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Muscle & Nerve|January 1, 1981
Increased rates of myofibrillar protein breakdown in muscle-wasting diseasesD M Warnes, F M Tomas, F J BallardMuscle & Nerve|January 1, 1981
Supernormal excitability of human sensory fibers after ischemiaM Stöhr, R W Gilliatt, R G WillisonMuscle & Nerve|July 1, 1981
Congenital myasthenia: end-plate acetylcholine receptors and electrophysiology in five casesA Vincent, S G Cull-Candy, J Newsom-Davis, et al.Muscle & Nerve|September 1, 1981
Idiopathic torticollis: sternocleidomastoid myopathy and accessory neuropathyH B Sarnat, R T MorrissyMuscle & Nerve|October 26, 2019
Loss of appetite in amyotrophic lateral sclerosis is associated with weight loss and decreased calorie consumption independent of dysphagiaTaylor Mezoian, Emily Belt, Jamie Garry, et al.Muscle & Nerve|October 26, 2019
Comparative value and determinants of suitability of outcome measures in treated chronic inflammatory demyelinating polyneuropathyYusuf A Rajabally, Majid GhasemiMuscle & Nerve|October 26, 2019
Response to treatment in pediatric ocular myasthenia gravisLori Xu, Diana Castro, Joan S Reisch, et al.Muscle & Nerve|October 26, 2019
Neurodevelopmental, behavioral, and emotional symptoms in Becker muscular dystrophyJoshua T Lambert, Andrew J Darmahkasih, Paul S Horn, et al.Muscle & Nerve|October 26, 2019
Cryptogenic small-fiber neuropathies: Serum autoantibody binding to trisulfated heparan disaccharide and fibroblast growth factor receptor-3Todd D Levine, Jafar Kafaie, Lawrence A Zeidman, et al.Muscle & Nerve|April 10, 2020
Guidelines on clinical presentation and management of nondystrophic myotoniasBas C Stunnenberg, Samantha LoRusso, W David Arnold, et al.Pageof 898