Muscle & Nerve is an international and interdisciplinary publication of original contributions, in both health and disease, concerning studies of the muscle, the neuromuscular junction, the peripheral motor, sensory and autonomic neurons, and the central nervous system where the behavior of the peripheral nervous system is clarified. Appearing monthly, Muscle & Nerve publishes clinical studies and clinically relevant research reports in the fields of anatomy, biochemistry, cell biology, electrophysiology and electrodiagnosis, epidemiology, genetics, immunology, pathology, pharmacology, physiology, toxicology, and virology. The Journal welcomes articles and reports on basic clinical electrophysiology and electrodiagnosis. We expedite some papers dealing with timely topics to keep up with the fast-moving pace of science, based on the referees' recommendation.
《肌肉与神经》是一本国际性、跨学科的出版物，收录了有关肌肉、神经肌肉接头、外周运动神经元、感觉神经元和自主神经元以及中枢神经系统的健康和疾病方面的原创性论文，其中阐明了外周神经系统的行为。《肌肉与神经》月刊出版解剖学、生物化学、细胞生物学、电生理学和电诊断学、流行病学、遗传学、免疫学、病理学、药理学、生理学、毒理学和病毒学领域的临床研究和临床相关研究报告。该杂志欢迎文章和报告的基础临床电生理学和电诊断。根据评审员的推荐，我们加快了一些涉及及时主题的论文，以跟上科学的快速发展步伐。
Impact of expiratory strength training in amyotrophic lateral sclerosis: Results of a randomized, sham‐controlled trial
来源期刊：Muscle & NerveDOI：10.1002/mus.26292
Rasagiline for amyotrophic lateral sclerosis: A randomized, controlled trial
来源期刊：Muscle & NerveDOI：10.1002/mus.26335
4‐Aminopyridine attenuates muscle atrophy after sciatic nerve crush injury in mice
来源期刊：Muscle & NerveDOI：10.1002/mus.26516
A pilot study of neuromuscular ultrasound as a biomarker for amyotrophic lateral sclerosis
来源期刊：Muscle & NerveDOI：10.1002/mus.26360
Development of grading scales of pedal sensory loss using Mokken scale analysis on the Rotterdam Diabetic Foot Study Test Battery data
来源期刊：Muscle & NerveDOI：10.1002/mus.26628
Validation of diagnostic methods for traumatic sensory neuropathy and neuropathic pain
来源期刊：Muscle & NerveDOI：10.1002/mus.26400
Fascicular constrictions above elbow typify anterior interosseous nerve syndrome
来源期刊：Muscle & NerveDOI：10.1002/mus.26768
Longitudinal follow‐up of biopsy‐proven small fiber neuropathy
来源期刊：Muscle & NerveDOI：10.1002/mus.26648
Muscle endurance deficits in myositis patients despite normal manual muscle testing scores
来源期刊：Muscle & NerveDOI：10.1002/mus.26307
Muscle thickness measured by ultrasound is reduced in neuromuscular disorders and correlates with clinical and electrophysiological findings
来源期刊：Muscle & NerveDOI：10.1002/mus.26693
MiRNAs as biomarkers of phenotype in neutral lipid storage disease with myopathy
来源期刊：Muscle & NerveDOI：10.1002/mus.26761
Magnetic resonance imaging of the anterior compartment of the lower leg is a biomarker for weakness, disability, and impaired gait in childhood Charcot–Marie–Tooth disease
来源期刊：Muscle & NerveDOI：10.1002/mus.26352
Spinocerebellar ataxia type 2—neuronopathy or neuropathy?
