Journal of the Peripheral Nervous System

Papers
(The median citation count of Journal of the Peripheral Nervous System is 1. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
70
51
Abstracts38
28
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?”26
Safety and Cost Analysis of Immunoglobulin Cessation Trials in Chronic Inflammatory Demyelinating Polyradiculoneuropathy24
PNS Abstracts 202321
Identifying Predictors of Idiopathic Small‐Fiber Neuropathy in Adolescent Patients With Chronic Pain19
Prospective Evaluation of Machine‐Assisted Electrophysiologic and Online Clinical Diagnostic Support Tools in Chronic Inflammatory Demyelinating Polyradiculoneuropathy19
Toxic medications in Charcot–Marie–Tooth patients: A systematic review19
18
Abstracts of the 33rd annual meeting of the Japanese peripheral nerve society (JPNS)18
Loss of MEGF10 Decreases the Number of Perisynaptic Schwann Cells and Innervation of Neuromuscular Junctions in Aging Mice17
Incidence and risk factors for developing chemotherapy‐induced neuropathic pain in 500 cancer patients: A file‐based observational study17
Nerve ultrasound as a screening tool for inherited sensory neuronopathy16
Ofatumumab for treating autoimmune nodopathy16
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders16
Corneal confocal microscopy in small and mixed fiber neuropathy—Comparison with skin biopsy and cold detection in a large prospective cohort15
Variability in Conduction Block Definitions Affects the Sensitivity of Diagnostic Criteria for Multifocal Motor Neuropathy14
Abstracts of the 35th Annual Meeting of the Japanese Peripheral Nerve Society (JPNS)14
Issue Information14
Effectiveness of exercise therapy for individuals diagnosed with Charcot–Marie–Tooth disease: A systematic review of randomized clinical trials13
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy12
Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy12
Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology12
Feasibility, Validity, and Reliability of the Virtual CMT Infant Toddler Scale (vCMTInfS): A Remote Evaluation of Infants/Toddlers With CMT12
Parent‐proxy pediatric CMT quality of life outcome measure: Validation of the Italian version11
Issue Information11
Association of dynamic hepatic metabolism with clinical outcomes in patients with severe Guillain‐Barré syndrome: A prospective cohort study from multi‐centers in China11
Novel Dominant Splicing Variant in MPZ Associated With Unusual Charcot–Marie–Tooth Disease11
Pain hypersensitivity, sensorimotor impairment, and decreased muscle force in a novel rat model of radiation‐induced peripheral neuropathy11
Patient‐reported disease burden in the Accelerate Clinical Trials in Charcot–Marie–Tooth Disease Study10
Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A10
Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia10
Issue Information10
IgM anti‐MAG± peripheral neuropathy (IMAGiNe) study protocol: An international, observational, prospective registry of patients with IgM M‐protei10
Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis10
A Novel Case of Nerve Biopsy Proven Wild Type Transthyretin (TTR) Amyloidosis10
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy10
Rethinking Neuropathy in TTC19 Mutations: The Need for Broader Differential Diagnosis9
Peter James Dyck: In Memoriam9
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
Frequent De Novo Mutations in Korean Patients With Charcot–Marie–Tooth Disease9
8
Issue Information8
8
Benefit of high‐dose oral riboflavin therapy in riboflavin transporter deficiency8
Issue Information8
Intravenous Immunoglobulin Elevates Regulatory T Cells in Guillain‐Barré Syndrome: A Potential Biomarker of Therapeutic Response7
Glucose‐lowering medication associated with weight loss may limit the progression of diabetic neuropathy in type 2 diabetes7
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers7
Issue Information7
Dapagliflozin for Small Nerve Fibre Regeneration in Diabetic Peripheral Neuropathy: A Randomised Controlled Study (DINE)6
An innovative phase 2 proof‐of‐concept trial design to evaluate SAR445088, a monoclonal antibody targeting complement C1s in chronic inflammatory demyelinating polyneuropathy6
6
Issue Information6
ABSTRACT6
Reply to “Nerve ultrasound as a screening tool for inherited sensory neuronopathy”6
The autoimmune vulnerability of the node of Ranvier6
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies5
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
The small fiber neuropathy—symptom inventory questionnaire (SFN‐SIQ) does not discriminate between patients with or without small fiber neuropathy5
Impact of High‐Dose Tafamidis on Hereditary ATTR ( ATTRv ) Amyloidosis With Central Nervous System5
Molecular Characterization of Oxaliplatin‐Induced Peripheral Neurotoxicity: The Complex Spectrum of Painful Manifestations5
5
Digenesis in Charcot–Marie–Tooth Disease: Impact of Combined Mutations in the MFN2 and GDAP1 Genes5
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease5
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis5
5
Correction to “Polyneuropathy in Kidney Transplant Recipients: Accuracy of a New Clinical Diagnostic Scoring System”5
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
