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 2020-03-01 to 2024-03-01.)
ArticleCitations
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision168
Guillain‐Barré syndrome during SARS‐CoV‐2 pandemic: A case report and review of recent literature147
Guillain‐Barré syndrome associated with SARS‐CoV‐2 infection: A systematic review and individual participant data meta‐analysis44
COVID‐19 and the peripheral nervous system. A 2‐year review from the pandemic to the vaccine era44
KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement39
Evolving concepts on the role of dyslipidemia, bioenergetics, and inflammation in the pathogenesis and treatment of diabetic peripheral neuropathy37
Incidence and characteristics of neurotoxicity in immune checkpoint inhibitors with focus on neuromuscular events: Experience beyond the clinical trials31
The neuropathy in hereditary transthyretin amyloidosis: A narrative review29
Platinum accumulation in oxaliplatin‐induced peripheral neuropathy27
Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics26
Prospectively assessing serum neurofilament light chain levels as a biomarker of paclitaxel‐induced peripheral neurotoxicity in breast cancer patients21
Peripheral neuropathy symptoms in wild type transthyretin amyloidosis21
Perisynaptic Schwann cells phagocytose nerve terminal debris in a mouse model of Guillain‐Barré syndrome20
Small and large fiber sensory polyneuropathy in type 2 diabetes: Influence of diagnostic criteria on neuropathy subtypes19
Description of a large cohort of Caucasian patients with V122I ATTRv amyloidosis: Neurological and cardiological features18
Guillain‐Barré syndrome decreases in Singapore during the COVID‐19 pandemic17
Pathological, ultrasonographic, and electrophysiological characterization of clinically diagnosed cases of pure neuritic leprosy17
A longitudinal and cross‐sectional study of plasma neurofilament light chain concentration in Charcot‐Marie‐Tooth disease16
Loss of function MPZ mutation causes milder CMT1B neuropathy15
Acute and chronic inflammatory neuropathies and COVID‐19 vaccines: Practical recommendations from the task force of the Italian Peripheral Nervous System Association (ASNP)15
Relevance of diagnostic investigations in chronic inflammatory demyelinating poliradiculoneuropathy: Data from the Italian CIDP database15
Motor chronic inflammatory demyelinating polyneuropathy (CIDP) in 17 patients: Clinical characteristics, electrophysiological study, and response to treatment14
Placebo effect in chronic inflammatory demyelinating polyneuropathy: The PATH study and a systematic review14
Enhancing peripheral nerve regeneration with neurotrophic factors and bioengineered scaffolds: A basic science and clinical perspective14
Acquired and inherited amyloidosis: Knowledge driving patients' care12
Home monitoring of maintenance intravenous immunoglobulin therapy in patients with chronic inflammatory neuropathy12
Diabetic polyneuropathy: Bridging the translational gap12
An international multicenter efficacy and safety study of IqYmune in initial and maintenance treatment of patients with chronic inflammatory demyelinating polyradiculoneuropathy: PRISM12
Cold intolerance and neuropathic pain after peripheral nerve injury in upper extremity12
Report of a fulminant anti‐pan‐neurofascin‐associated neuropathy responsive to rituximab and bortezomib11
Cutaneous and muscular afferents from the foot and sensory fusion processing: Physiology and pathology in neuropathies11
Antecedent infections in Guillain‐Barré syndrome in endemic areas of arbovirus transmission: A multinational case‐control study11
Antecedent infections inGuillain‐Barrésyndrome patients from south India11
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: Suggestive features and diagnostic challenges10
Incidence and mortality rates of Guillain‐Barré syndrome in Serbia10
The Hippo pathway: Horizons for innovative treatments of peripheral nerve diseases10
Associations of Guillain‐Barré syndrome with coronavirus disease 2019 vaccination: Disproportionality analysis using the World Health Organization pharmacovigilance database9
The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ) for identifying pure small fiber neuropathy9
