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 2022-05-01 to 2026-05-01.)
ArticleCitations
AANEM News and Insights108
AANEM Calender of Events108
Join AANEM94
AANEM News & Insights89
AANEM News & Insights70
Issue Information45
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy44
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey44
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects40
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course39
Join AANEM39
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine38
Neuroma morphology: A macroscopic classification system37
Pilot study of a virtual weight management program for Duchenne muscular dystrophy37
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure36
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle33
Diagnosis and management of metabolic myopathies33
Comorbidities and Treatment Patterns in People With Myasthenia Gravis in Denmark, Finland and Sweden: A Population‐Based Observational Study32
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method31
Neuromuscular ultrasound: Impact on diagnosis and management31
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study30
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study29
Prognosis After Discontinuation of Azathioprine or Mycophenolate Mofetil in Well‐Controlled Myasthenia Gravis: A Retrospective Analysis29
Radial Mononeuropathy: Clinical and Electrodiagnostic Characteristics in 177 Patients28
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy27
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis26
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials26
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia25
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis25
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma25
Emerging Upper Extremity Muscle Ultrasound Patterns as a Diagnostic Aid in TTN ‐Related Myopathies23
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts23
Diagnosis of Primary Mitochondrial Diseases22
AANEM Application21
Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression21
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AANEM News and Comments21
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy20
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates20
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier20
The Disparities in Myasthenia Gravis Clinical Trial Enrollment in the United States and Canada20
Peripheral nerve injuries in the performing artist20
AANEM News & Insights20
Rasch analysis of the Unidimensional Self‐Efficacy Scale in Neuromuscular Disorders and comparison between sex, age, and diagnoses20
Physiology of Abnormal Muscle Fiber Generators19
Integrating Serum Neurofilament Light Chain Into Amyotrophic Lateral Sclerosis Diagnostic Criteria19
Atypical presentation of hypokalemic periodic paralysis: A case report18
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis18
Issue Highlights18
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report18
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change18
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy18
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 sclerosis17
Effect of Capsaicin (8%) Topical System on Sensory Function in Patients With Diabetic Peripheral Neuropathy: Analysis of the PACE Study17
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis17
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry17
Amyotrophic lateral sclerosis mimics16
The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study16
Predictive Values of Preoperative Compound Muscle Action Potential Amplitude for Surgical Outcomes in Idiopathic Ulnar Neuropathy at the Elbow16
Response to the Letter From Gaul‐Muller and Bach on NIV Intolerance, NIV Settings and Mortality in MND Patients With Gastrostomy16
Join AANEM15
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus15
AANEM News and Insights15
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis15
MRI of Neurogenic Human Motor Units Following Poliomyelitis15
Pregnancy outcomes in patients with congenital myasthenic syndromes15
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury14
Congenital Myopathies and Muscular Dystrophies: A Single Tertiary Center Experience and Factors Associated With Long‐Term Outcomes14
Calendar of Events14
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis14
Predictors of Outcome in Myasthenic Crisis14
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis13
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
Issue Highlights13
A‐waves are associated with neuropathic pain in leprosy13
Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen13
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment13
AANEM News and Insights13
Motor Unit Number Index (MUNIX) in Control Children: Reference Values and Reliability12
Paraproteinemic neuropathies12
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions12
Motor Nerve Conduction of the Hypoglossal Nerve With F‐Waves in Healthy Adults12
Ultrasound Guidance to Augment Needle Electromyography Precision in the Complex Nerve Injury Setting12
Focal Neurogenic Muscle Hypertrophy and Focal Neurogenic Myositis12
Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment12
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation Defects12
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene12
Broadening the Comorbidity Landscape in Facioscapulohumeral Dystrophy: Beyond the Usual Suspects11
AANEM 2024 Annual Meeting Abstracts Guide11
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults11
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 201811
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Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region11
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP11
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock11
Calendar of Events11
Extraocular muscle volume on time‐of‐flight magnetic resonance angiography in patients with myasthenia gravis11
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies11
Evaluation of mechanomyogram efficacy as a tool for assessing paired‐pulse inhibition of blink reflex early R1 component11
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study11
Short‐term educational value of online neuromuscular ultrasound courses10
Utility of Far‐Field Potentials as a Biomarker of Neurodegeneration in Spinal Muscular Atrophy10
Oral Health in Amyotrophic Lateral Sclerosis: Feasibility of Oral Screening and Determinants of Poor Outcomes10
Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms10
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study10
Join AANEM10
AANEM News & Insights10
Standardization of Myasthenia Gravis Outcome Measures in Clinical Practice: A Report of the MGFA Task Force10
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy10
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 10
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up10
Issue Information10
Issue Information10
Calendar of Events10
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari10
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy10
Observational Evaluation of Muscle Echointensity and EMG Insertional Activity in Poststroke Spasticity10
AANEM News and Comments10
Issue Information10
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study9
