SALSANO, ETTORE
SALSANO, ETTORE
DIPARTIMENTO DI SCIENZE NEUROLOGICHE (attivo dal 01/01/2001 al 27/04/2012)
Identification of a new candidate gene in the insurgence of leukodystrophies
2022 A. Pezzotta, M. Spreafico, S. Magri, F. Balistreri, D. Di Bella, C. Gellera, E. Salsano, F. Taroni, A. Pistocchi
RARS1-related hypomyelinating leukodystrophy : Expanding the spectrum
2020 M.I. Mendes, L.M.C. Green, E. Bertini, D. Tonduti, C. Aiello, D. Smith, E. Salsano, S. Beerepoot, J. Hertecant, S. von Spiczak, J.H. Livingston, L. Emrick, J. Fraser, L. Russell, G. Bernard, S. Magri, D. Di Bella, F. Taroni, M.K. Koenig, I. Moroni, G. Cappuccio, N. Brunetti-Pierri, J. Rhee, B.A. Mendelsohn, I. Helbig, K. Helbig, H. Muhle, O. Ismayl, A.L. Vanderver, G.S. Salomons, M.S. van der Knaap, N.I. Wolf
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency
2019 S. Masnada, S. Groenweg, V. Saletti, L. Chiapparini, B. Castellotti, E. Salsano, W.E. Visser, D. Tonduti
Human adipose-derived mesenchymal stem cells as a new model of spinal and bulbar muscular atrophy
2014 M. Dossena, G. Bedini, P. Rusmini, E. Giorgetti, A. Canazza, V. Tosetti, E. Salsano, A. Sagnelli, C. Mariotti, C. Gellera, S.E. Navone, G. Marfia, G. Alessandri, F. Corsi, E.A. Parati, D. Pareyson, A. Poletti
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features
2014 G. Rossi, A. Bastone, E. Piccoli, M. Morbin, G. Mazzoleni, V. Fugnanesi, M. Beeg, E. Del Favero, L. Cantù, S. Motta, E. Salsano, D. Pareyson, A. Erbetta, A. Elia, V. Silani, C. Morelli, M. Salmona, F. Tagliavini
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease
2014 A. Sagnelli, M. Savoiardo, C. Marchesi, L. Morandi, M. Mora, M. Morbin, L. Farina, A. Mazzeo, A. Toscano, S. Pagliarani, S. Lucchiari, G.P. Comi, E. Salsano, D. Pareyson
One gene, two clinical profiles:novel GBE1 mutations in GSD type IV and Adult Polyglucosan Body Disease.
2009 S. Pagliarani, C. Marchesi, C. Lamperti, S. Lucchiari, L. Morandi, E. Salsano, M. Savoiardo, A. Bordoni, M. Moggio, G.P. Comi, Pareyson
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients.
2009 F. Magri, A. Govoni, M.G. D’Angelo, R. Del Bo, S. Tedeschi, S. Ghezzi, R. Virgilio, S. Bonato, S. Gandossini, A. Bordoni, S. Corti, V. Crugnola, A. Prelle, C. Lamperti, M. Moggio, N. Bresolin, G.P. Comi, C. Marchesi, S. Pagliarani, S. Lucchiari, E. Salsano
Phenotypic heterogeneity of GBE1 mutations: congenital glycogen storage disease type IV and adult polyglucosan body disease.
2009 C. Marchesi, S. Pagliarani, S. Lucchiari, L. Morandi, E. Salsano, M. Savoiardo, A. Bordoni, M. Moggio, D. Pareyson, G.P. Comi