Acute small fiber neuropathy after Oxford‐AstraZeneca ChAdOx1‐S vaccination: A report of three cases and review of the literature9
Acute nitrous oxide‐induced neuropathy mimicking Guillain‐Barré syndrome9
Ataxia pancytopenia syndrome due to SAMD9L mutation presenting as demyelinating neuropathy9
Recent advances in the treatment of Charcot‐Marie‐Tooth neuropathies9
Real world, open label experience with lacosamide against acute painful oxaliplatin‐induced peripheral neurotoxicity8
Reliability of the Charcot‐Marie‐Tooth functional outcome measure8
Impact of drug formulations on kinetics and toxicity in a preclinical model of paclitaxel‐induced neuropathy8
Diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy in clinical practice: A survey among Dutch neurologists8
Sensory neuronopathies: A case series and literature review7
Charcot–Marie–Toothneuropathies: Current gene therapy advances and the route toward translation7
Charcot‐Marie‐Tooth disease: Genetic profile of patients from a large Brazilian neuromuscular reference center7
Clinical features of inherited neuropathy with BSCL2 mutations in Japan7
From pathogenesis to personalized treatments of neuropathies in hematological malignancies7
ABSTRACT7
The Brighton Collaboration case definition: Comparison in a retrospective and prospective cohort of children with Guillain‐Barré syndrome7
Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study7
Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot‐Marie‐Tooth disease7
Proximal weakness involvement in the first Italian case of Charcot‐Marie‐Tooth 2CC harboring a novel frameshift variant in NEFH6
Early onset demyelinating Charcot‐Marie‐Tooth disease caused by a novel in‐frame isoleucine deletion in peripheral myelin protein 26
Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin‐related amyloidosis—A Swiss reference center experience6
Feasibility of assessing progression of transthyretin amyloid polyneuropathy using nerve conduction studies: Findings from the Transthyretin Amyloidosis Outcomes Survey (THAOS)5
Diagnosis of Guillain‐Barré syndrome and validation of the Brighton criteria in Malaysia5
Focal chronic inflammatory demyelinating polyradiculoneuropathy: Onset, course, and distinct features5
Frequency dependent, reversible focused ultrasound suppression of evoked potentials in the reflex arc in an anesthetized animal5
A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?5
Oxaliplatin rechallenge in metastatic colorectal cancer patients with clinically significant oxaliplatin‐induced peripheral neurotoxicity5
Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands5
Validation of the Italian version of the Charcot‐Marie‐Tooth disease Pediatric Scale5
Variations within Toll‐like receptor (TLR) and TLR signaling pathway‐related genes and their synergistic effects on the risk of Guillain‐Barré syndrome5
Comorbidities, anthropometric, demographic, and lifestyle risk factors for ulnar neuropathy at the elbow: A case control study5
Comparing neuropathy in multiple myeloma and AL amyloidosis5
Riveting hammer vibration damages mechanosensory nerve endings5
Vitamin B6 levels do not correlate with severity of neuropathy in chronic idiopathic axonal polyneuropathy5
The epidemiology of Guillain‐Barré syndrome in Thailand over 13 years (2005‐2017): A nationwide population‐based retrospective cohort study4
Severe distinct dysautonomia in RFC1‐related disease associated with Parkinsonism4
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy4
A novel HSPB1 mutation associated with a late onset CMT2 phenotype: Case presentation and systematic review of the literature4
An innovative phase 2 proof‐of‐concept trial design to evaluate SAR445088, a monoclonal antibody targeting complement C1s in chronic inflammatory demyelinating polyneuropathy4
Vibratory testing with the 64 Hz Rydel‐Seiffer tuning fork and its relation to the sural nerve action potential4
2021 Peripheral Nerve Society virtual event4
Expanding the spectrum of SPTLC1‐related disorders beyond hereditary sensory and autonomic neuropathies: A novel case of the distinct “S331 syndrome”4
Expanding the phenotypic spectrum of TRIM2‐associated Charcot‐Marie‐Tooth disease4
