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

by Zago, S., Poletti, B., Corbo, M., Adobbati, L., Silani, V.
Published in Behav Neurol (2008)

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

by Sassone, J, Maraschi, A, Sassone, F, Silani, V, Ciammola, A
Published 2013

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

by Ciammola, A., Sassone, J., Poletti, B., Mencacci, N., Benti, R., Silani, V.
Published 2011

cDNA sequence of human beta-NGF.

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

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

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

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

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

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

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

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

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

The Present and the Future of Neuroimaging in Amyotrophic Lateral Sclerosis

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

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

by 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.
Published in Sci Rep (2020)

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

by 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.
Published 1996

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

by 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.
Published 2009