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COL6A1 related muscular dystrophy in Landseer dogs: A canine model for Ullrich congenital muscular dystrophy
Brands J, Steffen F, Spennes J, et al.
Muscle & Nerve, 2020
12-Month progression of motor and functional outcomes in congenital myotonic dystrophy
Quigg KH, Berggren KN, McIntyre M, et al.
Muscle & Nerve, 2020
Safety, feasibility, and efficacy of strengthening exercise in Duchenne muscular dystrophy
Lott DJ, Taivassalo T, Cooke KD, et al.
Muscle & Nerve, 2020
Early experiences of Nusinersen for the Treatment of Spinal Muscular Atrophy: Results from a large survey of patients and caregivers
Chen E, Dixon S, Naik R, et al.
Muscle & Nerve, 2020
Skeletal muscle magnetic resonance imaging in Pompe disease
Diaz-Manera J, Walter G, Straub V
Muscle & Nerve, 2020
Multisystem proteinopathy: Where myopathy and motor neuron disease converge
Korb MK, Kimonis VE, Mozaffar T
Muscle & Nerve, 2020
Patient compliance with orthotic use- can we do better? An editorial for Zuccarino et al. "Satisfaction with Ankle Foot Orthoses in Individuals with Charcot-Marie-Tooth"
Hachisuka A, Hubenig L, Chan KM
Muscle & Nerve, 2020
(-)-Epicatechin induces mitochondrial biogenesis and markers of muscle regeneration in adults with Becker muscular dystrophy
McDonald CM, Ramirez-Sanchez I, Oskarsson B, et al.
Muscle & Nerve, 2020
Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy
Manokaran RK, Aggarwala S, Kumar R, et al.
Muscle & Nerve, 2020
Combination molecular therapies for type 1 spinal muscular atrophy
Harada Y, Rao VK, Arya K, et al.
Muscle & Nerve, 2020
Clinical features of LRP4/agrin-antibody-positive myasthenia gravis: A multicenter study
Rivner MH, Quarles BM, Pan JX, et al.
Muscle & Nerve, 2020
The CINRG Becker Natural History Study: Baseline Characteristics
Clemens PR, Niizawa G, Feng J, et al.
Muscle & Nerve, 2020
Whole blood survival motor neuron protein levels correlate with severity of denervation in spinal muscular atrophy
Alves CRR, Zhang R, Johnstone AJ, et al.
Muscle & Nerve, 2020
A Telephonic Single Breath Count Test For Screening Of Exacerbations Of Myasthenia Gravis : A Pilot Study
Kukulka K, Gummi RR, Govindarajan R
Muscle & Nerve, 2020
The effects of concentric and eccentric training in murine models of dysferlin-associated muscular dystrophy
Begam M, Roche R, Hass JJ, et al.
Muscle & Nerve, 2020
Update on immune-mediated therapies for myasthenia gravis
Habib AA, Ahmadi Jazi G, Mozaffar T
Muscle & Nerve, 2020
Guidelines on clinical presentation and management of non-dystrophic myotonias
Stunnenberg B, LoRusso S, Arnold WD, et al.
Muscle & Nerve, 2020
Histone acetyltransferase inhibition rescues differentiation of emerin-deficient myogenic progenitors
Bossone KA, Ellis JA, Holaska JM
Muscle & Nerve, 2020
Rituximab in late-onset myasthenia gravis is safe and effective
Sahai SK, Maghzi AH, Lewis RA
Muscle & Nerve, 2020
Spinal muscular atrophy care in the COVID-19 pandemic era
Veerapandiyan A, Connolly AM, Finkel RS, et al.
Muscle & Nerve, 2020
A study of impairments in Oculopharyngeal Muscular Dystrophy
Brisson JD, Gagnon C, Brais B, et al.
Muscle & Nerve, 2020
The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic
Veerapandiyan A, Wagner KR, Apkon S, et al.
Muscle & Nerve, 2020
Ultrasound can differentiate inclusion body myositis from disease mimics
Leeuwenberg KE, van Alfen N, Christopher-Stine L, et al.
Muscle & Nerve, 2020
Validity of the Mini-BESTest in adults with myotonic dystrophy type 1
Duchesne E, Hebert LJ, Mathieu J, et al.
Muscle & Nerve, 2020
Long-term strength and functional status in inclusion body myositis and identification of trajectory subgroups
Oldroyd AGS, Lilleker JB, Williams J, et al.
Muscle & Nerve, 2020
