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Items: 7

1.

Video-polygraphy in Rett syndrome.

d'Orsi G, La Selva L, Specchio LM.

Pediatr Neurol. 2014 Feb;50(2):e5. doi: 10.1016/j.pediatrneurol.2013.07.006. Epub 2013 Nov 20. No abstract available.

PMID:
24269129
2.

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.

Epilepsy Behav. 2012 Nov;25(3):401-7. doi: 10.1016/j.yebeh.2012.08.033. Epub 2012 Oct 26.

PMID:
23103540
3.

Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children.

Vignoli A, Canevini MP, Darra F, La Selva L, Fiorini E, Piazzini A, Lazzarotto F, Zucca C, Dalla Bernardina B.

Epilepsia. 2009 Nov;50(11):2420-7. doi: 10.1111/j.1528-1167.2009.02176.x. Epub 2009 Jul 2.

4.

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.

Neurology. 2003 Jun 24;60(12):1961-7.

PMID:
12821740
5.

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.

Epilepsy Res. 2003 Mar;53(3):196-200.

PMID:
12694927
6.

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.

Epilepsia. 1994 Nov-Dec;35(6):1187-93.

PMID:
7988509
7.

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.

Neuropediatrics. 1989 Nov;20(4):223-9. Review.

PMID:
2514400

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