Journal of the Peripheral Nervous System

Article	Citations
Abstracts	310
PNS Abstracts 2023	58
	49
	33
	31
Antecedent infections in Guillain‐Barré syndrome in endemic areas of arbovirus transmission: A multinational case‐control study	25
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?”	23
Toxic medications in Charcot–Marie–Tooth patients: A systematic review	19
Safety and Cost Analysis of Immunoglobulin Cessation Trials in Chronic Inflammatory Demyelinating Polyradiculoneuropathy	19
Nerve ultrasound as a screening tool for inherited sensory neuronopathy	18
Corneal confocal microscopy in small and mixed fiber neuropathy—Comparison with skin biopsy and cold detection in a large prospective cohort	16
Abstracts of the 33rd annual meeting of the Japanese peripheral nerve society (JPNS)	16
Genetic, electrophysiological, and pathological studies on patients with SCN9A‐related pain disorders	16
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Ofatumumab for treating autoimmune nodopathy	14
Loss of MEGF10 Decreases the Number of Perisynaptic Schwann Cells and Innervation of Neuromuscular Junctions in Aging Mice	14
Incidence and risk factors for developing chemotherapy‐induced neuropathic pain in 500 cancer patients: A file‐based observational study	14
Effectiveness of exercise therapy for individuals diagnosed with Charcot–Marie–Tooth disease: A systematic review of randomized clinical trials	13
Proximal weakness involvement in the first Italian case of Charcot‐Marie‐Tooth 2CC harboring a novel frameshift variant in NEFH	12
Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology	12
Assessing corneal dendritic cells in glucose dysregulation small‐fibre neuropathy	11
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Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy	10
Abstracts of the 35th Annual Meeting of the Japanese Peripheral Nerve Society (JPNS)	10

Parent‐proxy pediatric CMT quality of life outcome measure: Validation of the Italian version	9
Association of dynamic hepatic metabolism with clinical outcomes in patients with severe Guillain‐Barré syndrome: A prospective cohort study from multi‐centers in China	9
Sensory neuronopathies: A case series and literature review	9
A robust framework for characterising diffusion metrics of the median and ulnar nerves: Exploiting state‐of‐the‐art tracking methods	9
Pain hypersensitivity, sensorimotor impairment, and decreased muscle force in a novel rat model of radiation‐induced peripheral neuropathy	9
Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis	8
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision	8
Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A	8
Nerve biopsy in acquired neuropathies	8
Techniques for the standard histological and ultrastructural assessment of nerve biopsies	8
IgM anti‐MAG± peripheral neuropathy (IMAGiNe) study protocol: An international, observational, prospective registry of patients with IgM M‐protei	8
Patient‐reported disease burden in the Accelerate Clinical Trials in Charcot–Marie–Tooth Disease Study	8
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Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy	7
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Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia	7
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Benefit of high‐dose oral riboflavin therapy in riboflavin transporter deficiency	7
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers	6
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An innovative phase 2 proof‐of‐concept trial design to evaluate SAR445088, a monoclonal antibody targeting complement C1s in chronic inflammatory demyelinating polyneuropathy	6
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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 po	5
Retrospective analysis of response to rituximab in chronic inflammatory demyelinating polyneuropathy refractory to first‐line therapy	5
Reply to “Nerve ultrasound as a screening tool for inherited sensory neuronopathy”	5
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Dapagliflozin for Small Nerve Fibre Regeneration in Diabetic Peripheral Neuropathy: A Randomised Controlled Study (DINE)	5
VitaminB6levels do not correlate with severity of neuropathy in chronic idiopathic axonal polyneuropathy	5
Glucose‐lowering medication associated with weight loss may limit the progression of diabetic neuropathy in type 2 diabetes	5
ABSTRACT	5
