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Page 1
Rud syndrome with focal cortical dysplasia: a case report.
Marconi S, Cantalupo G, Marliani F, Toni F, Capovilla G, Lorenzetti E, Romeo A, Michelucci R, Rubboli G. Marconi S, et al. Among authors: capovilla g. Brain Dev. 2011 Sep;33(8):683-6. doi: 10.1016/j.braindev.2010.10.011. Epub 2010 Nov 12. Brain Dev. 2011. PMID: 21074957
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: capovilla g. 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.
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myoclonia.
Capovilla G, Striano P, Gambardella A, Beccaria F, Hirsch E, Casellato S, Romeo A, Rubboli G, Sofia V, Teutonico F, Valenti MP, Striano S. Capovilla G, et al. Epilepsia. 2009 Jun;50(6):1536-41. doi: 10.1111/j.1528-1167.2008.02002.x. Epub 2009 May 20. Epilepsia. 2009. PMID: 19490056 Free article.
223 results