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Page 1
Myoclonus: Differential diagnosis and current management.
Riva A, D'Onofrio G, Ferlazzo E, Pascarella A, Pasini E, Franceschetti S, Panzica F, Canafoglia L, Vignoli A, Coppola A, Badioni V, Beccaria F, Labate A, Gambardella A, Romeo A, Capovilla G, Michelucci R, Striano P, Belcastro V. Riva A, et al. Among authors: capovilla g. Epilepsia Open. 2024 Apr;9(2):486-500. doi: 10.1002/epi4.12917. Epub 2024 Feb 9. Epilepsia Open. 2024. PMID: 38334331 Free PMC article. Review.
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
Canafoglia L, Gennaro E, Capovilla G, Gobbi G, Boni A, Beccaria F, Viri M, Michelucci R, Agazzi P, Assereto S, Coviello DA, Di Stefano M, Rossi Sebastiano D, Franceschetti S, Zara F. Canafoglia L, et al. Among authors: capovilla g. Epilepsia. 2012 Dec;53(12):2120-7. doi: 10.1111/j.1528-1167.2012.03718.x. Epilepsia. 2012. PMID: 23205931 Free article.
Relevance of clinical context in the diagnostic-therapeutic approach to status epilepticus.
Aguglia U, Sueri C, Gasparini S, Beghi E, Labate A, Gambardella A, Specchio LM, Ferlazzo E; Epilepsy Study Group of the Italian Neurological Society and of the Subcommission on Status Epilepticus of the Italian League Against Epilepsy. Aguglia U, et al. Epilepsia. 2016 Sep;57(9):1527-9. doi: 10.1111/epi.13475. Epilepsia. 2016. PMID: 27594403 Free article. No abstract available.
Photosensitive benign myoclonic epilepsy in infancy.
Capovilla G, Beccaria F, Gambardella A, Montagnini A, Avantaggiato P, Seri S. Capovilla G, et al. Epilepsia. 2007 Jan;48(1):96-100. doi: 10.1111/j.1528-1167.2006.00836.x. Epilepsia. 2007. PMID: 17241214 Free article.
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.
Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, LePiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria F, Annesi G, Striano S, Aguglia U, Guerrini R, Quattrone A. Annesi F, et al. Among authors: capovilla g. Epilepsia. 2007 Sep;48(9):1686-1690. doi: 10.1111/j.1528-1167.2007.01173.x. Epub 2007 Jul 18. Epilepsia. 2007. PMID: 17634063 Free article.
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.
Changes in Panayiotopoulos syndrome over time.
Capovilla G, Striano P, Beccaria F. Capovilla G, et al. Epilepsia. 2009 May;50 Suppl 5:45-8. doi: 10.1111/j.1528-1167.2009.02120.x. Epilepsia. 2009. PMID: 19469846 Free article. Review.
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.
The system epilepsies: a pathophysiological hypothesis.
Avanzini G, Manganotti P, Meletti S, Moshé SL, Panzica F, Wolf P, Capovilla G. Avanzini G, et al. Among authors: capovilla g. Epilepsia. 2012 May;53(5):771-8. doi: 10.1111/j.1528-1167.2012.03462.x. Epilepsia. 2012. PMID: 22533642 Free article. Review.
219 results