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Telephone-induced seizures: a new type of reflex epilepsy.
Michelucci R, Gardella E, de Haan GJ, Bisulli F, Zaniboni A, Cantalupo G, Alberto Tassinari C, Tinuper P, Nobile C, Nichelli P, Kasteleijn-Nolst Trenité DG. Michelucci R, et al. Epilepsia. 2004 Mar;45(3):280-3. doi: 10.1111/j.0013-9580.2004.39703.x. Epilepsia. 2004. PMID: 15009231 Free article.
Genetics of epilepsy and relevance to current practice.
Michelucci R, Pasini E, Riguzzi P, Volpi L, Dazzo E, Nobile C. Michelucci R, et al. Curr Neurol Neurosci Rep. 2012 Aug;12(4):445-55. doi: 10.1007/s11910-012-0281-8. Curr Neurol Neurosci Rep. 2012. PMID: 22618127 Review.
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
Michelucci R, Pasini E, Malacrida S, Striano P, Bonaventura CD, Pulitano P, Bisulli F, Egeo G, Santulli L, Sofia V, Gambardella A, Elia M, de Falco A, Neve Al, Banfi P, Coppola G, Avoni P, Binelli S, Boniver C, Pisano T, Marchini M, Dazzo E, Fanciulli M, Bartolini Y, Riguzzi P, Volpi L, de Falco FA, Giallonardo AT, Mecarelli O, Striano S, Tinuper P, Nobile C. Michelucci R, et al. Epilepsia. 2013 Jul;54(7):1288-97. doi: 10.1111/epi.12194. Epub 2013 Apr 26. Epilepsia. 2013. PMID: 23621105 Free article.
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.
Striano P, Serioli E, Santulli L, Manna I, Labate A, Dazzo E, Pasini E, Gambardella A, Michelucci R, Striano S, Nobile C. Striano P, et al. Among authors: michelucci r. Epilepsia. 2015 Oct;56(10):e168-71. doi: 10.1111/epi.13094. Epub 2015 Jul 27. Epilepsia. 2015. PMID: 26216793 Free article.
In response: DEPDC5 mutations in epilepsy with auditory features.
Striano P, Michelucci R, Striano S, Nobile C. Striano P, et al. Among authors: michelucci r. Epilepsia. 2016 Feb;57(2):336; discussion 336-7. doi: 10.1111/epi.13255. Epilepsia. 2016. PMID: 26849479 Free article. No abstract available.
CNTNAP2 mutations and autosomal dominant epilepsy with auditory features.
Leonardi E, Dazzo E, Aspromonte MC, Tabaro F, Pascarelli S, Tosatto SCE, Michelucci R, Murgia A, Nobile C. Leonardi E, et al. Among authors: michelucci r. Epilepsy Res. 2018 Jan;139:51-53. doi: 10.1016/j.eplepsyres.2017.11.006. Epub 2017 Nov 21. Epilepsy Res. 2018. PMID: 29179159
Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy.
Dazzo E, Rehberg K, Michelucci R, Passarelli D, Boniver C, Vianello Dri V, Striano P, Striano S, Pasterkamp RJ, Nobile C. Dazzo E, et al. Among authors: michelucci r. Ann Neurol. 2018 Mar;83(3):483-493. doi: 10.1002/ana.25167. Epub 2018 Mar 13. Ann Neurol. 2018. PMID: 29394500
215 results