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Risk factors for Lumbosacral Radiculoplexus Neuropathy
Abstract Introduction/Aims Recently, our group found an association between diabetes mellitus (DM) and lumbosacral radicul...
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Immune‐mediated Necrotizing Myopathy following BNT162b2 Vaccination in a Patient with Antibodies against Receptor‐binding Domain of SARS‐CoV‐2 and Signal Recognition Particle
Corresponding Author Jian-Qiang Lu MD, PhD Department of P...
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Time course of capillary regression and an expression balance between vascular endothelial growth factor‐A and thrombospondin‐1 in the soleus muscle of hindlimb unloaded rats
Abstract Introduction/Aims Skeletal muscle capillaries regress with disuse; however, information on time-dependent changes...
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COVID‐19 Infection in Patients with Late‐Onset Pompe Disease
Abstract Introduction/Aims Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2/COVID-19) is frequently more severe...
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Opinions on pneumocystis jirovecci prophylaxis in autoimmune neuromuscular disorders
Abstract Pneumocystis jirovecci (PJ) is ubiquitously present in the environment and capable of causing an interstitial pne...
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Weak shoulder and arm sparing signs in amyotrophic lateral sclerosis
Abstract Introduction/Aims A number of signs of selective involvement have been reported in amyotrophic lateral sclerosis ...
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A pilot study of a novel transmembranous electromyography device for assessment of oral cavity and oropharyngeal muscles
Abstract Introduction/Aims Electromyography (EMG) can provide valuable insights into the pathophysiology of oropharyngeal ...
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GNE myopathy: Don’t sleep on the platelets
Corresponding Author Teerin Liewluck MD Division of Neurom...
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Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments
Abstract Introduction/Aims Becker muscular dystrophy (BMD) is characterized by variable disease severity and progression, ...
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Evidence‐based guideline: Neuromuscular ultrasound for the diagnosis of ulnar neuropathy at the elbow
Abstract Introduction/Aims The purpose of this literature review is to develop an evidence-based guideline for the use of ...
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Calendar of Events
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A Randomized Placebo‐Controlled Phase 3 Study of Mesenchymal stem cells induced to secrete high levels of neurotrophic factors in Amyotrophic Lateral Sclerosis
Abstract Introduction/Aims Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative illness with great unmet patie...
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Myonuclear apoptosis via cleaved caspase‐3 upregulation is related to macrophage accumulation underlying immobilization‐induced muscle fibrosis
Abstract Introduction/Aims Although macrophage accumulation plays a key role in the development of immobilization-induced ...
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The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review
Abstract Duchenne muscular dystrophy (DMD) is associated with progressive muscle weakness, loss of ambulation (LOA), and e...
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A novel homozygous ALPK3 variant associated with cardiomyopathy and skeletal muscle involvement
Corresponding Author 1st Department of Neurology, Eginition Hospital, Medical S...
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Radial motor nerve conduction studies recorded from triceps brachii and extensor carpi radialis longus: Techniques and reference values
Abstract Introduction/Aims Optimal timing of nerve transfer surgery in cervical spinal cord injury (SCI) depends upon the ...
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Motor Unit Integrity in Multifocal Motor Neuropathy: A Systematic Evaluation with CMAP Scans
Abstract Introduction/Aims Progressive axonal loss in multifocal motor neuropathy (MMN) is often assessed with nerve condu...
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Optimal stimulation site of the femoral nerve to record F‐waves from the vastus lateralis muscle
Abstract Introduction/Aims: The conventional recording of F-waves from the vastus lateralis muscle may not accurately meas...
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Home‐based gait analysis as an exploratory endpoint during a multicenter phase 1 trial in limb girdle muscular dystrophy type R2 and facioscapulohumeral muscular dystrophy
Abstract Introduction/Aims Limb girdle muscular dystrophy type 2B (LGMDR2) and facioscapulohumeral muscular dystrophy (FSH...
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The long exercise test as a functional marker of periodic paralysis
Abstract Introduction/Aims The aim of this study was to evaluate the sensitivity of the long exercise test (LET) in the di...
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Laryngospasm in Amyotrophic Lateral Sclerosis
Abstract Introduction Laryngospasm is an involuntary sustained closure of sphincter musculature that leads to an unpleasan...
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Slowing the Loss of Physical Function in Amyotrophic Lateral Sclerosis With Edaravone: Post hoc Analysis of ALSFRS‐R Item Scores in Pivotal Study MCI186‐19
Abstract Introduction Phase 3 study MCI186-19 demonstrated less loss of physical function with edaravone versus placebo, a...
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Transcutaneous CO2 monitoring as indication for inpatient non‐invasive ventilation initiation in patients with amyotrophic lateral sclerosis
Abstract Introduction/Aims Amyotrophic lateral sclerosis (ALS) is characterized by profound muscle weakness, including dia...
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Documentation of Advance Care Planning Forms in Patients with Amyotrophic Lateral Sclerosis
Abstract Documentation of Advance Care Planning Forms in Patients with Amyotrophic Lateral Sclerosis Introduction/Aims Amy...
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A Population‐based Study of Scoliosis among Males Diagnosed with a Dystrophinopathy Identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)
Abstract INTRODUCTION/AIMS Scoliosis is a common comorbidity among individuals diagnosed with a dystrophinopathy. We exami...
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Acute‐onset polyradiculoneuropathy after SARS‐CoV2 vaccine in the West and North Midlands, United Kingdom
Abstract Introduction/Aims We aimed to determine whether specific SARS-CoV2 vaccines may be associated with acute-onset po...
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Small Fiber Neuropathy Associated with SARS‐CoV‐2 Infection
Abstract Introduction/Aims The development and persistence of neurological symptoms following SARS-CoV-2 infection is refe...
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Demographics, clinical characteristics, and prognostic factors of amyotrophic lateral sclerosis in Midwest
Abstract Introduction/Aims The Midwest has the highest regional prevalence of self-reported amyotrophic lateral sclerosis ...
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Transcutaneous CO2 Monitoring as Indication for Inpatient NIV Initiation in Patients with ALS
Abstract Introduction/Aims Amyotrophic lateral sclerosis (ALS) is characterized by profound muscle weakness, including dia...
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Combining multiple measures into a summary index ‐ a step toward more reliable measurement
This article has been accepted for publication and undergone full peer review but has not been through the co...
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