来源期刊：Muscle & NerveDOI：10.1002/mus.26613
Adipose‐derived stem cells delay muscle atrophy after peripheral nerve injury in the rodent model
来源期刊：Muscle & NerveDOI：10.1002/mus.26432
Treatment outcome in juvenile‐onset myasthenia gravis
来源期刊：Muscle & NerveDOI：10.1002/mus.26445
Impaired short‐ and long‐latency afferent inhibition in amyotrophic lateral sclerosis
来源期刊：Muscle & NerveDOI：10.1002/mus.26464
Comparing electrical stimulation and tacrolimus (FK506) to enhance treating nerve injuries
来源期刊：Muscle & NerveDOI：10.1002/mus.26659
Vibration testing: Optimizing methods to improve reliability
来源期刊：Muscle & NerveDOI：10.1002/mus.26373
Diaphragm involvement in immune checkpoint inhibitor‐related myositis
来源期刊：Muscle & NerveDOI：10.1002/mus.26640
Pregnancy‐associated respiratory failure in muscle specific kinase congenital myasthenic syndrome
来源期刊：Muscle & NerveDOI：10.1002/mus.26410
The motor unit and quantitative electromyography
来源期刊：Muscle & NerveDOI：10.1002/mus.26718
When should you order genetic testing for patients with cryptogenic neuropathy? Let the data do the talking
来源期刊：Muscle & NerveDOI：10.1002/mus.26409
A model to predict ventilator requirement in myotonic dystrophy type 1
来源期刊：Muscle & NerveDOI：10.1002/mus.26471
Repetitive nerve stimulation testing in myasthenic crisis
来源期刊：Muscle & NerveDOI：10.1002/mus.26472
Neurodevelopmental, behavioral, and emotional symptoms in Becker muscular dystrophy
来源期刊：Muscle & NerveDOI：10.1002/mus.26750
Limitations of 6‐minute walk test reference values for spinal muscular atrophy
来源期刊：Muscle & NerveDOI：10.1002/mus.26794
Bilateral nerve conduction studies in the evaluation of distal symmetric polyneuropathy
来源期刊：Muscle & NerveDOI：10.1002/mus.26616
A modified multiple point stimulation method for motor unit number estimation of the hypothenar muscles
来源期刊：Muscle & NerveDOI：10.1002/mus.26391
Viral vector delivery of follistatin enhances recovery of reinnervated muscle
来源期刊：Muscle & NerveDOI：10.1002/mus.26653
Far‐field potentials in the compound muscle action potential
来源期刊：Muscle & NerveDOI：10.1002/mus.26743
Dual innervation may occur in a partially denervated muscle
来源期刊：Muscle & NerveDOI：10.1002/mus.26323
Clinical and neurophysiological variability in Andersen‐Tawil syndrome
来源期刊：Muscle & NerveDOI：10.1002/mus.26705
Diffusion‐weighted magnetic resonance imaging is useful for assessing inflammatory myopathies
来源期刊：Muscle & NerveDOI：10.1002/mus.26438
Local FK506 delivery at the direct nerve repair site improves nerve regeneration
来源期刊：Muscle & NerveDOI：10.1002/mus.26656
Family with primary periodic paralysis and a mutation in MCM3AP, a gene implicated in mRNA transport
来源期刊：Muscle & NerveDOI：10.1002/mus.26622
Cross‐sectional area reference values for sonography of nerves in the upper extremities
来源期刊：Muscle & NerveDOI：10.1002/mus.26781
Reducing glucose variability with continuous subcutaneous insulin infusion is associated with reversal of axonal dysfunction in type 1 diabetes mellitus
来源期刊：Muscle & NerveDOI：10.1002/mus.26738
Apoptotic changes in a full‐lengthened immobilization model of rat soleus muscle
来源期刊：Muscle & NerveDOI：10.1002/mus.26359
TFG: At the crossroads of motor neuron disease and myopathy
来源期刊：Muscle & NerveDOI：10.1002/mus.26692
A pilot study of the responsiveness of wireless motion analysis in facioscapulohumeral muscular dystrophy
来源期刊：Muscle & NerveDOI：10.1002/mus.26681
Chaperones in sporadic inclusion body myositis—Validation of proteomic data
来源期刊：Muscle & NerveDOI：10.1002/mus.26742
What system controls balance in children with charcot‐marie‐tooth disease?
来源期刊：Muscle & NerveDOI：10.1002/mus.26612
Safety of intravenous immune globulin in an outpatient setting for patients with neuromuscular disease
来源期刊：Muscle & NerveDOI：10.1002/mus.26678
Cladribine in myasthenia gravis: A case urging for prudence
来源期刊：Muscle & NerveDOI：10.1002/mus.26446
Body composition in patients with congenital myotonic dystrophy
来源期刊：Muscle & NerveDOI：10.1002/mus.26509
Nerve high‐resolution ultrasonography in tangier disease
来源期刊：Muscle & NerveDOI：10.1002/mus.26427
Parameters derived from compound muscle action potential scan for discriminating amyotrophic lateral sclerosis‐related denervation
来源期刊：Muscle & NerveDOI：10.1002/mus.26644
Optimal stimulation site selection for H‐reflex measurement: Comments on previously published paper
来源期刊：Muscle & NerveDOI：10.1002/mus.26615
Take two: Utility of the repeat skeletal muscle biopsy
来源期刊：Muscle & NerveDOI：10.1002/mus.26484
Cost of illness, cost of immunoglobulin therapy and their determinants in chronic inflammatory demyelinating polyneuropathy
来源期刊：Muscle & NerveDOI：10.1002/mus.26407
