Neuromuscular Disorders : Impact Factor & More

eISSN: 1873-2364pISSN: 0960-8966

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Aims and Scope of Neuromuscular Disorders

Neuromuscular Disorders is a peer-reviewed medical journal that focuses on neuromuscular disease, including muscular dystrophy, spinal muscular atrophy, and myasthenia. It is the official journal of the World Muscle Society. It was established in 1991 and is published by Elsevier. Less

Neuromuscular Disorders Key Metrics

CiteScore
5.8
Eigenfactor
0.005 - 0.01
Impact Factor
< 5
SJR
Q2Neurology
SNIP
1.31
Time to Accept
3
 Mo
Time to Publish
time-to-publish View Chart
3
 Mo
Time to Publish

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% of papers by time taken from submission to publication
0 to 3 months
36%
4 to 6 months
51%
7 to 9 months
11%
Above 9 months
2%

Topics Covered on Neuromuscular Disorders

Neuromuscular Disorders Journal Specifications

Indexed in the following public directories

  • Web of Science Web of Science
  • Scopus Scopus
  • SJR SJR
Overview
Publisher PERGAMON-ELSEVIER SCIENCE LTD
Language English
Frequency Monthly
General Details
LanguageEnglish
FrequencyMonthly
Publication Start Year1991
Publisher URLVisit website
Website URLVisit website
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Recently Published Papers in Neuromuscular Disorders

Obituary
  • 1 Jun 2025
  • Neuromuscular Disorders
Biallelic variants in the RFC4 gene cause a rapidly progressive congenital myopathy with severe hypotonia and axial weakness.
  • 1 Jun 2025
  • Neuromuscular disorders : NMD
The involvement of central nervous system across the phenotypic spectrum of Pompe disease: a systematic review.
  • 1 Jun 2025
  • Neuromuscular disorders : NMD
New insight in lipid storage myopathy.
  • 1 Jun 2025
  • Neuromuscular disorders : NMD
Corrigendum to "Assessing disease progression in Spinal Muscular Atrophy, current gaps, and opportunities: a narrative review" [NMD, volume 49, article 105341
  • 22 May 2025
  • Neuromuscular disorders : NMD
Aseptic meningoencephalitis during nusinersen therapy in a patient with type III spinal muscular atrophy: a case report.
  • 1 May 2025
  • Neuromuscular disorders : NMD
Obituary
  • 1 Jun 2025
  • Neuromuscular Disorders
Biallelic variants in the RFC4 gene cause a rapidly progressive congenital myopathy with severe hypotonia and axial weakness.
  • 1 Jun 2025
  • Neuromuscular disorders : NMD
The involvement of central nervous system across the phenotypic spectrum of Pompe disease: a systematic review.
  • 1 Jun 2025
  • Neuromuscular disorders : NMD
New insight in lipid storage myopathy.
  • 1 Jun 2025
  • Neuromuscular disorders : NMD
Corrigendum to "Assessing disease progression in Spinal Muscular Atrophy, current gaps, and opportunities: a narrative review" [NMD, volume 49, article 105341
  • 22 May 2025
  • Neuromuscular disorders : NMD
Aseptic meningoencephalitis during nusinersen therapy in a patient with type III spinal muscular atrophy: a case report.
  • 1 May 2025
  • Neuromuscular disorders : NMD
View all papers for this journal

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