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

E Mercuri

Showing results (131-140 of 150) with videos related to

Pageof 15
Sort By:
European Journal of Neurology|October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersenV A Sansone, G Coratti, M C Pera, et al.
Neurology|July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with coresH Jungbluth, C R Müller, B Halliger-Keller, et al.
Neurology|June 16, 2005
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathyS Lucioli, B Giusti, E Mercuri, et al.
Neurology|June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patientsM Scoto, S Cirak, R Mein, 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.
Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
European Journal of Pediatrics|September 28, 2025
Pediatric acute respiratory distress syndrome in children with type I - spinal muscular atrophy: a 12-year case seriesM Piastra, G Zito, A M Orr, 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.
Neurology|January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophyM Kinali, V Arechavala-Gomeza, S Cirak, et al.
Pageof 15

Showing results (131-140 of 150) with videos related to

Sort By:
Pageof 15
European Journal of Neurology|October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersenV A Sansone, G Coratti, M C Pera, et al.
Neurology|July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with coresH Jungbluth, C R Müller, B Halliger-Keller, et al.
Neurology|June 16, 2005
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathyS Lucioli, B Giusti, E Mercuri, et al.
Neurology|June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patientsM Scoto, S Cirak, R Mein, 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.
Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
European Journal of Pediatrics|September 28, 2025
Pediatric acute respiratory distress syndrome in children with type I - spinal muscular atrophy: a 12-year case seriesM Piastra, G Zito, A M Orr, 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.
Neurology|January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophyM Kinali, V Arechavala-Gomeza, S Cirak, et al.
Pageof 15