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 2022-05-01 to 2026-05-01.)
ArticleCitations
69
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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?”30
Safety and Cost Analysis of Immunoglobulin Cessation Trials in Chronic Inflammatory Demyelinating Polyradiculoneuropathy29
PNS Abstracts 202324
Identifying Predictors of Idiopathic Small‐Fiber Neuropathy in Adolescent Patients With Chronic Pain21
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Toxic medications in Charcot–Marie–Tooth patients: A systematic review21
Prospective Evaluation of Machine‐Assisted Electrophysiologic and Online Clinical Diagnostic Support Tools in Chronic Inflammatory Demyelinating Polyradiculoneuropathy21
Abstracts21
Incidence and risk factors for developing chemotherapy‐induced neuropathic pain in 500 cancer patients: A file‐based observational study20
Abstracts of the 33rd annual meeting of the Japanese peripheral nerve society (JPNS)20
Nerve ultrasound as a screening tool for inherited sensory neuronopathy18
Issue Information18
Loss of MEGF10 Decreases the Number of Perisynaptic Schwann Cells and Innervation of Neuromuscular Junctions in Aging Mice16
Ofatumumab for treating autoimmune nodopathy15
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders15
Variability in Conduction Block Definitions Affects the Sensitivity of Diagnostic Criteria for Multifocal Motor Neuropathy14
Broadening the Clinical Spectrum of Axonal Hereditary Neuropathies: A Comparative Case Study on DNAJB2‐ and HINT1‐ 14
Corneal confocal microscopy in small and mixed fiber neuropathy—Comparison with skin biopsy and cold detection in a large prospective cohort14
Abstracts of the 35th Annual Meeting of the Japanese Peripheral Nerve Society (JPNS)13
Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy13
Effectiveness of exercise therapy for individuals diagnosed with Charcot–Marie–Tooth disease: A systematic review of randomized clinical trials13
Feasibility, Validity, and Reliability of the Virtual CMT Infant Toddler Scale (vCMTInfS): A Remote Evaluation of Infants/Toddlers With CMT13
Issue Information13
Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology13
Behavioral Thermoceptive Responses and Morphologic Correlates in Mouse Models of CMT1A , HNPP , an12
Association of dynamic hepatic metabolism with clinical outcomes in patients with severe Guillain‐Barré syndrome: A prospective cohort study from multi‐centers in China12
Issue Information12
Issue Information11
Parent‐proxy pediatric CMT quality of life outcome measure: Validation of the Italian version11
A Novel Case of Nerve Biopsy Proven Wild Type Transthyretin (TTR) Amyloidosis11
IgM anti‐MAG± peripheral neuropathy (IMAGiNe) study protocol: An international, observational, prospective registry of patients with IgM M‐protei11
Pain hypersensitivity, sensorimotor impairment, and decreased muscle force in a novel rat model of radiation‐induced peripheral neuropathy11
Cranial Nerve Involvement With Diplopia as Presenting Feature of CMT1H Caused by Recurring FBLN5 Varia11
Novel Dominant Splicing Variant in MPZ Associated With Unusual Charcot–Marie–Tooth Disease11
Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia11
Rethinking Neuropathy in TTC19 Mutations: The Need for Broader Differential Diagnosis10
Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A10
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy10
Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis9
Patient‐reported disease burden in the Accelerate Clinical Trials in Charcot–Marie–Tooth Disease Study9
Benefit of high‐dose oral riboflavin therapy in riboflavin transporter deficiency9
Frequent De Novo Mutations in Korean Patients With Charcot–Marie–Tooth Disease9
Unveiling a Regional Variant of Demyelinating Guillain–Barré Syndrome: Nerve Conduction Study Evidence in Bifacial Weakness With Paresthesias9
Peter James Dyck: In Memoriam9
Issue Information8
Issue Information8
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Glucose‐lowering medication associated with weight loss may limit the progression of diabetic neuropathy in type 2 diabetes7
