Muscle & Nerve

Papers
(The TQCC of Muscle & Nerve is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
AANEM Calender of Events112
AANEM News and Insights108
Join AANEM97
AANEM News & Insights91
AANEM News & Insights71
Issue Information48
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey45
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy40
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects39
Join AANEM39
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine38
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course38
Neuroma morphology: A macroscopic classification system37
Pilot study of a virtual weight management program for Duchenne muscular dystrophy37
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle34
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study34
Prognosis After Discontinuation of Azathioprine or Mycophenolate Mofetil in Well‐Controlled Myasthenia Gravis: A Retrospective Analysis33
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study32
Radial Mononeuropathy: Clinical and Electrodiagnostic Characteristics in 177 Patients32
Neuromuscular ultrasound: Impact on diagnosis and management31
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy31
Emerging Upper Extremity Muscle Ultrasound Patterns as a Diagnostic Aid in TTN ‐Related Myopathies30
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis29
Comorbidities and Treatment Patterns in People With Myasthenia Gravis in Denmark, Finland and Sweden: A Population‐Based Observational Study29
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia28
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials27
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma27
Diagnosis of Primary Mitochondrial Diseases25
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis25
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts25
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure24
Diagnosis and management of metabolic myopathies23
23
AANEM Application22
AANEM News and Comments22
Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression21
AANEM News & Insights20
Peripheral nerve injuries in the performing artist20
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier20
Rasch analysis of the Unidimensional Self‐Efficacy Scale in Neuromuscular Disorders and comparison between sex, age, and diagnoses20
The Disparities in Myasthenia Gravis Clinical Trial Enrollment in the United States and Canada20
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates20
Issue Highlights19
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy19
Atypical presentation of hypokalemic periodic paralysis: A case report19
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report19
Physiology of Abnormal Muscle Fiber Generators19
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy19
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change18
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry18
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis18
Response to the Letter From Gaul‐Muller and Bach on NIV Intolerance, NIV Settings and Mortality in MND Patients With Gastrostomy18
Estimation of diaphragm depth based on waist circumference in the Thai population18
The utility of diaphragm ultrasound thickening indices for assessing respiratory decompensation in amyotrophic lateral sclerosis18
Integrating Serum Neurofilament Light Chain Into Amyotrophic Lateral Sclerosis Diagnostic Criteria17
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis17
Effect of Capsaicin (8%) Topical System on Sensory Function in Patients With Diabetic Peripheral Neuropathy: Analysis of the PACE Study17
Congenital Myopathies and Muscular Dystrophies: A Single Tertiary Center Experience and Factors Associated With Long‐Term Outcomes17
Predictive Values of Preoperative Compound Muscle Action Potential Amplitude for Surgical Outcomes in Idiopathic Ulnar Neuropathy at the Elbow16
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus16
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis16
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury15
AANEM News and Insights15
Calendar of Events15
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis15
Predictors of Outcome in Myasthenic Crisis15
Join AANEM14
Pregnancy outcomes in patients with congenital myasthenic syndromes14
Visible Tongue Fasciculations With Electromyographic Denervation in Autopsy‐Proven Progressive Supranuclear Palsy Mimicking Amyotrophic Lateral Sclerosis14
MRI of Neurogenic Human Motor Units Following Poliomyelitis14
The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study14
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis14
A‐waves are associated with neuropathic pain in leprosy14
Issue Highlights13
Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen13
Evaluation of the applicability of weak shoulder and arm sparing signs in amyotrophic lateral sclerosis by multiple neurologists and neurology residents: A single‐center study13
AANEM News and Insights13
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment13
Motor Unit Number Index (MUNIX) in Control Children: Reference Values and Reliability12
Ultrasound Guidance to Augment Needle Electromyography Precision in the Complex Nerve Injury Setting12