The autoimmune vulnerability of the node of Ranvier	5
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Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin‐related amyloidosis—A Swiss reference center experience	4
The small fiber neuropathy—symptom inventory questionnaire (SFN‐SIQ) does not discriminate between patients with or without small fiber neuropathy	4
Predicting long‐term trends in inflammatory neuropathy outcome measures using latent class modelling	4
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Do corticosteroids aggravate pure motor chronic inflammatory demyelinating polyneuropathy?	4
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis	4
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies	4
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease	4
2021 Peripheral Nerve Society virtual event	4
Cytokines and chemokines in patients with chronic inflammatory demyelinating polyradiculoneuropathy and multifocal motor neuropathy: A systematic review	3
Assessing deterioration using impairment and functional outcome measures in chronic inflammatory demyelinating polyneuropathy: A post‐hoc analysis of the immunoglobulin overtreatment in CIDP trial	3
Anxiety and depression in small fiber neuropathy	3
Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study	3
Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy	3
Genetic and clinical profile of 15 Chinese families with GDAP1‐related Charcot–Marie–Tooth disease and identification of H256R as a frequent mutation	3
COVID‐19 and the peripheral nervous system. A 2‐year review from the pandemic to the vaccine era	3

The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ): Reply to letter to the Editor	3
Macrophages influence Schwann cell myelin autophagy after nerve injury and in a model of Charcot‐Marie‐Tooth disease	3
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Validation of the parent‐proxy version of the pediatric Charcot‐Marie‐Tooth disease quality of life instrument for children aged 0–7 years	2
Feasibility of assessing progression of transthyretin amyloid polyneuropathy using nerve conduction studies: Findings from the Transthyretin Amyloidosis Outcomes Survey (THAOS)	2
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Hyaluronidase‐facilitated subcutaneous immunoglobulin 10% as maintenance therapy for chronic inflammatory demyelinating polyradiculoneuropathy: The ADVANCE‐CIDP 1 randomized controlled tria	2
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Incidence of Guillain‐Barré syndrome in an Uruguayan population. A prospective cohort study	2
Clinical, histologic, and immunologic signatures of Small Fiber Neuropathy in Systemic Lupus Erythematosus	2
The epidemiology of Guillain‐Barré syndrome in Thailand over 13 years (2005‐2017): A nationwide population‐based retrospective cohort study	2
Focal slowing of nerve conduction velocity in leprosy patients unveiled through multisegmented nerve analysis	2
Neurological Performance and Clinical Outcomes Related to Patients With Oropouche‐Associated Guillain–Barré Syndrome	2
CIDP Treatment Outcomes Correlation With First Nerve Conduction Changes: Ascertainment of Initial and Long‐Term Responders	2
Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian children	2
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Ultrasound Shear Wave Velocity of Peripheral Nerves: A Possible Non‐Invasive Biomarker for Demyelinating Neuropathies	2
Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies	2
Earlier diagnosis of peripheral neuropathy in primary care: A call to action	2
Recent advances in the treatment of Charcot‐Marie‐Tooth neuropathies	2
Imbalance and lower limb tremor in chronic inflammatory demyelinating polyradiculoneuropathy: Reply to Letter to the Editor	2
Abstract	2
Frequency dependent, reversible focused ultrasound suppression of evoked potentials in the reflex arc in an anesthetized animal	2
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Identical late motor responses in early Guillain‐Barré syndrome: A‐waves and repeater F‐waves	2
Phase 2a randomized controlled study investigating the safety and efficacy of PDA‐002 in diabetic peripheral neuropathy	2
The NCX1 calcium exchanger is implicated in delayed axotomy after peripheral nerve stretch injury	2
Cutaneous biomarkers of therapeutic efficacy in early treatment of hereditary ATTR amyloid polyneuropathy with tafamidis	2
