BRESOLIN, NEREO
BRESOLIN, NEREO
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
5 ' azacytidine enhances exogenous gene expression in skeletal muscle
1999 M. D'Angelo, C. Ausenda, Y. Torrente, A. Bordoni, S. Corti, R. Del Bo, M. Perini, M. Colucci, G. Comi, N. Bresolin, G. Scarlato
5'azacytidine enhances exogenous gene expression in muscle
1997 M. Dangelo, C. Ausenda, Y. Torrente, S. Corti, M. Perini, M. Colucci, G. Comi, N. Bresolin, G. Scarlato
[Expression of a defect in the respiratory chain in cultured human cells]
1991 G. Meola, G. Rotondo, M. Velicogna, R. Toppi, V. Sansone, N. Bresolin, G. Comi, A. Bordoni, P. Amati, C. Ausenda
A 175 million year history of T cell regulatory molecules reveals widespread selection, with adaptive evolution of disease alleles
2013 D. Forni, R. Cagliani, U. Pozzoli, M. Colleoni, S. Riva, M. Biasin, G. Filippi, L. De Gioia, F. Gnudi, G.P. Comi, N. Bresolin, M. Clerici, M. Sironi
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation
2012 L. Ghezzi, E. Scarpini, M. Rango, A. Arighi, M.T. Bassi, E. Tenderini, M. De Riz, F. Jacini, G.G. Fumagalli, A.M. Pietroboni, D. Galimberti, N. Bresolin
A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation
2012 L. Ghezzi, M.T. Bassi, A.M. Pietroboni, G.G. Fumagalli, A. Arighi, M. Rango, M. De Riz, F. Jacini, D. Galimberti, N. Bresolin, E. Scarpini
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy
2005 M. Sciacco, A. Prelle, G. Fagiolari, A. Bordoni, M.Crimi, A. Di Fonzo, P. Ciscato, C. Lamperti, E. D'Adda, S. Jann, N. Bresolin, G.P. Comi, M. Moggio
A CASE OF MITOCHONDRIAL MYOPATHY, LACTIC-ACIDOSIS AND COMPLEX-I DEFICIENCY
1990 L. Bet, N. Bresolin, M. Moggio, G. Meola, A. Prelle, A. Schapira, T. Binzoni, A. Chomyn, F. Fortunato, P. Cerretelli, G. Scarlato
A case of vanishing white-matter disease due to the c.260C>T (p.Ala87Val) EIF2B3 mutation
2012 L. Ghezzi, M. Bassi, A. Pietroboni, G. Fumagalli, A. Arighi, M. Rango, M. De Riz, F. Jacini, D. Galimberti, N. Bresolin, E. Scarpini
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation
2020 A. Manini, T. Bocci, A. Migazzi, E. Monfrini, D. Ronchi, G. Franco, A. De Rosa, F. Sartucci, A. Priori, S. Corti, G.P. Comi, N. Bresolin, M. Basso, A. Di Fonzo
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
2003 R. Cagliani, N. Bresolin, A. Prelle, A. Gallanti, F. Fortunato, M. Sironi, P. Ciscato, G. Fagiolari, S. Bonato, S. Galbiati, S. Corti, C. Lamperti, M. Moggio, G. Comi
A clinical, genetic and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia
2008 A. Arnoldi, A. Tonelli, F. Crippa, G. Villani, C. Pacelli, M. Sironi, U. Bozzoli, M.G. D’Angelo, G. Meola, A. Martinuzzi, C. Crivella, F. Redaelli, C. Panzeri, A. Renieri, G.P. Comi, A.C. Turioni, N. Bresolin, M.T. Bassi
A complex selection signature at the human AVPR1B gene
2009 R. Cagliani, M. Fumagalli, U. Pozzoli, S. Riva, M. Cereda, G. Comi, L. Pattini, N. Bresolin, M. Sironi
A cortically blind patient with preserved visual imagery
2010 S. Zago, S.P. Corti, A. Bersano, P. Baron, G. Conti, E. Ballabio, S. Lanfranconi, C.M. Cinnante, A. Costa, A. Cappellari, N. Bresolin
A de novo C19orf12 heterozygous mutation in a patient with MPAN
2017 E. Monfrini, V. Melzi, G. Buongarzone, G. Franco, D. Ronchi, R. Dilena, E. Scola, P. Vizziello, A. Bordoni, N. Bresolin, G.P. Comi, S. Corti, A. Di Fonzo
A functional variant in ERAP1 predisposes to multiple sclerosis
2012 F.R. Guerini, R. Cagliani, D. Forni, C. Agliardi, D. Caputo, A. Cassinotti, D. Galimberti, C. Fenoglio, M. Biasin, R. Asselta, E. Scarpini, G.P. Comi, N. Bresolin, M.S. Clerici, M. Sironi
A Late Role of ANT-1 Overexpression in the Pathogenesis of FSHD
2008 C. Lamperti, V. Crugnola, M. Servida, G. Fagiolari, M. Serafini, A. Prelle, M. Sciacco, F. Fortunato, L. Napoli, A. Di Fonzo, G.P. Comi, R.G. Tupler, N. Bresolin, M. Moggio
A model for motor neuron degeneration and treatment of Spinal Muscular Atrophy using human induced pluripotent stem cells
2011 S. Corti, F. Magri, M. Nizzardo, C. Simone, M. Falcone, S. Salani, C. Donadoni, M. Nardini, G. Riboldi, G. Menozzi, C. Bonaglia, F. Rizzo, N. Bresolin, G. Comi
A mouse model of facioscapulohumeral muscular dystrophy
2005 C. Lamperti, A. Naini, V. Lucchini, C. Zecca, P. Ciscato, M. Serafini, A. Prelle, N. Bresolin, S. Di Mauro, M. Moggio
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature
2018 R. Brusa, F. Magri, D. Papadimitriou, A. Govoni, R. Del Bo, P. Ciscato, M. Savarese, C. Cinnante, M.C. Walter, A. Abicht, S. Bulst, S. Corti, M. Moggio, N. Bresolin, V. Nigro, G.P. Comi