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Results: 1-8 |
Results: 8
Clinical and genetic study of essential tremor in the Italian population
Authors: Abbruzzese, G Pigullo, S Di Maria, E Martinelli, P Barone, P Marchese, R Scaglione, C Assini, A Lucetti, C Berardelli, A Calzetti, S Bellone, E Ajmar, F Mandich, P
Citation: G. Abbruzzese et al., Clinical and genetic study of essential tremor in the Italian population, NEUROL SCI, 22(1), 2001, pp. 39-40
The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter
Authors: Musso, M Balestra, P Bellone, E Cassandrini, D Di Maria, E Doria, LL Grandis, M Mancardi, G Schenone, A Levi, G Ajmar, F Mandich, P
Citation: M. Musso et al., The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter, NEUROBIOL D, 8(4), 2001, pp. 700-706
No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients
Authors: Pigullo, S Di Maria, E Marchese, R Assini, A Bellone, E Scaglione, C Vitale, C Bonuccelli, U Barone, P Ajmar, F Martinelli, P Abbruzzese, G Mandich, P
Citation: S. Pigullo et al., No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients, J NEURAL TR, 108(3), 2001, pp. 297-304
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
Authors: Di Maria, E Tabaton, M Vigo, T Abbruzzese, G Bellone, E Donati, C Frasson, E Marchese, R Montagna, P Munoz, DG Pramstaller, PP Zanusso, G Ajmar, F Mandich, P
Citation: E. Di Maria et al., Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy, ANN NEUROL, 47(3), 2000, pp. 374-377
Family and molecular data for a fine analysis of age at onset in Huntington disease
Authors: Squitieri, F Sabbadini, G Mandich, P Gellera, C Di Maria, E Bellone, E Castellotti, B Nargi, E de Grazia, U Frontali, M Novelletto, A
Citation: F. Squitieri et al., Family and molecular data for a fine analysis of age at onset in Huntington disease, AM J MED G, 95(4), 2000, pp. 366-373
Congenital hypomyelination due to myelin protein zero Q215X mutation
Authors: Mandich, P Mancardi, GL Varese, A Soriani, S Di Maria, E Bellone, E Bado, M Gross, L Windebank, AJ Ajmar, F Schenone, A
Citation: P. Mandich et al., Congenital hypomyelination due to myelin protein zero Q215X mutation, ANN NEUROL, 45(5), 1999, pp. 676-678
Mental function in males and females
Authors: Ajmar, F Di Maria, E Padovani, L
Citation: F. Ajmar et al., Mental function in males and females, AM J MED G, 88(6), 1999, pp. 593-593
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II
Authors: Mandich, P Bellone, E Di Maria, E Pigullo, S Pizzuti, A Schenone, A Soriani, S Varese, A Windebank, AJ Ajmar, F
Citation: P. Mandich et al., Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II, AM J MED G, 83(5), 1999, pp. 409-410
Risultati: 1-8 |