Journal of the Peripheral Nervous System

Papers
(The TQCC of Journal of the Peripheral Nervous System is 3. 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 2021-06-01 to 2025-06-01.)
ArticleCitations
Abstracts323
60
33
33
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 Polyradiculoneuropathy24
PNS Abstracts 202319
Antecedent infections in Guillain‐Barré syndrome in endemic areas of arbovirus transmission: A multinational case‐control study19
Toxic medications in Charcot–Marie–Tooth patients: A systematic review18
Nerve ultrasound as a screening tool for inherited sensory neuronopathy17
Loss of MEGF10 Decreases the Number of Perisynaptic Schwann Cells and Innervation of Neuromuscular Junctions in Aging Mice16
Ofatumumab for treating autoimmune nodopathy16
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Corneal confocal microscopy in small and mixed fiber neuropathy—Comparison with skin biopsy and cold detection in a large prospective cohort15
Abstracts of the 33rd annual meeting of the Japanese peripheral nerve society (JPNS)14
Incidence and risk factors for developing chemotherapy‐induced neuropathic pain in 500 cancer patients: A file‐based observational study13
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders13
Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy12
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy12
Issue Information12
Abstracts of the 35th Annual Meeting of the Japanese Peripheral Nerve Society (JPNS)12
Issue Information11
Effectiveness of exercise therapy for individuals diagnosed with Charcot–Marie–Tooth disease: A systematic review of randomized clinical trials11
Feasibility, Validity, and Reliability of the Virtual CMT Infant Toddler Scale (vCMTInfS): A Remote Evaluation of Infants/Toddlers With CMT11
Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology11
Pain hypersensitivity, sensorimotor impairment, and decreased muscle force in a novel rat model of radiation‐induced peripheral neuropathy10
Association of dynamic hepatic metabolism with clinical outcomes in patients with severe Guillain‐Barré syndrome: A prospective cohort study from multi‐centers in China10
A robust framework for characterising diffusion metrics of the median and ulnar nerves: Exploiting state‐of‐the‐art tracking methods9
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
Sensory neuronopathies: A case series and literature review9
Patient‐reported disease burden in the Accelerate Clinical Trials in Charcot–Marie–Tooth Disease Study9
Parent‐proxy pediatric CMT quality of life outcome measure: Validation of the Italian version9
IgM anti‐MAG± peripheral neuropathy (IMAGiNe) study protocol: An international, observational, prospective registry of patients with IgM M‐protei9
Nerve biopsy in acquired neuropathies8
Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia8
Techniques for the standard histological and ultrastructural assessment of nerve biopsies8
Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis8
Issue Information8
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Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A7
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Benefit of high‐dose oral riboflavin therapy in riboflavin transporter deficiency7
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy7
Dapagliflozin for Small Nerve Fibre Regeneration in Diabetic Peripheral Neuropathy: A Randomised Controlled Study (DINE)7
Issue Information6
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A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers6
Glucose‐lowering medication associated with weight loss may limit the progression of diabetic neuropathy in type 2 diabetes6
An innovative phase 2 proof‐of‐concept trial design to evaluate SAR445088, a monoclonal antibody targeting complement C1s in chronic inflammatory demyelinating polyneuropathy6
ABSTRACT6
The autoimmune vulnerability of the node of Ranvier5
Reply to “Nerve ultrasound as a screening tool for inherited sensory neuronopathy”5
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies5
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 po5
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Retrospective analysis of response to rituximab in chronic inflammatory demyelinating polyneuropathy refractory to first‐line therapy5
Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin‐related amyloidosis—A Swiss reference center experience4
4
Issue Information4
COVID‐19 and the peripheral nervous system. A 2‐year review from the pandemic to the vaccine era4
VitaminB6levels do not correlate with severity of neuropathy in chronic idiopathic axonal polyneuropathy4
Acquired Transthyretin Amyloidosis in Domino Liver Transplantation Treated With Gene‐Silencers4
Do corticosteroids aggravate pure motor chronic inflammatory demyelinating polyneuropathy?4
Anxiety and depression in small fiber neuropathy4
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease4
The small fiber neuropathy—symptom inventory questionnaire (SFN‐SIQ) does not discriminate between patients with or without small fiber neuropathy4
2021 Peripheral Nerve Society virtual event4
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis4
Assessing deterioration using impairment and functional outcome measures in chronic inflammatory demyelinating polyneuropathy: A post‐hoc analysis of the immunoglobulin overtreatment in CIDP trial3
Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies3
Macrophages influence Schwann cell myelin autophagy after nerve injury and in a model of Charcot‐Marie‐Tooth disease3
Cutaneous biomarkers of therapeutic efficacy in early treatment of hereditary ATTR amyloid polyneuropathy with tafamidis3
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Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy3
Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study3
Clinical and Electrophysiological Characterization of Diabetic Neuropathy in a Sub‐Saharan African Cohort3
Genetic and clinical profile of 15 Chinese families with GDAP1‐related Charcot–Marie–Tooth disease and identification of H256R as a frequent mutation3
Recent advances in the treatment of Charcot‐Marie‐Tooth neuropathies3
Issue Information3
Predicting long‐term trends in inflammatory neuropathy outcome measures using latent class modelling3
Issue Information3
The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ): Reply to letter to the Editor3
Cytokines and chemokines in patients with chronic inflammatory demyelinating polyradiculoneuropathy and multifocal motor neuropathy: A systematic review3
The NCX1 calcium exchanger is implicated in delayed axotomy after peripheral nerve stretch injury3
Earlier diagnosis of peripheral neuropathy in primary care: A call to action3
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