Muscle & Nerve

Papers
(The median citation count of Muscle & Nerve is 0. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
AANEM News and Insights110
AANEM Calender of Events86
Pain reduction method in recording F‐waves from the vastus lateralis muscle60
Issue Information59
Diagnoses of muscular dystrophy in a veterans health system58
Sodium phenylbutyrate–taurursodiol access, adherence and adverse event in patients with amyotrophic lateral sclerosis: Experience at one center in the United States56
Appendicular lean mass index and motor function in ambulatory patients with Duchenne muscular dystrophy55
Multifocal acquired demyelinating sensory and motor neuropathy presenting with a unilateral radial neuropathy54
Hydrodissection With or Without Corticosteroid Versus Corticosteroid‐Only Injection for Carpal Tunnel Syndrome: Double‐Blind Randomized Controlled Trial48
Cancer in myotonic dystrophy: A new discovery in an old disease47
47
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy40
Hypogammaglobulinemia and infection risk in myotonic dystrophy type 136
Usefulness of somatosensory evoked potentials for monitoring the clinical course of patients with chronic inflammatory demyelinating polyradiculoneuropathy35
Sensory Nerve Action Potential Analysis in a Cohort of Patients With Spinal Muscular Atrophy Aged 12 Years and Older32
Orbicularis Oculi Stimulated Jitter Analysis in Children With Autoimmune Myasthenia Gravis32
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study31
Join AANEM30
Establishing Reference Values in the Neuromuscular Ultrasound Laboratory Using the e‐Norms Method: A Feasibility Study30
Thoracic Electric Impedance Tomography Detects Lung Volume Changes in Amyotrophic Lateral Sclerosis28
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure28
AANEM News & Insights27
26
Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome25
Open‐label pilot study of ranolazine for cramps in amyotrophic lateral sclerosis24
Issue Information24
The cumulative incidence of dysphagia and dysphagia‐free survival in persons diagnosed with amyotrophic lateral sclerosis23
Thumbs up for electrodiagnosis in neonatal brachial plexopathy23
AANEM Application23
Diagnostic yield of advanced genetic testing in patients with hereditary neuropathies: A retrospective single‐site study22
Advancing electrical impedance myography one small step at a time21
A longitudinal study of disease progression in facioscapulohumeral muscular dystrophy (FSHD)21
Response to: “Pulmonary care for ALS: There is more to the story”: We agree more than we disagree20
Issue Highlights20
Join AANEM19
Does SARS‐CoV2 vaccine exposure trigger acute‐onset polyradiculopathy characterized by more common facial paralysis?19
RETRACTED: Utility of phrenic nerve conduction studies for identification of patients with neuromuscular diseases requiring invasive mechanical ventilation18
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Issue Information18
Comparison of the United Kingdom and United States approaches to approval of new neuromuscular therapies18
Thank You to Our Reviewers18
Issue Information17
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle17
Calendar of Events17
AANEM News and Insights17
High‐resolution ultrasound demonstrates in vivo effects of wrist movement on the median nerve along the forearm16
Neuromuscular ultrasound findings in gunshot wounds16
AANEM News and Comments16
Issue Information15
In Memorium: Jun Kimura, MD15
Atypical presentations of immune‐mediated necrotizing myopathy: Clues and caveats15
Interstitial amyloidosis in sporadic inclusion body myositis15
AANEM News and Comments15
AANEM Application15
Issue Highlights14
Neuromuscular ultrasound standardized scanning techniques and protocols: Expert panel recommendations14
Evidence of nerve hypertrophy in patients with inclusion body myositis on lower limb MRI14
Pain perception during electrodiagnostic studies and the impact of learners14
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis14
Refining quality measures for electrodiagnostic testing in suspected carpal tunnel syndrome to account for acceptable variations in practice: Expert review process13
Clinical and neurophysiological biomarkers of disease progression in amyotrophic lateral sclerosis13
A single ALS center experience with clinical use of sodium phenylbutyrate‐taurursodiol13
Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants13
Causes and consequences of diagnostic delay in Guillain‐Barré syndrome in a UK tertiary center13
Risdiplam in non‐sitter patients aged 16 years and older with 5q spinal muscular atrophy13
Axial muscle involvement in patients with limb girdle muscular dystrophy type R913
Real world experience with sodium phenylbutyrate‐taurursodiol for ALS: Lessons learned from a failed drug12
Ted M. Burns MD12
Paradoxical thinning of the diaphragm on ultrasound is a risk factor for requiring non‐invasive ventilation in patients with neuromuscular diaphragmatic dysfunction12
Issue Highlights12
