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 2021-06-01 to 2025-06-01.)
ArticleCitations
115
Join AANEM97
AANEM News and Insights68
AANEM Calender of Events64
Issue Information63
AANEM News & Insights60
Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single‐site study56
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials53
The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review49
Neuroma morphology: A macroscopic classification system41
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study41
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy37
Diagnosis of Primary Mitochondrial Diseases36
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study35
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects33
Join AANEM32
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle32
Neuromuscular ultrasound: Impact on diagnosis and management31
Axial muscle involvement in patients with limb girdle muscular dystrophy type R929
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method28
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis27
Pilot study of a virtual weight management program for Duchenne muscular dystrophy27
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine27
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course27
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia25
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy25
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis25
The neuromuscular fellowship portal and match25
Diagnosis and management of metabolic myopathies24
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure24
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts23
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma23
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey22
Volumetric muscle composition analysis in sporadic inclusion body myositis using fat‐referenced magnetic resonance imaging: Disease pattern, repeatability, and natural progression20
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AANEM Application19
AANEM News and Comments19
The strength of associations between ultrasound measures of upper limb muscle morphology and isometric muscle strength: An exploratory study19
Issue Information19
The utility of diaphragm ultrasound thickening indices for assessing respiratory decompensation in amyotrophic lateral sclerosis18
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates18
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy18
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy18
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis18
Pembrolizumab‐induced radiation recall myopathy with fasciopathy: A case report18
Atypical presentation of hypokalemic periodic paralysis: A case report18
Amyotrophic lateral sclerosis mimics18
Nerve ultrasound characteristics of immunoglobulin M neuropathy associated with anti‐myelin‐associated glycoprotein antibodies17
Pregnancy outcomes in patients with congenital myasthenic syndromes17
Positive acetylcholine receptor antibody in nonmyasthenic patients17
A case of neuroleukemiosis: The usefulness of nerve ultrasound as a diagnostic tool17
Optimal placement for needle electromyography of the supinator muscle: Cadaveric studies17
Estimation of diaphragm depth based on waist circumference in the Thai population16
Diagnostic criteria in amyotrophic lateral sclerosis: Time for a change16
Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury16
Intermittent versus daily regimen of prednisolone in ambulatory boys with Duchenne muscular dystrophy: A randomized, open‐label trial15
AANEM News and Insights15
Rasch analysis of the Unidimensional Self‐Efficacy Scale in Neuromuscular Disorders and comparison between sex, age, and diagnoses15
Bilateral hemidiaphragm atrophy and electrical myotonia in anti‐muscle specific tyrosine kinase myasthenia gravis15
Issue Highlights15
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Impact of COVID‐19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy15
Redundant nerve roots on magnetic resonance imaging can predict ongoing denervation in patients with lumbar spinal stenosis15
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier15
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophy14
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis14
Peripheral nerve injuries in the performing artist14
Psychometric evaluation of modified spinal muscular atrophy functional rating scale (SMAFRS) in adult patients using Rasch analysis14
Low T3 syndrome is associated with peripheral neuropathy in patients with type 2 diabetes mellitus14
Utilization of MG‐ADL in myasthenia gravis clinical research and care13
Issue Highlights13
