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 2021-11-01 to 2025-11-01.)
ArticleCitations
Issue Information107
AANEM Calender of Events85
AANEM News and Insights83
81
Join AANEM79
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma70
AANEM News & Insights66
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy50
AANEM News & Insights48
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis43
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle39
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method36
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study35
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure34
Axial muscle involvement in patients with limb girdle muscular dystrophy type R932
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials31
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis29
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia27
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects25
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey25
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy25
Neuroma morphology: A macroscopic classification system25
The neuromuscular fellowship portal and match23
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course23
Join AANEM23
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study22
Diagnosis of Primary Mitochondrial Diseases21
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts21
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine21
Pilot study of a virtual weight management program for Duchenne muscular dystrophy21
Neuromuscular ultrasound: Impact on diagnosis and management20
Diagnosis and management of metabolic myopathies20
The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review20
AANEM Application19
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Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression18
AANEM News and Comments18
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 Emirates17
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis17
Peripheral nerve injuries in the performing artist17
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier17
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis17
Issue Highlights16
A case of neuroleukemiosis: The usefulness of nerve ultrasound as a diagnostic tool16
Pregnancy outcomes in patients with congenital myasthenic syndromes16
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy16
Atypical presentation of hypokalemic periodic paralysis: A case report16
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry16
Predictors of Outcome in Myasthenic Crisis16
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy16
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report16
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis15
Optimal placement for needle electromyography of the supinator muscle: Cadaveric studies15
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change15
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis15
Estimation of diaphragm depth based on waist circumference in the Thai population15
The utility of diaphragm ultrasound thickening indices for assessing respiratory decompensation in amyotrophic lateral sclerosis14
Join AANEM14
Predictive Values of Preoperative Compound Muscle Action Potential Amplitude for Surgical Outcomes in Idiopathic Ulnar Neuropathy at the Elbow14
Response to the Letter From Gaul‐Muller and Bach on NIV Intolerance, NIV Settings and Mortality in MND Patients With Gastrostomy14
AANEM News and Insights14
Amyotrophic lateral sclerosis mimics14
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury14
Nerve ultrasound characteristics of immunoglobulin M neuropathy associated with anti‐myelin‐associated glycoprotein antibodies13
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis13
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies13
The supraclavicular nerve13
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus13
Physiology of Abnormal Muscle Fiber Generators13
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
Utilization of MG‐ADL in myasthenia gravis clinical research and care13
Positive acetylcholine receptor antibody in nonmyasthenic patients13
Issue Highlights13
The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study13
Issue Highlights12
Broadening the Comorbidity Landscape in Facioscapulohumeral Dystrophy: Beyond the Usual Suspects12
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment12
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study12
Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen12
AANEM News and Insights12
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock12
Evaluation of the applicability of weak shoulder and arm sparing signs in amyotrophic lateral sclerosis by multiple neurologists and neurology residents: A single‐center study12
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 201812
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy12
A‐waves are associated with neuropathic pain in leprosy12
Issue Highlights12
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene11
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Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region11
Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms11
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up11
Evaluation of mechanomyogram efficacy as a tool for assessing paired‐pulse inhibition of blink reflex early R1 component11
Focal Neurogenic Muscle Hypertrophy and Focal Neurogenic Myositis11
Guidelines for ethical behavior relating to clinical practice issues in neuromuscular and electrodiagnostic medicine11
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions11
AANEM 2024 Annual Meeting Abstracts Guide11
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study11
Extraocular muscle volume on time‐of‐flight magnetic resonance angiography in patients with myasthenia gravis10
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults10
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP10
AANEM News and Comments10
Motor Unit Number Index (MUNIX) in Control Children: Reference Values and Reliability10
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari10
Ultrasound‐guided transforaminal approach for nusinersen delivery in adult spinal muscle atrophy patients with challenging access10
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy10
Issue Information10
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
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
Paraproteinemic neuropathies10
Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment10
Join AANEM10
Calendar of Events10
Short‐term educational value of online neuromuscular ultrasound courses9
Milestones of progression in myotonic dystrophy type 1 and type 29
Neuromuscular Ultrasound Training: Bridging the Gap9
Assessment of clinical skills in electrodiagnostic medicine9
Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve9
Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies9
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study9
