Muscle & Nerve

Papers
(The TQCC of Muscle & Nerve is 3. 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 2021-05-01 to 2025-05-01.)
ArticleCitations
110
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis95
Join AANEM68
AANEM News and Insights62
The neuromuscular fellowship portal and match60
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course59
AANEM Calender of Events58
Issue Information55
AANEM News & Insights52
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study47
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method41
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy40
Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single‐site study37
Pilot study of a virtual weight management program for Duchenne muscular dystrophy35
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects32
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia32
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey32
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials31
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle31
Diagnosis of Primary Mitochondrial Diseases28
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy28
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine27
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis26
Diagnosis and management of metabolic myopathies25
Neuromuscular ultrasound: Impact on diagnosis and management25
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure25
The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review25
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study24
Axial muscle involvement in patients with limb girdle muscular dystrophy type R924
Neuroma morphology: A macroscopic classification system24
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts23
Estimation of diaphragm depth based on waist circumference in the Thai population22
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Nerve ultrasound characteristics of immunoglobulin M neuropathy associated with anti‐myelin‐associated glycoprotein antibodies21
Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression20
A case of neuroleukemiosis: The usefulness of nerve ultrasound as a diagnostic tool19
Issue Information19
The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study19
AANEM News and Comments18
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury18
AANEM Application18
Optimal placement for needle electromyography of the supinator muscle: Cadaveric studies18
Value and pitfalls of imaging and electrodiagnosis in neurogenic thoracic outlet syndrome: Lessons learned from present and past18
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy17
Atypical presentation of hypokalemic periodic paralysis: A case report17
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis17
Pregnancy outcomes in patients with congenital myasthenic syndromes17
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis16
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change16
Quantitative muscle echointensity: A practical approach using ultrasound to evaluate children with suspected neuromuscular disorders16
Amyotrophic lateral sclerosis mimics16
Impact of COVID‐19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy15
Rasch analysis of the Unidimensional Self‐Efficacy Scale in Neuromuscular Disorders and comparison between sex, age, and diagnoses15
Peripheral nerve injuries in the performing artist15
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis15
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates15
Join AANEM15
Issue Highlights15
Positive acetylcholine receptor antibody in nonmyasthenic patients15
The utility of diaphragm ultrasound thickening indices for assessing respiratory decompensation in amyotrophic lateral sclerosis15
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report15
AANEM News and Insights15
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis15
Intermittent versus daily regimen of prednisolone in ambulatory boys with Duchenne muscular dystrophy: A randomized, open‐label trial15
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus14
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier14
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis14
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy14
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Utilization of MG‐ADL in myasthenia gravis clinical research and care13
Issue Highlights13
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophy13
The supraclavicular nerve13
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry13
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari12
Issue Highlights12
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment12
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up12
A‐waves are associated with neuropathic pain in leprosy12
Clinical profile and impact of comorbidities in patients with very‐late‐onset myasthenia gravis11
Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study11
AANEM News and Insights11
Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment11
Effects of cardiac medications on ventricular function in patients with Duchenne muscular dystrophy–related cardiomyopathy11
Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms11
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene11
Pain in acute motor axonal neuropathy11
Issue Highlights11
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 201811
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP11
Guidelines for ethical behavior relating to clinical practice issues in neuromuscular and electrodiagnostic medicine11
Implications of median sensory study to the thumb and deltoid/biceps motor unit recruitment on identifying C6 root avulsion in upper neonatal brachial plexus palsy11
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions11
Issue Highlights11
Ultrasound‐guided transforaminal approach for nusinersen delivery in adult spinal muscle atrophy patients with challenging access11
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies11
Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen11
Extraocular muscle volume on time‐of‐flight magnetic resonance angiography in patients with myasthenia gravis10
Evaluation of mechanomyogram efficacy as a tool for assessing paired‐pulse inhibition of blink reflex early R1 component10
AANEM 2024 Annual Meeting Abstracts Guide10
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study10
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults10
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock10
Voluntary and magnetically evoked muscle contraction protocol in males with Duchenne muscular dystrophy: Safety, feasibility, reliability, and validity10
10
Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region10
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy10
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy10
Calendar of Events10
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study10
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
9
Measuring treatment response to chronic inflammatory demyelinating polyneuropathy in clinical practice: More than just asking9
Standardization of Myasthenia Gravis Outcome Measures in Clinical Practice: A Report of the MGFA Task Force9
Radial motor nerve conduction studies recorded from triceps brachii and extensor carpi radialis longus: Techniques and reference values9
Issue Information9
Issue Information9
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”9
A phase Ib/IIa, open‐label, multiple ascending‐dose trial of domagrozumab in fukutin‐related protein limb‐girdle muscular dystrophy9
AANEM News and Comments9
Assessment of clinical factors affecting outcome of myasthenia gravis9
Paraproteinemic neuropathies9
Milestones of progression in myotonic dystrophy type 1 and type 29
MScanFit motor unit number estimation of human anconeus muscle8
Join AANEM8
Mass effect of the distal triceps brachii muscle on ulnar nerve movement during elbow flexion8
Calendar of Events8
