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The ENIGMA-Epilepsy working group: Mapping disease from large data sets.
Sisodiya SM, Whelan CD, Hatton SN, Huynh K, Altmann A, Ryten M, Vezzani A, Caligiuri ME, Labate A, Gambardella A, Ives-Deliperi V, Meletti S, Munsell BC, Bonilha L, Tondelli M, Rebsamen M, Rummel C, Vaudano AE, Wiest R, Balachandra AR, Bargalló N, Bartolini E, Bernasconi A, Bernasconi N, Bernhardt B, Caldairou B, Carr SJA, Cavalleri GL, Cendes F, Concha L, Desmond PM, Domin M, Duncan JS, Focke NK, Guerrini R, Hamandi K, Jackson GD, Jahanshad N, Kälviäinen R, Keller SS, Kochunov P, Kowalczyk MA, Kreilkamp BAK, Kwan P, Lariviere S, Lenge M, Lopez SM, Martin P, Mascalchi M, Moreira JCV, Morita-Sherman ME, Pardoe HR, Pariente JC, Raviteja K, Rocha CS, Rodríguez-Cruces R, Seeck M, Semmelroch MKHG, Sinclair B, Soltanian-Zadeh H, Stein DJ, Striano P, Taylor PN, Thomas RH, Thomopoulos SI, Velakoulis D, Vivash L, Weber B, Yasuda CL, Zhang J, Thompson PM, McDonald CR; ENIGMA Consortium Epilepsy Working Group. Sisodiya SM, et al. Among authors: striano p. Hum Brain Mapp. 2020 May 29;43(1):113-28. doi: 10.1002/hbm.25037. Online ahead of print. Hum Brain Mapp. 2020. PMID: 32468614 Free PMC article. Review.
Neuroimaging and neuropathology of Dravet syndrome.
Guerrini R, Striano P, Catarino C, Sisodiya SM. Guerrini R, et al. Among authors: striano p. Epilepsia. 2011 Apr;52 Suppl 2:30-4. doi: 10.1111/j.1528-1167.2011.02998.x. Epilepsia. 2011. PMID: 21463276 Free article. Review.
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Zumsteg D, Duncan S, Kälviäinen RK, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Théâtre E, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Chaves J, Costa PP, Silva BM, da Silva AM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Rössler K, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME; UK Brain Expression Consortium; Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM. Kasperaviciute D, et al. Among authors: striano p. Brain. 2013 Oct;136(Pt 10):3140-50. doi: 10.1093/brain/awt233. Epub 2013 Sep 6. Brain. 2013. PMID: 24014518 Free PMC article.
The α2B-adrenergic receptor is mutant in cortical myoclonus and epilepsy.
De Fusco M, Vago R, Striano P, Di Bonaventura C, Zara F, Mei D, Kim MS, Muallem S, Chen Y, Wang Q, Guerrini R, Casari G. De Fusco M, et al. Among authors: striano p. Ann Neurol. 2014 Jan;75(1):77-87. doi: 10.1002/ana.24028. Epub 2014 Jan 2. Ann Neurol. 2014. PMID: 24114805 Free PMC article.
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
Mumoli L, Tarantino P, Michelucci R, Bianchi A, Labate A, Franceschetti S, Marini C, Striano P, Gagliardi M, Ferlazzo E, Sofia V, Pennese L, Annesi G, Aguglia U, Guerrini R, Zara F, Gambardella A; Genetic Commission, Italian League Against Epilepsy. Mumoli L, et al. Among authors: striano p. Epilepsia. 2015 Apr;56(4):e40-3. doi: 10.1111/epi.12944. Epub 2015 Mar 6. Epilepsia. 2015. PMID: 25752200 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: striano s. Epilepsia. 2015 Oct;56(10):e168-71. doi: 10.1111/epi.13094. Epub 2015 Jul 27. Epilepsia. 2015. PMID: 26216793 Free article.
Genetics of reflex seizures and epilepsies in humans and animals.
Italiano D, Striano P, Russo E, Leo A, Spina E, Zara F, Striano S, Gambardella A, Labate A, Gasparini S, Lamberti M, De Sarro G, Aguglia U, Ferlazzo E. Italiano D, et al. Among authors: striano p, striano s. Epilepsy Res. 2016 Mar;121:47-54. doi: 10.1016/j.eplepsyres.2016.01.010. Epub 2016 Feb 2. Epilepsy Res. 2016. PMID: 26875109 Review.
Dravet syndrome: Not just epilepsy.
Guerrini R, Striano P. Guerrini R, et al. Among authors: striano p. Neurology. 2016 Jul 19;87(3):245-6. doi: 10.1212/WNL.0000000000002873. Epub 2016 Jun 17. Neurology. 2016. PMID: 27316245 No abstract available.
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors.
Ferlazzo E, Gasparini S, Beghi E, Sueri C, Russo E, Leo A, Labate A, Gambardella A, Belcastro V, Striano P, Paciaroni M, Pisani LR, Aguglia U; Epilepsy Study Group of the Italian Neurological Society. Ferlazzo E, et al. Among authors: striano p. Epilepsia. 2016 Aug;57(8):1205-14. doi: 10.1111/epi.13448. Epub 2016 Jul 6. Epilepsia. 2016. PMID: 27381481 Free article. Review.
815 results