BALLABIO, ELENA
BALLABIO, ELENA
DIPARTIMENTO DI SCIENZE NEUROLOGICHE (attivo dal 01/01/2001 al 27/04/2012)
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant
2012 A. Bersano, M. Ranieri, A. Ciammola, C. Cinnante, S. Lanfranconi, M.T. Dotti, L. Candelise, C. Baschirotto, I. Ghione, E. Ballabio, N. Bresolin, M.T. Bassi
Transthyretin asn90 variant: amyloidogenic or non-amyloidogenic role
2009 A. Bersano, R. Del Bo, E. Ballabio, C. Cinnante, S. Lanfranconi, G.P. Comi, P. Baron, N. Bresolin, L. Candelise
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation
2009 A. Bersano, R. Del Bo, C. Lamperti, S. Ghezzi, G. Fagiolari, F. Fortunato, E. Ballabio, M. Moggio, L. Candelise, D. Galimberti, R. Virgilio, S. Lanfranconi, Y. Torrente, M. Carpo, N. Bresolin, G.P. Comi, S. Corti
Stem cell therapy in stroke
2009 F. Locatelli, A. Bersano, E. Ballabio, S. Lanfranconi, D. Papadimitriou, S. Strazzer, N. Bresolin, G.P. Comi, S. Corti
Recovery after L-DOPA treatment in peg-interferon and ribavirin induced parkinsonism
2008 A. Bersano, A. Aghemo, M. Rumi, E. Ballabio, L. Candelise, M. Colombo
Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene
2007 A. Bersano, R. Del Bo, C. Lamperti, S. Ghezzi, N. Bresolin, L. Napoli, E. Ballabio, M. Moggio, L. Candelise, G.P. Comi, S. Corti
TWO NOVEL MUTATIONS IN THE AMINO TERMINUS OF ATP1A2 ASSOCIATED TO A MILD PHENOTYPE OF HEMIPLEGIC MIGRAINE
2007 A. Bersano, M.T. Bassi, A. Tonelli, A. Gallanti, V. Cardin, E. Ballabio, G. Airoldi, F. Redaelli, N. Bresolin, L. Candelise
Clinical and pathological aspects of an Italian patient with inclusion body myopathy and frontotemporal dementia carrying a novel mutation in valosin-containing protein gene
2007 A. Bersano, R. Del Bo, C. Lamperti, S. Ghezzi, N. Bresolin, L. Napoli, E. Ballabio, M. Moggio, L. Candelise, G.P. Comi, S. Corti
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine
2007 A. Tonelli, A. Gallanti, A. Bersano, V. Cardin, E. Ballabio, G. Airoldi, F. Redaelli, L. Candelise, N. Bresolin, M. Bassi