Standardization of Myasthenia Gravis Outcome Measures in Clinical Practice: A Report of the MGFA Task Force13
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry13
Intravenous immunoglobulin and plasma exchange prescribing patterns for Guillain‐Barre Syndrome in the United States—2001 to 201813
Issue Highlights13
Value and pitfalls of imaging and electrodiagnosis in neurogenic thoracic outlet syndrome: Lessons learned from present and past13
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Fatigue and Fatigability in Spinal Muscular Atrophy; a Proposed Taxonomy to Enhance Assessment and Treatment13
Associations between lower extremity muscle fat fraction and motor performance in myotonic dystrophy type 2: A pilot study12
Acquired hyperexcitable peripheral nerve disorders: Clinical and laboratory features, therapeutic responses, and long‐term follow‐up12
Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study12
Assessing perspectives of disease burden and clinically meaningful changes using the Spinal Muscular Atrophy Health Index in adolescents and young adults12
A‐waves are associated with neuropathic pain in leprosy12
Effects of hypobaric hypoxia during a simulated ultra‐long‐haul flight on inflammation and regeneration after muscle trauma and muscle trauma‐hemorrhagic shock12
Effects of cardiac medications on ventricular function in patients with Duchenne muscular dystrophy–related cardiomyopathy12
The supraclavicular nerve12
Autologous hematopoietic stem cell transplant for the treatment of refractory myasthenia gravis with anti‐muscle specific kinase antibodies12
Serial electrodiagnostic studies in acute partial conduction block from cyclist's palsy12
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
Evaluation of the applicability of weak shoulder and arm sparing signs in amyotrophic lateral sclerosis by multiple neurologists and neurology residents: A single‐center study11
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Factors associated with increased health‐related quality‐of‐life benefits in hereditary transthyretin amyloidosis polyneuropathy patients treated with inotersen11
Prevalence of Pathogenic Transthyretin Gene Variants in the Rocky Mountain Region11
Segmental motor neuron dysfunction in amyotrophic lateral sclerosis: Insights from H reflex paradigms11
Calendar of Events11
Issue Highlights11
Guidelines for ethical behavior relating to clinical practice issues in neuromuscular and electrodiagnostic medicine11
Extraocular muscle volume on time‐of‐flight magnetic resonance angiography in patients with myasthenia gravis11
Voluntary and magnetically evoked muscle contraction protocol in males with Duchenne muscular dystrophy: Safety, feasibility, reliability, and validity11
AANEM 2024 Annual Meeting Abstracts Guide11
Paraproteinemic neuropathies11
Clinical profile and impact of comorbidities in patients with very‐late‐onset myasthenia gravis11
AANEM News and Insights11
Ultrasound‐guided transforaminal approach for nusinersen delivery in adult spinal muscle atrophy patients with challenging access11
Understanding the role of the lower motor neuron in spinal cord injury and its impact on electrodiagnostic assessment11
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
Exercise as Medicine in Neuromuscular Disorders: Changing Attitudes, Ongoing Challenges, and Future Research Directions11
Prevalence of cardiovascular implantable electronic devices in children with type 1 myotonic dystrophy11
Issue Highlights11
Utility of Carpal Tunnel Release and Ulnar Decompression in CMT1A and HNPP10
Issue Information10
Join AANEM10
Calendar of Events10
AANEM News and Comments10
Epidemiology of seropositive myasthenia gravis in Sardinia: A population‐based study in the district of Sassari10
Measuring treatment response to chronic inflammatory demyelinating polyneuropathy in clinical practice: More than just asking10
The Enigma of the Motor Nerve Conduction Study10
Effectiveness and Safety of IVIG for the Treatment of HMGCR Immune‐Mediated Necrotizing Myopathy10
Adult‐onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene10
Pain in acute motor axonal neuropathy10
Details Matter: The Difference Between NIV and NVS10
Issue Information10
Issue Information10
Incidence and causes of overdiagnosis of myasthenia gravis9
Changes in electrophysiological findings suggestive of demyelination following Guillain‐Barré syndrome: A retrospective study9
Assessment of clinical skills in electrodiagnostic medicine9
Racial Disparities in ALS Progression: Time to Clinical Events Observed in a Single Center9
Radial motor nerve conduction studies recorded from triceps brachii and extensor carpi radialis longus: Techniques and reference values9
Reply to “Intravenous saline may not be a placebo in patients with small fiber neuropathy”9
