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:
Vanacore, N
Bonifati, V
Colosimo, C
Fabbrini, G
De Michele, G
Marconi, R
Nicholl, D
Locuratolo, N
Romano, S
Talarico, G
Stocchi, F
Bonuccelli, U
Lamberti, P
Vieregge, P
Meco, G
Citation: N. Vanacore et al., Epidemiology of progressive supranuclear palsy, NEUROL SCI, 22(1), 2001, pp. 101-103
Authors:
Lucking, CB
Bonifati, V
Periquet, M
Vanacore, N
Brice, A
Meco, G
Citation: Cb. Lucking et al., Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations, NEUROLOGY, 57(5), 2001, pp. 924-927
Authors:
Casali, C
Bonifati, V
Santorelli, FM
Casari, G
Fortini, D
Patrignani, A
Fabbrini, G
Carrozzo, R
D'Amati, G
Locuratolo, N
Vanacore, N
Damiano, M
Pierallini, A
Pierelli, F
Amabile, GA
Meco, G
Citation: C. Casali et al., Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family, NEUROLOGY, 56(6), 2001, pp. 802-805
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:
Vanacore, N
Bonifati, V
Fabbrini, G
Colosimo, C
Marconi, R
Nicholl, D
Bonuccelli, U
Stocchi, F
Lamberti, P
Volpe, G
De Michele, G
Iavarone, I
Bennett, P
Vieregge, P
Meco, G
Citation: N. Vanacore et al., Smoking habits in multiple system atrophy and progressive supranuclear palsy, NEUROLOGY, 54(1), 2000, pp. 114-119
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
Authors:
Nicholl, DJ
Bennett, P
Hiller, L
Bonifati, V
Vanacore, N
Fabbrini, G
Marconi, R
Colosimo, C
Lamberti, P
Stocchi, F
Bonuccelli, U
Vieregge, P
Ramsden, DB
Meco, G
Williams, AC
Citation: Dj. Nicholl et al., A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders, NEUROLOGY, 53(7), 1999, pp. 1415-1421
Authors:
Mastrocola, C
Vanacore, N
Giovani, A
Locuratolo, N
Vella, C
Alessandri, A
Baratta, L
Tubani, L
Meco, G
Citation: C. Mastrocola et al., Twenty-four-hour heart rate variability to assess autonomic function in Parkinson's disease, ACT NEUR SC, 99(4), 1999, pp. 245-247