Neutrophil‐lymphocyte ratio in Guillain‐Barré syndrome: A prognostic biomarker of severe disease and mechanical ventilation in Bangladesh4
SARM1 knockout does not rescue neuromuscular phenotypes in a Charcot‐Marie‐Tooth disease Type 1A mouse model4
Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Macular Telangiectasia type 2 ‐ implications for retinal screening in HSN14
Wearables, sensors, and smart devices for the detection and monitoring of chemotherapy‐induced peripheral neurotoxicity: Systematic review and directions for future research4
Hyaluronidase‐facilitated subcutaneous immunoglobulin 10% as maintenance therapy for chronic inflammatory demyelinating polyradiculoneuropathy: The ADVANCE‐CIDP 1 randomized controlled tria4
Clinical and serological prognostic factors in childhood Guillain‐Barré syndrome: A prospective cohort study in Bangladesh3
B‐cell and T‐cell receptor repertoire in chronic inflammatory demyelinating polyneuropathy, a prospective cohort study3
Utility of stimulus induced after discharges in the evaluation of peripheral nerve hyperexcitability: Old wine in a new bottle?3
Assessing deterioration using impairment and functional outcome measures in chronic inflammatory demyelinating polyneuropathy: A post‐hoc analysis of the immunoglobulin overtreatment in CIDP trial3
Long‐term walking ability and patient satisfaction after lower limb functional surgery in patients affected by Charcot‐Marie‐Tooth disease: A retrospective study3
Retrospective analysis of response to rituximab in chronic inflammatory demyelinating polyneuropathy refractory to first‐line therapy3
A recurrent MORC2 mutation causes Charcot‐Marie‐Tooth disease type 2Z3
Convergent pathological and ultrasound features in hereditary syndromic and non‐syndromic minifascicular neuropathy related to DHH3
Techniques for the standard histological and ultrastructural assessment of nerve biopsies3
Anxiety and depression in small fiber neuropathy3
Predicting long‐term trends in inflammatory neuropathy outcome measures using latent class modelling3
Identical late motor responses in early Guillain‐Barré syndrome: A‐waves and repeater F‐waves3
Relation of exercise and pain in patients with idiopathic distal axonal polyneuropathies3
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 po3
An approach to assessing immunoglobulin dependence in chronic inflammatory demyelinating inflammatory polyneuropathy3
Validation of the Italian version of the Charcot‐Marie‐Tooth Health Index3
Co‐expression gene modules involved in cisplatin‐induced peripheral neuropathy according to sensitivity, status, and severity3
Liver‐directed drugs for transthyretin‐mediated amyloidosis3
2020 Peripheral Nerve Society Virtual Event3
Validation of a new hand function outcome measure in individuals with Charcot‐Marie‐Tooth disease3
Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review3
Spontaneous activity of specific C‐nociceptor subtypes from diabetic patients and mice: Involvement of reactive dicarbonyl compounds and (sensitized) transient receptor potential channel A12
Clinical scoring systems for the risk of cardiovascular autonomic neuropathy in type 1 and type 2 diabetes: A simple tool2
Nerve biopsy in acquired neuropathies2
A robust framework for characterising diffusion metrics of the median and ulnar nerves: Exploiting state‐of‐the‐art tracking methods2
A prospective study on surgical management of foot deformities in Charcot Marie tooth disease2
Quantitative sensory testing and skin biopsy findings in late‐onset ATTRv presymptomatic carriers: Relationships with predicted time of disease onset (PADO)2
2
Autoimmune nodo‐paranodopathies 10 years later: Clinical features, pathophysiology and treatment2
Abstracts2
Validation of the Italian version of the pediatric CMT quality of life outcome measure2
HINT1‐related neuropathy in Greek patients with Charcot‐Marie‐Tooth disease2
Abstracts of the Eleventh Annual Meeting of the Associazione Italiana Sistema Nervoso Periferico (ASNP)2
Imbalance and lower limb tremor in chronic inflammatory demyelinating polyradiculoneuropathy2
Targeting translation: A review of preclinical animal models in the development of treatments for chemotherapy‐induced peripheral neuropathy2