Neuromuscular Ultrasound Training: Bridging the Gap9
Short‐term educational value of online neuromuscular ultrasound courses9
MScanFit motor unit number estimation of human anconeus muscle9
The use and misuse of sonographic reference values in neuromuscular disease8
Correction to “Myositis‐Related Autoantibody Profile and Clinical Characteristics Stratified by Anti‐Cytosolic 5′‐Nucleotidase 1A Status in Connective Tissue Diseases”8
Mass effect of the distal triceps brachii muscle on ulnar nerve movement during elbow flexion8
Issue Highlights8
Issue Highlights8
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The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy8
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3‐related muscular dystrophy8
Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey8
Three‐dimensional quantitative muscle ultrasound in patients with facioscapulohumeral dystrophy and myotonic dystrophy8
Electrodiagnostic and ultrasound evaluation of respiratory weakness8
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Single center experience with hourglass‐like constriction neuropathy of suprascapular nerve8
Could posturography be a useful outcome measure for chronic inflammatory demyelinating polyneuropathy?8
Chronic ataxic neuropathy, ophthalmoplegia, immunoglobulin M paraprotein, cold agglutinins, and disialosyl antibodies presenting after COVID19 mRNA vaccination8
Perceived exertion is not a substitute for fatiguability in spinal muscular atrophy8
Hyperhomocysteinemia in patients with riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency8
Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment8
AANEM News and Comments8
Ten years of riluzole use in a tertiary ALS clinic8
Milestones of progression in myotonic dystrophy type 1 and type 28
AANEM Application8
Phantom radiculopathy: An electrodiagnostic challenge8
Myotonic dystrophy type 1: A comparison between the adult‐ and late‐onset subtype8
Ultrasonic evidence of mononeuritis multiplex caused by Lyme neuroborreliosis7
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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
Serious Neurologic Adverse Events in Tofersen Clinical Trials for Amyotrophic Lateral Sclerosis7
The quality of occupational healthcare for carpal tunnel syndrome, healthcare expenditures, and disability outcomes: A prospective observational study7
Age‐related sensory neuropathy in patients with spinal muscular atrophy type 17
Electrophysiology to identify disease mechanisms in CIDP: Reliability and value7
Utility of Median Nerve Electrophysiological Parameters in Differentiating Immune‐Mediated Demyelination From Compressive Median Neuropathy at the Wrist7
High prevalence of paraspinal muscle involvement in adults with McArdle disease7
Thymoma Associated Myasthenia Gravis Successfully Treated With Ravulizumab7
GNE myopathy: Don't sleep on the platelets7
AANEM Calender of Events7
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Burden of illness and costs in patients with myasthenia gravis currently receiving treatment in the United States7
Pregnancy planning may impact maternal and neonatal outcomes in people with myasthenia gravis7
“An Ounce of Prevention…”7
Lung volume recruitment improves volitional airway clearance in amyotrophic lateral sclerosis7
Updated consensus statement: Intravenous immunoglobulin in the treatment of neuromuscular disorders report of the AANEM ad hoc committee7
Combining multiple measures into a summary index: A step toward more reliable measurement7
A novel homozygous ALPK3 variant associated with cardiomyopathy and skeletal muscle involvement7
Laryngospasm in amyotrophic lateral sclerosis7
Issue Information7
AANEM News & Insights7
Issue Information7
Calendar of Events7
Relationship Between Quantitative Magnetic Resonance Imaging Measures and Functional Changes in Patients With Duchenne Muscular Dystrophy7
Prognostic factors, disease course, and treatment efficacy in Duchenne muscular dystrophy: A systematic review and meta‐analysis7
Nerve Ultrasound Detects Nerve Atrophy in Patients With Ataxia‐Telangiectasia: A Pilot Study7
Infiltrative arteriovenous malformation of the sciatic nerve: Imaging and management7
The diagnosis of myasthenia gravis: The sensitive issue of specificity7
The effect of methocarbamol and mexiletine on murine muscle spindle function7
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
Cubital tunnel perfusion in different postures—An anatomical investigation6
Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy6
Cardiopulmonary exercise performance and factors associated with aerobic capacity in neuromuscular diseases6
Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype6
