GUGLIERI, MICHELA ESTER
GUGLIERI, MICHELA ESTER
DIPARTIMENTO DI SCIENZE NEUROLOGICHE (attivo dal 01/01/2001 al 27/04/2012)
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
2020 J. Alonso-Perez, L. Gonzalez-Quereda, L. Bello, M. Guglieri, V. Straub, P. Gallano, C. Semplicini, E. Pegoraro, V. Zangaro, A. Nascimento, C. Ortez, G.P. Comi, L.T. Dam, M. De Visser, A.J. van der Kooi, C. Garrido, M. Santos, U. Schara, A. Gangfuss, N. Lokken, J.H. Storgaard, J. Vissing, B. Schoser, G. Dekomien, B. Udd, J. Palmio, A. D'Amico, L. Politano, V. Nigro, C. Bruno, C. Panicucci, A. Sarkozy, O. Abdel-Mannan, A. Alonso-Jimenez, K.G. Claeys, D. Gomez-Andres, F. Munell, L. Costa-Comellas, J. Haberlova, M. Rohlenova, V. Elke, J.L. De Bleecker, C. Dominguez-Gonzalez, G. Tasca, C. Weiss, N. Deconinck, R. Fernandez-Torron, A. Lopez de Munain, A. Camacho-Salas, B. Melegh, K. Hadzsiev, L. Leonardis, B. Koritnik, M. Garibaldi, J.C. de Leon-Hernandez, E. Malfatti, A. Fraga-Bau, I. Richard, I. Illa, J. Diaz-Manera
Neurocognitive profiles in duchenne muscular dystrophy and gene mutation site
2011 M. D'Angelo, M. Lorusso, F. Civati, G. Comi, F. Magri, R. Del Bo, M. Guglieri, M. Molteni, A. Turconi, N. Bresolin
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
2008 R. Del Bo, M. Moggio, M. Rango, S. Bonato, M.G. D'Angelo, S. Ghezzi, G. Airoldi, M.T. Bassi, M. Guglieri, L. Napoli, C. Lamperti, S. Corti, A. Federico, N. Bresolin, G.P. Comi
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients
2008 M. Guglieri, F. Magri, M.G. D’Angelo, A. Prelle, L. Morandi, C. Rodolico, R. Cagliani, M. Mora, F. Fortunato, A. Bordoni, R. Del Bo, S. Ghezzi, S. Pagliarani, S. Lucchiari, S. Salani, C. Zecca, C. Lamperti, D. Ronchi, M. Aguennouz, P. Ciscato, C. Di Blasi, A. Ruggieri, I. Moroni, A. Turconi, M. Moggio, A. Toscano, N. Bresolin, G.P. Comi
Novel Q23R SOD1 mutation associated with muscle mitochondrial dysfunction
2007 D. Ronchi, S. Corti, A. Bordoni, D. Santoro, D. Papadimitriou, C. Lamperti, V. Lucchini, M. Magri, M. Guglieri, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi
Autosomal dominant and recessive limb-girdle muscular dystrophies : clinical, genetic relative frequency in a large Italian population
2007 M. Guglieri, F. Magri, R. Cagliani, M.G. D'Angelo, A. Prelle, F. Fortunato, S. Lucchiari, S. Salani, R. Del Bo, S. Ghezzi, C. Zecca, C. Lamperti, L. Morandi, M. Mora, M. Moggio, N. Bresolin, G.P. Comi
Clinical and genetical variability in a large sample of LGMD Italian patients
2007 F. Magri, M. Guglieri, M. D’Angelo, R. Cagliani, R. Del Bo, S. Ghezzi, D. Ronchi, A. Prelle, C. Lamperti, F. Fortunato, L. Morandi, M. Mora, M. Moggio, N. Bresolin, G.P. Comi
Autologous transplantation of muscle-derived CD133+ stem cells in Duchenne muscle patients
2007 Y. Torrente, M. Belicchi, C. Marchesi, G. Dantona, F. Cogiamanian, F. Pisati, M. Gavina, R. Giordano, R. Tonlorenzi, G. Fagiolari, C. Lamperti, L. Porretti, R. Lopa, M. Sampaolesi, L. Vicentini, N. Grimoldi, F. Tiberio, V. Songa, P. Baratta, A. Prelle, L. Forzenigo, M. Guglieri, O. Pansarasa, C. Rinaldi, V. Mouly, G.S. Butler Browne, G.P. Comi, P. Biondetti, M. Moggio, S.M. Gaini, N. Stocchetti, A. Priori, M.G. D'Angelo, A. Turconi, R. Bottinelli, G. Cossu, P. Rebulla, N. Bresolin