A longitudinal and cross‐sectional study of plasma neurofilament light chain concentration in Charcot‐Marie‐Tooth disease	1
A call to action for peripheral neuropathy research funding—Time to consolidate funding under one NIH initiative?	1
Results From a Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of ANX005, a C1q Inhibitor, in Patients With Guillain–Barré Syndrome	1
Correction to “Automated immunohistochemistry of intra‐epidermal nerve fibres in skin biopsies: A proof‐of‐concept study”	1
Serum neurofilament light chain measurements following nerve trauma	1
Laura Feltri: In memoriam	1
Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study	1
Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation	1
Monoclonal gammopathy‐associated peripheral neuropathies: Uncovering pearls and challenges	1
Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Macular Telangiectasia type 2 ‐ implications for retinal screening in HSN1	1
Expanding the genetic and clinical spectrum of SORD‐related peripheral neuropathy by reporting a novel variant c.210T>G and evidence of subclinical muscle involvement	1
Plasma proteomic analysis on neuropathic pain in idiopathic peripheral neuropathy patients	1
Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review	1
Leptospirosis‐induced acute acquired inflammatory neuropathy	1
Altered Cellular Pathways in the Blood of Patients With Guillain‐Barre Syndrome	1
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Caspr1 antibodies autoimmune paranodopathy with severe tetraparesis: Potential relevance of antibody titers in monitoring treatment response	1
Changes in axonal and clinical function during intravenous and subcutaneous immunoglobulin therapy in chronic inflammatory demyelinating polyneuropathy	1
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Charcot‐Marie‐Tooth disease: Genetic profile of patients from a large Brazilian neuromuscular reference center	1
Axolemmal nanoruptures arising from paranodal membrane injury induce secondary axon degeneration in murine Guillain‐Barré syndrome	1
Differential Impact of Metabolic Factors and Comorbidities on Peripheral Neuropathy	1
Digital nerve reconstruction with a new composite silk fibroin nerve conduit	1
Unusual upper limb features in SORD neuropathy	1
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Effect of age on metabolomic changes in a model of paclitaxel‐induced peripheral neurotoxicity	1
Rasch‐built overall disability scale for POEMS syndrome (POEMS‐RODS)	1
Plasma neurofilament light chain concentrations are elevated in youth‐onset type 2 diabetes and associated with neuropathy	1
Normal structure and pathological features in peripheral neuropathies	1
B‐cell and T‐cell receptor repertoire in chronic inflammatory demyelinating polyneuropathy, a prospective cohort study	1
Adult‐onset Krabbe disease presenting as isolated sensorimotor demyelinating polyneuropathy: A case report	1
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New Approaches Based on Serial‐Block Face Electron Microscopy to Investigate the Peripheral Nervous System	1
Targeting translation: A review of preclinical animal models in the development of treatments for chemotherapy‐induced peripheral neuropathy	1
Identification of cellular and noncellular components of mature intact human peripheral nerve	1
Initial findings using high‐resolution magnetic resonance imaging for visualisation of the sural nerve and surrounding anatomy in healthy volunteers at 7 Tesla	1
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Nodes of Ranvier in health and disease	0
Abstracts of the 32nd Annual Meeting of the Japanese Peripheral Nerve Society (JPNS)	0
DNMT1‐associated sensory neuropathy and cerebellar ataxia: A novel variant and review of genotype–phenotype correlation	0
Feasibility and Reliability of a Monitoring App for Chronic Inflammatory Neuropathies	0
Abstracts of the Eleventh Annual Meeting of the Associazione Italiana Sistema Nervoso Periferico (ASNP)	0
Wearables, sensors, and smart devices for the detection and monitoring of chemotherapy‐induced peripheral neurotoxicity: Systematic review and directions for future research	0
Unveiling the clinical and electrophysiological profile of CMTX6: Insights from two Brazilian families	0
Morphofunctional characterisation of axonal damage in different rat models of chemotherapy‐induced peripheral neurotoxicity: The role of nerve excitability testing	0
A 21‐bp deletion in the complement regulator CD55 promotor region is associated with multifocal motor neuropathy and its disease course	0
