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

por Zago, S., Poletti, B., Corbo, M., Adobbati, L., Silani, V.
Publicado en Behav Neurol (2008)

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

por Sassone, J, Maraschi, A, Sassone, F, Silani, V, Ciammola, A
Publicado 2013

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

por Ciammola, A., Sassone, J., Poletti, B., Mencacci, N., Benti, R., Silani, V.
Publicado 2011

cDNA sequence of human beta-NGF.

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

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

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

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

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

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

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

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

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

The Present and the Future of Neuroimaging in Amyotrophic Lateral Sclerosis

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

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

por 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.
Publicado en Sci Rep (2020)

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

por 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.
Publicado 1996

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

por 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.
Publicado 2009