This journal publishes research on neuromuscular diseases, including amyotrophic lateral sclerosis (ALS), Duchenne muscular dystrophy (DMD), myotonic dystrophy type 2 (DM2), immune-mediated necrotizing myopathy (IMNM), and generalized myasthenia gravis (gMG). Studies investigate disease mechanisms, diagnostic methods such as electrodiagnostic studies and muscle biopsy, and therapeutic interventions including gene therapy, experimental treatments, and palliative care. The scope also encompasses patient care, quality of life, and the impact of multidisciplinary clinics and home health services.
Based on the Think.Check.Submit framework by DOAJ, COPE & OASPA. All data from verified open sources.
Publication & Citation Trend
Articles published
Times cited
2019
2020
2021
2022
2023
2024
2025
2026
Source: OpenAlex · Note: citations accumulate over time so older years appear higher
SJR Quartile by Discipline
Scimago ranks this journal separately in each subject category — its quartile can differ by discipline.
Neurology (clinical)Q1
PhysiologyQ1
Physiology (medical)Q1
Cellular and Molecular NeuroscienceQ2
Subject Classification
Web of Science Categories
Clinical NeurologyNeurosciences
Scopus Categories
Physiology (medical)Neurology (clinical)Cellular and Molecular NeurosciencePhysiology
Research Topics (OpenAlex)
Peripheral Nerve DisordersMuscle Physiology and DisordersMuscle activation and electromyography studiesPeripheral Neuropathies and DisordersMyasthenia Gravis and ThymomaHereditary Neurological DisordersGenetic Neurodegenerative DiseasesNeurogenetic and Muscular Disorders ResearchAmyotrophic Lateral Sclerosis ResearchNerve Injury and Rehabilitation