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Results:
1-10
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Results: 10
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
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
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
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
Authors:
Origone, P
Bonioli, E
Panucci, E
Costabel, S
Ajmar, F
Coviello, DA
Citation: P. Origone et al., The Genoa experience of prenatal diagnosis in NF1, PRENAT DIAG, 20(9), 2000, pp. 719-724
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
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
Authors:
Penco, S
Schenone, A
Bordo, D
Bolognesi, M
Abbruzzese, M
Bugiani, O
Ajmar, F
Garre, C
Citation: S. Penco et al., A SOD1 gene mutation in a patient with slowly progressing familial ALS, NEUROLOGY, 53(2), 1999, pp. 404-406
Authors:
Ghiorzo, P
Ciotti, P
Mantelli, M
Heouaine, A
Queirolo, P
Rainero, ML
Ferrari, C
Santi, PL
De Marchi, R
Farris, A
Ajmar, F
Bruzzi, P
Bianchi-Scarra, G
Citation: P. Ghiorzo et al., Characterization of Ligurian melanoma families and risk of occurrence of other neoplasia, INT J CANC, 83(4), 1999, pp. 441-448
Risultati:
1-10
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