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Appropriate use of generic and branded antiseizure medications in epilepsy: Updated recommendations from the Italian League Against Epilepsy (LICE).
Roberti R, Casarella A, Iudice A, La Neve A, Beghi E, Capovilla G, Di Bonaventura C, Giorgi FS, Grosso S, Iannone LF, Romigi A, Specchio LM, Zaccara G, Mecarelli O, Russo E; Antiseizure Medications Commission of the Italian League against Epilepsy LICE. Roberti R, et al. Among authors: di bonaventura c. Epilepsy Behav. 2021 Mar;116:107804. doi: 10.1016/j.yebeh.2021.107804. Epub 2021 Feb 10. Epilepsy Behav. 2021. PMID: 33581599 Review.
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome).
Striano P, Sofia V, Capovilla G, Rubboli G, Di Bonaventura C, Coppola A, Vitale G, Fontanillas L, Giallonardo AT, Biondi R, Romeo A, Viri M, Zara F, Striano S. Striano P, et al. Among authors: di bonaventura c. Epilepsia. 2008 Mar;49(3):425-30. doi: 10.1111/j.1528-1167.2007.01524.x. Epub 2008 Jan 29. Epilepsia. 2008. PMID: 18248445 Free article. Clinical Trial.
Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy.
Specchio N, Boero G, Michelucci R, Gambardella A, Giallonardo AT, Fattouch J, Di Bonaventura C, de Palo A, Ladogana M, Lamberti P, Vigevano F, La Neve A, Specchio LM. Specchio N, et al. Among authors: di bonaventura c. Epilepsia. 2008 Apr;49(4):663-9. doi: 10.1111/j.1528-1167.2007.01523.x. Epub 2008 Feb 5. Epilepsia. 2008. PMID: 18266754 Free article. Clinical Trial.
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
Diani E, Di Bonaventura C, Mecarelli O, Gambardella A, Elia M, Bovo G, Bisulli F, Pinardi F, Binelli S, Egeo G, Castellotti B, Striano P, Striano S, Bianchi A, Ferlazzo E, Vianello V, Coppola G, Aguglia U, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Diani E, et al. Among authors: di bonaventura c. Epilepsy Res. 2008 Jul;80(1):1-8. doi: 10.1016/j.eplepsyres.2008.03.001. Epub 2008 Apr 28. Epilepsy Res. 2008. PMID: 18440780
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy.
Busolin G, Malacrida S, Bisulli F, Striano P, Di Bonaventura C, Egeo G, Pasini E, Cianci V, Ferlazzo E, Bianchi A, Coppola G, Elia M, Mecarelli O, Gobbi G, Casellato S, Marchini M, Binelli S, Freri E, Granata T, Posar A, Parmeggiani A, Vigliano P, Boniver C, Aguglia U, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Busolin G, et al. Among authors: di bonaventura c. Epilepsy Res. 2011 Mar;94(1-2):110-6. doi: 10.1016/j.eplepsyres.2011.01.010. Epub 2011 Feb 18. Epilepsy Res. 2011. PMID: 21333500
Recurrent partial seizures with ictal yawning as atypical presentation of Hashimoto's encephalopathy (steroid-responsive encephalopathy associated with autoimmune thyroiditis).
Casciato S, Di Bonaventura C, Lapenta L, Fattouch J, Ferrazzano G, Fanella M, Di Fabio F, Pasquini M, Amendolea MA, Manfredi M, Prencipe M, Giallonardo AT. Casciato S, et al. Among authors: di bonaventura c, di fabio f. Epilepsy Behav. 2011 Dec;22(4):799-803. doi: 10.1016/j.yebeh.2011.09.023. Epub 2011 Oct 24. Epilepsy Behav. 2011. PMID: 22030535
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy.
Rigon L, Vettori A, Busolin G, Egeo G, Pulitano P, Santulli L, Pasini E, Striano P, la Neve A, Vianello Dri V, Boniver C, Gambardella A, Banfi P, Binelli S, Di Bonaventura C, Striano S, de Falco F, Giallonardo AT, Mecarelli O, Michelucci R, Nobile C. Rigon L, et al. Among authors: di bonaventura c. Epilepsy Res Treat. 2011;2011:258365. doi: 10.1155/2011/258365. Epub 2010 Dec 21. Epilepsy Res Treat. 2011. PMID: 22937229 Free PMC article.
187 results