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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
November 3, 2021
Correction to: Reldesemtiv in Patients with Spinal Muscular Atrophy: a Phase 2 Hypothesis-Generating Study
Stacy A Rudnicki, Jinsy A Andrews, Tina Duong, et al.
Journal of Neuromuscular Diseases
|
June 14, 2021
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial
Richard S Finkel, Craig M McDonald, H Lee Sweeney, et al.
Translational Neurodegeneration
|
October 29, 2025
Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases
Gang Wu, Wenan Chen, Joanne Wuu, et al.
Brain : a Journal of Neurology
|
September 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy
Richard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
September 24, 2020
A Phase 2, Double-Blind, Randomized, Dose-Ranging Trial Of <i>Reldesemtiv</i> In Patients With ALS
Jeremy M Shefner, Jinsy A Andrews, Angela Genge, et al.
Neurology. Clinical Practice
|
December 28, 2018
Consensus-based care recommendations for adults with myotonic dystrophy type 1
Tetsuo Ashizawa, Cynthia Gagnon, William J Groh, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
February 19, 2021
Preface: promoting research in PLS: current knowledge and future challenges
Hiroshi Mitsumoto, Martin R Turner, , et al.
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Search research articles
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Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
November 3, 2021
Correction to: Reldesemtiv in Patients with Spinal Muscular Atrophy: a Phase 2 Hypothesis-Generating Study
Stacy A Rudnicki, Jinsy A Andrews, Tina Duong, et al.
Journal of Neuromuscular Diseases
|
June 14, 2021
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial
Richard S Finkel, Craig M McDonald, H Lee Sweeney, et al.
Translational Neurodegeneration
|
October 29, 2025
Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases
Gang Wu, Wenan Chen, Joanne Wuu, et al.
Brain : a Journal of Neurology
|
September 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy
Richard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
September 24, 2020
A Phase 2, Double-Blind, Randomized, Dose-Ranging Trial Of <i>Reldesemtiv</i> In Patients With ALS
Jeremy M Shefner, Jinsy A Andrews, Angela Genge, et al.
Neurology. Clinical Practice
|
December 28, 2018
Consensus-based care recommendations for adults with myotonic dystrophy type 1
Tetsuo Ashizawa, Cynthia Gagnon, William J Groh, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
February 19, 2021
Preface: promoting research in PLS: current knowledge and future challenges
Hiroshi Mitsumoto, Martin R Turner, , et al.
Page
of 4