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

C Minetti

Showing results (101-110 of 114) with videos related to

Pageof 12
Sort By:
Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.
Nature Medicine|September 19, 2006
Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitorsG C Minetti, C Colussi, R Adami, et al.
Neurology|May 4, 2011
West syndrome associated with 14q12 duplications harboring FOXG1P Striano, R Paravidino, F Sicca, et al.
Neurology|September 29, 2004
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)C Bruno, O P van Diggelen, D Cassandrini, et al.
Neuromuscular Disorders : NMD|April 17, 2007
The Hammersmith functional score correlates with the SMN2 copy number: a multicentric studyF D Tiziano, E Bertini, S Messina, et al.
Neurology|November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyE Mercuri, E Bertini, S Messina, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric studyE Mercuri, S Messina, R Battini, et al.
European Journal of Neurology|October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolutionS Agostinelli, M Traverso, P Accorsi, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyC Wallgren-Pettersson, K Pelin, P Hilpelä, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.
Nature Medicine|September 19, 2006
Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitorsG C Minetti, C Colussi, R Adami, et al.
Neurology|May 4, 2011
West syndrome associated with 14q12 duplications harboring FOXG1P Striano, R Paravidino, F Sicca, et al.
Neurology|September 29, 2004
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)C Bruno, O P van Diggelen, D Cassandrini, et al.
Neuromuscular Disorders : NMD|April 17, 2007
The Hammersmith functional score correlates with the SMN2 copy number: a multicentric studyF D Tiziano, E Bertini, S Messina, et al.
Neurology|November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyE Mercuri, E Bertini, S Messina, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric studyE Mercuri, S Messina, R Battini, et al.
European Journal of Neurology|October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolutionS Agostinelli, M Traverso, P Accorsi, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyC Wallgren-Pettersson, K Pelin, P Hilpelä, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.
Pageof 12