Authors:
Bonifati, V
De Michele, G
Lucking, CB
Durr, A
Fabrizio, E
Ambrosio, G
Vanacore, N
De Mari, M
Marconi, R
Capus, L
Breteler, MMB
Gasser, T
Oostra, B
Wood, N
Agid, Y
Filla, A
Meco, G
Brice, A
Citation: V. Bonifati et al., The parkin gene and its phenotype, NEUROL SCI, 22(1), 2001, pp. 51-52
Authors:
Vanacore, N
Bonifati, V
Fabbrini, G
Colosimo, C
De Michele, G
Marconi, R
Nicholl, D
Locuratolo, N
Talarico, G
Romano, S
Stocchi, F
Bonuccelli, U
De Mari, M
Vieregge, P
Meco, G
Citation: N. Vanacore et al., Epidemiology of multiple system atrophy, NEUROL SCI, 22(1), 2001, pp. 97-99
Authors:
Colosimo, C
Vanacore, N
Bonifati, V
Fabbrini, G
Rum, A
De Michele, G
De Mari, M
Bonuccelli, U
Nicholl, DJ
Meco, G
Citation: C. Colosimo et al., Clinical diagnosis of multiple system atrophy: level of agreement between Quinn's criteria and the consensus conference guidelines, ACT NEUR SC, 103(4), 2001, pp. 261-264
Authors:
Defazio, G
De Mari, M
De Salvia, R
Lamberti, P
Giorelli, M
Livrea, P
Citation: G. Defazio et al., "Apraxia of eyelid opening" induced by levodopa therapy and apomorphine inatypical parkinsonism (possible progressive supranuclear palsy): A case report, CLIN NEUROP, 22(5), 1999, pp. 292-294
Authors:
Bonifati, V
Joosse, M
Nicholl, DJ
Vanacore, N
Bennett, P
Rizzu, P
Fabbrini, G
Marconi, R
Colosimo, C
Locuratolo, N
Stocchi, F
Bonuccelli, U
De Mari, M
Wenning, G
Vieregge, P
Oostra, B
Meco, G
Heutink, P
Citation: V. Bonifati et al., The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronicvariant of the disease-associated H1 haplotype in Italian cases, NEUROSCI L, 274(1), 1999, pp. 61-65