Electrical impedance myography in healthy volunteers6
Recurrent motor branch neuropathy in carpal tunnel syndrome: An ultrasound study6
No sex‐based differences in odds of starting or time to treatment of generalized myasthenia gravis: A single center cohort study6
The impact of myasthenia gravis severity on work and daily activities6
Time course of capillary regression and an expression balance between vascular endothelial growthfactor‐Aand thrombospondin‐1 in the soleus muscle of hindlimb unloaded rats6
Late‐onset Becker muscular dystrophy with distal muscle weakness and rimmed vacuoles6
Neuromuscular Ultrasound Training in Neuromuscular Fellowship Programs in Canada: Minding the Gap6
AANEM News & Insights6
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
The use of electrical stimulation to enhance recovery following peripheral nerve injury6
Does specificity of electrodiagnostic test referrals predict test outcome in children?6
Brachial multisegmental muscle weakness and atrophy caused by a spinal CSF leak after lumbo‐peritoneal shunting6
Gene transfer therapy in children with spinal muscular atrophy: A single‐center experience with a cohort of 25 children6
Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab: subgroup analysis of REGAIN and its extension study6
Alterations in fast‐twitch muscle membrane conductance regulation do not explain decreased muscle function of SOD1G93A rats6
A cross‐sectional study of memory and executive functions in patients with sporadic inclusion body myositis6
Sarcolemmal Excitability Properties of the Trapezius6
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Transcutaneous carbon dioxide monitoring in ALS: Assessment of hypoventilation heats up6
The best and worst of times in therapy development for myasthenia gravis6
Respiratory considerations in patients with neuromuscular disorders6
Nasal cannulas for pediatric neuromuscular respiratory home management—Perhaps a too well‐kept secret?6
Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy6
Myasthenia gravis Lambert–Eaton overlap syndrome: Recommended modification for the diagnostic criteria6
Quantifying adverse events: The burden is on us!6
Which combined nerve conduction study scores are best suited for polyneuropathy in diabetic patients?6
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
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations6
ALS patient and caregiver attitudes toward physician‐hastened death in California6
Longitudinal relationships between free‐living activities, fatigue, and symptom severity in myasthenia gravis using cohort and individualized models5
Issue Information5
Visual versus quantitative analysis of muscle ultrasound in neuromuscular disease5
Relative effects of forced vital capacity and ALSFRS‐R on survival in ALS5
Limb‐girdle muscular dystrophies: A scoping review and overview of currently available rehabilitation strategies5
Issue Information5
Imaging of neuralgic amyotrophy in the acute phase5
Orbicularis Oculi Stimulated Jitter Analysis in Children With Autoimmune Myasthenia Gravis5
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study5
Gene replacement therapy for spinal muscular atrophy unmasking occult hepatitis C in a pediatric patient5
Correlates of night‐time and exercise‐associated lower limb cramps in healthy adults5
Neuralgic amyotrophy: An update in evaluation, diagnosis, and treatment approaches5
Longitudinal motor function in proximal versus distal DMD pathogenic variants5
Transverse interlaminar ultrasound‐guided C1‐C2 puncture for the intrathecal administration of nusinersen in patients with spinal muscular atrophy5
Persistent post–COVID‐19 neuromuscular symptoms5
COVID‐19–accelerated disease progression in two patients with amyotrophic lateral sclerosis5
Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy5
COVID‐19 infection in patients with late‐onset Pompe disease5
AANEM Annual Meeting Abstract Guide Nashville, TN | September, 21–24, 20225
Issue Information5
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Proceedings of the 22nd Annual Meeting of the Northeast ALS Consortium5
Small Fiber Neuropathy and SARS‐CoV‐2 Infection. Another piece in the long COVID puzzle?5
Differences in corneal nerve fiber density and fiber length in patients with painful chronic idiopathic axonal polyneuropathy and diabetic polyneuropathy5
Efgartigimod alfa‐fcab use in a pregnant woman with generalized myasthenia gravis: A case report5
RETRACTED: Utility of phrenic nerve conduction studies for identification of patients with neuromuscular diseases requiring invasive mechanical ventilation5
Urinary titin in myotonic dystrophy type 15
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