Journal Report

JOURNAL OF NEUROMUSCULAR DISEASES

Download PDF
Journal Information
Journal Title
JOURNAL OF NEUROMUSCULAR DISEASES
Publisher
SAGE PUBLICATIONS INC
ISSN
2214-3599
E-ISSN
2214-3602
Database
Clarivate
Domain
Health Sciences, Life Sciences, Physical 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
Caregivers perspectives on multidisciplinary clinic visits for Duchenne and Becker muscular dystrophy
Cade Haynie, Ruthwik Duvuru, Chary Akmyradov et al.
2026-10-29
DOI: 10.1177/22143602261502976
Diagnostic approach and management strategy for patients with exertional rhabdomyolysis – Results from an international survey of healthcare professionals
Mads Godtfeldt Stemmerik, Nick Kruijt, Felix Kleefeld et al.
2026-10-28
DOI: 10.1177/22143602261493649
Exploring the gut microbiome in children and young adults with myotonic dystrophy type 1
Anne M. van Uden, Heidi Zweers, Alejandro Arias Vasquez et al.
2026-10-26
DOI: 10.1177/22143602261496624
<i>RYR1</i> -related diseases patient-led international research workshop: Novel perspectives, treatments and interventions
Pomi Yun, Lourdes Figueroa, Chang Seok Lee et al.
2026-10-21
DOI: 10.1177/22143602261463646
Machine learning predicts treatment response to nusinersen in non-sitter spinal muscular atrophy (SMA)
Georgia Stimpson, Emer O’Reilly, Giorgia Coratti et al.
2026-10-20
DOI: 10.1177/22143602261496327
Neurofilaments in cerebrospinal fluid and/or serum as a possible biomarker of pediatric spinal muscular atrophy
Markéta Kumhera, Eva Vrsčaj, Tanja Loboda et al.
2026-10-17
DOI: 10.1177/22143602261488135
The cognitive-behavioral missing link in myotonic dystrophy type 1: Rethinking social cognition assessment
Emanuele Maria Costantini, Silvi Cadri, Alice Ciattaglia et al.
2026-10-15
DOI: 10.1177/22143602261494687
Managing growth and puberty concerns in individuals with Duchenne muscular dystrophy: Updated guidance and future directions
Meilan M. Rutter, Janet L. Crane, Funmbi Babalola et al.
2026-10-10
DOI: 10.1177/22143602261486896
Combined qualitative and quantitative MRI reveals short-term progression in facioscapulohumeral muscular dystrophy
Anna-Lena Mayer, Anika Starke, Valentina Schunk et al.
2026-10-9
DOI: 10.1177/22143602261491510
An international patient survey of RYR1-related diseases: The patient perspective on clinical trial participation
Lizan Stinissen, Sanne A.J.H. van de Camp, Brentney Simon et al.
2026-9-29
DOI: 10.1177/22143602261493651
Articles retrieved from Crossref.
Green Journals | https://www.green-journals.com | info@green-journals.com
Printed: November 1, 2026 19:32