Journal of the Peripheral Nervous System

Papers
(The TQCC of Journal of the Peripheral Nervous System is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-12-01 to 2025-12-01.)
ArticleCitations
66
49
Abstracts38
31
Broadening Research Priorities in Peripheral Neuropathy: A Response to “A Call to Action for Peripheral Neuropathy Research Funding—Time to Consolidate Funding Under One NIH Initiative?”27
Safety and Cost Analysis of Immunoglobulin Cessation Trials in Chronic Inflammatory Demyelinating Polyradiculoneuropathy26
PNS Abstracts 202323
Toxic medications in Charcot–Marie–Tooth patients: A systematic review21
Identifying Predictors of Idiopathic Small‐Fiber Neuropathy in Adolescent Patients With Chronic Pain19
19
Abstracts of the 33rd annual meeting of the Japanese peripheral nerve society (JPNS)18
Nerve ultrasound as a screening tool for inherited sensory neuronopathy17
Corneal confocal microscopy in small and mixed fiber neuropathy—Comparison with skin biopsy and cold detection in a large prospective cohort17
Loss of MEGF10 Decreases the Number of Perisynaptic Schwann Cells and Innervation of Neuromuscular Junctions in Aging Mice16
Ofatumumab for treating autoimmune nodopathy16
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders16
Incidence and risk factors for developing chemotherapy‐induced neuropathic pain in 500 cancer patients: A file‐based observational study15
Feasibility, Validity, and Reliability of the Virtual CMT Infant Toddler Scale (vCMTInfS): A Remote Evaluation of Infants/Toddlers With CMT15
Variability in Conduction Block Definitions Affects the Sensitivity of Diagnostic Criteria for Multifocal Motor Neuropathy15
Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy14
Issue Information14
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy14
Abstracts of the 35th Annual Meeting of the Japanese Peripheral Nerve Society (JPNS)13
Issue Information12
Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology12
Effectiveness of exercise therapy for individuals diagnosed with Charcot–Marie–Tooth disease: A systematic review of randomized clinical trials12
Pain hypersensitivity, sensorimotor impairment, and decreased muscle force in a novel rat model of radiation‐induced peripheral neuropathy11
IgM anti‐MAG± peripheral neuropathy (IMAGiNe) study protocol: An international, observational, prospective registry of patients with IgM M‐protei11
A robust framework for characterising diffusion metrics of the median and ulnar nerves: Exploiting state‐of‐the‐art tracking methods11
Patient‐reported disease burden in the Accelerate Clinical Trials in Charcot–Marie–Tooth Disease Study11
Association of dynamic hepatic metabolism with clinical outcomes in patients with severe Guillain‐Barré syndrome: A prospective cohort study from multi‐centers in China11
Parent‐proxy pediatric CMT quality of life outcome measure: Validation of the Italian version11
Peter James Dyck: In Memoriam10
Benefit of high‐dose oral riboflavin therapy in riboflavin transporter deficiency10
A Novel Case of Nerve Biopsy Proven Wild Type Transthyretin (TTR) Amyloidosis10
Frequent De Novo Mutations in Korean Patients With Charcot–Marie–Tooth Disease10
Issue Information10
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy9
Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia9
Issue Information9
Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A9
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision9
Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis9
Rethinking Neuropathy in TTC19 Mutations: The Need for Broader Differential Diagnosis9
An innovative phase 2 proof‐of‐concept trial design to evaluate SAR445088, a monoclonal antibody targeting complement C1s in chronic inflammatory demyelinating polyneuropathy8
8
Glucose‐lowering medication associated with weight loss may limit the progression of diabetic neuropathy in type 2 diabetes8
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Issue Information8
Issue Information8
Reply to “Nerve ultrasound as a screening tool for inherited sensory neuronopathy”7
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers7
Issue Information7
Intravenous Immunoglobulin Elevates Regulatory T Cells in Guillain‐Barré Syndrome: A Potential Biomarker of Therapeutic Response7
Dapagliflozin for Small Nerve Fibre Regeneration in Diabetic Peripheral Neuropathy: A Randomised Controlled Study (DINE)7
ABSTRACT6
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6
Validation of an Artificial Intelligence driven framework to automatically detect red flag symptoms in screening for rare diseases in electronic health records: hereditary transthyretin amyloidosis po6
The autoimmune vulnerability of the node of Ranvier6
Molecular Characterization of Oxaliplatin‐Induced Peripheral Neurotoxicity: The Complex Spectrum of Painful Manifestations6
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies5
Correction to “Polyneuropathy in Kidney Transplant Recipients: Accuracy of a New Clinical Diagnostic Scoring System”5
The small fiber neuropathy—symptom inventory questionnaire (SFN‐SIQ) does not discriminate between patients with or without small fiber neuropathy5
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis5
VitaminB6levels do not correlate with severity of neuropathy in chronic idiopathic axonal polyneuropathy5
Influence of Genomic Ancestry and Other Traditional Risk Factors on the Prevalence of Diabetic Peripheral Neuropathy in Admixed Individuals With Type 1 Diabetes in Brazil: A Pioneer Multicenter Study5
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease5
Do corticosteroids aggravate pure motor chronic inflammatory demyelinating polyneuropathy?5
5
Digenesis in Charcot–Marie–Tooth Disease: Impact of Combined Mutations in the MFN2 and GDAP1 Genes5
Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin‐related amyloidosis—A Swiss reference center experience5
Acquired Transthyretin Amyloidosis in Domino Liver Transplantation Treated With Gene‐Silencers5
Genetic and clinical profile of 15 Chinese families with GDAP1‐related Charcot–Marie–Tooth disease and identification of H256R as a frequent mutation4
Cutaneous biomarkers of therapeutic efficacy in early treatment of hereditary ATTR amyloid polyneuropathy with tafamidis4
High‐Fat Diet Disrupt Nerve Function by Targeting Schwann Cells4
COVID‐19 and the peripheral nervous system. A 2‐year review from the pandemic to the vaccine era4
Issue Information4
Clinical and Electrophysiological Characterization of Diabetic Neuropathy in a Sub‐Saharan African Cohort4
The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ): Reply to letter to the Editor4
Assessing deterioration using impairment and functional outcome measures in chronic inflammatory demyelinating polyneuropathy: A post‐hoc analysis of the immunoglobulin overtreatment in CIDP trial4
GDAP1‐Related Charcot–Marie–Tooth Disease: Axonal or Demyelinating Subtype? Autosomal Recessive or Autosomal Dominant Inheritance?4
Predicting long‐term trends in inflammatory neuropathy outcome measures using latent class modelling4
Macrophages influence Schwann cell myelin autophagy after nerve injury and in a model of Charcot‐Marie‐Tooth disease4
Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies4
Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy4
Issue Information4
Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study4
Anxiety and depression in small fiber neuropathy4
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