Showing results (11-20 of 21) with videos related to
Sort By:
Pageof 3
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.Human Molecular Genetics|August 1, 2000
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiencyY Torrente, M G D'Angelo, Z Li, et al.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.Cell Transplantation|August 12, 1999
Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx miceY Torrente, M G D'Angelo, R Del Bo, et al.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 18, 2020
Upper-limb actuated exoskeleton for muscular dystrophy patients: preliminary results.S Dalla Gasperina, M Gfoehler, M Puchinger, 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.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.The Journal of Cell Biology|March 27, 2001
Intraarterial injection of muscle-derived CD34(+)Sca-1(+) stem cells restores dystrophin in mdx miceY Torrente, J P Tremblay, F Pisati, et al.Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.Pageof 3