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 2021-08-01 to 2025-08-01.)
ArticleCitations
101
Join AANEM72
AANEM News and Insights70
AANEM Calender of Events68
Issue Information63
AANEM News & Insights61
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia58
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey46
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials42
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study41
Neuroma morphology: A macroscopic classification system37
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy35
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects34
Join AANEM32
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle32
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method31
Pilot study of a virtual weight management program for Duchenne muscular dystrophy29
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course28
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis28
The neuromuscular fellowship portal and match26
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy25
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine25
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis23
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure22
Diagnosis of Primary Mitochondrial Diseases22
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts21
The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review20
Axial muscle involvement in patients with limb girdle muscular dystrophy type R920
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma20
Diagnosis and management of metabolic myopathies19
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study19
Neuromuscular ultrasound: Impact on diagnosis and management19
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The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study18
AANEM Application18
Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression18
Issue Information18
AANEM News and Comments17
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy17
Amyotrophic lateral sclerosis mimics17
Atypical presentation of hypokalemic periodic paralysis: A case report17
A case of neuroleukemiosis: The usefulness of nerve ultrasound as a diagnostic tool16
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy16
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report16
Positive acetylcholine receptor antibody in nonmyasthenic patients15
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury15
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis15
Pregnancy outcomes in patients with congenital myasthenic syndromes15
Optimal placement for needle electromyography of the supinator muscle: Cadaveric studies15
Impact of COVID‐19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy15
Estimation of diaphragm depth based on waist circumference in the Thai population15
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis15
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change15
Join AANEM14
Issue Highlights14
AANEM News and Insights14
Nerve ultrasound characteristics of immunoglobulin M neuropathy associated with anti‐myelin‐associated glycoprotein antibodies14
Rasch analysis of the Unidimensional Self‐Efficacy Scale in Neuromuscular Disorders and comparison between sex, age, and diagnoses14
Intermittent versus daily regimen of prednisolone in ambulatory boys with Duchenne muscular dystrophy: A randomized, open‐label trial14
Value and pitfalls of imaging and electrodiagnosis in neurogenic thoracic outlet syndrome: Lessons learned from present and past13
Predictors of Outcome in Myasthenic Crisis13
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus13
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier13
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis13
Utilization of MG‐ADL in myasthenia gravis clinical research and care13
The utility of diaphragm ultrasound thickening indices for assessing respiratory decompensation in amyotrophic lateral sclerosis13
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis13
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry13
Peripheral nerve injuries in the performing artist13
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis13
Response to the Letter From Gaul‐Muller and Bach on NIV Intolerance, NIV Settings and Mortality in MND Patients With Gastrostomy12
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Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms12
The supraclavicular nerve12
A‐waves are associated with neuropathic pain in leprosy12
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates12
Issue Highlights12
Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment12
Implications of median sensory study to the thumb and deltoid/biceps motor unit recruitment on identifying C6 root avulsion in upper neonatal brachial plexus palsy12
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment12
Issue Highlights12
Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen12
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy12
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock12
Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study12
AANEM 2024 Annual Meeting Abstracts Guide11
Ultrasound‐guided transforaminal approach for nusinersen delivery in adult spinal muscle atrophy patients with challenging access11
Evaluation of mechanomyogram efficacy as a tool for assessing paired‐pulse inhibition of blink reflex early R1 component11
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study11
AANEM News and Insights11
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Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region11
Extraocular muscle volume on time‐of‐flight magnetic resonance angiography in patients with myasthenia gravis11
Issue Highlights11
Calendar of Events11
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene10
Standardization of Myasthenia Gravis Outcome Measures in Clinical Practice: A Report of the MGFA Task Force10
Pain in acute motor axonal neuropathy10
Paraproteinemic neuropathies10
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies10
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up10
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions10
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari10
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
Guidelines for ethical behavior relating to clinical practice issues in neuromuscular and electrodiagnostic medicine10
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy10
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP10
Motor Unit Number Index (MUNIX) in Control Children: Reference Values and Reliability10
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults10
Evaluation of the applicability of weak shoulder and arm sparing signs in amyotrophic lateral sclerosis by multiple neurologists and neurology residents: A single‐center study10
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Radial motor nerve conduction studies recorded from triceps brachii and extensor carpi radialis longus: Techniques and reference values9
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study9
Issue Information9
Ten years of riluzole use in a tertiary ALS clinic9
Neuromuscular Ultrasound Training: Bridging the Gap9
AANEM News & Insights9
Calendar of Events9
Issue Information9
Issue Information9
Join AANEM9
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center9
MScanFit motor unit number estimation of human anconeus muscle9
Incidence and causes of overdiagnosis of myasthenia gravis9
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 20189
AANEM News and Comments9
The Enigma of the Motor Nerve Conduction Study9
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy9
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”8
Assessment of clinical skills in electrodiagnostic medicine8
Join AANEM8
Issue Highlights8
Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial8
A novel homozygous ALPK3 variant associated with cardiomyopathy and skeletal muscle involvement8
Issue Information8
Issue Highlights8
Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies8
