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Electrical status epilepticus during sleep in Mowat-Wilson syndrome.
Bonanni P, Negrin S, Volzone A, Zanotta N, Epifanio R, Zucca C, Osanni E, Petacchi E, Fabbro F. Bonanni P, et al. Among authors: epifanio r. Brain Dev. 2017 Oct;39(9):727-734. doi: 10.1016/j.braindev.2017.04.013. Epub 2017 May 10. Brain Dev. 2017. PMID: 28501473
Partial deletion of DEPDC5 in a child with focal epilepsy.
Bonaglia MC, Giorda R, Epifanio R, Bertuzzo S, Marelli S, Gerard M, Andrieux J, Zanotta N, Zucca C. Bonaglia MC, et al. Among authors: epifanio r. Epilepsia Open. 2016 Aug 25;1(3-4):140-144. doi: 10.1002/epi4.12012. eCollection 2016 Dec. Epilepsia Open. 2016. PMID: 29588938 Free PMC article.
Novel epilepsy phenotype associated to a known SCN8A mutation.
Epifanio R, Zanotta N, Giorda R, Bardoni A, Zucca C. Epifanio R, et al. Seizure. 2019 Apr;67:15-17. doi: 10.1016/j.seizure.2019.01.017. Epub 2019 Mar 4. Seizure. 2019. PMID: 30851583 Free article. No abstract available.
Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
Zucca C, Redaelli F, Epifanio R, Zanotta N, Romeo A, Lodi M, Veggiotti P, Airoldi G, Panzeri C, Romaniello R, De Polo G, Bonanni P, Cardinali S, Baschirotto C, Martorell L, Borgatti R, Bresolin N, Bassi MT. Zucca C, et al. Among authors: epifanio r. Arch Neurol. 2008 Apr;65(4):489-94. doi: 10.1001/archneur.65.4.489. Arch Neurol. 2008. PMID: 18413471 Free article.
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature.
Vignoli A, Borgatti R, Peron A, Zucca C, Ballarati L, Bonaglia C, Bellini M, Giordano L, Romaniello R, Bedeschi MF, Epifanio R, Russo S, Caselli R, Giardino D, Darra F, La Briola F, Banderali G, Canevini MP. Vignoli A, et al. Among authors: epifanio r. Epilepsia. 2012 Jul;53(7):1146-55. doi: 10.1111/j.1528-1167.2012.03501.x. Epub 2012 May 11. Epilepsia. 2012. PMID: 22578097 Free article. Review.
32 results