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
Predicting long‐term trends in inflammatory neuropathy outcome measures using latent class modelling4
Assessing deterioration using impairment and functional outcome measures in chronic inflammatory demyelinating polyneuropathy: A post‐hoc analysis of the immunoglobulin overtreatment in CIDP trial4
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
Anxiety and depression in small fiber neuropathy4
Do corticosteroids aggravate pure motor chronic inflammatory demyelinating polyneuropathy?4
GDAP1‐Related Charcot–Marie–Tooth Disease: Axonal or Demyelinating Subtype? Autosomal Recessive or Autosomal Dominant Inheritance?4
Nonsystemic Vasculitic Neuropathy—A Brazilian Case Series4
Issue Information4
Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies4
Issue Information4
Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study4
COVID‐19 and the peripheral nervous system. A 2‐year review from the pandemic to the vaccine era4
Macrophages influence Schwann cell myelin autophagy after nerve injury and in a model of Charcot‐Marie‐Tooth disease4
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
3
Recent advances in the treatment of Charcot‐Marie‐Tooth neuropathies3
Clinical, histologic, and immunologic signatures of Small Fiber Neuropathy in Systemic Lupus Erythematosus3
Issue Information3
Neurological Performance and Clinical Outcomes Related to Patients With Oropouche‐Associated Guillain–Barré Syndrome3
Etiologic Diagnosis of Neuropathies Based on First‐Line Screening of TTR Gene Mutations3
Validation of the parent‐proxy version of the pediatric Charcot‐Marie‐Tooth disease quality of life instrument for children aged 0–7 years3
Focal slowing of nerve conduction velocity in leprosy patients unveiled through multisegmented nerve analysis3
Earlier diagnosis of peripheral neuropathy in primary care: A call to action3
Rasch‐Built Overall Disability Scale for IgM‐Associated Polyneuropathy With and Without Anti‐MAG Antibodies: IgMRODS3
Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy3
Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian children3
Hyaluronidase‐facilitated subcutaneous immunoglobulin 10% as maintenance therapy for chronic inflammatory demyelinating polyradiculoneuropathy: The ADVANCE‐CIDP 1 randomized controlled tria3
Frequency dependent, reversible focused ultrasound suppression of evoked potentials in the reflex arc in an anesthetized animal3
The NCX1 calcium exchanger is implicated in delayed axotomy after peripheral nerve stretch injury3
Issue Information3
A Case of Retinopathy–Sensory Neuropathy Syndrome With a Novel Compound Heterozygous FLVCR1 Varian3
Genetic and clinical profile of 15 Chinese families with GDAP1‐related Charcot–Marie–Tooth disease and identification of H256R as a frequent mutation3
Cytokines and chemokines in patients with chronic inflammatory demyelinating polyradiculoneuropathy and multifocal motor neuropathy: A systematic review3
Ultrasound Shear Wave Velocity of Peripheral Nerves: A Possible Non‐Invasive Biomarker for Demyelinating Neuropathies3
Identical late motor responses in early Guillain‐Barré syndrome: A‐waves and repeater F‐waves3
Blood 1‐Deoxysphingolipid Levels Are Associated With Epidermal Denervation in Small Fiber Neuropathy3
Longitudinal Assessment of Quality of Life and Functionality by CAPPRI in Patients With Active 3
New Approaches Based on Serial‐Block Face Electron Microscopy to Investigate the Peripheral Nervous System2
Epidemiology, Presentation, Management and Outcomes in Chronic Inflammatory Demyelinating Polyneuropathy in Birmingham, UK : The Impact of Ethnicity2
Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review2
Plasma proteomic analysis on neuropathic pain in idiopathic peripheral neuropathy patients2
Initial findings using high‐resolution magnetic resonance imaging for visualisation of the sural nerve and surrounding anatomy in healthy volunteers at 7 Tesla2
CIDP Treatment Outcomes Correlation With First Nerve Conduction Changes: Ascertainment of Initial and Long‐Term Responders2
Leptospirosis‐induced acute acquired inflammatory neuropathy2
Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation2
Altered Cellular Pathways in the Blood of Patients With Guillain‐Barre Syndrome2
Issue Information2
Expanding the genetic and clinical spectrum of SORD‐related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement2
Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Macular Telangiectasia type 2 ‐ implications for retinal screening in HSN12
Advanced Hybrid Closed‐Loop Insulin Delivery Is Associated With Improved Glycemic Indicators and Normalization of Small Nerve Fibre Structure in Adults With Type 1 Diabetes2
Correction to “The Correlation Between Functional and Morphometric Small Fiber Assessment in Mixed Etiology Polyneuropathy”2
2
Abstract2
Identification of cellular and noncellular components of mature intact human peripheral nerve2
Differential Impact of Metabolic Factors and Comorbidities on Peripheral Neuropathy2
Issue Information2
Effect of age on metabolomic changes in a model of paclitaxel‐induced peripheral neurotoxicity2