Familial amyotrophic lateral sclerosis with a novel Q23R mutation in the copper/zinc superoxide dismutase gene associated with muscle mitochondrial dysfunction
2007 S. Corti, A. Bordoni, D. Ronchi, D. Santoro, D. Papadimitriou, C. Lamperti, V. Lucchini, F. Magri, M. Guglieri, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi
Dysferlinopathies: clinical and genetic correlation in a large population
2006 M. Guglieri, F. Magri, R. Cagliani, M.G. D'Angelo, A. Prelle, F. Fortunato, R. Del Bo, S. Ghezzi, C. Zecca, C. Lamperti, L. Morandi, M. Mora, M. Moggio, N. Bresolin, G.P. Comi
Autosomal recessive myopathy without inclusion bodies caused by GNE gene mutation.
2006 R. DEL BO, M. Guglieri, M.G. D'Angelo, S. Ghezzi, F. Magri, L. Napoli, A. Prelle, A.C. Turconi, M. Moggio, N. Bresolin, G.P. Comi
Linguistic abilities in a group of Italian children affected by Duchenne Muscular Dystrophy
2006 M.G. D'Angelo, F. Civati, M. Lorusso, A. Marini, M. Guglieri, A. Turconi, F. Fabbro, N. Bresolin
Evaluation of linguistic abilities in a group of Italian children affected by Duchenne muscular dystrophy.
2006 F. Civati, M.G. D'Angelo, M.L. Lorusso, A. Marini, M. Guglieri, A.C. Turconi, F. Fabbro, N. Bresolin
Functional and structural modifications of dystrophic muscles after autologous transplantation of muscle-derived AC133+ stem cells
2006 M. Belicchi, C. Marchesi, R. Benchaouir, G. D'Antona, G. Fagiolari, C. Lamperti, A. Prelle, M. Guglieri, M. Moggio, A. Priori, M.G. D'Angelo, R. Bottinelli, G. Cossu, N. Bresolin, L. Garcia, Y. Torrente
A novel GENE mutations causes familial recessive myopathy without inclusion bodies
2006 R. Del Bo, M. Guglieri, M.G. D'Angelo, S. Ghezzi, F. Magri, L. Napoli, A. Prelle, M. Moggio, M. Mora, N. Bresolin, G.P. Comi
Limb-Girdle muscular dystrophies : clinical features and genetic frequency in a large Italian population
2006 M. Guglieri, F. Magri, R. Cagliani, M.G. D'Angelo, A. Prelle, F. Fortunato, S. Lucchiari, S. Salani, R. Del Bo, S. Ghezzi, C. Zecca, C. Lamperti, L. Morandi, M. Mora, M. Moggio, N. Bresolin, G.P. Comi
Molecular etiopathogenesis of Limb Girdle Muscular and Congenital Muscular Dystrophies: boundaries and contiguities
2005 M.Guglieri , F. Magri,G.P. Comi
The limb girdle muscular dystrophies: clinical, biochemical and genetic evaluation of a large Italian population
2005 M. Guglieri, F. Magri, M.G. D'Angelo, R. Cagliani, A. Bordoni, D. Ronchi, S. Grezzi, R. Del Bo, A. Prelle, M. Moggio, T. Mongini, M. Mora, A.C. Turconi, N. Bresolin, G.P. Comi
Autosomal dominant and recessive limb-girdle muscular dystrophies: relative frequency in a large Italian population
2005 M. Guglieri, F. Magri, R. Cagliani, M.G. D'Angelo, A. Prelle, F. Fortunato, S. Lucchiari, S. Salani, R. Del Bo, A. Bordoni, S. Ghezzi, C. Zecca, C. Lamperti, M. Moggio, N. Bresolin, G.P. Comi
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