Milestones of progression in myotonic dystrophy type 1 and type 29
9
Risk of Infection Following Clearance of Immunoglobulin G by Plasma Exchange in Myasthenia Gravis9
Practical Approach to Managing SCIg Treatment in Patients With Chronic Inflammatory Demyelinating Polyneuropathy9
The Antibody‐Microbiota Interface in Autoimmune Diseases9
Incidence and causes of overdiagnosis of myasthenia gravis9
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Introduction to the Supplement9
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
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy9
Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve9
Spectrum of Anti‐Neurofascin Neuropathies: A Retrospective Indian Cohort9
Reply to: “Beyond Prevalence: The Importance of Multifactorial Assessment in Cancer Risk Among Myotonic Dystrophy Patients”9
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”9
Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies9
Fascial Border Absence Between the Extensor Carpi Radialis Longus and Brachioradialis Muscles9
Phantom radiculopathy: An electrodiagnostic challenge9
Issue Highlights9
Neuromuscular Ultrasound Training: Bridging the Gap9
Join AANEM9
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center9
Details Matter: The Difference Between NIV and NVS9
AANEM News & Insights9
Assessment of clinical skills in electrodiagnostic medicine9
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3‐related muscular dystrophy8
AANEM News & Insights8
Utility of Median Nerve Electrophysiological Parameters in Differentiating Immune‐Mediated Demyelination From Compressive Median Neuropathy at the Wrist8
Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial8
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy8
Nerve Ultrasound in Patients With Friedreich Ataxia8
Join AANEM8
The quality of occupational healthcare for carpal tunnel syndrome, healthcare expenditures, and disability outcomes: A prospective observational study8
Issue Information8
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy8
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab8
Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States8
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy8
Electrophysiological Changes in Pediatric Spinal Muscular Atrophy: Results From an Observational Study8
AANEM News & Insights8
Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management8
“An Ounce of Prevention…”8
Join AANEM8
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value8
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connectiv8
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis8
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
The diagnosis of myasthenia gravis: The sensitive issue of specificity8
True Chronic Immune Sensorimotor Polyradiculopathy Localized Using Tibial Nerve Somatosensory Evoked Potentials7
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis7
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Sarcolemmal Excitability Properties of the Trapezius7
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study7
Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria7
Issue Information7
AANEM Calender of Events7
Quantifying adverse events: The burden is on us!7
Calendar of Events7
Electrical impedance myography in healthy volunteers7
The use and misuse of sonographic reference values in neuromuscular disease7
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy7
Rhabdomyolysis7
AANEM News & Insights7
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype7
Response to Letter to the Editor: Explanation of Surveillance Data Used in Hearing Loss, Retinal Abnormality, and Seizures in Facioscapulohumeral Muscular Dystrophy Study7
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap7
Issue Information7
Issue Information7
2025 ANNUAL MEETING ABSTRACTS GUIDE7
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee7
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting7
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency7
AANEM News & Insights7
Electrodiagnostic and ultrasound evaluation of respiratory weakness7
Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study7
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles7
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy7
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy7
Respiratory considerations in patients with neuromuscular disorders7
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis7
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy7
Join AANEM7
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?7
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Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey7
Diagnoses of muscular dystrophy in a veterans health system6
Issue Information6
Isolated Periodic‐Paralysis‐Like Syndrome in a Kinship With a Pathogenic MT‐ATP6 Variant: A Case Report6
Transverse interlaminar ultrasound‐guided C1‐C2 puncture for the intrathecal administration of nusinersen in patients with spinal muscular atrophy6
Less Social Contact During the Pandemic Could Explain the Lower Prevalence of GBS During This Time6
Increased Glycogenin‐Exposed Residual Glycogen in Lysosomes Is the Early Pathological Finding in Asymptomatic Pompe Disease6
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study6
Ted M. Burns MD6
Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome6
AANEM News and Insights6
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study6
Elevated Serum SIRT2 Is Associated With Rapid Progression and Cognitive Impairment in Amyotrophic Lateral Sclerosis6
The best and worst of times in therapy development for myasthenia gravis6
AANEM News & Insights6
Electrodiagnostic and Functional Biomarkers for Non‐Ambulatory Children With Late‐Onset Spinal Muscular Atrophy6
Examining Complication Rates to Inform the Consent Process in Needle Electromyography: A Quality Improvement Project6
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
Refining quality measures for electrodiagnostic testing in suspected carpal tunnel syndrome to account for acceptable variations in practice: Expert review process6
Issue Information6
AANEM News and Insights6
Neuromuscular ultrasound findings in gunshot wounds6
Are Cannabis and/or Cannabinoids a Potential Therapy for ALS ?6
The impact of myasthenia gravis severity on work and daily activities6
Calendar of Events6
Does the ACT Have ImpACT for ALS ?6
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
Diabetic Neuropathies6
Issue Information6
Calendar of Events6
Skeletal Muscle Microbiopsies in Children and Adults—Tolerability, Sample Yield, and Analyzability6
Issue Information6
Issue Information6
Join AANEM6
Issue Information6
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children6
Appendicular lean mass index and motor function in ambulatory patients with Duchenne muscular dystrophy6
The use of electrical stimulation to enhance recovery following peripheral nerve injury6
Dynamics of Nerve Conduction Studies in Patients With Guillain–Barré Syndrome5
Join AANEM5
Associations between the ALSFRS‐R score and urate levels during 12 months of edaravone treatment for amyotrophic lateral sclerosis: Post hoc analysis of ALSFRS‐R scores in clinic5
Issue Information5
Calendar of Events5
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