Axolemmal nanoruptures arising from paranodal membrane injury induce secondary axon degeneration in murine Guillain‐Barré syndrome2
Unusual upper limb features in SORD neuropathy2
2
Incidence of Guillain‐Barré syndrome in an Uruguayan population. A prospective cohort study2
Translating diabetic peripheral neuropathy2
The endogenous calpain inhibitor calpastatin attenuates axon degeneration in murine Guillain‐Barré syndrome2
IgM anti‐MAG± peripheral neuropathy (IMAGiNe) study protocol: An international, observational, prospective registry of patients with IgM M‐protei2
GJB1 variants in Charcot‐Marie‐Tooth disease X‐linked type 1 in Mali2
INF2 mutations in patients with a broad phenotypic spectrum of Charcot‐Marie‐Tooth disease and focal segmental glomerulosclerosis2
No evidence of improvement in neuropathy after renal transplantation in patients with end stage kidney disease2
Electrodiagnostic subtyping in Guillain‐Barré syndrome: Use of criteria in practice based on a survey study in IGOS2
Analysis of relapse by inflammatory Rasch‐built overall disability scale status in the PATH study of subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy2
Chronic inflammatory demyelinating polyneuropathy with hypertrophic nerves1
A severe case of neuroleukemiosis caused by B cell chronic lymphocytic leukemia, presenting as mononeuritis multiplex1
Inter‐rater reliability of the Rasch‐modified medical research council scoring criteria for manual muscle testing in neuromuscular diseases1
Validation of the parent‐proxy version of the pediatric Charcot‐Marie‐Tooth disease quality of life instrument for children aged 0–7 years1
Normal structure and pathological features in peripheral neuropathies1
Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A1
Ophthalmological involvement in wild‐type transthyretin amyloidosis: A multimodal imaging study1
A novel homozygous variant extending the peripheral myelin protein 22 by 9 amino acids causes early‐onset Charcot‐Marie‐Tooth disease with predominant severe sensory ataxia1
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease1
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain–Barré syndrome1
Validation of the parent‐proxy pediatric Charcot‐Marie‐Tooth disease quality of life outcome measure1
The autoimmune vulnerability of the node of Ranvier1
Toxic medications in Charcot–Marie–Tooth patients: A systematic review1
Mitofusin 1 overexpression rescues the abnormal mitochondrial dynamics caused by the Mitofusin 2 K357T mutation in vitro1
Evidence for spontaneous regulation of the humoral IgM anti‐GM1 autoimmune response by IgG antibodies in multifocal motor neuropathy patients1
Assessing diabetic polyneuropathy in Spanish‐speaking patients: Translation and validation of the Toronto Clinical Neuropathy Score1
Two new mouse models of Gjb1‐associated Charcot–Marie–Tooth disease type 1X1
Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia1
1
The effect of tremor on disability assessment in chronic inflammatory demyelinating polyradiculoneuropathy1
Mutational screening of Greek patients with axonal Charcot‐Marie‐Tooth disease using targeted next‐generation sequencing: Clinical and molecular spectrum delineation1
Adult‐onset Krabbe disease presenting as isolated sensorimotor demyelinating polyneuropathy: A case report1
Imbalance and lower limb tremor in chronic inflammatory demyelinating polyradiculoneuropathy: Reply to Letter to the Editor1
Sural nerve biopsy utility by masked assessment of individual histologic preparations1
Lessons from late onset Charcot‐Marie‐Tooth disease1
Phase 2a randomized controlled study investigating the safety and efficacy of PDA‐002 in diabetic peripheral neuropathy1
Changes in axonal and clinical function during intravenous and subcutaneous immunoglobulin therapy in chronic inflammatory demyelinating polyneuropathy1
Rasch‐built overall disability scale for POEMS syndrome (POEMS‐RODS)1
Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis1
Plasma neurofilament light chain concentrations are elevated in youth‐onset type 2 diabetes and associated with neuropathy1
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision1
Hereditary neuropathies: A pathological perspective1
1
1
High glucose level as a modifier factor in CMT1A patients1
1
0.064283132553101