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course12
An expanded access protocol of RT001 in amyotrophic lateral sclerosis—Initial experience with a lipid peroxidation inhibitor11
Transverse interlaminar ultrasound‐guided C1‐C2 puncture for the intrathecal administration of nusinersen in patients with spinal muscular atrophy11
AANEM News and Comments11
Issue Highlights11
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COVID‐19–accelerated disease progression in two patients with amyotrophic lateral sclerosis11
Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts11
AANEM Application11
Differences in corneal nerve fiber density and fiber length in patients with painful chronic idiopathic axonal polyneuropathy and diabetic polyneuropathy11
Issue Information11
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis11
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine10
Three‐dimensional quantitative muscle ultrasound in a healthy population10
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey10
Cardiac atrial pathology in Duchenne muscular dystrophy10
Join AANEM10
Pathological features of reinnervated skeletal muscles after crush injury of the sciatic nerve in ob/ob mice10
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia10
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method10
Calendar of Events10
Pilot study of a novel transmembranous electromyography device for assessment of oral cavity and oropharyngeal muscles10
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Small Fiber Neuropathy and SARS‐CoV‐2 Infection. Another piece in the long COVID puzzle?10
Sensitivity and specificity of the Amyotrophic Lateral Sclerosis Functional Rating Scale—Revised to detect dysarthria in individuals with amyotrophic lateral sclerosis9
Latency and distance9
AANEM Calender of Events9
Initial validation of the Mass. General Neuropathy Exam Tool (MAGNET) for evaluation of distal small‐fiber neuropathy9
Sonographic reference values of cranial nerve size: A systematic review and meta‐analysis9
Pilot study of a virtual weight management program for Duchenne muscular dystrophy9
Issue Information9
Changes in the excitability of anterior horn cells in a mental rotation task of body parts9
Protective effect of alpha‐lipoic acid and epalrestat on oxaliplatin‐induced peripheral neuropathy in zebrafish9
Asymptomatic common extensor tendon pathology in patients with carpal tunnel syndrome9
Epidemiology and features of non–length‐dependent small fiber neuropathy9
Clinical outcome in chronic inflammatory demyelinating polyneuropathy: Facing variability8
Issue Information8
Feasibility of intrathecal therapeutic injections in spinal muscular atrophy patients via a percutaneous transsacral hiatus route: An initial neuroimaging morphometric study8
AANEM News and Comments8
Safety and immunogenicity of mRNA COVID‐19 vaccine in inpatients with muscular dystrophy8
Neuralgic amyotrophy: An update in evaluation, diagnosis, and treatment approaches8
Issue Information8
Diagnostic characteristics of nerve conduction study parameters for vasculitic neuropathy8
Optimal needle electromyography approach to the serratus anterior muscle8
Muscle Contractility in Hypokalemic Periodic Paralysis8
Calendar of Events8
Issue Information8
Safety and efficacy of an injectable nerve‐specific hydrogel in a rodent crush injury model8
COVID‐19 infection in patients with late‐onset Pompe disease8
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Issue Highlights8
Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy8
Electrical Interference in Clinical Practice: A Conceptual and Practical Approach8
Longitudinal Efficacy of Nusinersen Treatment on Health‐Related Quality of Life and Independence in Children With Later‐Onset Spinal Muscular Atrophy8
Perceived utility of electrodiagnostic testing in critical illness myopathy and polyneuropathy: A survey of intensive care unit providers8
Defective E2 electrode lead gives low‐amplitude compound muscle action potential8
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Join AANEM8
AANEM News and Insights8
Motor unit recruitment and firing rate at low force of contraction8
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects7
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study7
The neuromuscular fellowship portal and match7
AANEM News and Insights7
Gene replacement therapy for spinal muscular atrophy unmasking occult hepatitis C in a pediatric patient7
Survival analyses from the CENTAUR trial in amyotrophic lateral sclerosis: Evaluating the impact of treatment crossover on outcomes7
Myotonic Dystrophy (DM) Burden of Disease: A Retrospective Study of Healthcare Costs and Utilization by Individuals With DM7
Direct costs of adhering to selected Duchenne muscular dystrophy Care Considerations: Estimates from a midwestern state7
Single‐ and multiple‐dose safety, tolerability, pharmacokinetic, and pharmacodynamic profiles of ASP0367, or bocidelpar sulfate, a novel modulator of peroxisome proliferator‐activated recep7
