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Protocadherin 19 mutations in girls with infantile-onset epilepsy.
Marini C, Mei D, Parmeggiani L, Norci V, Calado E, Ferrari A, Moreira A, Pisano T, Specchio N, Vigevano F, Battaglia D, Guerrini R. Marini C, et al. Among authors: specchio n. Neurology. 2010 Aug 17;75(7):646-53. doi: 10.1212/WNL.0b013e3181ed9e67. Neurology. 2010. PMID: 20713952
Therapeutic approach to epileptic encephalopathies.
Vigevano F, Arzimanoglou A, Plouin P, Specchio N. Vigevano F, et al. Among authors: specchio n. Epilepsia. 2013 Nov;54 Suppl 8:45-50. doi: 10.1111/epi.12423. Epilepsia. 2013. PMID: 24571117 Free article. Review.
Epilepsy in patients with duplications of chromosome 14 harboring FOXG1.
Pontrelli G, Cappelletti S, Claps D, Sirleto P, Ciocca L, Petrocchi S, Terracciano A, Serino D, Fusco L, Vigevano F, Specchio N. Pontrelli G, et al. Among authors: specchio n. Pediatr Neurol. 2014 May;50(5):530-5. doi: 10.1016/j.pediatrneurol.2014.01.022. Epub 2014 Jan 11. Pediatr Neurol. 2014. PMID: 24731847 Review.
Seizing control of epileptic activity can improve outcome.
Chapman KE, Specchio N, Shinnar S, Holmes GL. Chapman KE, et al. Among authors: specchio n. Epilepsia. 2015 Oct;56(10):1482-5. doi: 10.1111/epi.13109. Epub 2015 Aug 21. Epilepsia. 2015. PMID: 26293783 Free article. Review.
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations.
Cetica V, Chiari S, Mei D, Parrini E, Grisotto L, Marini C, Pucatti D, Ferrari A, Sicca F, Specchio N, Trivisano M, Battaglia D, Contaldo I, Zamponi N, Petrelli C, Granata T, Ragona F, Avanzini G, Guerrini R. Cetica V, et al. Among authors: specchio n. Neurology. 2017 Mar 14;88(11):1037-1044. doi: 10.1212/WNL.0000000000003716. Epub 2017 Feb 15. Neurology. 2017. PMID: 28202706 Free PMC article.
244 results