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Mechanisms Inducing Low Bone Density in Duchenne Muscular Dystrophy in Mice and HumansRUFO, Anna; DEL FATTORE, Andrea; BERTINI, Enrico et al.Journal of bone and mineral research (Print). 2011, Vol 26, Num 8, pp 1891-1903, issn 0884-0431, 13 p.Article

Impaired oxygen extraction in metabolic myopathies : Detection and quantification by near-infrared spectroscopyGRASSI, Bruno; MARZORATI, Mauro; LANFRANCONI, Francesca et al.Muscle & nerve. 2007, Vol 35, Num 4, pp 510-520, issn 0148-639X, 11 p.Article

Metabolic Myopathies: Functional Evaluation by Analysis of Oxygen Uptake KineticsGRASSI, Bruno; PORCELLI, Simone; MARZORATI, Mauro et al.Medicine and science in sports and exercise. 2009, Vol 41, Num 12, pp 2120-2127, issn 0195-9131, 8 p.Article

Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skippingDI BLASI, Claudia; YI HE; MORANDI, Lucia et al.Brain. 2001, Vol 124, pp 698-704, issn 0006-8950, 4Article

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Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondriaSPELBRINK, Johannes N; LI, Fang-Yuan; SANTORO, Lucio et al.Nature genetics. 2001, Vol 28, Num 3, pp 223-231, issn 1061-4036Article

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Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosisZANOTTI, Simona; GIBERTINI, Sara; DI BLASI, Claudia et al.Histopathology. 2011, Vol 59, Num 6, pp 1215-1228, issn 0309-0167, 14 p.Article

FUKUTIN GENE MUTATIONS IN AN ITALIAN PATIENT WITH EARLY ONSET MUSCULAR DYSTROPHY BUT NO CENTRAL NERVOUS SYSTEM INVOLVEMENTSAREDI, Simona; RUGGIERI, Alessandra; MOTTARELLI, Elisa et al.Muscle & nerve. 2009, Vol 39, Num 6, pp 845-848, issn 0148-639X, 4 p.Article

Proteomic investigation of the molecular pathophysiology of dysferlinopathyDE PALMA, Sara; MORANDI, Lucia; MARIANI, Elena et al.Proteomics (Weinheim. Print). 2006, Vol 6, Num 1, pp 379-385, issn 1615-9853, 7 p.Article

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