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Targeting translation: A review of preclinical animal models in the development of treatments for chemotherapy‐induced peripheral neuropathy2
Adult‐onset Krabbe disease presenting as isolated sensorimotor demyelinating polyneuropathy: A case report2
Digital nerve reconstruction with a new composite silk fibroin nerve conduit2
A call to action for peripheral neuropathy research funding—Time to consolidate funding under one NIH initiative?2
Unusual upper limb features in SORD neuropathy2
Validation and Reliability of the Thai Pediatric Charcot–Marie–Tooth Quality of Life Outcome Measure2
Imbalance and lower limb tremor in chronic inflammatory demyelinating polyradiculoneuropathy: Reply to Letter to the Editor2
Axolemmal nanoruptures arising from paranodal membrane injury induce secondary axon degeneration in murine Guillain‐Barré syndrome2
Issue Information2
Designing and Implementing a Web‐Based Platform for Accurate and Reliable Clinical Outcome Measures and Global Certification for Evaluating Charcot–Marie–Tooth disease2
Pseudodominant Inheritance of Biallelic RFC1 Expansions—Revisiting the 3p22‐p24 2
Patient‐Reported Outcome Measures for Assessing Health‐Related Quality of Life in Patients With Polyneuropathies, Focusing on Guillain‐Barré Syndrome and Chronic Inflammatory Demyelinating Polyneuropa2
Real‐World Multinational Survey of Chronic Inflammatory Demyelinating Polyneuropathy: Disease Characteristics and Therapeutic Landscape1
Peripheral Neuropathy as an Early Marker in Newborn‐Screened Krabbe Disease: The Value of Pre‐Confirmatory Neurophysiological Testing1
Long‐Term Functional Outcomes in Immunoglobulin‐Treated Multifocal Motor Neuropathy Evaluated Through the MMN ‐Rasch‐Built Overall Disability Scale1
Plasma neurofilament light chain concentrations are elevated in youth‐onset type 2 diabetes and associated with neuropathy1
Changes in axonal and clinical function during intravenous and subcutaneous immunoglobulin therapy in chronic inflammatory demyelinating polyneuropathy1
Issue Information1
Correction to “Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study”1
Minimal invasive biopsies are highly sensitive for amyloid detection in hereditary transthyretin amyloidosis with polyneuropathy1
Abstract1
Vitamin D levels do not correlate with severity of idiopathic peripheral neuropathy1
Motor Neuropathy in a Patient With Mitochondrial Disease and a Novel TTC19 Variant: An Underrecognized Phenotypic Feature1
Genetic Deletion of Sarm1 in Mouse Models of Three Neurological Diseases1
1
Human Cytomegalovirus Associated Neuropathies: A Comprehensive Review From Pathophysiology to Clinical and Therapeutic Considerations1
Polyneuropathy in Kidney Transplant Recipients: Accuracy of a New Clinical Diagnostic Scoring System1
Laura Feltri: In memoriam1
Issue Information1
Spontaneous activity of specific C‐nociceptor subtypes from diabetic patients and mice: Involvement of reactive dicarbonyl compounds and (sensitized) transient receptor potential channel A11
1
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain–Barré syndrome1
Rasch‐built overall disability scale for POEMS syndrome (POEMS‐RODS)1
A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot–Marie–Tooth neuropathy 1A1
Intrathecal Antibody Synthesis in Autoimmune Nodopathy1
Hip Dysplasia in Charcot–Marie–Tooth Disease: Insights From a Large Cohort of Children and Adolescents1
Prognostic value of neurofilament light in blood in patients with polyneuropathy: A systematic review1
Somatosensory profiling of patients undergoing alcohol withdrawal: Do neuropathic pain and sensory loss represent a problem?1
Eculizumab as a Disease‐Modifying Therapy in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Case Report1
B‐cell and T‐cell receptor repertoire in chronic inflammatory demyelinating polyneuropathy, a prospective cohort study1
EGR2 gene‐linked hereditary neuropathies present with a bimodal age distribution at symptoms onset1
Serum neurofilament light chain measurements following nerve trauma1
Monoclonal gammopathy‐associated peripheral neuropathies: Uncovering pearls and challenges1
Caspr1 antibodies autoimmune paranodopathy with severe tetraparesis: Potential relevance of antibody titers in monitoring treatment response1
Sural nerve biopsy utility by masked assessment of individual histologic preparations1
Feasibility and Reliability of a Monitoring App for Chronic Inflammatory Neuropathies1
ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren Syndrome1
Results From a Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of ANX005, a C1q Inhibitor, in Patients With Guillain–Barré Syndrome1
A 21‐bp deletion in the complement regulator CD55 promotor region is associated with multifocal motor neuropathy and its disease course1
Issue Information1
The Easy Handgrip Test as a Tool for Assessing Motor Fatigability in Children With Charcot‐Marie‐Tooth Disease Type 1A1
Validation of the Korean version of inflammatory Rasch‐built Overall Disability Scale in patients with inflammatory neuropathy1
Variations within Toll‐like receptor (TLR) and TLR signaling pathway‐related genes and their synergistic effects on the risk of Guillain‐Barré syndrome1
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