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998 results

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Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox-Gastaut Syndrome.
Iannone LF, Arena G, Battaglia D, Bisulli F, Bonanni P, Boni A, Canevini MP, Cantalupo G, Cesaroni E, Contin M, Coppola A, Cordelli DM, Cricchiuti G, De Giorgis V, De Leva MF, De Rinaldis M, d'Orsi G, Elia M, Galimberti CA, Morano A, Granata T, Guerrini R, Lodi MAM, La Neve A, Marchese F, Masnada S, Michelucci R, Nosadini M, Pilolli N, Pruna D, Ragona F, Rosati A, Santucci M, Spalice A, Pietrafusa N, Striano P, Tartara E, Tassi L, Papa A, Zucca C, Russo E, Mecarelli O; CBD LICE Italy Study Group. Iannone LF, et al. Among authors: coppola a. Front Neurol. 2021 May 20;12:673135. doi: 10.3389/fneur.2021.673135. eCollection 2021. Front Neurol. 2021. PMID: 34093420 Free PMC article.
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy.
Striano P, Coppola A, Pezzella M, Ciampa C, Specchio N, Ragona F, Mancardi MM, Gennaro E, Beccaria F, Capovilla G, Rasmini P, Besana D, Coppola GG, Elia M, Granata T, Vecchi M, Vigevano F, Viri M, Gaggero R, Striano S, Zara F. Striano P, et al. Among authors: coppola gg, coppola a. Neurology. 2007 Jul 17;69(3):250-4. doi: 10.1212/01.wnl.0000265222.24102.db. Neurology. 2007. PMID: 17636062 Clinical Trial.
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.
Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R. Striano P, et al. Among authors: coppola a. J Neurol. 2008 Jan;255(1):16-23. doi: 10.1007/s00415-007-0653-1. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004642
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: coppola a. 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.
West syndrome associated with 14q12 duplications harboring FOXG1.
Striano P, Paravidino R, Sicca F, Chiurazzi P, Gimelli S, Coppola A, Robbiano A, Traverso M, Pintaudi M, Giovannini S, Operto F, Vigliano P, Granata T, Coppola G, Romeo A, Specchio N, Giordano L, Osborne LR, Gimelli G, Minetti C, Zara F. Striano P, et al. Among authors: coppola a, coppola g. Neurology. 2011 May 3;76(18):1600-2. doi: 10.1212/WNL.0b013e3182194bbf. Neurology. 2011. PMID: 21536641 No abstract available.
A clinical and genetic study of 33 new cases with early-onset absence epilepsy.
Giordano L, Vignoli A, Accorsi P, Galli J, Pezzella M, Traverso M, Battaglia S, Baglietto MG, Beccaria F, Cerminara C, Gambara S, Del Giudice E, Crichiutti G, Bisulli F, Pinci M, Tinuper P, Briatore E, Calzolari S, Coppola A, Canevini MP, Capovilla G, Striano S, Zara F, Minetti C, Striano P. Giordano L, et al. Among authors: coppola a. Epilepsy Res. 2011 Aug;95(3):221-6. doi: 10.1016/j.eplepsyres.2011.03.017. Epub 2011 May 4. Epilepsy Res. 2011. PMID: 21546213 Free article.
998 results