Muscle & Nerve

Papers
(The median citation count of Muscle & Nerve is 1. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
Issue Information89
AANEM News and Insights87
AANEM Calender of Events87
Join AANEM86
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma73
AANEM News & Insights72
Neuromuscular ultrasound: Impact on diagnosis and management55
AANEM News & Insights51
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method43
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia39
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey38
Neuroma morphology: A macroscopic classification system36
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy35
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects34
Join AANEM32
The neuromuscular fellowship portal and match30
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course30
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine28
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study28
Diagnosis of Primary Mitochondrial Diseases27
Pilot study of a virtual weight management program for Duchenne muscular dystrophy26
Issue Information24
Radial Mononeuropathy: Clinical and Electrodiagnostic Characteristics in 177 Patients23
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis23
Prognosis After Discontinuation of Azathioprine or Mycophenolate Mofetil in Well‐Controlled Myasthenia Gravis: A Retrospective Analysis23
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study23
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure23
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts22
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials21
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy21
Axial muscle involvement in patients with limb girdle muscular dystrophy type R921
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle20
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis20
Diagnosis and management of metabolic myopathies20
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AANEM News and Comments19
AANEM Application19
Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression18
Peripheral nerve injuries in the performing artist18
Issue Information18
Rasch analysis of the Unidimensional Self‐Efficacy Scale in Neuromuscular Disorders and comparison between sex, age, and diagnoses18
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates18
Pregnancy outcomes in patients with congenital myasthenic syndromes17
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier17
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry17
Issue Highlights17
Predictors of Outcome in Myasthenic Crisis17
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy16
Estimation of diaphragm depth based on waist circumference in the Thai population16
Atypical presentation of hypokalemic periodic paralysis: A case report16
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy16
A case of neuroleukemiosis: The usefulness of nerve ultrasound as a diagnostic tool16
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report16
Optimal placement for needle electromyography of the supinator muscle: Cadaveric studies16
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change15
AANEM News and Insights15
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus15
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis15
Join AANEM15
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis15
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury15
Predictive Values of Preoperative Compound Muscle Action Potential Amplitude for Surgical Outcomes in Idiopathic Ulnar Neuropathy at the Elbow14
The utility of diaphragm ultrasound thickening indices for assessing respiratory decompensation in amyotrophic lateral sclerosis14
MRI of Neurogenic Human Motor Units Following Poliomyelitis14
Response to the Letter From Gaul‐Muller and Bach on NIV Intolerance, NIV Settings and Mortality in MND Patients With Gastrostomy14
Positive acetylcholine receptor antibody in nonmyasthenic patients14
Physiology of Abnormal Muscle Fiber Generators14
The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study14
Nerve ultrasound characteristics of immunoglobulin M neuropathy associated with anti‐myelin‐associated glycoprotein antibodies14
The Disparities in Myasthenia Gravis Clinical Trial Enrollment in the United States and Canada14
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
Amyotrophic lateral sclerosis mimics13
Utilization of MG‐ADL in myasthenia gravis clinical research and care13
A‐waves are associated with neuropathic pain in leprosy13
Issue Highlights13
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis13
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis13
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment13
Implications of median sensory study to the thumb and deltoid/biceps motor unit recruitment on identifying C6 root avulsion in upper neonatal brachial plexus palsy13
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis13
Issue Highlights13
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up12
AANEM News and Insights12
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene12
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 201812
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions12
Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen12
Broadening the Comorbidity Landscape in Facioscapulohumeral Dystrophy: Beyond the Usual Suspects12
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies11
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
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The supraclavicular nerve11
Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms11
Calendar of Events11
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
Guidelines for ethical behavior relating to clinical practice issues in neuromuscular and electrodiagnostic medicine11
AANEM 2024 Annual Meeting Abstracts Guide11
Paraproteinemic neuropathies11
Ultrasound Guidance to Augment Needle Electromyography Precision in the Complex Nerve Injury Setting10
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP10
Focal Neurogenic Muscle Hypertrophy and Focal Neurogenic Myositis10
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy10
Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment10
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation Defects10
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari10
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock10
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy10
Evaluation of mechanomyogram efficacy as a tool for assessing paired‐pulse inhibition of blink reflex early R1 component10
Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study10
Standardization of Myasthenia Gravis Outcome Measures in Clinical Practice: A Report of the MGFA Task Force10
Motor Unit Number Index (MUNIX) in Control Children: Reference Values and Reliability10
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study10
Ultrasound‐guided transforaminal approach for nusinersen delivery in adult spinal muscle atrophy patients with challenging access10
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study10
AANEM News and Comments9
Issue Information9
Issue Information9
Short‐term educational value of online neuromuscular ultrasound courses9
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study9
