Journal Report

NEUROMUSCULAR DISORDERS

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Journal Information
Journal Title
NEUROMUSCULAR DISORDERS
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
ISSN
0960-8966
E-ISSN
1873-2364
Database
Clarivate
Domain
Health Sciences, Life Sciences, Physical Sciences, Social Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Dual ultrasound detection of facial muscle changes in FSHD1: thickness and echo intensity findings - a cross-sectional comparison with healthy adults
Havvanur Albayrak, Ahmet Peker, Gulshan Yunisova et al.
2026-12 Vol. 69 Pages 107457
DOI: 10.1016/j.nmd.2026.107457
Generalized edema as the initial manifestation of Anti-TIF1γ-positive dermatomyositis associated with ovarian cancer
Sumin Kim, Seung-Ah Lee
2026-12 Vol. 69 Pages 107452
DOI: 10.1016/j.nmd.2026.107452
Non-invasive assessment of microvascular changes in a Duchenne muscular dystrophy rat model with near-infrared spectroscopy
Margarita Egiian, Rasa Eskandari, Susan Tyler et al.
2026-12 Vol. 69 Pages 107463
DOI: 10.1016/j.nmd.2026.107463
Interindividual variability of muscle involvement on imaging in a family with FLNC c.577G>A (p.A193T)-related myopathy
Wakako Yoshioka, Satoru Noguchi, Hotake Takizawa et al.
2026-12 Vol. 69 Pages 107454
DOI: 10.1016/j.nmd.2026.107454
Pathogen identification by shotgun metagenomics in inflammatory myopathies: a prospective observational study reporting the first European case of Anncaliia algerae myositis
Andrei-Valentin Brîncuș, Cécile Angebault, Nadège Wesner et al.
2026-12 Vol. 69 Pages 107458
DOI: 10.1016/j.nmd.2026.107458
Validation of non-instrumental clinical outcome assessments for dysphagia in OPMD: A structured, COSMIN-guided assessment
Claudia Côté, Hanns Lochmüller, Bernard Brais et al.
2026-12 Vol. 69 Pages 107453
DOI: 10.1016/j.nmd.2026.107453
Juvenile dermatomyositis across diagnostic eras: treatment evolution and long-term outcomes in a 25-year cohort
Mehmet Orhan Erkan, Hulya Ercan Emreol, Mehmet Besrek et al.
2026-12 Vol. 69 Pages 107459
DOI: 10.1016/j.nmd.2026.107459
A late-onset slowly progressive dystrophic–myasthenic phenotype expands the clinical spectrum of TOR1AIP1-related disease
Carolina Cunha, Danilo Alves, Luís Ferreira et al.
2026-12 Vol. 69 Pages 107455
DOI: 10.1016/j.nmd.2026.107455
Development of Italian centile curves for the North Star Ambulatory Assessment and timed items
Sophia Paolucci, Nicolò Lentini, Giorgia Coratti et al.
2026-12 Vol. 69 Pages 107456
DOI: 10.1016/j.nmd.2026.107456
Twenty years of givinostat in Duchenne muscular dystrophy: a patient-organisation perspective
Filippo Buccella, Patricia Furlong
2026-12 Vol. 69 Pages 107451
DOI: 10.1016/j.nmd.2026.107451
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Printed: November 4, 2026 04:23