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Muscle & Nerve|May 19, 2022
Quantitative muscle analysis in facioscapulohumeral muscular dystrophy using whole-body fat-referenced MRI: Protocol development, multicenter feasibility, and repeatabilityPer Widholm, André Ahlgren, Markus Karlsson, et al.Muscle & Nerve|January 1, 1987
An examination of some factors influencing creatine kinase in the blood of patients with muscular dystrophyM J Jackson, J M Round, D J Newham, et al.Muscle & Nerve|January 1, 1987
Practical analysis of variability of muscle function measurements in Duchenne muscular dystrophyR H Edwards, S J Chapman, D J Newham, et al.Muscle & Nerve|July 1, 2021
Interstitial amyloidosis in sporadic inclusion body myositisMazen Alamr, Margherita Milone, Elie Naddaf, et al.Muscle & Nerve|January 19, 2018
Effect of dys-1 mutation on gene expression profile in space-flown Caenorhabditis elegansDan Xu, Ying Gao, Lin Guo, et al.Muscle & Nerve|December 12, 2018
Differences in muscle contraction onset as determined by ultrasound and electromyographyAndrew J Tweedell, Matthew S Tenan, Courtney A HaynesMuscle & Nerve|December 15, 2018
Validation of diagnostic methods for traumatic sensory neuropathy and neuropathic painTuija Teerijoki-Oksa, Heli Forssell, Satu K JääskeläinenMuscle & Nerve|December 23, 2018
Disease duration and disability in dysfeRlinopathy can be described by muscle imaging using heatmaps and random forestsDavid Gómez-Andrés, Jorge Díaz, Francina Munell, et al.Muscle & Nerve|December 22, 2018
Quantitative myotonia assessment with a commercially available dynamometer in myotonic dystrophy types 1 and 2Magda Horáková, Tomáš Horák, Olesja Parmová, et al.Muscle & Nerve|December 25, 2018
The utility of a point-of-care sural nerve conduction device for detection of diabetic polyneuropathy: A cross-sectional studyMustafa A Kural, Signe T Andersen, Niels T Andersen, et al.Pageof 898