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Results: 1-11 |
Results: 11
Ictal and nonictal paroxysmal events in infantile neuroaxonal dystrophy: Polygraphic study of a case
Authors: Santucci, M Ambrosetto, G Scaduto, MC Morbin, M Tzolas, EV Rossi, PG
Citation: M. Santucci et al., Ictal and nonictal paroxysmal events in infantile neuroaxonal dystrophy: Polygraphic study of a case, EPILEPSIA, 42(8), 2001, pp. 1074-1077
Guidelines for the diagnosis of dementia and Alzheimer's disease
Authors: Sorbi, S Alberoni, M Alfieri, P Vesuviana, S Amici, S Antana, D Appollonio, I Avanzi, S Bartoli, A Bergamasco, B Bracco, L Bruni, A Terme, L Bugiani, O Caffarra, P Caltagirone, C Carolei, A Casini, AR Ciannella, L Citterio, A Daniele, A D'Achille, G Del Curatolo, G Dell'Agnello, G Durante, D Farina, E Ferrero, P Forleo, P Gainotti, G Gabriele, P Galante, E Gallai, V Gallassi, R Gasparini, M Ghetti, B Giaccone, G Girotti, F Grimaldi, L Grioli, S Guarnieri, BM Grottoli, S Iemolo, F Latorraca, S Le Pira, F Lenzi, GL Lorusso, S Mariani, C Marcon, G Mascia, V Mearelli, S Morante, M Morbin, M Musicco, M Nardelli, E Nichelli, P Padovani, A Paganini, M Pantieri, R Parisen, P Parnetti, L Passerella, B Pettenati, C Piacentini, S Piccoli, F Piccolini, C Pizzolato, G Provinciali, L Pugliese, N Redi, F Ruggieri, RM Ruggiero, U Saetta, M Schoenuber, R Silveri, MC Sorbi, S Sorrentino, G Sucapane, P Stracciari, A Tabaton, M Tagliavini, F Toso, V Valluzzi, F
Citation: S. Sorbi et al., Guidelines for the diagnosis of dementia and Alzheimer's disease, NEUROL SCI, 21(4), 2000, pp. 187-194
Neuronal ceroid lipofuscinosis: detection of atypical forms
Authors: Nardocci, N Morbin, M Bugiani, M Lamantea, E Bugiani, O
Citation: N. Nardocci et al., Neuronal ceroid lipofuscinosis: detection of atypical forms, NEUROL SCI, 21(3), 2000, pp. S57-S61
Neuropathology of Gerstmann-Straussler-Scheinker disease
Authors: Bugiani, O Giaccone, G Piccardo, P Morbin, M Tagliavini, F Ghetti, B
Citation: O. Bugiani et al., Neuropathology of Gerstmann-Straussler-Scheinker disease, MICROSC RES, 50(1), 2000, pp. 10-15
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
Authors: Pareyson, D Taroni, F Botti, S Morbin, M Baratta, S Lauria, G Ciano, C Sghirlanzoni, A
Citation: D. Pareyson et al., Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation, NEUROLOGY, 54(8), 2000, pp. 1696-1698
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22
Authors: Simonati, A Fabrizi, GM Pasquinelli, A Taioli, F Cavallaro, T Morbin, M Marcon, G Papini, M Rizzuto, N
Citation: A. Simonati et al., Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22, NEUROMUSC D, 9(4), 1999, pp. 257-261
Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients
Authors: Farina, L Nardocci, N Bruzzone, MG D'Incerti, L Zorzi, G Verga, L Morbin, M Savoiardo, M
Citation: L. Farina et al., Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients, NEURORADIOL, 41(5), 1999, pp. 376-380
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a pointmutation of peripheral myelin protein-22
Authors: Fabrizi, GM Cavallaro, T Taioli, F Orrico, D Morbin, M Simonati, A Rizzuto, N
Citation: Gm. Fabrizi et al., Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a pointmutation of peripheral myelin protein-22, NEUROLOGY, 53(4), 1999, pp. 846-851
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau
Authors: Bugiani, O Murrell, JR Giaccone, G Hasegawa, M Ghigo, G Tabaton, M Morbin, M Primavera, A Carella, F Solaro, C Grisoli, M Savoiardo, M Spillantini, MG Tagliavini, F Goedert, M Ghetti, B
Citation: O. Bugiani et al., Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau, J NE EXP NE, 58(6), 1999, pp. 667-677
Novel mutation of the P-0 extracellular domain causes a Dejerine-Sottas syndrome
Authors: Fabrizi, GM Cavallaro, T Morbin, M Simonati, A Taioli, F Rizzuto, N
Citation: Gm. Fabrizi et al., Novel mutation of the P-0 extracellular domain causes a Dejerine-Sottas syndrome, J NE NE PSY, 66(3), 1999, pp. 386-389
HIV-associated PML presenting as epilepsia partialis continua
Authors: Ferrari, S Monaco, S Morbin, M Zanusso, G Bertolasi, L Cerini, R Rizzuto, N
Citation: S. Ferrari et al., HIV-associated PML presenting as epilepsia partialis continua, J NEUR SCI, 161(2), 1998, pp. 180-184
Risultati: 1-11 |