Dysgraphia in Patients with Primary Lateral Sclerosis: A Speech-Based Rehearsal Deficit?

per Zago, S., Poletti, B., Corbo, M., Adobbati, L., Silani, V.
Publicat a Behav Neurol (2008)

Defining the role of the Bcl-2 family proteins in Huntington's disease

per Sassone, J, Maraschi, A, Sassone, F, Silani, V, Ciammola, A
Publicat 2013

Atypical Parkinsonism Revealing a Late Onset, Rigid and Akinetic Form of Huntington's Disease

per Ciammola, A., Sassone, J., Poletti, B., Mencacci, N., Benti, R., Silani, V.
Publicat 2011

cDNA sequence of human beta-NGF.

per Borsani, G, Pizzuti, A, Rugarli, E I, Falini, A, Silani, V, Sidoli, A, Scarlato, G, Baralle, F E
Publicat 1990

Mutant Huntingtin induces activation of the Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3)

per Sassone, J, Colciago, C, Marchi, P, Ascardi, C, Alberti, L, Di Pardo, A, Zippel, R, Sipione, S, Silani, V, Ciammola, A
Publicat 2010

EFNS guidelines on the use of neuroimaging in the management of motor neuron diseases

per Filippi, M., Agosta, F., Abrahams, S., Fazekas, F., Grosskreutz, J., Kalra, S., Kassubek, J., Silani, V., Turner, M. R., Masdeu, J. C.
Publicat 2010

Noninvasive near-infrared live imaging of human adult mesenchymal stem cells transplanted in a rodent model of Parkinson’s disease

per Bossolasco, P, Cova, L, Levandis, G, Diana, V, Cerri, S, Deliliers, G Lambertenghi, Polli, E, Silani, V, Blandini, F, Armentero, MT
Publicat 2012

Inefficient skeletal muscle oxidative function flanks impaired motor neuron recruitment in Amyotrophic Lateral Sclerosis during exercise

per Lanfranconi, F., Ferri, A., Corna, G., Bonazzi, R., Lunetta, C., Silani, V., Riva, N., Rigamonti, A., Maggiani, A., Ferrarese, C., Tremolizzo, L.
Publicat a Sci Rep (2017)

The Present and the Future of Neuroimaging in Amyotrophic Lateral Sclerosis

per Agosta, F., Chiò, A., Cosottini, M., De Stefano, N., Falini, A., Mascalchi, M., Rocca, M.A., Silani, V., Tedeschi, G., Filippi, M.
Publicat a AJNR Am J Neuroradiol (2010)

Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral Sclerosis

per Carlomagno, C., Banfi, P. I., Gualerzi, A., Picciolini, S., Volpato, E., Meloni, M., Lax, A., Colombo, E., Ticozzi, N., Verde, F., Silani, V., Bedoni, M.
Publicat a Sci Rep (2020)

Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

per Pizzuti, A., Novelli, G., Mari, A., Ratti, A., Colosimo, A., Amati, F., Penso, D., Sangiuolo, F., Calabrese, G., Palka, G., Silani, V., Gennarelli, M., Mingarelli, R., Scarlato, G., Scambler, P., Dallapiccola, B.
Publicat 1996

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

per Ticozzi, N, Silani, V, LeClerc, A L., Keagle, P, Gellera, C, Ratti, A, Taroni, F, Kwiatkowski, T J., McKenna-Yasek, D M., Sapp, P C., Brown, R H., Landers, J E.
Publicat 2009