VIRGILIO, ROBERTA
VIRGILIO, ROBERTA
DIPARTIMENTO DI SCIENZE NEUROLOGICHE (attivo dal 01/01/2001 al 27/04/2012)
A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment
2007 R. Virgilio, A. Bordoni, D. Ronchi, F. Saladino, N. Bresolin, M. Sciacco, G.P. Comi
A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype
2008 F. Magri, R. Virgilio, R. Del Bo, F. Fortunato, S. Ghezzi, R. Cagliani, M. Sironi, M.G. D'Angelo, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi
Association between VEGF gene and sporadic Alzheimer's disease.
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli-Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Association between VEGF gene and sporadic Alzheimer’s Disease
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene
2008 D. Ronchi, A. Bordoni, R. Virgilio, E. Fassone, A. DiFonzo, M. Servida, M. Ronconi, V. Lucchini, M. Matteoli, N. Bresolin, G.P. Comi
Cognitive evaluation in Duchenne Muscular Dystrophy
2005 A. Russo, F. Civati, R. Virgilio, M. Guglieri, M. Lo Russo, F. Fabbro, M.G. D'Angelo, A.C. Turconi, N. Bresolin
Comprehensive genetic analysis and clinical follow-up findings in 203 DMD patients
2008 R. Virgilio, F. Magri, R. Del Bo, S. Ghezzi, S. Tedeschi, M.G. D’Angelo, D. Coviello, A. Prelle, A. Bordoni, M. Sciacco, C. Lamperti, S. Corti, Y. Torrente, M. Moggio, N. Bresolin, G.P. Comi
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies
2009 R. Virgilio, S.P. Corti, P. Agazzi, D. Santoro, S. Lanfranconi, L. Candelise, N. Bresolin, G.P. Comi, A. Bersano
Evaluation of bone mineral density with quantitative ultrasound in children affected by Duchenne Muscular Dystrophy
2005 G. Cerina, M. Guglieri, R. Virgilio, A. Russo, P. Fraschini, F. De Terlizzi, M.G. D'Angelo, A.C. Turconi, N. Bresolin
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
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients
2005 I. Guidi, D. Galimberti, E. Venturelli, C. Lovati, R. Del Bo, C. Fenoglio, A. Gatti, R. Dominici, S. Galbiati, R. Virgilio, S. Pomati, G.P. Comi, C. Mariani, G. Forloni, N. Bresolin, E.A. Scarpini
Is M129V of PRNP gene associated with Alzheimer's disease? A case control study and a meta-analysis
2005 S. Ghezzi, R. Del BO, M. Scarlato, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Mitochondrial DNA G8363A mutation in the tRNA Lys gene : clinical features of a new family
2008 R. Virgilio, D. Ronchi, A. Bordoni, E. Fassone, M. Moggio, S. Bonato, G. Conti, C. Donadoni, L. Barbetta, G. Torgano, S. Corti, N. Bresolin, G.P. Comi
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study
2009 R. Virgilio, D. Ronchi, A. Bordoni, E. Fassone, S. Bonato, C. Donadoni, G. Torgano, M. Moggio, S. Corti, N. Bresolin, G.P. Comi
Mitochondrial DNA microarray resequencing in Leber's hereditary optic neuropathy and other mitochondrial encephalomyopathies
2007 F. Saladino, R. Virgilio, I. Cifola, A. Bordoni, S. Galbiati, C. Battaglia, N. Bresolin, G.P. Comi
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
Muscle mitochondrial oxidative defects in Amyotrophic Lateral Scelosis
2007 V. Crugnola, V. Lucchini, S. Corti, L. Adobbati, A. Ciammola, N. Ticozzi, M.E. Fruguglietti, A. Prelle, D. Santoro, R. Virgilio, V. Silani, N. Bresolin, M. Moggio, G.P. Comi
Neuropsychological profile in Duchenne Muscular Dystrophy
2005 M.G. D'Angelo, F. Civati, M.L. Lo Russo, A.M. Russo, R. Virgilio, A. Tavano, F. Fabbro, A.C. Turconi, N. Bresolin
New twinkle gene mutations in PEO patients with multiple mitochondrial DNA deletions
2006 R. Virgilio, A. Bordoni, D. Ronchi, G.M. Hadjigeorgiou, R. Del Bo, V. Crugnola, D. Kafetsouli, E. Tsironi, A. Papadimitriou, N. Bresolin, G.P. Comi
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia
2008 R. Virgilio, D. Ronchi, G.M. Hadjigeorgiou, A. Bordoni, F. Saladino, M. Moggio, L. Adobbati, D. Kafetsouli, E. Tsironi, S. Previtali, A. Papadimitriou, N. Bresolin, G.P. Comi