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Featured Cover	0
Correction to ‘Serum neurofilament light chain measurements following nerve trauma’	0

Correction to “Rasch‐built overall disability scale for POEMS syndrome (POEMS‐RODS)”	0
Hereditary neuropathies: A pathological perspective	0
A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing	0
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Report of a fulminant anti‐pan‐neurofascin‐associated neuropathy responsive to rituximab and bortezomib	0
Hip Dysplasia in Charcot–Marie–Tooth Disease: Insights From a Large Cohort of Children and Adolescents	0
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The density of hepatic autonomic innervation differs between compensatory and direct hyperplasia rat models	0
Correction to “Earlier diagnosis of peripheral neuropathy in primary care: A call to action”	0
Physical exercise halts further functional decline in an animal model for Charcot–Marie–Tooth disease 1X at an advanced disease stage	0
The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ) for identifying pure small fiber neuropathy	0
The neuropathy in hereditary transthyretin amyloidosis: A narrative review	0
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Sural nerve biopsy utility by masked assessment of individual histologic preparations	0
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Prediction of respiratory failure and prolonged mechanical ventilation in Guillain‐Barré syndrome: A prospective cohort study in Bangladesh	0
PNS 2022 Abstract Supplement	0
Eculizumab as a Disease‐Modifying Therapy in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Case Report	0
No evidence of improvement in neuropathy after renal transplantation in patients with end stage kidney disease	0
Paclitaxel alters the microvascular network in the central and peripheral nervous system of rats with chemotherapy‐induced painful peripheral neuropathy	0
Clinical and laboratory findings in scrub typhus associated Guillain‐Barré syndrome in South Korea	0
Somatosensory profiling of patients undergoing alcohol withdrawal: Do neuropathic pain and sensory loss represent a problem?	0
Development of a functional outcome measure for riboflavin transporter deficiency	0
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Two new mouse models of Gjb1‐associated Charcot–Marie–Tooth disease type 1X	0
Spontaneous activity of specific C‐nociceptor subtypes from diabetic patients and mice: Involvement of reactive dicarbonyl compounds and (sensitized) transient receptor potential channel A1	0
Differences in the ultrastructure of neurons in the spinal ganglion and dorsal rootlet between rats treated with cisplatin only versus co‐administration with a sphingosine 1‐phosphate receptor 2 agoni	0
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Mitofusin 1 overexpression rescues the abnormal mitochondrial dynamics caused by the Mitofusin 2 K357T mutation in vitro	0
Distinguishing Chronic Inflammatory Demyelinating Polyneuropathy From Mimic Disorders: The Role of Statistical Modeling	0
Variations within Toll‐like receptor (TLR) and TLR signaling pathway‐related genes and their synergistic effects on the risk of Guillain‐Barré syndrome	0
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Recruiting for an International Rare Disease Clinical Trial Readiness Study during the COVID‐19 pandemic: Challenges and solutions	0
Minimal invasive biopsies are highly sensitive for amyloid detection in hereditary transthyretin amyloidosis with polyneuropathy	0
Noncanonical splice‐site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies	0
Electrodiagnostic subtyping in Guillain‐Barré syndrome: Use of criteria in practice based on a survey study in IGOS	0
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Nodal–paranodal antibodies in HIV‐immune mediated radiculo‐neuropathies: Clinical phenotypes and relevance	0
Genotype–phenotype correlations of AR‐CMT2S in a cohort of axonal Charcot–Marie–Tooth patients from Central South China	0
Knowledge gaps in diagnosing chronic polyneuropathy: Review of national guidelines	0
Inter‐rater reliability of the Rasch‐modified medical research council scoring criteria for manual muscle testing in neuromuscular diseases	0
GJB1 variants in Charcot‐Marie‐Tooth disease X‐linked type 1 in Mali	0
Vestibular impairment in Guillain‐Barré syndrome	0
