FVEPs in Creutzfeldt–Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis

Autor: Visani, E., Agazzi, P., Scaioli, V., Giaccone, G., Binelli, S., Canafoglia, L., Panzica, F. ^*, Tagliavini, F., Bugiani, O., Avanzini, G., Franceschetti, S.

Publikováno v: In Clinical Neurophysiology 2005 116(4):895-904

Electroencephalographic features in a series of patients with neuronal ceroid lipofuscinoses.

Autor: Binelli, S., Canafoglia, L., Panzica, F., Pozzi, A., Francescheti, A.

Publikováno v: Neurological Sciences. Sep2000 Supplement 1, Vol. 21, pS83. 5p. 3 Diagrams.

Spectral and Coherence Analysis of EEG during Intermittent Photic Stimulation in Patients with Photosensitive Epilepsy

Autor: Visani, E., Varotto, G., Binelli, S., Fratello, L., Franceschetti, S., Avanzini, G., Panzica, F.

Publikováno v: Clinical Neurophysiology; Vol 121

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=ec_fp7health::b8d5cda5d9ba76b951abdba911e005da

Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy

Autor: 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, Nobile C. Bovo G, Giallonardo AT, Miche

Publikováno v: Neuroscience letters
436 (2008): 23–26.
info:cnr-pdr/source/autori: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, Nobile C. 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, Miche/titolo:Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy./doi:/rivista:Neuroscience letters (Print)/anno:2008/pagina_da:23/pagina_a:26/intervallo_pagine:23–26/volume:436

Autosomal dominant lateral temporal epilepsy (ADTLE) is a genetically transmitted epileptic syndrome characterized by focal seizures with predominant auditory symptoms likely originating from the lateral region of the temporal lobe. Mutations in codi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::cb94bd27642f1aae75ac1377190817f8
http://www.cnr.it/prodotto/i/170520

CONCORDANCE OF CLINICAL FORMS OF EPILEPSY IN FAMILIES WITH SEVERAL AFFECTED MEMBERS

Autor: BIANCHI A, AVANZINI G, DALLA BERNARDINA B, CANGER R, TASSINARI CA, VIGEVANO F, TIEZZI A, BUZZI G, FANI C, DEVERMANDOIS ROSSI C, ZOLO P, ANTONELLI A, BINELLI S, BUTI D, CANEVINI MP, CARULLO A, CIARMATORI C, COPPOLA G, D'ALESSANDRO P, DE FEO MR, DI DONATO S, DURISOTTI C, ROSO FILATI C, FRANCIA A, GALIMBERTI CA, GALLI R, GAROFALO P, GIOVANARDI ROSSI P, IANI C, MAIER R, MANFREDI M, MARGIOTTA N, MASSETANI R, MAZZA S, MECARELLI O, PARMEGGIANI A, RICCI S, ROCCHI R, ROMANO G, SALTARELLI A, SANTUCCI M, SIDERI G, SPECCHIO L, TARTARA A, TIACCI C., PASCOTTO, Antonio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3977::d0ab4e6dfbf8863a8290afee1de02a07
http://hdl.handle.net/11591/184595