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Clinical Genetics|July 23, 2021
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype-phenotype spectrum and functional impact on GPI-anchored proteinsSmrithi Salian, Marcello Scala, Thi Tuyet Mai Nguyen, et al.Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 27, 2021
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsiesSimona Balestrini, Daniela Chiarello, Maria Gogou, et al.Epilepsia|March 17, 2022
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetamCiarán Campbell, Mark McCormack, Sonn Patel, et al.Epilepsy Research|February 22, 2011
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsyGiorgia Busolin, Sandro Malacrida, Francesca Bisulli, et al.Epilepsia|September 17, 2013
Clinical dissection of early onset absence epilepsy in children and prognostic implicationsSergio Agostinelli, Patrizia Accorsi, Francesca Beccaria, et al.Epilepsia|March 31, 2023
Long-term effectiveness of add-on perampanel in patients with Lennox-Gastaut syndrome: A multicenter retrospective studySara Matricardi, Elisabetta Cesaroni, Paolo Bonanni, et al.Human Genetics|July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.Epilepsia|March 27, 2007
Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlationsPasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, et al.Pageof 68