Journal of Neuromuscular Diseases
ISSN:2214-3599

Journal of Neuromuscular Diseases

学科领域:医学
是否预警:不在预警名单内
是否OA:
录用周期:-
新锐分区:医学2区
年发文量:100
影响因子:3.4
JCR分区:Q2

基本信息

-
2214-3599SCIE/Scopus收录
3.4
3.3
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学2区
CLINICAL NEUROLOGY 临床神经病学
3区
NEUROSCIENCES 神经科学
3区
N/A
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科:CLINICAL NEUROLOGY
SCIE
Q2
78/286
学科:NEUROSCIENCES
SCIE
Q2
116/314
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科:CLINICAL NEUROLOGY
SCIE
Q2
94/286
学科:NEUROSCIENCES
SCIE
Q2
118/314
暂无h-index数据
100
----Medicine-Neurology (clinical)
11.8%
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
85.00%62.5%-
CiteScore:5.60
SJR:1.016
SNIP:1.053
学科类别分区排名百分位
大类:Medicine
小类:Neurology (clinical)
Q2
112 / 400
大类:Medicine
小类:Neurology
Q2
59 / 194

期刊高被引文献

Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 – A Prospective Observational Study
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190416
Exploration of New Contrasts, Targets, and MR Imaging and Spectroscopy Techniques for Neuromuscular Disease – A Workshop Report of Working Group 3 of the Biomedicine and Molecular Biosciences COST Action BM1304 MYO-MRI
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-180333
Phase 1 Study of Edasalonexent (CAT-1004), an Oral NF-κB Inhibitor, in Pediatric Patients with Duchenne Muscular Dystrophy
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-180341
Report of a TREAT-NMD/World Duchenne Organisation Meeting on Dystrophin Quantification Methodology
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-180357
Clinical Presentation, Diagnosis and Treatment of TTR Amyloidosis
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-180371
Advances in Treatment of Spinal Muscular Atrophy – New Phenotypes, New Challenges, New Implications for Care
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190424
Discovery of Novel Therapeutics for Muscular Dystrophies using Zebrafish Phenotypic Screens
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190389
Perspectives on Spinraza (Nusinersen) Treatment Study: Views of Individuals and Parents of Children Diagnosed with Spinal Muscular Atrophy.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180330
Perceived Fatigue in Spinal Muscular Atrophy: A Pilot Study.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180342
Defects in Axonal Transport in Inherited Neuropathies
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190427
Management of Adrenal Insufficiency Risk After Long-term Systemic Glucocorticoid Therapy in Duchenne Muscular Dystrophy: Clinical Practice Recommendations
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-180346
Brain Structural Features of Myotonic Dystrophy Type 1 and their Relationship with CTG Repeats
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190397
Homozygous Nonsense Mutation p.Q274X in TRIM63 (MuRF1) in a Patient with Mild Skeletal Myopathy and Cardiac Hypertrophy.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180350
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190377
Intra-Rater Reliability and Concurrent Validity of Quantified Muscle Testing for Maximal Knee Extensors Strength in Men with Myotonic Dystrophy Type 1.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190388
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180376
Advancements in AAV-mediated Gene Therapy for Pompe Disease
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190426
Treatment with Nusinersen - Challenges Regarding the Indication for Children with SMA Type 1.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/jnd-190441
Spinal Stenosis in Familial Transthyretin Amyloidosis.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180348
Responsiveness to Change of 5-point MRC scale, Endurance and Functional Evaluation for Assessing Myositis in Daily Clinical Practice.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180358
Molecular and Clinical Characteristics of a National Cohort of Paediatric Duchenne Muscular Dystrophy Patients in Norway.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190402
A Mutation in the Mitochondrial Aspartate/Glutamate Carrier Leads to a More Oxidizing Intramitochondrial Environment and an Inflammatory Myopathy in Dutch Shepherd Dogs
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190421
The Added Value of Cardiac Magnetic Resonance in Muscular Dystrophies
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190415
Ocular Weakness in Myasthenia Gravis: Changes in Affected Muscles are a Distinct Clinical Feature
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190407
The Position of Neuromuscular Patients in Shared Decision Making. Report from the 235th ENMC Workshop: Milan, Italy, January 19-20, 2018.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180368
Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190379
A Novel De Novo Heterozygous SCN4a Mutation Causing Congenital Myopathy, Myotonia and Multiple Congenital Anomalies.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/jnd-190425
Echographic Assessment of Diaphragmatic Function in Duchenne Muscular Dystrophy from Childhood to Adulthood.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180326
MuscleViz: Free Open-Source Software for Muscle Weakness Visualization.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190385
Muscle Strength and Aerobic Capacity in Patients with CIDP One Year after Participation in an Exercise Trial.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180344
Caregiver Burden and Related Factors Among Caregivers of Patients with Myotonic Dystrophy Type 1.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/jnd-190386
Implementing a Global Expanded Access Program (EAP) for Infantile-Onset Spinal Muscular Atrophy (Type I): Understanding the Imperative, Impact and Challenges
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190387
A Novel Mutation in MARS in a Patient with Charcot-Marie-Tooth Disease, Axonal, Type 2U with Congenital Onset
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190404
Increased Blood Pressure and Body Mass Index as Potential Modifiable Factors in The Progression of Myocardial Dysfunction in Duchenne Muscular Dystrophy.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180340
Identification of a Novel Deep Intronic Mutation in CAPN3 Presenting a Promising Target for Therapeutic Splice Modulation.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190414
Lower Extremity Functional Outcome Measures in Duchenne Muscular Dystrophy-A Delphi Survey.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180337
Abnormal Excitation-Contraction Coupling and Calcium Homeostasis in Myopathies and Cardiomyopathies.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180314
Myo-Glyco disease Biology: Genetic Myopathies Caused by Abnormal Glycan Synthesis and Degradation
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-180369
Dihydropyridine Receptor Congenital Myopathy In A Consangineous Turkish Family.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190383
The Dog Model in the Spotlight: Legacy of a Trustful Cooperation
来源期刊:Journal of Neuromuscular DiseasesDOI:10.3233/JND-190394
Muscular, Ocular and Brain Involvement Associated with a De Novo 11q13.2q14.1 Duplication: Contribution to the Differential Diagnosis of Muscle-Eye-Brain Congenital Muscular Dystrophy.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/jnd-190413
Dysautonomia as the Presenting Symptom in Anti-Muscle-Specific Kinase Antibody Myasthenia Gravis.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-190411
Myotubular Trust - 2019 Call for Projects (Open to International Applications).
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-189002
A Phenotypic Description of Congenital Myotonic Dystrophy using PhenoStacks.
来源期刊:Journal of neuromuscular diseasesDOI:10.3233/JND-180345

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