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M Pane

Showing results (31-40 of 46) with videos related to

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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|June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patientsM Scoto, S Cirak, R Mein, 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.
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.
Journal of Neurology|April 28, 2026
X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort studyA Elkoush, R Giossi, G Gadaleta, et al.
Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.
Neuromuscular Disorders : NMD|July 2, 2013
Six minute walk test in type III spinal muscular atrophy: a 12month longitudinal studyE Mazzone, F Bianco, M Main, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
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|June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patientsM Scoto, S Cirak, R Mein, 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.
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.
Journal of Neurology|April 28, 2026
X-linked Emery-Dreifuss muscular dystrophy: a multicenter, Italian, cohort studyA Elkoush, R Giossi, G Gadaleta, et al.
Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.
Neuromuscular Disorders : NMD|July 2, 2013
Six minute walk test in type III spinal muscular atrophy: a 12month longitudinal studyE Mazzone, F Bianco, M Main, et al.
Pageof 5