoardo Ferlazzo, Sabrina Neri, et al.
Epilepsia Open|August 23, 2024
Italian report on RARE epilepsies (i-RARE): A consensus on multidisciplinarityAntonella Riva, Antonietta Coppola, Francesca Bisulli, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Pathogenic variants in TMEM184B cause a neurodevelopmental syndrome via alteration of metabolic signalingKimberly A Chapman, Farid Ullah, Zachary A Yahiku, et al.
Epilepsy Research|May 7, 2011
A clinical and genetic study of 33 new cases with early-onset absence epilepsyLucio Giordano, Aglaia Vignoli, Patrizia Accorsi, et al.
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