Intravenous Immunoglobulin Elevates Regulatory T Cells in Guillain‐Barré Syndrome: A Potential Biomarker of Therapeutic Response7
Issue Information7
Dapagliflozin for Small Nerve Fibre Regeneration in Diabetic Peripheral Neuropathy: A Randomised Controlled Study (DINE)7
Molecular Characterization of Oxaliplatin‐Induced Peripheral Neurotoxicity: The Complex Spectrum of Painful Manifestations6
Correction to “Polyneuropathy in Kidney Transplant Recipients: Accuracy of a New Clinical Diagnostic Scoring System”6
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A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers6
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 neuropathies6
Measurement of Red Blood Cell Sorbitol Dehydrogenase Activity for Fast Screening of SORD ‐Related Neuropathies6
An innovative phase 2 proof‐of‐concept trial design to evaluate SAR445088, a monoclonal antibody targeting complement C1s in chronic inflammatory demyelinating polyneuropathy6
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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
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Overall Diagnostic Performance of Multiple Versus Single Physical Examination Tests for the Prediction of Future Diabetic Neuropathy Risk6
Issue Information6
ABSTRACT6
Acquired Transthyretin Amyloidosis in Domino Liver Transplantation Treated With Gene‐Silencers5
Impact of High‐Dose Tafamidis on Hereditary ATTR ( ATTRv ) Amyloidosis With Central Nervous System5
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease5
High‐Fat Diet Disrupt Nerve Function by Targeting Schwann Cells5
Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study5
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis5
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
GDAP1‐Related Charcot–Marie–Tooth Disease: Axonal or Demyelinating Subtype? Autosomal Recessive or Autosomal Dominant Inheritance?5
Nonsystemic Vasculitic Neuropathy—A Brazilian Case Series5
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
Issue Information5
Assessing deterioration using impairment and functional outcome measures in chronic inflammatory demyelinating polyneuropathy: A post‐hoc analysis of the immunoglobulin overtreatment in CIDP trial5
Do corticosteroids aggravate pure motor chronic inflammatory demyelinating polyneuropathy?5
SOX5 Overexpression in Schwann Cell Combined With Chitosan‐Based Conduit Promotes Peripheral Nerve Regeneration4
Clinical and Electrophysiological Characterization of Diabetic Neuropathy in a Sub‐Saharan African Cohort4
Rasch‐Built Overall Disability Scale for IgM‐Associated Polyneuropathy With and Without Anti‐MAG Antibodies: IgMRODS4
Cytokines and chemokines in patients with chronic inflammatory demyelinating polyradiculoneuropathy and multifocal motor neuropathy: A systematic review4
A Case of Retinopathy–Sensory Neuropathy Syndrome With a Novel Compound Heterozygous FLVCR1 Varian4
A New Simple SCreening Tool for Painful Diabetic Neuropathy ( ACT ) in Ecuador4
Earlier diagnosis of peripheral neuropathy in primary care: A call to action4
Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies4
Recent advances in the treatment of Charcot‐Marie‐Tooth neuropathies4
Anxiety and depression in small fiber neuropathy4
Macrophages influence Schwann cell myelin autophagy after nerve injury and in a model of Charcot‐Marie‐Tooth disease4
Pathological Features of Vasculitic Neuropathy and the Role of Nerve Biopsy4
Genetic and clinical profile of 15 Chinese families with GDAP1‐related Charcot–Marie–Tooth disease and identification of H256R as a frequent mutation4
Issue Information4
Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy4
Cutaneous biomarkers of therapeutic efficacy in early treatment of hereditary ATTR amyloid polyneuropathy with tafamidis4
The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ): Reply to letter to the Editor4
Elucidating Causal Associations Between Immune Cells, Circulating Inflammatory Proteins, and Chronic Inflammatory Demyelinating Polyneuropathy: A Two‐Sample Two‐Step Mendelian Randomization Study4
