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211 results

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Page 1
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy.
Bovo G, Diani E, Bisulli F, Di Bonaventura C, Striano P, Gambardella A, Ferlazzo E, Egeo G, Mecarelli O, Elia M, Bianchi A, Bortoluzzi S, Vettori A, Aguglia U, Binelli S, De Falco A, Coppola G, Gobbi G, Sofia V, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Bovo G, et al. Among authors: ferlazzo e. Neurosci Lett. 2008 May 2;436(1):23-6. doi: 10.1016/j.neulet.2008.02.045. Epub 2008 Mar 4. Neurosci Lett. 2008. PMID: 18355961
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
Diani E, Di Bonaventura C, Mecarelli O, Gambardella A, Elia M, Bovo G, Bisulli F, Pinardi F, Binelli S, Egeo G, Castellotti B, Striano P, Striano S, Bianchi A, Ferlazzo E, Vianello V, Coppola G, Aguglia U, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Diani E, et al. Among authors: ferlazzo e. Epilepsy Res. 2008 Jul;80(1):1-8. doi: 10.1016/j.eplepsyres.2008.03.001. Epub 2008 Apr 28. Epilepsy Res. 2008. PMID: 18440780
Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy.
Busolin G, Malacrida S, Bisulli F, Striano P, Di Bonaventura C, Egeo G, Pasini E, Cianci V, Ferlazzo E, Bianchi A, Coppola G, Elia M, Mecarelli O, Gobbi G, Casellato S, Marchini M, Binelli S, Freri E, Granata T, Posar A, Parmeggiani A, Vigliano P, Boniver C, Aguglia U, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Busolin G, et al. Among authors: ferlazzo e. Epilepsy Res. 2011 Mar;94(1-2):110-6. doi: 10.1016/j.eplepsyres.2011.01.010. Epub 2011 Feb 18. Epilepsy Res. 2011. PMID: 21333500
Progressive myoclonic epilepsies: definitive and still undetermined causes.
Franceschetti S, Michelucci R, Canafoglia L, Striano P, Gambardella A, Magaudda A, Tinuper P, La Neve A, Ferlazzo E, Gobbi G, Giallonardo AT, Capovilla G, Visani E, Panzica F, Avanzini G, Tassinari CA, Bianchi A, Zara F; Collaborative LICE study group on PMEs. Franceschetti S, et al. Among authors: ferlazzo e. Neurology. 2014 Feb 4;82(5):405-11. doi: 10.1212/WNL.0000000000000077. Epub 2014 Jan 2. Neurology. 2014. PMID: 24384641 Free PMC article.
Mild Lafora disease: clinical, neurophysiologic, and genetic findings.
Ferlazzo E, Canafoglia L, Michelucci R, Gambardella A, Gennaro E, Pasini E, Riguzzi P, Plasmati R, Volpi L, Labate A, Gasparini S, Villani F, Casazza M, Viri M, Zara F, Minassian BA, Turnbull J, Serratosa JM, Guerrero-López R, Franceschetti S, Aguglia U. Ferlazzo E, et al. Epilepsia. 2014 Dec;55(12):e129-33. doi: 10.1111/epi.12806. Epub 2014 Sep 30. Epilepsia. 2014. PMID: 25270369 Free article.
An educational campaign about epilepsy among Italian primary school teachers. 2. The results of a focused training program.
Mecarelli O, Messina P, Capovilla G, Michelucci R, Romeo A, Beghi E; Epischool Collaborative Group of the Lega Italiana contro l'Epilessia (LICE); De Simone R, Cerquiglini A, Vecchi M, Boniver C, Monti F, Ferlazzo E, Gasparini S, Baldassarri C, Cesaroni E, Stranci G, Elia M, Severi S, Pizzanelli C, Ausserer H, Montalenti E, Pieri I, Germano M, Cantisani T, Casellato S, Pruna D. Mecarelli O, et al. Among authors: ferlazzo e. Epilepsy Behav. 2015 Jan;42:93-7. doi: 10.1016/j.yebeh.2014.07.022. Epub 2014 Dec 12. Epilepsy Behav. 2015. PMID: 25500360
Validation Study of Italian Version of Inventory for Déjà Vu Experiences Assessment (I-IDEA): A Screening Tool to Detect Déjà Vu Phenomenon in Italian Healthy Individuals.
Mumoli L, Tripepi G, Aguglia U, Augimeri A, Baggetta R, Bisulli F, Bruni A, Cavalli SM, D'Aniello A, Daniele O, Di Bonaventura C, Di Gennaro G, Fattouch J, Ferlazzo E, Ferrari A, Giallonardo A, Gasparini S, Nigro S, Romigi A, Sofia V, Tinuper P, Vaccaro MG, Zummo L, Quattrone A, Gambardella A, Labate A. Mumoli L, et al. Among authors: ferlazzo e. Behav Sci (Basel). 2017 Aug 7;7(3):50. doi: 10.3390/bs7030050. Behav Sci (Basel). 2017. PMID: 28783090 Free PMC article.
211 results