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Experimental Neurology|November 14, 2002
Modulated generation of neuronal cells from bone marrow by expansion and mobilization of circulating stem cells with in vivo cytokine treatmentS Corti, F Locatelli, S Strazzer, et al.Brain : a Journal of Neurology|February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlatesG P Comi, A Prelle, N Bresolin, et al.Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.Neurology|August 23, 2000
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophyG Felisari, F Martinelli Boneschi, A Bardoni, et al.Journal of the Neurological Sciences|September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansionS Lucchiari, S Pagliarani, S Corti, et al.Neurology|April 10, 2003
A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafnessM Crimi, S Galbiati, M P Perini, et al.Acta Neuropathologica|February 18, 2020
Synaptotagmin 13 is neuroprotective across motor neuron diseasesM Nizzardo, M Taiana, F Rizzo, et al.Neurology|January 5, 2002
A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO familyL Napoli, A Bordoni, M Zeviani, et al.Journal of Hematotherapy & Stem Cell Research|February 24, 2004
Neuronal differentiation of murine bone marrow Thy-1- and Sca-1-positive cellsF Locatelli, S Corti, C Donadoni, et al.Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.Pageof 10