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Epileptic seizures, movement disorders, and breathing disturbances in Rett syndrome: diagnostic relevance of video-polygraphy.
d'Orsi G, Trivisano M, Luisi C, Demaio V, Di Claudio MT, Pascarella MG, Sciruicchio V, Galeone D, La Neve A, Scarpelli F, Calvario T, Minervini M, La Selva L, Specchio LM. d'Orsi G, et al. Among authors: la selva l. Epilepsy Behav. 2012 Nov;25(3):401-7. doi: 10.1016/j.yebeh.2012.08.033. Epub 2012 Oct 26. Epilepsy Behav. 2012. PMID: 23103540
Video-polygraphy in Rett syndrome.
d'Orsi G, La Selva L, Specchio LM. d'Orsi G, et al. Among authors: la selva l. Pediatr Neurol. 2014 Feb;50(2):e5. doi: 10.1016/j.pediatrneurol.2013.07.006. Epub 2013 Nov 20. Pediatr Neurol. 2014. PMID: 24269129 No abstract available.
Imaging studies in partial epilepsy in children and adolescents.
Resta M, Palma M, Dicuonzo F, Spagnolo P, Specchio LM, Laneve A, Bellomo R, Lauriero F, La Selva L. Resta M, et al. Among authors: la selva l. Epilepsia. 1994 Nov-Dec;35(6):1187-93. doi: 10.1111/j.1528-1157.1994.tb01787.x. Epilepsia. 1994. PMID: 7988509
GM3 synthase deficiency in non-Amish patients.
Heide S, Jacquemont ML, Cheillan D, Renouil M, Tallot M, Schwartz CE, Miquel J, Bintner M, Rodriguez D, Darcel F, Buratti J, Haye D, Passemard S, Gras D, Perrin L, Capri Y, Gérard B, Piton A, Keren B, Thauvin-Robinet C, Duffourd Y, Faivre L, Poe C, Pervillé A, Héron D, Thévenon J, Arnaud L, LeGuern E, La Selva L, Vetro A, Guerrini R, Nava C, Mignot C. Heide S, et al. Among authors: la selva l. Genet Med. 2022 Feb;24(2):492-498. doi: 10.1016/j.gim.2021.10.007. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906476 Free article.
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F. Nabbout R, et al. Among authors: la selva l. Neurology. 2003 Jun 24;60(12):1961-7. doi: 10.1212/01.wnl.0000069463.41870.2f. Neurology. 2003. PMID: 12821740
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy.
Madia F, Gennaro E, Cecconi M, Buti D, Capovilla G, Dalla Bernardina B, Elia M, Ferrari A, Fontana E, Gaggero R, Giannotta M, Giordano L, Granata T, La Selva L, Luisa Lispi M, Santucci M, Vanadia F, Veggiotti P, Vigliano P, Viri M, Dagna Bricarelli F, Bianchi A, Zara F. Madia F, et al. Among authors: la selva l. Epilepsy Res. 2003 Mar;53(3):196-200. doi: 10.1016/s0920-1211(03)00022-6. Epilepsy Res. 2003. PMID: 12694927
Progressive myoclonic encephalopathy in X-linked hypogamma-globulinemia. Case report, review of the literature and its relationship with progressive encephalopathy in children with A.I.D.S.
Colamaria V, Marradi P, Boner A, Pajno-Ferrara F, Procacci C, Cesaro G, La Selva L, Capovilla G, Fontana E, Dalla Bernardina B. Colamaria V, et al. Among authors: la selva l. Neuropediatrics. 1989 Nov;20(4):223-9. doi: 10.1055/s-2008-1071298. Neuropediatrics. 1989. PMID: 2514400 Review.
First-aid management of tonic-clonic seizures among healthcare personnel: A survey by the Apulian section of the Italian League Against Epilepsy.
Martino T, Lalla A, Carapelle E, Di Claudio MT, Avolio C, d'Orsi G; #SorprenderEpilessia Collaborative Group of Apulian Section of Italian League Against Epilepsy (LICE). Martino T, et al. Epilepsy Behav. 2018 Mar;80:321-325. doi: 10.1016/j.yebeh.2017.11.017. Epub 2018 Feb 3. Epilepsy Behav. 2018. PMID: 29402633