Mass effect of the distal triceps brachii muscle on ulnar nerve movement during elbow flexion8
Could posturography be a useful outcome measure for chronic inflammatory demyelinating polyneuropathy?8
Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States8
Chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M paraprotein, cold agglutinins, and disialosyl antibodies presenting after COVID19 mRNA vaccination8
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis8
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connective Tissue Diseases”8
Milestones of progression in myotonic dystrophy type 1 and type 28
Details Matter: The Difference Between NIV and NVS8
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study8
Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve8
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Phantom radiculopathy: An electrodiagnostic challenge8
Electrodiagnostic and ultrasound evaluation of respiratory weakness8
AANEM Application8
Short‐term educational value of online neuromuscular ultrasound courses8
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy7
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis7
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy7
Ultrasonic evidence of mononeuritis multiplex caused by Lyme neuroborreliosis7
Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype7
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency7
“An Ounce of Prevention…”7
The effect of methocarbamol and mexiletine on murine muscle spindle function7
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy7
Combining multiple measures into a summary index: A step toward more reliable measurement7
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3‐related muscular dystrophy7
The quality of occupational healthcare for carpal tunnel syndrome, healthcare expenditures, and disability outcomes: A prospective observational study7
Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey7
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee7
The diagnosis of myasthenia gravis: The sensitive issue of specificity7
Utility of Median Nerve Electrophysiological Parameters in Differentiating Immune‐Mediated Demyelination From Compressive Median Neuropathy at the Wrist7
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value7
Home‐based gait analysis as an exploratory endpoint during a multicenter phase 1 trial in limb girdle muscular dystrophy type R2 and facioscapulohumeral muscular dystrophy7
High prevalence of paraspinal muscle involvement in adults with McArdle disease7
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis7
Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment7
Age‐related sensory neuropathy in patients with spinal muscular atrophy type 17
Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study7
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy7
GNE myopathy: Don't sleep on the platelets7
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab7
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Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management7
Lung volume recruitment improves volitional airway clearance in amyotrophic lateral sclerosis7
Laryngospasm in amyotrophic lateral sclerosis7
AANEM News & Insights7
The use and misuse of sonographic reference values in neuromuscular disease7
Cubital tunnel perfusion in different postures—An anatomical investigation6
Which combined nerve conduction study scores are best suited for polyneuropathy in diabetic patients?6
Time course of capillary regression and an expression balance between vascular endothelial growthfactor‐Aand thrombospondin‐1 in the soleus muscle of hindlimb unloaded rats6
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study6
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?6
Transcutaneous carbon dioxide monitoring in ALS: Assessment of hypoventilation heats up6
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy6
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype6
Does specificity of electrodiagnostic test referrals predict test outcome in children?6
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Issue Information6
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Statin‐associated anti–3‐hydroxy‐3‐methyl‐glutaryl‐coenzyme A reductase (HMGCR) myopathy: Imaging findings on thigh‐muscle magnetic resonance imaging (MRI) in six patients6
Alterations in fast‐twitch muscle membrane conductance regulation do not explain decreased muscle function of SOD1G93A rats6
Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab: subgroup analysis of REGAIN and its extension study6
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy6
Electrical impedance myography in healthy volunteers6
Quantifying adverse events: The burden is on us!6
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap6
The use of electrical stimulation to enhance recovery following peripheral nerve injury6
Calendar of Events6
Join AANEM6
A cross‐sectional study of memory and executive functions in patients with sporadic inclusion body myositis6
The best and worst of times in therapy development for myasthenia gravis6
Cardiopulmonary exercise performance and factors associated with aerobic capacity in neuromuscular diseases6
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy6
Slowing the loss of physical function in amyotrophic lateral sclerosis with edaravone: Post hoc analysis of ALSFRS‐R item scores in pivotal study MCI186‐196
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting6
The impact of myasthenia gravis severity on work and daily activities6
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children6
Respiratory considerations in patients with neuromuscular disorders6
Sarcolemmal Excitability Properties of the Trapezius6
AANEM News & Insights6
AANEM Calender of Events6
Refining quality measures for electrodiagnostic testing in suspected carpal tunnel syndrome to account for acceptable variations in practice: Expert review process5
Urinary titin in myotonic dystrophy type 15
Imaging of neuralgic amyotrophy in the acute phase5
Proceedings of the 22nd Annual Meeting of the Northeast ALS Consortium5
Persistent post–COVID‐19 neuromuscular symptoms5
COVID‐19 infection in patients with late‐onset Pompe disease5
Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria5
Issue Information5
Issue Information5
Ted M. Burns MD5
RETRACTED: Utility of phrenic nerve conduction studies for identification of patients with neuromuscular diseases requiring invasive mechanical ventilation5
Differences in corneal nerve fiber density and fiber length in patients with painful chronic idiopathic axonal polyneuropathy and diabetic polyneuropathy5
Examining Complication Rates to Inform the Consent Process in Needle Electromyography: A Quality Improvement Project5
Neuralgic amyotrophy: An update in evaluation, diagnosis, and treatment approaches5
Efgartigimod alfa‐fcab use in a pregnant woman with generalized myasthenia gravis: A case report5
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study5
Calendar of Events5
Issue Information5
AANEM News and Insights5
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study5
Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome5
Issue Information5
Comparison of the United Kingdom and United States approaches to approval of new neuromuscular therapies5
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?5
Transverse interlaminar ultrasound‐guided C1‐C2 puncture for the intrathecal administration of nusinersen in patients with spinal muscular atrophy5
Limb‐girdle muscular dystrophies: A scoping review and overview of currently available rehabilitation strategies5
Gene replacement therapy for spinal muscular atrophy unmasking occult hepatitis C in a pediatric patient5
AANEM News & Insights5
AANEM News and Insights5
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles5
Neuromuscular ultrasound findings in gunshot wounds5
Small Fiber Neuropathy and SARS‐CoV‐2 Infection. Another piece in the long COVID puzzle?5
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