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Ictal haemodynamic changes in a patient affected by "subtle" Epilepsia Partialis Continua.
Vaudano AE, Di Bonaventura C, Carni M, Rodionov R, Lapenta L, Casciato S, Fattouch J, Egeo G, Pantano P, Nucciarelli V, Maraviglia B, Prencipe M, Lemieux L, Giallonardo AT. Vaudano AE, et al. Among authors: egeo g. Seizure. 2012 Jan;21(1):65-9. doi: 10.1016/j.seizure.2011.09.003. Epub 2011 Sep 29. Seizure. 2012. PMID: 21958459 Free article.
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy.
Rigon L, Vettori A, Busolin G, Egeo G, Pulitano P, Santulli L, Pasini E, Striano P, la Neve A, Vianello Dri V, Boniver C, Gambardella A, Banfi P, Binelli S, Di Bonaventura C, Striano S, de Falco F, Giallonardo AT, Mecarelli O, Michelucci R, Nobile C. Rigon L, et al. Among authors: egeo g. Epilepsy Res Treat. 2011;2011:258365. doi: 10.1155/2011/258365. Epub 2010 Dec 21. Epilepsy Res Treat. 2011. PMID: 22937229 Free PMC article.
Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings.
Di Bonaventura C, Carni M, Diani E, Fattouch J, Vaudano EA, Egeo G, Pantano P, Maraviglia B, Bozzao L, Manfredi M, Prencipe M, Giallonardo TA, Nobile C. Di Bonaventura C, et al. Among authors: egeo g. Epilepsia. 2009 Nov;50(11):2481-6. doi: 10.1111/j.1528-1167.2009.02181.x. Epub 2009 Jun 22. Epilepsia. 2009. PMID: 19552651 Free article.
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: egeo g. 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
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: egeo g. 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
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: egeo g. 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
Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy.
Di Bonaventura C, Operto FF, Busolin G, Egeo G, D'Aniello A, Vitello L, Smaniotto G, Furlan S, Diani E, Michelucci R, Giallonardo AT, Coppola G, Nobile C. Di Bonaventura C, et al. Among authors: egeo g. Epilepsia. 2011 Jul;52(7):1258-64. doi: 10.1111/j.1528-1167.2011.03071.x. Epub 2011 Apr 19. Epilepsia. 2011. PMID: 21504429 Free article.
94 results