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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.
Italian Journal of Pediatrics|April 18, 2024
Adolescent gender dysphoria management: position paper from the Italian Academy of Pediatrics, the Italian Society of Pediatrics, the Italian Society for Pediatric Endocrinology and Diabetes, the Italian Society of Adolescent Medicine and the Italian Society of Child and Adolescent NeuropsychiatryValeria Calcaterra, Gianluca Tornese, Gianvincenzo Zuccotti, et al.
Epilepsia|February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history studyIngrid E Scheffer, M Scott Perry, Joseph Sullivan, 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.
American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Epilepsia Open|September 11, 2020
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study groupJoerg Klepper, Cigdem Akman, Marisa Armeno, et al.
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