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Results: 1-5 |
Results: 5

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
Risultati: 1-5 |