Focal slowing of nerve conduction velocity in leprosy patients unveiled through multisegmented nerve analysis3
The NCX1 calcium exchanger is implicated in delayed axotomy after peripheral nerve stretch injury3
Longitudinal Assessment of Quality of Life and Functionality by CAPPRI in Patients With Active 3
Frequency dependent, reversible focused ultrasound suppression of evoked potentials in the reflex arc in an anesthetized animal3
Clinical, histologic, and immunologic signatures of Small Fiber Neuropathy in Systemic Lupus Erythematosus3
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Neurological Performance and Clinical Outcomes Related to Patients With Oropouche‐Associated Guillain–Barré Syndrome3
Validation of the parent‐proxy version of the pediatric Charcot‐Marie‐Tooth disease quality of life instrument for children aged 0–7 years3
Blood 1‐Deoxysphingolipid Levels Are Associated With Epidermal Denervation in Small Fiber Neuropathy3
Etiologic Diagnosis of Neuropathies Based on First‐Line Screening of TTR Gene Mutations3
Issue Information3
Issue Information3
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
Validation and Reliability of the Thai Pediatric Charcot–Marie–Tooth Quality of Life Outcome Measure3
Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian children3
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
Digital nerve reconstruction with a new composite silk fibroin nerve conduit2
CIDP Treatment Outcomes Correlation With First Nerve Conduction Changes: Ascertainment of Initial and Long‐Term Responders2
Hyaluronidase‐facilitated subcutaneous immunoglobulin 10% as maintenance therapy for chronic inflammatory demyelinating polyradiculoneuropathy: The ADVANCE‐CIDP 1 randomized controlled tria2
Differential Impact of Metabolic Factors and Comorbidities on Peripheral Neuropathy2
Cytokine Dynamics in Bortezomib‐Induced Peripheral Neuropathy: Challenges in Translating Preclinical Findings to Humans2
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
Targeting translation: A review of preclinical animal models in the development of treatments for chemotherapy‐induced peripheral neuropathy2
Leptospirosis‐induced acute acquired inflammatory neuropathy2
Imbalance and lower limb tremor in chronic inflammatory demyelinating polyradiculoneuropathy: Reply to Letter to the Editor2
A call to action for peripheral neuropathy research funding—Time to consolidate funding under one NIH initiative?2
Abstract2
Correction to “The Correlation Between Functional and Morphometric Small Fiber Assessment in Mixed Etiology Polyneuropathy”2
A Next‐Generation ELISA for the Detection of Anti‐(Para)Nodal Antibodies in Autoimmune Nodopathy and COVID 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
Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Macular Telangiectasia type 2 ‐ implications for retinal screening in HSN12
Axolemmal nanoruptures arising from paranodal membrane injury induce secondary axon degeneration in murine Guillain‐Barré syndrome2
Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation2
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
Evaluation of Nicotinamide Riboside in Prevention of Small Nerve Fiber Axon Degeneration and Promotion of Nerve Regeneration2
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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
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Adult‐onset Krabbe disease presenting as isolated sensorimotor demyelinating polyneuropathy: A case report2
Somatosensory profiling of patients undergoing alcohol withdrawal: Do neuropathic pain and sensory loss represent a problem?1
Effect of age on metabolomic changes in a model of paclitaxel‐induced peripheral neurotoxicity1
Serum neurofilament light chain measurements following nerve trauma1
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
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Long‐Term Functional Outcomes in Immunoglobulin‐Treated Multifocal Motor Neuropathy Evaluated Through the MMN ‐Rasch‐Built Overall Disability Scale1
Rasch‐built overall disability scale for POEMS syndrome (POEMS‐RODS)1