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis8
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study8
Incidence and causes of overdiagnosis of myasthenia gravis8
Details Matter: The Difference Between NIV and NVS8
Issue Information8
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center8
Ten years of riluzole use in a tertiary ALS clinic8
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy8
Laryngospasm in amyotrophic lateral sclerosis8
Issue Highlights8
Could posturography be a useful outcome measure for chronic inflammatory demyelinating polyneuropathy?8
Neuromuscular Ultrasound Training: Bridging the Gap8
The Enigma of the Motor Nerve Conduction Study8
Assessment of clinical skills in electrodiagnostic medicine8
Short‐term educational value of online neuromuscular ultrasound courses8
Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management8
Ultrasonic evidence of mononeuritis multiplex caused by Lyme neuroborreliosis8
Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve8
The effect of methocarbamol and mexiletine on murine muscle spindle function7
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connective Tissue Diseases”7
GNE myopathy: Don't sleep on the platelets7
Electrodiagnostic and ultrasound evaluation of respiratory weakness7
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value7
Join AANEM7
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab7
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy7
Phantom radiculopathy: An electrodiagnostic challenge7
Age‐related sensory neuropathy in patients with spinal muscular atrophy type 17
AANEM Application7
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3‐related muscular dystrophy7
AANEM News and Comments7
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency7
Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment7
High prevalence of paraspinal muscle involvement in adults with McArdle disease7
The use and misuse of sonographic reference values in neuromuscular disease7
Utility of Median Nerve Electrophysiological Parameters in Differentiating Immune‐Mediated Demyelination From Compressive Median Neuropathy at the Wrist7
The quality of occupational healthcare for carpal tunnel syndrome, healthcare expenditures, and disability outcomes: A prospective observational study7
7
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy7
Issue Highlights7
A novel homozygous ALPK3 variant associated with cardiomyopathy and skeletal muscle involvement7
Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey7
Chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M paraprotein, cold agglutinins, and disialosyl antibodies presenting after COVID19 mRNA vaccination7
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee6
Lung volume recruitment improves volitional airway clearance in amyotrophic lateral sclerosis6
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
Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study6
Quantifying adverse events: The burden is on us!6
The diagnosis of myasthenia gravis: The sensitive issue of specificity6
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AANEM Calender of Events6
A cross‐sectional study of memory and executive functions in patients with sporadic inclusion body myositis6
Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States6
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis6
Home‐based gait analysis as an exploratory endpoint during a multicenter phase 1 trial in limb girdle muscular dystrophy type R2 and facioscapulohumeral muscular dystrophy6
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“An Ounce of Prevention…”6
Issue Information6
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype6
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting6
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy6
Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial6
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis6
Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria6
Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype6
Cardiopulmonary exercise performance and factors associated with aerobic capacity in neuromuscular diseases6
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy6
Combining multiple measures into a summary index: A step toward more reliable measurement6
Join AANEM6
ALS patient and caregiver attitudes toward physician‐hastened death in California6
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy6
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy5
Issue Information5
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap5
The best and worst of times in therapy development for myasthenia gravis5
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study5
Ted M. Burns MD5
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study5
AANEM News and Insights5
Respiratory considerations in patients with neuromuscular disorders5
Proceedings of the 22nd Annual Meeting of the Northeast ALS Consortium5
COVID‐19 infection in patients with late‐onset Pompe disease5
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Issue Information5
Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab: subgroup analysis of REGAIN and its extension study5
Electrical impedance myography in healthy volunteers5
Calendar of Events5
Time course of capillary regression and an expression balance between vascular endothelial growthfactor‐Aand thrombospondin‐1 in the soleus muscle of hindlimb unloaded rats5
AANEM News & Insights5
Pathological features of reinnervated skeletal muscles after crush injury of the sciatic nerve in ob/ob mice5
In Memorium: Jun Kimura, MD5
Small Fiber Neuropathy and SARS‐CoV‐2 Infection. Another piece in the long COVID puzzle?5
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles5
Refining quality measures for electrodiagnostic testing in suspected carpal tunnel syndrome to account for acceptable variations in practice: Expert review process5
Alterations in fast‐twitch muscle membrane conductance regulation do not explain decreased muscle function of SOD1G93A rats5
Differences in corneal nerve fiber density and fiber length in patients with painful chronic idiopathic axonal polyneuropathy and diabetic polyneuropathy5
AANEM Application5
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children5
Which combined nerve conduction study scores are best suited for polyneuropathy in diabetic patients?5
Slowing the loss of physical function in amyotrophic lateral sclerosis with edaravone: Post hoc analysis of ALSFRS‐R item scores in pivotal study MCI186‐195
Cubital tunnel perfusion in different postures—An anatomical investigation5
Does specificity of electrodiagnostic test referrals predict test outcome in children?5
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study5
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy5
Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome5
AANEM News & Insights5
The impact of myasthenia gravis severity on work and daily activities5
Issue Information5
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations5
COVID‐19–accelerated disease progression in two patients with amyotrophic lateral sclerosis5
AANEM News and Insights5
Sarcolemmal Excitability Properties of the Trapezius5
The use of electrical stimulation to enhance recovery following peripheral nerve injury5
Transcutaneous carbon dioxide monitoring in ALS: Assessment of hypoventilation heats up5
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?5
Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterations4
Issue Highlights4
Oculopharyngodistal myopathy: The recent discovery of an old disease4
Issue Information4
Calendar of Events4
Ultrasound‐guided motor unit scanning electromyography4
Longitudinal relationships between free‐living activities, fatigue, and symptom severity in myasthenia gravis using cohort and individualized models4
Ultrasonographic evaluation of ulnar nerve morphology in patients with ulnar nerve instability4
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