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S Finkel

Showing results (221-230 of 289) with videos related to

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Plos One|March 20, 2018
Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophyAlison M Barnard, Rebecca J Willcocks, Erika L Finanger, et al.
JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Annals of Clinical and Translational Neurology|September 12, 2019
Dominant collagen XII mutations cause a distal myopathyPayam Mohassel, Teerin Liewluck, Ying Hu, et al.
Nature Medicine|December 8, 2025
Intrathecal onasemnogene abeparvovec in treatment-naive patients with spinal muscular atrophy: a phase 3, randomized controlled trialCrystal M Proud, Dũng Chí Vũ, Jo M Wilmshurst, et al.
Muscle & Nerve|April 27, 2019
Balance impairment in pediatric charcot-marie-tooth diseaseTimothy Estilow, Allan M Glanzman, Joshua Burns, et al.
Neuromuscular Disorders : NMD|January 2, 2018
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional careEugenio Mercuri, Richard S Finkel, Francesco Muntoni, et al.
The New England Journal of Medicine|August 13, 2025
Risdiplam in Presymptomatic Spinal Muscular AtrophyRichard S Finkel, Laurent Servais, Dmitry Vlodavets, et al.
Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.
Neuromuscular Disorders : NMD|January 7, 2018
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethicsRichard S Finkel, Eugenio Mercuri, Oscar H Meyer, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
Pageof 29

Showing results (221-230 of 289) with videos related to

Sort By:
Pageof 29
Plos One|March 20, 2018
Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophyAlison M Barnard, Rebecca J Willcocks, Erika L Finanger, et al.
JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Annals of Clinical and Translational Neurology|September 12, 2019
Dominant collagen XII mutations cause a distal myopathyPayam Mohassel, Teerin Liewluck, Ying Hu, et al.
Nature Medicine|December 8, 2025
Intrathecal onasemnogene abeparvovec in treatment-naive patients with spinal muscular atrophy: a phase 3, randomized controlled trialCrystal M Proud, Dũng Chí Vũ, Jo M Wilmshurst, et al.
Muscle & Nerve|April 27, 2019
Balance impairment in pediatric charcot-marie-tooth diseaseTimothy Estilow, Allan M Glanzman, Joshua Burns, et al.
Neuromuscular Disorders : NMD|January 2, 2018
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional careEugenio Mercuri, Richard S Finkel, Francesco Muntoni, et al.
The New England Journal of Medicine|August 13, 2025
Risdiplam in Presymptomatic Spinal Muscular AtrophyRichard S Finkel, Laurent Servais, Dmitry Vlodavets, et al.
Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.
Neuromuscular Disorders : NMD|January 7, 2018
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethicsRichard S Finkel, Eugenio Mercuri, Oscar H Meyer, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
Pageof 29