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European Journal of Neurology
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October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen
V A Sansone, G Coratti, M C Pera, et al.
Neurology
|
July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores
H 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 myopathy
S Lucioli, B Giusti, E Mercuri, et al.
Neurology
|
June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patients
M 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 study
F 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 deficiency
M 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 series
M Piastra, G Zito, A M Orr, et al.
Neurology
|
November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E 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 study
E Mercuri, S Messina, R Battini, et al.
Neurology
|
January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophy
M Kinali, V Arechavala-Gomeza, S Cirak, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 150) with videos related to
Sort By:
Page
of 15
European Journal of Neurology
|
October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen
V A Sansone, G Coratti, M C Pera, et al.
Neurology
|
July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores
H 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 myopathy
S Lucioli, B Giusti, E Mercuri, et al.
Neurology
|
June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patients
M 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 study
F 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 deficiency
M 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 series
M Piastra, G Zito, A M Orr, et al.
Neurology
|
November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E 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 study
E Mercuri, S Messina, R Battini, et al.
Neurology
|
January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophy
M Kinali, V Arechavala-Gomeza, S Cirak, et al.
Page
of 15