Phosphorylated Tau at Threonine 181 Is Elevated in Amyotrophic Lateral Sclerosis Plasma12
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation Defects12
Motor Nerve Conduction of the Hypoglossal Nerve With F‐Waves in Healthy Adults12
Paraproteinemic neuropathies12
AANEM News & Insights12
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions12
Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment12
Broadening the Comorbidity Landscape in Facioscapulohumeral Dystrophy: Beyond the Usual Suspects12
Utility of Far‐Field Potentials as a Biomarker of Neurodegeneration in Spinal Muscular Atrophy12
Focal Neurogenic Muscle Hypertrophy and Focal Neurogenic Myositis12
Oral Health in Amyotrophic Lateral Sclerosis: Feasibility of Oral Screening and Determinants of Poor Outcomes11
Calendar of Events11
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock11
Evaluation of mechanomyogram efficacy as a tool for assessing paired‐pulse inhibition of blink reflex early R1 component11
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy11
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari11
Extraocular muscle volume on time‐of‐flight magnetic resonance angiography in patients with myasthenia gravis11
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy11
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies11
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults11
11
Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region11
A Phase 1, Double‐Blind, Placebo‐Controlled Trial of Sevasemten (EDG‐5506), a Selective Modulator of Fast Skeletal Muscle Contraction, in Healthy Volunteers and Adults With Becker Muscular 11
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 201811
Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms11
Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies10
Assessment of clinical skills in electrodiagnostic medicine10
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study10
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene10
AANEM 2024 Annual Meeting Abstracts Guide10
Issue Information10
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”10
Short‐term educational value of online neuromuscular ultrasound courses10
Improving ALS Clinic Care Through Experience‐Based Co‐Design: A Participatory Action Research Study10
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up10
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study10
Join AANEM10
Issue Information10
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study10
Calendar of Events10
Observational Evaluation of Muscle Echointensity and EMG Insertional Activity in Poststroke Spasticity10
Standardization of Myasthenia Gravis Outcome Measures in Clinical Practice: A Report of the MGFA Task Force10
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP10
AANEM News & Insights10
10
Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve9
Spectrum of Anti‐Neurofascin Neuropathies: A Retrospective Indian Cohort9
Join AANEM9
Phantom radiculopathy: An electrodiagnostic challenge9
Issue Highlights9
9
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center9
Introduction to the Supplement9
Reply to: “Beyond Prevalence: The Importance of Multifactorial Assessment in Cancer Risk Among Myotonic Dystrophy Patients”9
Milestones of progression in myotonic dystrophy type 1 and type 29
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy9
Risk of Infection Following Clearance of Immunoglobulin G by Plasma Exchange in Myasthenia Gravis9
“An Ounce of Prevention…”9
Join AANEM9
Details Matter: The Difference Between NIV and NVS9
The Antibody‐Microbiota Interface in Autoimmune Diseases9
Practical Approach to Managing SCIg Treatment in Patients With Chronic Inflammatory Demyelinating Polyneuropathy9
Neuromuscular Ultrasound Training: Bridging the Gap9
The Enigma of the Motor Nerve Conduction Study9
Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype9
Chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M paraprotein, cold agglutinins, and disialosyl antibodies presenting after COVID19 mRNA vaccination9
Distribution of Infralesional Lower Motor Neuron Injury in Traumatic Cervical Spinal Cord Injury Candidates for Upper Limb Reconstruction: A Single Center Experience9
Fascial Border Absence Between the Extensor Carpi Radialis Longus and Brachioradialis Muscles9
Incidence and causes of overdiagnosis of myasthenia gravis9
AANEM News & Insights9
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab8
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3‐related muscular dystrophy8
Issue Information8
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value8
Ultrasound‐Guided Near‐Nerve Needle Assessment of the End‐to‐Side Anterior Interosseous to Ulnar Motor Nerve Transfer Contribution to Hand Intrinsic Reinnervation in Compressive Ulnar Neuropathy8
Electrodiagnostic and ultrasound evaluation of respiratory weakness8
AANEM News & Insights8
Resistance Training in a Patient With Hypokalemic Periodic Paralysis and Permanent Weakness: A Case Report8
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy8
The diagnosis of myasthenia gravis: The sensitive issue of specificity8
Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management8
Utility of Median Nerve Electrophysiological Parameters in Differentiating Immune‐Mediated Demyelination From Compressive Median Neuropathy at the Wrist8
Nerve Ultrasound in Patients With Friedreich Ataxia8
AANEM News & Insights8
Rhabdomyolysis8
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy8
Join AANEM8
Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States8
The quality of occupational healthcare for carpal tunnel syndrome, healthcare expenditures, and disability outcomes: A prospective observational study8
AANEM News & Insights8
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connectiv8
Electrophysiological Changes in Pediatric Spinal Muscular Atrophy: Results From an Observational Study8
Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey8
True Chronic Immune Sensorimotor Polyradiculopathy Localized Using Tibial Nerve Somatosensory Evoked Potentials8
Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study8
Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria7
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap7
AANEM News & Insights7
2025 ANNUAL MEETING ABSTRACTS GUIDE7
Issue Information7
7
Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial7
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis7
Sarcolemmal Excitability Properties of the Trapezius7
Issue Information7
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children7
Response to Letter to the Editor: Explanation of Surveillance Data Used in Hearing Loss, Retinal Abnormality, and Seizures in Facioscapulohumeral Muscular Dystrophy Study7
Issue Information7
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy7
AANEM Calender of Events7
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype7
Join AANEM7
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis7
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy7
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy7
A Rare Biopsy‐Confirmed Case of Wild‐Type Transthyretin Amyloid Polyneuropathy and Autonomic Neuropathy7
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting7
Elevated Serum SIRT2 Is Associated With Rapid Progression and Cognitive Impairment in Amyotrophic Lateral Sclerosis7
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study7
Calendar of Events7
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis7
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy7
7
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?7
Calendar of Events7
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee7
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency7
The use and misuse of sonographic reference values in neuromuscular disease7
Quantifying adverse events: The burden is on us!7
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles7
Electrical impedance myography in healthy volunteers7
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy7
Refining quality measures for electrodiagnostic testing in suspected carpal tunnel syndrome to account for acceptable variations in practice: Expert review process6
Repetitive Nerve Stimulation (RNS) Studies in Infants: Are Infants Just “Little Adults” or Do They Deserve Their Own Parameters (or Cut‐Off Values) for RNS?6
AANEM News and Insights6
AANEM News and Insights6
Issue Information6
Does the ACT Have ImpACT for ALS ?6
The best and worst of times in therapy development for myasthenia gravis6
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study6
Appendicular lean mass index and motor function in ambulatory patients with Duchenne muscular dystrophy6
Proceedings of the 22nd Annual Meeting of the Northeast ALS Consortium6
Limb‐girdle muscular dystrophies: A scoping review and overview of currently available rehabilitation strategies6
Join AANEM6
Skeletal Muscle Microbiopsies in Children and Adults—Tolerability, Sample Yield, and Analyzability6
AANEM News & Insights6
Issue Information6
Are Cannabis and/or Cannabinoids a Potential Therapy for ALS ?6
Respiratory considerations in patients with neuromuscular disorders6
Issue Information6
Issue Information6
Less Social Contact During the Pandemic Could Explain the Lower Prevalence of GBS During This Time6
Calendar of Events6
Transverse interlaminar ultrasound‐guided C1‐C2 puncture for the intrathecal administration of nusinersen in patients with spinal muscular atrophy6
Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome6
Ted M. Burns MD6
Issue Information6
The use of electrical stimulation to enhance recovery following peripheral nerve injury6
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study6
The impact of myasthenia gravis severity on work and daily activities6
Diagnoses of muscular dystrophy in a veterans health system6
Issue Information6
Neuromuscular ultrasound findings in gunshot wounds6
Combat‐related peripheral nerve injuries5
Issue Information5
Carpal tunnel syndrome in pregnancy5
Calendar of Events5
Longitudinal relationships between free‐living activities, fatigue, and symptom severity in myasthenia gravis using cohort and individualized models5
Safety and Effectiveness of Eculizumab in Patients With Refractory Ocular or Ocular‐Predominant Myasthenia Gravis: A Case Series5
Join AANEM5
0.092466115951538