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E Mercuri

Showing results (141-150 of 150) with videos related to

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Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Refining functional phenotypes in an international cohort of untreated paediatric type 2 and 3 SMA patients using the Revised Hammersmith ScaleE Milev, G Stimpson, D Ramsey, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, 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.
Neuromuscular Disorders : NMD|February 5, 2014
Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patientsE Mazzone, R De Sanctis, L Fanelli, et al.
Neurology|March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population studyE Mercuri, S Messina, C Bruno, et al.
Neurology|July 8, 2011
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort studyE Mazzone, G Vasco, M P Sormani, et al.
Neuromuscular Disorders : NMD|June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric settingE S Mazzone, S Messina, G Vasco, et al.
Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Neuromuscular Disorders : NMD|February 4, 2026
Refining functional phenotypes in an international cohort of untreated paediatric type 2 and 3 SMA patients using the Revised Hammersmith ScaleE Milev, G Stimpson, D Ramsey, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, 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.
Neuromuscular Disorders : NMD|February 5, 2014
Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patientsE Mazzone, R De Sanctis, L Fanelli, et al.
Neurology|March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population studyE Mercuri, S Messina, C Bruno, et al.
Neurology|July 8, 2011
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort studyE Mazzone, G Vasco, M P Sormani, et al.
Neuromuscular Disorders : NMD|June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric settingE S Mazzone, S Messina, G Vasco, et al.
Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.
Pageof 15