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Results: 1-9 |
Results: 9
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping
Authors: Di Blasi, C He, Y Morandi, L Cornelio, F Guicheney, P Mora, M
Citation: C. Di Blasi et al., Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping, BRAIN, 124, 2001, pp. 698-704
Development of muscle pathology in canine X-linked muscular dystrophy. II.Quantitative characterization of histopathological progression during postnatal skeletal muscle development
Authors: Cozzi, F Cerletti, M Luvoni, GC Lombardo, R Brambilla, PG Faverzani, S Blasevich, F Cornelio, F Pozza, O Mora, M
Citation: F. Cozzi et al., Development of muscle pathology in canine X-linked muscular dystrophy. II.Quantitative characterization of histopathological progression during postnatal skeletal muscle development, ACT NEUROP, 101(5), 2001, pp. 469-478
Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis
Authors: Di Blasi, C Mora, M Pareyson, D Farina, L Sghirlanzoni, A Vignier, N Blasevich, F Cornelio, F Guicheney, P Morandi, L
Citation: C. Di Blasi et al., Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis, ANN NEUROL, 47(6), 2000, pp. 811-816
Increased expression of beta-chemokines in muscle of patients with inflammatory myopathies
Authors: Confalonieri, P Bernasconi, P Megna, P Galbiati, S Cornelio, F Mantegazza, R
Citation: P. Confalonieri et al., Increased expression of beta-chemokines in muscle of patients with inflammatory myopathies, J NE EXP NE, 59(2), 2000, pp. 164-169
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations
Authors: Barresi, R Di Blasi, C Negri, T Brugnoni, R Vitali, A Felisari, G Salandi, A Daniel, S Cornelio, F Morandi, L Mora, M
Citation: R. Barresi et al., Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations, J MED GENET, 37(2), 2000, pp. 102-107
Transforming growth factor-beta 1 and fibrosis in congenital muscular dystrophies
Authors: Bernasconi, P Di Blasi, C Mora, M Morandi, L Galbiati, S Confalonieri, P Cornelio, F Mantegazza, R
Citation: P. Bernasconi et al., Transforming growth factor-beta 1 and fibrosis in congenital muscular dystrophies, NEUROMUSC D, 9(1), 1999, pp. 28-33
Oral administration of an immunodominant T-cell epitope downregulates Th1/Th2 cytokines and prevents experimental myasthenia gravis
Authors: Baggi, F Andreetta, F Caspani, E Milani, M Longhi, R Mantegazza, R Cornelio, F Antozzi, C
Citation: F. Baggi et al., Oral administration of an immunodominant T-cell epitope downregulates Th1/Th2 cytokines and prevents experimental myasthenia gravis, J CLIN INV, 104(9), 1999, pp. 1287-1295
Clinical correlations in 16 patients with total or partial laminin alpha 2deficiency characterized using antibodies against 2 fragments of the protein
Authors: Morandi, L Di Blasi, C Farina, L Sorokin, L Uziel, G Azan, G Pini, A Toscano, A Lanfossi, M Galbiati, S Cornelio, F Mora, M
Citation: L. Morandi et al., Clinical correlations in 16 patients with total or partial laminin alpha 2deficiency characterized using antibodies against 2 fragments of the protein, ARCH NEUROL, 56(2), 1999, pp. 209-215
Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression
Authors: Lanfossi, M Cozzi, F Bugini, D Colombo, S Scarpa, P Morandi, L Galbiati, S Cornelio, F Pozza, O Mora, M
Citation: M. Lanfossi et al., Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression, ACT NEUROP, 97(2), 1999, pp. 127-138
Risultati: 1-9 |