Impact Factor
2.18
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
0.79
63 total citations
h5-index
13
h5 depth signal
Cited share
40.0%
32 of 80
Total citations
63
Citation footprint
Metric signal
0.70
External metric anchor
Self-citation
4.8%
3 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
290
India
25
Canada
13
Austria
12
Greece
9
Citing Fields of Research
Neuromuscular Disorders
262
Nervous System Disorders
197
Musculoskeletal Disorders
118
Auto-Inflammatory Disorders
49
Neurodegenerative Disorders
32
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
1,103
Articles tracked across the journal lifetime
Indexed publication set
80
32 cited publications
Last 12 months
39
7.8 publications/month
Open access share
2.6%
1 OA publications in the last year
Leading citing country
United States
290 citing publications
Leading citing field
Neuromuscular Disorders
262 citing publications
Latest tracked publication
3 September 2026
10 recent records available
Coverage & Indexing History
v9n1, Sept. 2007-
v9n1, Sept. 2007-
Research Focus & Classification
Indexed Subjects
Neuromuscular Disorders
Nervous System Disorders
Musculoskeletal Disorders
Neurodegenerative Disorders
Broad Categories
Neurology
Physiology
Neuromuscular Disorders
Musculoskeletal Disorders
Nervous System Disorders
MeSH Descriptors
Neuromuscular Diseases
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1097/cnd.0000000000000570
Open DOI
Chronic Inflammatory Demyelinating Polyneuropathy: Update on Diagnosis and Treatment
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired immune-mediated neuropathy characterized by progressive or relapsing weakness and sensory loss because of demyelination of peripheral nerves. CIDP has a higher preva...
02
DOI 10.1097/cnd.0000000000000568
Open DOI
Clinical Feature and Treatment Outcomes of Necrotizing Autoimmune Myopathy in a Referral Neurological Center in Thailand
Background: Necrotizing autoimmune myopathy (NAM) is classified into 3 subtypes according to antibodies. Data from Southeast Asian populations remain limited. Objective: To describe and compare clinical characteristics and treatment resp...
03
DOI 10.1097/cnd.0000000000000558
Open DOI
Acute Pharyngeal–Cervical–Brachial Weakness Associated With Urinary Retention and Anti-GD1a Antibodies: A Case Report
Was not provided for this article.
04
DOI 10.1097/cnd.0000000000000572
Open DOI
Ultrasound-Guided Perineural Corticosteroid Injection for Bell Palsy in a Patient Recovering From Diabetic Ketoacidosis: An Alternative When Systemic Corticosteroids Are Contraindicated
Was not provided for this article.
05
DOI 10.1097/cnd.0000000000000571
Open DOI
Fatal Myocarditis Relapse in a Patient with Myasthenia Gravis Treated with Efgartigimod Alfa: A Case Report
Myasthenia gravis (MG) is an autoimmune neuromuscular disorder primarily caused by autoantibodies against acetylcholine receptors (AChR), leading to muscle weakness. In 2021, efgartigimod was FDA-approved as the first neonatal Fc recepto...
06
DOI 10.1097/cnd.0000000000000567
Open DOI
Proteomic and Functional Signatures of Phenoconversion in Presymptomatic Amyotrophic Lateral Sclerosis
Background: Amyotrophic lateral sclerosis (ALS) likely has a prolonged presymptomatic phase. Identifying blood biomarkers that predict phenoconversion is critical for early intervention. Methods: We analyzed baseline serum proteomics in ...
07
DOI 10.1097/cnd.0000000000000555
Open DOI
Demyelination in Diabetic Distal Symmetric Polyneuropathy: A Retrospective Electrodiagnostic Study
Background: Features of acquired demyelination have been reported in diabetic distal symmetrical polyneuropathy (DDSP). Objectives: To characterize the natural history of demyelination in diabetic distal symmetric polyneuropathy (DDSP). ...
08
DOI 10.1097/cnd.0000000000000529
Open DOI
Diagnostic Tool Predicting Results of Electrodiagnostic Tests in Patients Presenting With Musculoskeletal Symptoms
Objectives: Patients presenting with musculoskeletal symptoms are fairly common in any neurologist practice, their presentation raises concern of underlying radiculopathy as a cause of their symptoms. The role of electrodiagnostic study ...
09
DOI 10.1097/cnd.0000000000000561
Open DOI
Letter to the Editor: Utility of Smartwatches in Neuromuscular Disease: Current Use and Barriers to Adoption
10
DOI 10.1097/cnd.0000000000000557
Open DOI
Acute Motor Axonal Neuropathy in Biotinidase Deficiency Complicated by Dietary Restriction
Bibliographical & Catalog Notes
Print issues ceased with 2024.
Also issued online.