Prospectively assessing serum neurofilament light chain levels as a biomarker of paclitaxel‐induced peripheral neurotoxicity in breast cancer patients	0
A previously unreported NARS1 variant causes dominant distal hereditary motor neuropathy in a French family	0
Quantitative sensory testing and skin biopsy findings in late‐onset ATTRv presymptomatic carriers: Relationships with predicted time of disease onset (PADO)	0
Clinical scoring systems for the risk of cardiovascular autonomic neuropathy in type 1 and type 2 diabetes: A simple tool	0
Diagnosis and Management of Multifocal Motor Neuropathy in the United Kingdom: A Multicentre Survey	0
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain–Barré syndrome	0
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Identification of blood metabolic biomarkers associated with diabetic distal symmetric sensorimotor polyneuropathy in patients with type 2 diabetes mellitus	0
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HINT1‐related neuropathy in Greek patients with Charcot‐Marie‐Tooth disease	0
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Autoimmune nodo‐paranodopathies 10 years later: Clinical features, pathophysiology and treatment	0
PNS Abstracts 2024	0
The effect of tremor on disability assessment in chronic inflammatory demyelinating polyradiculoneuropathy	0
Loss of function MPZ mutation causes milder CMT1B neuropathy	0
Cardiovascular autonomic neuropathy in patients with type 2 diabetes with and without sensorimotor polyneuropathy	0
CYBA allelic variants are associated with severity and recovery in Guillain–Barré syndrome	0
Dorsal root ganglia CSF1+ neuronal subtypes have different impact on macrophages and microglia after spared nerve injury	0
EGR2 gene‐linked hereditary neuropathies present with a bimodal age distribution at symptoms onset	0
An approach to assessing immunoglobulin dependence in chronic inflammatory demyelinating inflammatory polyneuropathy	0
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Electrodiagnostic methods to verify Guillain‐Barré syndrome subtypes in Istanbul: A prospective multicenter study	0
Nerve pathology in animal models of neuropathies	0
Corneal confocal microscopy detects early nerve regeneration after pharmacological and surgical interventions: Systematic review and meta‐analysis	0
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Imbalance and lower limb tremor in chronic inflammatory demyelinating polyradiculoneuropathy	0
The endogenous calpain inhibitor calpastatin attenuates axon degeneration in murineGuillain‐Barrésyndrome	0
Evidence for spontaneous regulation of the humoral IgM anti‐GM1 autoimmune response by IgG antibodies in multifocal motor neuropathy patients	0
Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands	0
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Serum anti‐GM2 and anti‐GalNAc‐GD1a ganglioside IgG antibodies are biomarkers for immune‐mediated polyneuropathies in cats	0
The neurological core features of the infantile‐onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family	0
Clinical features of a family with late‐onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1	0
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Severe distinct dysautonomia in RFC1‐related disease associated with Parkinsonism	0
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision	0
Ophthalmological involvement in wild‐type transthyretin amyloidosis: A multimodal imaging study	0
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Successful autologous hematopoietic stem cell transplantation in a refractory anti‐Caspr1 antibody nodopathy	0
Conduction block and temporal dispersion in a SIGMAR1‐related neuropathy	0
Charcot‐Marie‐Tooth disease in Africa	0
Prognostic value of neurofilament light in blood in patients with polyneuropathy: A systematic review	0
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Validation of the Korean version of inflammatory Rasch‐built Overall Disability Scale in patients with inflammatory neuropathy	0
Associations of Guillain‐Barré syndrome with coronavirus disease 2019 vaccination: Disproportionality analysis using the World Health Organization pharmacovigilance database	0
Management of Guillain–Barré syndrome in Bangladesh: Clinical practice, limitations and recommendations for low‐ and middle‐income countries	0
Nerve ultrasound in CANVAS‐spectrum disease: Reduced nerve size distinguishes genetically confirmed CANVAS from other axonal polyneuropathies	0