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N Bresolin

Showing results (161-170 of 206) with videos related to

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Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Scientific Reports|February 17, 2016
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotypeM Nizzardo, C Simone, F Rizzo, et al.
Journal of Neurology|June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophyA Prelle, G P Comi, C Rigoletto, et al.
Cellular and Molecular Life Sciences : CMLS|January 21, 2009
CD20-related signaling pathway is differently activated in normal and dystrophic circulating CD133(+) stem cellsD Parolini, M Meregalli, M Belicchi, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2008
MDC/CCL22 intrathecal levels in patients with multiple sclerosisD Galimberti, C Fenoglio, C Comi, et al.
Journal of Medical Genetics|August 3, 2004
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhoodM T Bassi, N Bresolin, A Tonelli, et al.
The European Respiratory Journal|October 21, 2009
Abdominal volume contribution to tidal volume as an early indicator of respiratory impairment in Duchenne muscular dystrophyA Lo Mauro, M G D'Angelo, M Romei, et al.
Cellular and Molecular Life Sciences : CMLS|March 7, 2001
T-antigen regulated expression reduces apoptosis of tag-transformed human myoblastsS Corti, S Salani, R Del Bo, 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.
Pageof 21

Showing results (161-170 of 206) with videos related to

Sort By:
Pageof 21
Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Scientific Reports|February 17, 2016
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotypeM Nizzardo, C Simone, F Rizzo, et al.
Journal of Neurology|June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophyA Prelle, G P Comi, C Rigoletto, et al.
Cellular and Molecular Life Sciences : CMLS|January 21, 2009
CD20-related signaling pathway is differently activated in normal and dystrophic circulating CD133(+) stem cellsD Parolini, M Meregalli, M Belicchi, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2008
MDC/CCL22 intrathecal levels in patients with multiple sclerosisD Galimberti, C Fenoglio, C Comi, et al.
Journal of Medical Genetics|August 3, 2004
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhoodM T Bassi, N Bresolin, A Tonelli, et al.
The European Respiratory Journal|October 21, 2009
Abdominal volume contribution to tidal volume as an early indicator of respiratory impairment in Duchenne muscular dystrophyA Lo Mauro, M G D'Angelo, M Romei, et al.
Cellular and Molecular Life Sciences : CMLS|March 7, 2001
T-antigen regulated expression reduces apoptosis of tag-transformed human myoblastsS Corti, S Salani, R Del Bo, 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.
Pageof 21