Reliability and construct validity of the Duchenne Video Assessment7
Burden and preparedness of care partners of people living with amyotrophic lateral sclerosis at home in Korea: A care partner survey7
Subclinical motor involvement in nonsystemic vasculitic neuropathy determined by the motor unit number estimation method MScanFit7
Amyotrophic Lateral Sclerosis, the Endocannabinoid System, and Exogenous Cannabinoids: Current State and Clinical Implications7
Early initiation of riluzole may improve absolute survival in amyotrophic lateral sclerosis7
AANEM Calender of Events7
Proceedings of the 22nd Annual Meeting of the Northeast ALS Consortium7
Combination therapy with onasemnogene and risdiplam in spinal muscular atrophy type 17
Conduction blocks of the median nerve at the wrist in pregnancy and postpartum carpal tunnel syndromes6
T‐box transcription factor 21 is expressed in terminal Schwann cells at the neuromuscular junction6
Imaging of neuralgic amyotrophy in the acute phase6
The impact of genotype on outcomes in individuals with Duchenne muscular dystrophy: A systematic review6
Calendar of Events6
Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments6
Non‐Hospitalized Patients With Post‐COVID Condition and Myopathic Electromyography Findings Show no Difference in Symptom Severity and Clinical Manifestations Compared to Those Without Myop6
Outcome in chronic inflammatory demyelinating polyneuropathy: A systematic review and meta‐analysis6
An overview of the non‐procedural treatment options for peripheral neuropathic pain6
Diagnostic workup of rhabdomyolysis: Genetic testing should precede neurophysiological testing6
Relationship between pulmonary, cough, and swallowing functions in individuals with amyotrophic lateral sclerosis6
Pregnancy in MuSK‐positive myasthenia gravis: A single‐center case series6
Autoantibody profile in myasthenia gravis patients with a refractory phase6
Urinary titin in myotonic dystrophy type 16
Screening for oropharyngeal dysphagia in adult patients with neuromuscular diseases using the Sydney Swallow Questionnaire6
Limb‐girdle muscular dystrophies: A scoping review and overview of currently available rehabilitation strategies6
Buprenorphine may be effective for treatment of paramyotonia congenita6
Maslow's hammer and nerve conduction studies: How best to use a powerful tool in the evaluation and treatment of diabetic neuropathy?6
Outcomes after intervention for enteral nutrition in patients with amyotrophic lateral sclerosis in multidisciplinary clinics6
Do nerve conduction studies or ultrasound imaging correlate more closely with subjective symptom severity in carpal tunnel syndrome?6
Oral and topical analgesia in pediatric electrodiagnostic studies6
Safety and outcomes of eculizumab for acetylcholine receptor‐positive generalized myasthenia gravis in clinical practice6
Exertional rhabdomyolysis in newly enrolled cadets of a military academy6
Correction to “Role of artificial intelligence in neuromuscular and electrodiagnostic medicine”6
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Health services utilization prior to amyotrophic lateral sclerosis diagnosis: A province‐wide study of individuals treated with riluzole in Ontario, Canada5
Focus on the role of Na(v)1.7 channel as molecular target of methocarbamol and its analgesic effects5
Assessment of the upper limb function, strength, and mobility in treatment‐naive children with spinal muscular atrophy Types 2 and 35
Value and pitfalls of imaging and electrodiagnosis in neurogenic thoracic outlet syndrome: Lessons learned from present and past5
The diagnostic role of magnetic resonance neurography in the neurological subtypes of thoracic outlet syndrome: Some answers and some additional questions5
Diagnosis and management of metabolic myopathies5
Efgartigimod alfa‐fcab use in a pregnant woman with generalized myasthenia gravis: A case report5
Lower limb nerve ultrasound: A four‐way comparison of acquired and inherited axonopathy, inherited neuronopathy and healthy controls5
Sensory nerve regeneration and reinnervation in muscle following peripheral nerve injury5
Neuromuscular ultrasound: Impact on diagnosis and management5
Identifying Daytime Hypercapnia Using Transcutaneous Carbon Dioxide Monitoring in Patients With Amyotrophic Lateral Sclerosis5
Assessing hepatitis B virus serologies when transitioning patients from intravenous immune globulin therapy to rituximab for the treatment of autoimmune neuromuscular diseases5
Retrospective review of patients with myasthenia gravis switched from plasma exchange therapy to efgartigimod treatment5
Secondary outcomes of scoliosis surgery in disease‐modifying treatment‐naïve patients with spinal muscular atrophy type 2 and nonambulant type 35
Electrical stimulation or tacrolimus (FK506) alone enhances nerve regeneration and recovery after nerve surgery, while dual use reduces variance and combines strengths of each in promoting 5
Methodological challenges in measuring meaningful change in individuals with spinal muscular atrophy5
