Muscle & Nerve

Papers
(The H4-Index of Muscle & Nerve is 23. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
Issue Information89
AANEM News and Insights87
AANEM Calender of Events87
Join AANEM86
Quality of Life of People With Neuromuscular Diseases: The Role of Stigma73
AANEM News & Insights72
Neuromuscular ultrasound: Impact on diagnosis and management55
AANEM News & Insights51
Longitudinal specialty palliative care for people with amyotrophic lateral sclerosis using a universal referral method43
Cardiopulmonary exercise testing on adaptive equipment in children and adults with Friedreich ataxia39
Electrodiagnostic reporting preferences of referring physicians: An exploratory survey38
Neuroma morphology: A macroscopic classification system36
Paraneoplastic Anti‐Contactin‐1 Autoimmune Nodopathy35
Concentric Needle Jitter Measurements in Voluntarily Activated Deltoid Muscle in Healthy Control Subjects34
Join AANEM32
The neuromuscular fellowship portal and match30
An atypical case of pure motor neuropathy with proximal limb weakness and polyphasic course30
Are Women Physicians Underrecognized for National Awards in Neuromuscular and Electrodiagnostic Medicine? An Observational Study28
Identifying amyotrophic lateral sclerosis through interactions with an internet search engine28
Diagnosis of Primary Mitochondrial Diseases27
Pilot study of a virtual weight management program for Duchenne muscular dystrophy26
Issue Information24
Radial Mononeuropathy: Clinical and Electrodiagnostic Characteristics in 177 Patients23
A clinical bulbar assessment scale (CBAS) for amyotrophic lateral sclerosis23
Prognosis After Discontinuation of Azathioprine or Mycophenolate Mofetil in Well‐Controlled Myasthenia Gravis: A Retrospective Analysis23
Longitudinal Outcomes Among Patients With Duchenne Muscular Dystrophy: A Canadian Retrospective Population‐Based Study23
Amyotrophic lateral sclerosis represents corticomotoneuronal system failure23
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