Muscle & Nerve

Papers
(The H4-Index of Muscle & Nerve is 26. 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 2022-05-01 to 2026-05-01.)
ArticleCitations
AANEM News and Insights108
AANEM Calender of Events108
Join AANEM94
AANEM News & Insights89
AANEM News & Insights70
Issue Information45
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey44
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy44
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects40
Join AANEM39
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course39
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine38
Pilot study of a virtual weight management program for Duchenne muscular dystrophy37
Neuroma morphology: A macroscopic classification system37
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure36
Diagnosis and management of metabolic myopathies33
Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle33
Comorbidities and Treatment Patterns in People With Myasthenia Gravis in Denmark, Finland and Sweden: A Population‐Based Observational Study32
Neuromuscular ultrasound: Impact on diagnosis and management31
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method31
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study30
Prognosis After Discontinuation of Azathioprine or Mycophenolate Mofetil in Well‐Controlled Myasthenia Gravis: A Retrospective Analysis29
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study29
Radial Mononeuropathy: Clinical and Electrodiagnostic Characteristics in 177 Patients28
Skeletal muscle symptoms and quantitative MRI in females with dystrophinopathy27
A 5‐year natural history cohort of patients with facioscapulohumeral muscular dystrophy determining disease progression and feasibility of clinical outcome assessments for clinical trials26
Combination of stem cells and nerve guide conduit for the treatment of peripheral nerve injury: A meta‐analysis26
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