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Muscle & Nerve|October 16, 2020
Long-term survival of participants in the CENTAUR trial of sodium phenylbutyrate-taurursodiol in amyotrophic lateral sclerosisSabrina Paganoni, Suzanne Hendrix, Samuel P Dickson, et al.Muscle & Nerve|October 12, 2020
Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3Stefan A Djordjevic, Vedrana Milic-Rasic, Vesna Brankovic, et al.Muscle & Nerve|October 12, 2020
Psychometric longitudinal evaluation of the Chronic Acquired Polyneuropathy Patient-Reported Index (CAPPRI) in patients with chronic inflammatory demyelinating polyneuropathyReza Sadjadi, Stojan Peric, Kelly Gwathmey, et al.Muscle & Nerve|July 30, 2021
Different trajectories in upper limb and gross motor function in spinal muscular atrophyGiorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.Muscle & Nerve|January 19, 2020
Quantitative muscle MRI study of patients with sporadic inclusion body myositisBehnaz Ansari, Emmanuelle Salort-Campana, Augustin Ogier, et al.Muscle & Nerve|February 1, 1985
Changes in intramuscular collagen and fibronectin in denervation atrophyV Salonen, M Lehto, M Kalimo, et al.Muscle & Nerve|June 6, 2022
Reachable workspace analysis is a potential measurement for impairment of the upper extremity in neuralgic amyotrophyJos IJspeert, Renee Lustenhouwer, Renske M Janssen, et al.Muscle & Nerve|June 18, 2022
Delays in pulmonary decline in eteplirsen-treated patients with Duchenne muscular dystrophyJoel Iff, Charles Gerrits, Yi Zhong, et al.Muscle & Nerve|June 16, 2022
National prescription patterns of antidepressants among patients with amyotrophic lateral sclerosis: An analysis of the Korean National Health Insurance databaseC Hyung Keun Park, Seok-Jin Choi, Ye-Jee Kim, et al.Muscle & Nerve|June 9, 2021
Safety, tolerability, and pharmacokinetics of casimersen in patients with Duchenne muscular dystrophy amenable to exon 45 skipping: A randomized, double-blind, placebo-controlled, dose-titration trialKathryn R Wagner, Nancy L Kuntz, Erica Koenig, et al.Pageof 898