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Respiratory Medicine|November 16, 2011
Low abdominal contribution to breathing as daytime predictor of nocturnal desaturation in adolescents and young adults with Duchenne Muscular DystrophyM Romei, M G D'Angelo, A LoMauro, et al.Annals of Neurology|August 17, 2001
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysisG P Comi, F Fortunato, S Lucchiari, et al.Acta Neuropathologica|November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patientsA Prelle, G P Comi, L Tancredi, et al.Rejuvenation Research|August 30, 2008
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degenerationB Borroni, S Ghezzi, C Agosti, et al.Clinical Neuropathology|August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterizationA Prelle, M Sciacco, G P Comi, et al.Journal of the Neurological Sciences|May 3, 2011
Respiratory pattern in an adult population of dystrophic patientsM G D'Angelo, M Romei, A Lo Mauro, et al.Annals of Neurology|August 12, 1999
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiencyV Tiranti, M Jaksch, S Hofmann, et al.Archives of Gerontology and Geriatrics|January 1, 1996
Late-onset mitochondrial neuromyopathy: an age-related phenomenon?A Toscano, M Santoro, G Vita, et al.Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, 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.Pageof 10