AAAAAA
Results:
1-11
|
Results: 11
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:
Bolino, A
Muglia, M
Conforti, FL
LeGuern, E
Salih, MAM
Georgiou, DM
Christodoulou, K
Hausmanowa-Petrusewicz, I
Mandich, P
Schenone, A
Gambardella, A
Bono, F
Quattrone, A
Devoto, M
Monaco, AP
Citation: A. Bolino et al., Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2, NAT GENET, 25(1), 2000, pp. 17-19
Authors:
Bolino, A
Levy, ER
Muglia, M
Conforti, FL
LeGuern, E
Salih, MAM
Georgiou, DM
Hausmanowa-Petrusewicz, I
Mandich, P
Gambardella, A
Quattrone, A
Devoto, M
Monaco, AP
Citation: A. Bolino et al., Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22, GENOMICS, 63(2), 2000, pp. 271-278
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:
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
Authors:
Pizzuti, A
Novelli, G
Ratti, A
Amati, F
Bordoni, R
Mandich, P
Bellone, E
Conti, E
Bengala, M
Mari, A
Silani, V
Dallapiccola, B
Citation: A. Pizzuti et al., Isolation and characterization of a novel transcript embedded within HIRA,a gene deleted in DiGeorge syndrome, MOL GEN MET, 67(3), 1999, pp. 227-235
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
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:
Bolino, A
Seri, M
Caroli, F
Eubanks, J
Srinivasan, J
Mandich, P
Schenone, A
Quattrone, A
Romeo, G
Catterall, WA
Devoto, M
Citation: A. Bolino et al., Exclusion of the SCN2B gene as candidate for CMT4B, EUR J HUM G, 6(6), 1998, pp. 629-634
Risultati:
1-11
|