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103 results

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Page 1
Ketogenic dietary therapies in epilepsy: recommendations of the Italian League against Epilepsy Dietary Therapy Study Group.
De Giorgis V, Tagliabue A, Bisulli F, Brambilla I, Camerini A, Cusmai R, Darra F, Dianin A, Domenica E, Lodi MAM, Matricardi S, Messana T, Operto F, Ragona F, Russo E, Varesio C, Volpi L, Zanaboni MP, Pasca L, Veggiotti P. De Giorgis V, et al. Among authors: darra f. Front Neurol. 2023 Jul 10;14:1215618. doi: 10.3389/fneur.2023.1215618. eCollection 2023. Front Neurol. 2023. PMID: 37497012 Free PMC article.
Gelastic seizures and "smiling spasms": A peculiar ictal pattern.
Lo Barco T, Corona L, Solazzi R, Fiorini E, Galati G, Cossu A, Proietti J, Francione S, Dalla Bernardina B, Darra F, Cantalupo G. Lo Barco T, et al. Among authors: darra f. Epileptic Disord. 2023 Apr;25(2):269-273. doi: 10.1002/epd2.20012. Epub 2023 May 16. Epileptic Disord. 2023. PMID: 37194193 No abstract available.
Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey.
Cossu A, Lo Barco T, Proietti J, Dalla Bernardina B, Cantalupo G, Ghobert L, Brambilla I, Giarola E, Costa A, De Benito T, Bethge S, Cardot S, Montwill I, Remonato E, Gramaglia S, Darra F. Cossu A, et al. Among authors: darra f. Epilepsy Behav. 2023 May;142:109153. doi: 10.1016/j.yebeh.2023.109153. Epub 2023 Mar 28. Epilepsy Behav. 2023. PMID: 36989566 Free article.
Adaptive behaviour in adolescents and adults with Dravet syndrome.
Lo Barco T, Offredi F, Castino E, Proietti J, Cossu A, Fiorini E, Fontana E, Cantalupo G, Dalla Bernardina B, Darra F. Lo Barco T, et al. Among authors: darra f. Dev Med Child Neurol. 2023 Jun;65(6):838-846. doi: 10.1111/dmcn.15448. Epub 2022 Oct 31. Dev Med Child Neurol. 2023. PMID: 36316303 Free article.
Periventricular heterotopia in fragile X syndrome.
Moro F, Pisano T, Bernardina BD, Polli R, Murgia A, Zoccante L, Darra F, Battaglia A, Pramparo T, Zuffardi O, Guerrini R. Moro F, et al. Among authors: darra f. Neurology. 2006 Aug 22;67(4):713-5. doi: 10.1212/01.wnl.0000230223.51595.99. Neurology. 2006. PMID: 16924033
Familial Ohtahara syndrome due to a novel ARX gene mutation.
Giordano L, Sartori S, Russo S, Accorsi P, Galli J, Tiberti A, Bettella E, Marchi M, Vignoli A, Darra F, Murgia A, Bernardina BD. Giordano L, et al. Among authors: darra f. Am J Med Genet A. 2010 Dec;152A(12):3133-7. doi: 10.1002/ajmg.a.33701. Am J Med Genet A. 2010. PMID: 21108397 Free article.
Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome.
Lenge M, Balestrini S, Mei D, Macconi L, Caligiuri ME, Cuccarini V, Aquino D, Mazzi F, d'Incerti L, Darra F, Bernardina BD, Guerrini R. Lenge M, et al. Among authors: darra f. Cereb Cortex. 2023 Aug 8;33(16):9532-9541. doi: 10.1093/cercor/bhad224. Cereb Cortex. 2023. PMID: 37344172 Free PMC article.
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome.
Specchio N, Trivisano M, Lenge M, Ferretti A, Mei D, Parrini E, Napolitano A, Rossi-Espagnet C, Talenti G, Longo D, Proietti J, Ragona F, Freri E, Solazzi R, Granata T, Darra F, Bernardina BD, Vigevano F, Guerrini R. Specchio N, et al. Among authors: darra f. Cereb Cortex. 2023 Aug 23;33(17):9709-9717. doi: 10.1093/cercor/bhad235. Cereb Cortex. 2023. PMID: 37429835 Free PMC article.
Quantitative EEG biomarkers for STXBP1-related disorders.
Cossu A, Furia F, Proietti J, Ancora C, Reale C, Darra F, Previtali R, Bernardina BD, Rubboli G, Beniczky S, Møller RS, Cantalupo G, Gardella E. Cossu A, et al. Among authors: darra f. Epilepsia. 2024 Dec;65(12):3595-3606. doi: 10.1111/epi.18154. Epub 2024 Oct 28. Epilepsia. 2024. PMID: 39463124 Free PMC article.
103 results