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Page 1
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.
Cerulli Irelli E, Cocchi E, Ramantani G, Riva A, Caraballo RH, Morano A, Giuliano L, Yilmaz T, Panagiotakaki E, Operto FF, Giraldez BG, Balestrini S, Silvennoinen K, Casciato S, Comajuan M, Fortunato F, Giallonardo AT, Gamirova R, Coppola A, Di Gennaro G, Labate A, Sofia V, Kluger GJ, Gambardella A, Kasteleijn-Nolst Trenite D, Baykan B, Sisodiya SM, Arzimanoglou A, Striano P, Di Bonaventura C; EMA study group. Cerulli Irelli E, et al. Among authors: fortunato f. Epilepsia. 2022 Oct 28. doi: 10.1111/epi.17450. Online ahead of print. Epilepsia. 2022. PMID: 36307934
A familial t(4;8) translocation segregates with epilepsy and migraine with aura.
Crippa M, Malatesta P, Bonati MT, Trapasso F, Fortunato F, Annesi G, Larizza L, Labate A, Finelli P, Perrotti N, Gambardella A. Crippa M, et al. Among authors: fortunato f. Ann Clin Transl Neurol. 2020 May;7(5):855-859. doi: 10.1002/acn3.51040. Epub 2020 Apr 21. Ann Clin Transl Neurol. 2020. PMID: 32315120 Free PMC article.
Focal neuromyotonia associated with a C9ORF72 expansion mutation.
Fortunato F, Bonapace G, Gullace R, Gagliardi M, Nisticò R, Valentino P, Gambardella A. Fortunato F, et al. Muscle Nerve. 2020 Oct;62(4):E63-E65. doi: 10.1002/mus.27009. Epub 2020 Aug 5. Muscle Nerve. 2020. PMID: 32578243 No abstract available.
392 results