Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Meola

Showing results (81-90 of 142) with videos related to

Pageof 15
Sort By:
European Journal of Histochemistry : EJH|November 11, 2011
Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidenceM Malatesta, M Giagnacovo, L V Renna, et al.
Journal of Neurology|June 1, 1986
Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophyG Meola, E Scarpini, M Velicogna, et al.
European Journal of Basic and Applied Histochemistry|January 1, 1991
Lysosomotropic agents induce morphological and functional changes in human muscle cells in vitroP L Baron, G Meola, E Scarpini, et al.
Molecular and Cellular Biology|April 1, 1991
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondriaA Chomyn, G Meola, N Bresolin, et al.
Muscle & Nerve|September 1, 1979
Treatment of denervated muscle by gangliosidesM R Caccia, G Meola, C Cerri, et al.
European Journal of Neurology|May 22, 2012
Measuring quality of life impairment in skeletal muscle channelopathiesV A Sansone, C Ricci, M Montanari, et al.
Proceedings of the Royal Society of London. Series B, Biological Sciences|July 22, 1989
Properties of acetylcholine-receptor activation in human Duchenne muscular dystrophy myotubesE Mancinelli, A Sardini, A D'Aumiller, et al.
Neuropediatrics|November 1, 1982
Familial nemaline myopathyG Scarlato, G Pellegrini, M Moggio, et al.
Neuromuscular Disorders : NMD|January 7, 2020
Fragility fractures and bone mineral density in male patients affected by type 1 and type 2 myotonic dystrophyE Passeri, V A Sansone, L M Sconfienza, et al.
European Journal of Histochemistry : EJH|October 30, 2009
RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical studyF Perdoni, M Malatesta, R Cardani, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
European Journal of Histochemistry : EJH|November 11, 2011
Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidenceM Malatesta, M Giagnacovo, L V Renna, et al.
Journal of Neurology|June 1, 1986
Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophyG Meola, E Scarpini, M Velicogna, et al.
European Journal of Basic and Applied Histochemistry|January 1, 1991
Lysosomotropic agents induce morphological and functional changes in human muscle cells in vitroP L Baron, G Meola, E Scarpini, et al.
Molecular and Cellular Biology|April 1, 1991
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondriaA Chomyn, G Meola, N Bresolin, et al.
Muscle & Nerve|September 1, 1979
Treatment of denervated muscle by gangliosidesM R Caccia, G Meola, C Cerri, et al.
European Journal of Neurology|May 22, 2012
Measuring quality of life impairment in skeletal muscle channelopathiesV A Sansone, C Ricci, M Montanari, et al.
Proceedings of the Royal Society of London. Series B, Biological Sciences|July 22, 1989
Properties of acetylcholine-receptor activation in human Duchenne muscular dystrophy myotubesE Mancinelli, A Sardini, A D'Aumiller, et al.
Neuropediatrics|November 1, 1982
Familial nemaline myopathyG Scarlato, G Pellegrini, M Moggio, et al.
Neuromuscular Disorders : NMD|January 7, 2020
Fragility fractures and bone mineral density in male patients affected by type 1 and type 2 myotonic dystrophyE Passeri, V A Sansone, L M Sconfienza, et al.
European Journal of Histochemistry : EJH|October 30, 2009
RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical studyF Perdoni, M Malatesta, R Cardani, et al.
Pageof 15