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Journal of Neuroscience Research|August 17, 2018
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1Michela Ripolone, Valeria Lucchini, Dario Ronchi, et al.
Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Brain : a Journal of Neurology|December 25, 2009
Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in miceStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Cell Transplantation|May 3, 2001
In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: evidence of programmed cell death after muscle cell transplantationR Del Bo, Y Torrente, S Corti, et al.
Acta Neuropathologica Communications|April 9, 2022
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophyMichela Ripolone, Daniele Velardo, Stefania Mondello, et al.
Experimental Neurology|February 8, 2011
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanismsMonica Nizzardo, Martina Nardini, Dario Ronchi, et al.
Neurology|October 27, 2015
Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophyLorenzo Peverelli, Silvia Testolin, Luisa Villa, et al.
Acta Neuropathologica|May 8, 2003
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiencyA Prelle, M Sciacco, L Tancredi, et al.
Neuromuscular Disorders : NMD|November 28, 2012
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseasesM Mancuso, C Angelini, E Bertini, et al.
Neuromuscular Disorders : NMD|January 2, 2014
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's diseaseA Sagnelli, M Savoiardo, C Marchesi, et al.
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