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Neurology
|
April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathies
M Sciacco, G Fagiolari, C Lamperti, et al.
Scientific Reports
|
February 17, 2016
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype
M Nizzardo, C Simone, F Rizzo, et al.
Journal of Neurology
|
June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophy
A 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 cells
D Parolini, M Meregalli, M Belicchi, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patient
R Cagliani, A Bardoni, M Sironi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
January 23, 2008
MDC/CCL22 intrathecal levels in patients with multiple sclerosis
D 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 childhood
M 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 dystrophy
A 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 myoblasts
S 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 mice
Y Torrente, M G D'Angelo, R Del Bo, et al.
Page
of 21
Search research articles
Search
Showing results (161-170 of 206) with videos related to
Sort By:
Page
of 21
Neurology
|
April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathies
M Sciacco, G Fagiolari, C Lamperti, et al.
Scientific Reports
|
February 17, 2016
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype
M Nizzardo, C Simone, F Rizzo, et al.
Journal of Neurology
|
June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophy
A 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 cells
D Parolini, M Meregalli, M Belicchi, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patient
R Cagliani, A Bardoni, M Sironi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
January 23, 2008
MDC/CCL22 intrathecal levels in patients with multiple sclerosis
D 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 childhood
M 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 dystrophy
A 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 myoblasts
S 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 mice
Y Torrente, M G D'Angelo, R Del Bo, et al.
Page
of 21