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Plasma neurofilament light chain concentrations are elevated in youth‐onset type 2 diabetes and associated with neuropathy1
Minimal invasive biopsies are highly sensitive for amyloid detection in hereditary transthyretin amyloidosis with polyneuropathy1
Laura Feltri: In memoriam1
Intrathecal Antibody Synthesis in Autoimmune Nodopathy1
CIDP With and Without Monoclonal Gammopathy of Undetermined Significance ( MGUS ): Comparison of Clinical Phenotype, D1
Issue Information1
Altered Cellular Pathways in the Blood of Patients With Guillain‐Barre Syndrome1
Motor Neuropathy in a Patient With Mitochondrial Disease and a Novel TTC19 Variant: An Underrecognized Phenotypic Feature1
Spontaneous activity of specific C‐nociceptor subtypes from diabetic patients and mice: Involvement of reactive dicarbonyl compounds and (sensitized) transient receptor potential channel A11
Sural nerve biopsy utility by masked assessment of individual histologic preparations1
Eculizumab as a Disease‐Modifying Therapy in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Case Report1
Polyneuropathy in Kidney Transplant Recipients: Accuracy of a New Clinical Diagnostic Scoring System1
Issue Information1
Peripheral Neuropathy as an Early Marker in Newborn‐Screened Krabbe Disease: The Value of Pre‐Confirmatory Neurophysiological Testing1
Real‐World Multinational Survey of Chronic Inflammatory Demyelinating Polyneuropathy: Disease Characteristics and Therapeutic Landscape1
Changes in axonal and clinical function during intravenous and subcutaneous immunoglobulin therapy in chronic inflammatory demyelinating polyneuropathy1
Issue Information1
Monoclonal gammopathy‐associated peripheral neuropathies: Uncovering pearls and challenges1
Vitamin D levels do not correlate with severity of idiopathic peripheral neuropathy1
Motor Neuronopathy With Widespread Fasciculations in MCM3AP ‐Related Disorder: Clinical and Muscle MRI 1
Hip Dysplasia in Charcot–Marie–Tooth Disease: Insights From a Large Cohort of Children and Adolescents1
Issue Information1
A 21‐bp deletion in the complement regulator CD55 promotor region is associated with multifocal motor neuropathy and its disease course1
Serum Neurofilament Light Chain and Glial Fibrillary Acidic Protein as Biomarkers in Hereditary Transthyretin Amyloidosis Polyneuropathy1
Prognostic value of neurofilament light in blood in patients with polyneuropathy: A systematic review1
The Easy Handgrip Test as a Tool for Assessing Motor Fatigability in Children With Charcot‐Marie‐Tooth Disease Type 1A1
Issue Information1
Genetic Deletion of Sarm1 in Mouse Models of Three Neurological Diseases1
Validation of the Korean version of inflammatory Rasch‐built Overall Disability Scale in patients with inflammatory neuropathy1
Human Cytomegalovirus Associated Neuropathies: A Comprehensive Review From Pathophysiology to Clinical and Therapeutic Considerations1
Identification of cellular and noncellular components of mature intact human peripheral nerve1
Caspr1 antibodies autoimmune paranodopathy with severe tetraparesis: Potential relevance of antibody titers in monitoring treatment response1
B‐cell and T‐cell receptor repertoire in chronic inflammatory demyelinating polyneuropathy, a prospective cohort study1
Feasibility and Reliability of a Monitoring App for Chronic Inflammatory Neuropathies1
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Correction to “Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study”1
A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot–Marie–Tooth neuropathy 1A1
Pseudodominant Inheritance of Biallelic RFC1 Expansions—Revisiting the 3p22‐p24 1
ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren Syndrome1
Issue Information1
Abstract1
Designing and Implementing a Web‐Based Platform for Accurate and Reliable Clinical Outcome Measures and Global Certification for Evaluating Charcot–Marie–Tooth disease1
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain–Barré syndrome1
EGR2 gene‐linked hereditary neuropathies present with a bimodal age distribution at symptoms onset1
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