Details Matter: The Difference Between NIV and NVS9
Ten years of riluzole use in a tertiary ALS clinic9
AANEM News & Insights9
Issue Information9
The Enigma of the Motor Nerve Conduction Study9
AANEM News & Insights9
Calendar of Events9
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”9
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MScanFit motor unit number estimation of human anconeus muscle9
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults9
Join AANEM9
Milestones of progression in myotonic dystrophy type 1 and type 29
Neuromuscular Ultrasound Training: Bridging the Gap9
Reply to: “Beyond Prevalence: The Importance of Multifactorial Assessment in Cancer Risk Among Myotonic Dystrophy Patients”9
Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve9
Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies9
Assessment of clinical skills in electrodiagnostic medicine9
“An Ounce of Prevention…”8
Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States8
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Issue Highlights8
Spectrum of Anti‐Neurofascin Neuropathies: A Retrospective Indian Cohort8
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy8
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis8
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3‐related muscular dystrophy8
Utility of Median Nerve Electrophysiological Parameters in Differentiating Immune‐Mediated Demyelination From Compressive Median Neuropathy at the Wrist8
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy8
AANEM News & Insights8
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connective Tissue Diseases”8
Join AANEM8
Fascial Border Absence Between the Extensor Carpi Radialis Longus and Brachioradialis Muscles8
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center8
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy8
Issue Information8
Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey8
Nerve Ultrasound in Patients With Friedreich Ataxia8
Phantom radiculopathy: An electrodiagnostic challenge8
Chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M paraprotein, cold agglutinins, and disialosyl antibodies presenting after COVID19 mRNA vaccination8
Incidence and causes of overdiagnosis of myasthenia gravis8
Mass effect of the distal triceps brachii muscle on ulnar nerve movement during elbow flexion8
AANEM Application8
The use and misuse of sonographic reference values in neuromuscular disease8
Electrodiagnostic and ultrasound evaluation of respiratory weakness8
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy7
AANEM News & Insights7
The effect of methocarbamol and mexiletine on murine muscle spindle function7
Issue Information7
True Chronic Immune Sensorimotor Polyradiculopathy Localized Using Tibial Nerve Somatosensory Evoked Potentials7
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GNE myopathy: Don't sleep on the platelets7
AANEM News & Insights7
The quality of occupational healthcare for carpal tunnel syndrome, healthcare expenditures, and disability outcomes: A prospective observational study7
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value7
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High prevalence of paraspinal muscle involvement in adults with McArdle disease7
Join AANEM7
Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study7
Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial7
Calendar of Events7
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis7
AANEM News & Insights7
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency7
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee7
Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management7
AANEM Calender of Events7
The diagnosis of myasthenia gravis: The sensitive issue of specificity7
Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype7
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy7
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis7
Rhabdomyolysis7
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab7
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Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria6
Issue Information6
Appendicular lean mass index and motor function in ambulatory patients with Duchenne muscular dystrophy6
Issue Information6
Issue Information6
2025 ANNUAL MEETING ABSTRACTS GUIDE6
Issue Information6
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy6
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype6
Does the ACT Have ImpACT for ALS ?6
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?6
Response to Letter to the Editor: Explanation of Surveillance Data Used in Hearing Loss, Retinal Abnormality, and Seizures in Facioscapulohumeral Muscular Dystrophy Study6
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy6
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles6
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy6
Issue Information6
Issue Information6
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study6
AANEM News & Insights6
AANEM News and Insights6
Transcutaneous carbon dioxide monitoring in ALS: Assessment of hypoventilation heats up6
AANEM News and Insights6
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study6
The best and worst of times in therapy development for myasthenia gravis6
The impact of myasthenia gravis severity on work and daily activities6
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap6
Issue Information6
Sarcolemmal Excitability Properties of the Trapezius6
Electrical impedance myography in healthy volunteers6
Time course of capillary regression and an expression balance between vascular endothelial growthfactor‐Aand thrombospondin‐1 in the soleus muscle of hindlimb unloaded rats6
Diagnoses of muscular dystrophy in a veterans health system6
Orbicularis Oculi Stimulated Jitter Analysis in Children With Autoimmune Myasthenia Gravis6
Ted M. Burns MD6
In Memorium: Jun Kimura, MD6
Does specificity of electrodiagnostic test referrals predict test outcome in children?6
The use of electrical stimulation to enhance recovery following peripheral nerve injury6
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children6
Quantifying adverse events: The burden is on us!6
Respiratory considerations in patients with neuromuscular disorders6
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting6
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study6
The neuromuscular evaluation of postural orthostatic tachycardia syndrome5
Combat‐related peripheral nerve injuries5
AANEM News & Insights5
Issue Highlights5
Join AANEM5
Oculopharyngodistal myopathy: The recent discovery of an old disease5
Elevated Cancer Prevalence Identified at Specific Anatomical Sites Among People With Myotonic Dystrophy Using a Population‐Based Sample5
Issue Information5
Calendar of Events5
Visual versus quantitative analysis of muscle ultrasound in neuromuscular disease5
Carpal tunnel syndrome in pregnancy5
Cryolipolysis‐associated radial mononeuropathy5
Ultrasonographic evaluation of ulnar nerve morphology in patients with ulnar nerve instability5
AANEM Annual Meeting Abstract Guide Nashville, TN | September, 21–24, 20225
Issue Information5
Characterization of Autonomic Involvement in Various Subtypes of Guillain‐Barré Syndrome and Association With Electrophysiological Parameters5
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