Issue Information9
Issue Information9
Calendar of Events9
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”9
Details Matter: The Difference Between NIV and NVS9
Ten years of riluzole use in a tertiary ALS clinic9
The Enigma of the Motor Nerve Conduction Study9
AANEM News & Insights9
Radial motor nerve conduction studies recorded from triceps brachii and extensor carpi radialis longus: Techniques and reference values9
Mass effect of the distal triceps brachii muscle on ulnar nerve movement during elbow flexion9
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Reply to: “Beyond Prevalence: The Importance of Multifactorial Assessment in Cancer Risk Among Myotonic Dystrophy Patients”9
Combining multiple measures into a summary index: A step toward more reliable measurement8
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
Phantom radiculopathy: An electrodiagnostic challenge8
Chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M paraprotein, cold agglutinins, and disialosyl antibodies presenting after COVID19 mRNA vaccination8
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy8
Issue Highlights8
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy8
The use and misuse of sonographic reference values in neuromuscular disease8
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee8
AANEM News & Insights8
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Incidence and causes of overdiagnosis of myasthenia gravis8
MScanFit motor unit number estimation of human anconeus muscle8
Laryngospasm in amyotrophic lateral sclerosis8
High prevalence of paraspinal muscle involvement in adults with McArdle disease8
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy8
Electrodiagnostic and ultrasound evaluation of respiratory weakness8
Issue Information8
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center8
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connective Tissue Diseases”8
Join AANEM8
AANEM Application8
“An Ounce of Prevention…”8
GNE myopathy: Don't sleep on the platelets7
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy7
Does specificity of electrodiagnostic test referrals predict test outcome in children?7
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
AANEM Calender of Events7
AANEM News & Insights7
Calendar of Events7
The diagnosis of myasthenia gravis: The sensitive issue of specificity7
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis7
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value7
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis7
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis7
AANEM News & Insights7
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy7
Sarcolemmal Excitability Properties of the Trapezius7
Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States7
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Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency7
Issue Information7
Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management7
The effect of methocarbamol and mexiletine on murine muscle spindle function7
Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype7
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Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study7
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Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial7
Join AANEM7
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab7
A novel homozygous ALPK3 variant associated with cardiomyopathy and skeletal muscle involvement7
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
Diagnoses of muscular dystrophy in a veterans health system6
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting6
Issue Information6
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy6
Quantifying adverse events: The burden is on us!6
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy6
Time course of capillary regression and an expression balance between vascular endothelial growthfactor‐Aand thrombospondin‐1 in the soleus muscle of hindlimb unloaded rats6
Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria6
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles6
The impact of myasthenia gravis severity on work and daily activities6
The best and worst of times in therapy development for myasthenia gravis6
Orbicularis Oculi Stimulated Jitter Analysis in Children With Autoimmune Myasthenia Gravis6
Ted M. Burns MD6
Issue Information6
Electrical impedance myography in healthy volunteers6
The use of electrical stimulation to enhance recovery following peripheral nerve injury6
Respiratory considerations in patients with neuromuscular disorders6
AANEM News and Insights6
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype6
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
Issue Information6
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study6
Issue Information6
Appendicular lean mass index and motor function in ambulatory patients with Duchenne muscular dystrophy6
Issue Information6
In Memorium: Jun Kimura, MD6
AANEM News and Insights6
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?6
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children6
2025 ANNUAL MEETING ABSTRACTS GUIDE6
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap6
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy6
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study6
Which combined nerve conduction study scores are best suited for polyneuropathy in diabetic patients?6
Transcutaneous carbon dioxide monitoring in ALS: Assessment of hypoventilation heats up6
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study6
AANEM News & Insights6
Longitudinal relationships between free‐living activities, fatigue, and symptom severity in myasthenia gravis using cohort and individualized models5
Visual versus quantitative analysis of muscle ultrasound in neuromuscular disease5
Urinary titin in myotonic dystrophy type 15
Carpal tunnel syndrome in pregnancy5
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
Sexual health and fertility in Duchenne muscular dystrophy—An exploratory study5
Issue Information5
Calendar of Events5
Join AANEM5
Neuralgic amyotrophy: An update in evaluation, diagnosis, and treatment approaches5
Evaluation and management of dyspnea as the dominant presenting feature in neuromuscular disorders5
The neuromuscular evaluation of postural orthostatic tachycardia syndrome5
Cryolipolysis‐associated radial mononeuropathy5
Design and pilot testing of a 26‐gauge impedance‐electromyography needle in wild‐type and ALS mice5
AANEM Annual Meeting Abstract Guide Nashville, TN | September, 21–24, 20225
Issue Information5
Combat‐related peripheral nerve injuries5
Imaging of neuralgic amyotrophy in the acute phase5
Issue Information5
Secondary outcomes of scoliosis surgery in disease‐modifying treatment‐naïve patients with spinal muscular atrophy type 2 and nonambulant type 35
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
AANEM News & Insights5
Issue Highlights5
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