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

بواسطة Zago, S., Poletti, B., Corbo, M., Adobbati, L., Silani, V.
الحاوية / القاعدة Behav Neurol (2008)

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

بواسطة Sassone, J, Maraschi, A, Sassone, F, Silani, V, Ciammola, A
منشور في 2013

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

بواسطة Ciammola, A., Sassone, J., Poletti, B., Mencacci, N., Benti, R., Silani, V.
منشور في 2011

cDNA sequence of human beta-NGF.

بواسطة Borsani, G, Pizzuti, A, Rugarli, E I, Falini, A, Silani, V, Sidoli, A, Scarlato, G, Baralle, F E
منشور في 1990

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

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

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

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

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

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

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

بواسطة Lanfranconi, F., Ferri, A., Corna, G., Bonazzi, R., Lunetta, C., Silani, V., Riva, N., Rigamonti, A., Maggiani, A., Ferrarese, C., Tremolizzo, L.
الحاوية / القاعدة Sci Rep (2017)

The Present and the Future of Neuroimaging in Amyotrophic Lateral Sclerosis

بواسطة Agosta, F., Chiò, A., Cosottini, M., De Stefano, N., Falini, A., Mascalchi, M., Rocca, M.A., Silani, V., Tedeschi, G., Filippi, M.
الحاوية / القاعدة AJNR Am J Neuroradiol (2010)

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

بواسطة 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.
الحاوية / القاعدة Sci Rep (2020)

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

بواسطة 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.
منشور في 1996

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

بواسطة 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.
منشور في 2009