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Page 1
Language Delay in Patients with CLN2 Disease: Could It Support Earlier Diagnosis?
Nickel M, Gissen P, Greenaway R, Cappelletti S, Hamborg C, Ragni B, Ribitzki T, Schulz A, Tondo I, Specchio N. Nickel M, et al. Among authors: specchio n. Neuropediatrics. 2023 Dec;54(6):402-406. doi: 10.1055/s-0043-1770143. Epub 2023 Jun 17. Neuropediatrics. 2023. PMID: 37329878 Free PMC 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
Neonatal hemifacial spasm and fourth ventricle mass.
Specchio N, Trivisano M, Bernardi B, Marras CE, Faggioli R, Fiumana E, Cappelletti S, Delalande O, Vigevano F, Fusco L. Specchio N, et al. Dev Med Child Neurol. 2012 Aug;54(8):697-703. doi: 10.1111/j.1469-8749.2012.04247.x. Epub 2012 Apr 30. Dev Med Child Neurol. 2012. PMID: 22548445 Free article. Review.
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
Epilepsy in ring 14 chromosome syndrome.
Specchio N, Trivisano M, Serino D, Cappelletti S, Carotenuto A, Claps D, Marras CE, Fusco L, Elia M, Vigevano F. Specchio N, et al. Epilepsy Behav. 2012 Dec;25(4):585-92. doi: 10.1016/j.yebeh.2012.09.032. Epub 2012 Nov 14. Epilepsy Behav. 2012. PMID: 23159383 Review.
264 results