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SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
Marini C, Scheffer IE, Nabbout R, Mei D, Cox K, Dibbens LM, McMahon JM, Iona X, Carpintero RS, Elia M, Cilio MR, Specchio N, Giordano L, Striano P, Gennaro E, Cross JH, Kivity S, Neufeld MY, Afawi Z, Andermann E, Keene D, Dulac O, Zara F, Berkovic SF, Guerrini R, Mulley JC. Marini C, et al. Among authors: specchio n. Epilepsia. 2009 Jul;50(7):1670-8. doi: 10.1111/j.1528-1167.2009.02013.x. Epub 2009 Mar 12. Epilepsia. 2009. PMID: 19400878 Free article.
Childhood refractory focal epilepsy following acute febrile encephalopathy.
Specchio N, Fusco L, Claps D, Trivisano M, Longo D, Cilio MR, Valeriani M, Cusmai R, Cappelletti S, Gentile S, Fariello G, Specchio LM, Vigevano F. Specchio N, et al. Among authors: specchio lm. Eur J Neurol. 2011 Jul;18(7):952-61. doi: 10.1111/j.1468-1331.2010.03253.x. Epub 2010 Nov 18. Eur J Neurol. 2011. PMID: 21087361
PRRT2 is mutated in familial and non-familial benign infantile seizures.
Specchio N, Terracciano A, Trivisano M, Cappelletti S, Claps D, Travaglini L, Cusmai R, Marras CE, Zara F, Fusco L, Bertini E, Vigevano F. Specchio N, et al. Eur J Paediatr Neurol. 2013 Jan;17(1):77-81. doi: 10.1016/j.ejpn.2012.07.006. Epub 2012 Aug 17. Eur J Paediatr Neurol. 2013. PMID: 22902423
Acute intralesional recording in hypothalamic hamartoma: description of 4 cases.
Specchio N, Rizzi M, Trivisano M, Fusco L, Rebessi E, Cappelletti S, De Palma L, Villani F, Savioli A, De Benedictis A, Marras CE, Vigevano F, Delalande O. Specchio N, et al. Acta Neurol Belg. 2015 Sep;115(3):233-9. doi: 10.1007/s13760-014-0374-z. Epub 2014 Oct 10. Acta Neurol Belg. 2015. PMID: 25300188
244 results