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Experimental Cell Research|July 20, 2001
Chemotactic factors enhance myogenic cell migration across an endothelial monolayerS Corti, S Salani, R Del Bo, et al.Acta Neuropathologica|January 1, 1994
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber levelA Prelle, G Fagiolari, N Checcarelli, et al.Journal of Neuromuscular Diseases|December 28, 2020
A Multidisciplinary Evaluation of Patients with DMD in An Italian Tertiary Care CenterA LoMauro, S Gandossini, A Russo, et al.Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.Journal of Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.Journal of the Neurological Sciences|August 1, 1991
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patientN Bresolin, P Martinelli, B Barbiroli, et al.Journal of Neurology|May 1, 1993
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiencyN Bresolin, G P Comi, F Fortunato, et al.Journal of Neuroscience Research|November 22, 2002
Neuroectodermal and microglial differentiation of bone marrow cells in the mouse spinal cord and sensory gangliaS Corti, F Locatelli, C Donadoni, et al.Pageof 10