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Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy".
Vetri L, Calì F, Vinci M, Amato C, Roccella M, Granata T, Freri E, Solazzi R, Romano V, Elia M. Vetri L, et al. Among authors: freri e. Neuropediatrics. 2021 Apr;52(2):153. doi: 10.1055/s-0040-1716904. Epub 2020 Oct 27. Neuropediatrics. 2021. PMID: 33111300 No abstract available.
Schizencephaly: clinical spectrum, epilepsy, and pathogenesis.
Granata T, Freri E, Caccia C, Setola V, Taroni F, Battaglia G. Granata T, et al. Among authors: freri e. J Child Neurol. 2005 Apr;20(4):313-8. doi: 10.1177/08830738050200040801. J Child Neurol. 2005. PMID: 15921232 Review.
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.
Mancardi MM, Striano P, Gennaro E, Madia F, Paravidino R, Scapolan S, Dalla Bernardina B, Bertini E, Bianchi A, Capovilla G, Darra F, Elia M, Freri E, Gobbi G, Granata T, Guerrini R, Pantaleoni C, Parmeggiani A, Romeo A, Santucci M, Vecchi M, Veggiotti P, Vigevano F, Pistorio A, Gaggero R, Zara F. Mancardi MM, et al. Among authors: freri e. Epilepsia. 2006 Oct;47(10):1629-35. doi: 10.1111/j.1528-1167.2006.00641.x. Epilepsia. 2006. PMID: 17054684 Free article.
ICTAL EEG fast activity in West syndrome: from onset to outcome.
Panzica F, Binelli S, Canafoglia L, Casazza M, Freri E, Granata T, Avanzini G, Franceschetti S. Panzica F, et al. Among authors: freri e. Epilepsia. 2007 Nov;48(11):2101-10. doi: 10.1111/j.1528-1167.2007.01264.x. Epub 2007 Sep 6. Epilepsia. 2007. PMID: 17825076 Free article.
Hemispherotomy and functional hemispherectomy: indications and outcome.
Marras CE, Granata T, Franzini A, Freri E, Villani F, Casazza M, De Curtis M, Ragona F, Ferroli P, D'Incerti L, Pincherle A, Spreafico R, Broggi G. Marras CE, et al. Among authors: freri e. Epilepsy Res. 2010 Mar;89(1):104-12. doi: 10.1016/j.eplepsyres.2009.09.006. Epub 2009 Nov 1. Epilepsy Res. 2010. PMID: 19883995
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
Ragona F, Granata T, Dalla Bernardina B, Offredi F, Darra F, Battaglia D, Morbi M, Brazzo D, Cappelletti S, Chieffo D, De Giorgi I, Fontana E, Freri E, Marini C, Toraldo A, Specchio N, Veggiotti P, Vigevano F, Guerrini R, Guzzetta F, Dravet C. Ragona F, et al. Among authors: freri e. Epilepsia. 2011 Feb;52(2):386-92. doi: 10.1111/j.1528-1167.2010.02925.x. Epub 2011 Jan 26. Epilepsia. 2011. PMID: 21269283 Free article.
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy.
Busolin G, Malacrida S, Bisulli F, Striano P, Di Bonaventura C, Egeo G, Pasini E, Cianci V, Ferlazzo E, Bianchi A, Coppola G, Elia M, Mecarelli O, Gobbi G, Casellato S, Marchini M, Binelli S, Freri E, Granata T, Posar A, Parmeggiani A, Vigliano P, Boniver C, Aguglia U, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Busolin G, et al. Among authors: freri e. Epilepsy Res. 2011 Mar;94(1-2):110-6. doi: 10.1016/j.eplepsyres.2011.01.010. Epub 2011 Feb 18. Epilepsy Res. 2011. PMID: 21333500
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