Longitudinal changes in respiratory and upper limb function in a pediatric type III spinal muscular atrophy cohort after loss of ambulation5
Join AANEM5
AANEM News & Insights5
Persistent post–COVID‐19 neuromuscular symptoms5
Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulation5
Neuroma morphology: A macroscopic classification system5
Incidence and prevalence of myasthenia gravis in the United States: A claims‐based analysis5
Rehabilitation is [still] necessary to optimize function in neuromuscular disorders5
Issue Highlights5
Ultrasound Evaluation of Upper Limb Sublesional Muscle Morphology in Cervical Spinal Cord Injury5
Relative effects of forced vital capacity and ALSFRS‐R on survival in ALS5
Nutrition outcomes of disease modifying therapies in spinal muscular atrophy: A systematic review5
Visual versus quantitative analysis of muscle ultrasound in neuromuscular disease5
Efficient and Rapid Histomorphometry of Regenerating Peripheral Nerve5
Continued benefit of nusinersen initiated in the presymptomatic stage of spinal muscular atrophy: 5‐year update of theNURTUREstudy5
Thank you to our reviewers5
Comment on Hydrodissection With or Without Corticosteroid Versus Corticosteroid‐Only Injection for Carpal Tunnel Syndrome: Double‐Blind Randomized Controlled Trial5
Long latency reflexes of the median nerves in healthy adults5
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials5
The impact of genotype on age at loss of ambulation in individuals with Duchenne muscular dystrophy treated with corticosteroids: A single‐center study of 555 patients5
Somatosensory temporal discrimination analysis reveals impaired processing in amyotrophic lateral sclerosis5
Magnetic resonance neurography in the diagnosis of neurological subtypes of thoracic outlet syndrome5
Musculoskeletal mimics for lumbosacral radiculopathy. Part 2: Specific disorders5
Non‐length‐dependent small fiber neuropathy: Not a matter of stockings and gloves5
Issue Information5
Investigating the Mechanism of Conditioning Versus Postoperative Electrical Stimulation to Enhance Nerve Regeneration: One Therapy, Two Distinct Effects5
Safety, tolerability, and pharmacokinetics of casimersen in patients with Duchenne muscular dystrophy amenable to exon 45 skipping: A randomized, double‐blind, placebo‐controlled5
Calendar of Events5
Prevalence of chronic inflammatory demyelinating polyneuropathy and multifocal motor neuropathy in two regions of Australia5
Initiation of noninvasive ventilation in patients with amyotrophic lateral sclerosis5
Neurophysiological patterns of acute and post‐acute foodborne botulism4
Issue Information4
Onasemnogene abeparvovec gene therapy for spinal muscular atrophy: A cohort study from the United Arab Emirates4
Stepping up for a practical biomarker of motor unit loss4
Treatment with patisiran of a patient with hereditary transthyretin‐mediated amyloidosis with stage 3 polyneuropathy4
Antibiotics in myasthenia gravis: Thinking outside the black box4
Self‐reported reduced sleep quality and excessive daytime sleepiness in facioscapulohumeral muscular dystrophy4
Carpal tunnel syndrome in pregnancy4
Atypical presentations of inclusion body myositis: Clinical characteristics and long‐term outcomes4
Autophagy in non–immune‐mediated rhabdomyolysis: Assessment of p62 immunohistochemistry4
Optimal stimulation site of the femoral nerve to record F waves from the vastus lateralis muscle4
Characterization of mononeuropathy of the lateral cutaneous nerve of the calf4
Calendar of Events4
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Categorization of the amyotrophic lateral sclerosis population via the clinical determinant of post‐onset ΔFS for study design and medical practice4
Assessment of the relationship between disease progression and goals of care by individuals with Duchenne muscular dystrophy and their caregivers4
AANEM Application4
Stability of serial platelet and urine protein measurements in patients receiving nusinersen for spinal muscular atrophy4
Reliability of confocal corneal microscopy for measurement of dendritic cell density in suspected small fiber neuropathy4
Revising nerve conduction reference limits4
Issue Information4
Primary perineuritis, a rare but treatable neuropathy: Review of perineurial anatomy, clinicopathological features, and differential diagnosis4
Issue Highlights4
Variable differences of nerve conduction amplitudes versus velocities and distal latencies of healthy subjects assessed in ethnic cohorts4
Opinions on Pneumocystis jirovecii prophylaxis in autoimmune neuromuscular disorders4
Issue Information4
Quantitative muscle echointensity: A practical approach using ultrasound to evaluate children with suspected neuromuscular disorders4
Peripheral nerve morphology and intraneural blood flow in chronic kidney disease with and without diabetes4
Join AANEM4
Issue Highlights4
Issue Information4
Clinical utility of far field motor potentials in amyotrophic lateral sclerosis4
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