Journal of the Peripheral Nervous System

Papers
(The TQCC of Journal of the Peripheral Nervous System is 5. 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 2020-05-01 to 2024-05-01.)
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 revision187
Guillain‐Barré syndrome during SARS‐CoV‐2 pandemic: A case report and review of recent literature149
COVID‐19 and the peripheral nervous system. A 2‐year review from the pandemic to the vaccine era46
Guillain‐Barré syndrome associated with SARS‐CoV‐2 infection: A systematic review and individual participant data meta‐analysis44
Evolving concepts on the role of dyslipidemia, bioenergetics, and inflammation in the pathogenesis and treatment of diabetic peripheral neuropathy40
The neuropathy in hereditary transthyretin amyloidosis: A narrative review33
Platinum accumulation in oxaliplatin‐induced peripheral neuropathy28
Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics26
Peripheral neuropathy symptoms in wild type transthyretin amyloidosis22
Small and large fiber sensory polyneuropathy in type 2 diabetes: Influence of diagnostic criteria on neuropathy subtypes22
Prospectively assessing serum neurofilament light chain levels as a biomarker of paclitaxel‐induced peripheral neurotoxicity in breast cancer patients21
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 pandemic18
A longitudinal and cross‐sectional study of plasma neurofilament light chain concentration in Charcot‐Marie‐Tooth disease17
Relevance of diagnostic investigations in chronic inflammatory demyelinating poliradiculoneuropathy: Data from the Italian CIDP database15
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
Enhancing peripheral nerve regeneration with neurotrophic factors and bioengineered scaffolds: A basic science and clinical perspective14
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
Antecedent infections in Guillain‐Barré syndrome in endemic areas of arbovirus transmission: A multinational case‐control study13
Diabetic polyneuropathy: Bridging the translational gap13
An international multicenter efficacy and safety study of IqYmune in initial and maintenance treatment of patients with chronic inflammatory demyelinating polyradiculoneuropathy: PRISM12
Acquired and inherited amyloidosis: Knowledge driving patients' care12
Report of a fulminant anti‐pan‐neurofascin‐associated neuropathy responsive to rituximab and bortezomib12
Home monitoring of maintenance intravenous immunoglobulin therapy in patients with chronic inflammatory neuropathy12
The diagnostic accuracy of the small fiber neuropathy symptoms inventory questionnaire (SFN‐SIQ) for identifying pure small fiber neuropathy12
Antecedent infections inGuillain‐Barrésyndrome patients from south India12
Cutaneous and muscular afferents from the foot and sensory fusion processing: Physiology and pathology in neuropathies11
The Hippo pathway: Horizons for innovative treatments of peripheral nerve diseases11
Serum neurofilament light chain as a reliable biomarker of hereditary transthyretin‐related amyloidosis—A Swiss reference center experience10
Incidence and mortality rates of Guillain‐Barré syndrome in Serbia10
Recent advances in the treatment of Charcot‐Marie‐Tooth neuropathies10
Neurolymphomatosis, a rare manifestation of peripheral nerve involvement in lymphomas: Suggestive features and diagnostic challenges10
Acute nitrous oxide‐induced neuropathy mimicking Guillain‐Barré syndrome9
Associations of Guillain‐Barré syndrome with coronavirus disease 2019 vaccination: Disproportionality analysis using the World Health Organization pharmacovigilance database9
Acute small fiber neuropathy after Oxford‐AstraZeneca ChAdOx1‐S vaccination: A report of three cases and review of the literature9
Diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy in clinical practice: A survey among Dutch neurologists9
Ataxia pancytopenia syndrome due to SAMD9L mutation presenting as demyelinating neuropathy9
Sensory neuronopathies: A case series and literature review8
A prospective study on surgical management of foot deformities in Charcot Marie tooth disease8
Impact of drug formulations on kinetics and toxicity in a preclinical model of paclitaxel‐induced neuropathy8
Charcot–Marie–Toothneuropathies: Current gene therapy advances and the route toward translation8
The Brighton Collaboration case definition: Comparison in a retrospective and prospective cohort of children with Guillain‐Barré syndrome8
Reliability of the Charcot‐Marie‐Tooth functional outcome measure8
Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study7
From pathogenesis to personalized treatments of neuropathies in hematological malignancies7
Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands7
Charcot‐Marie‐Tooth disease: Genetic profile of patients from a large Brazilian neuromuscular reference center7
Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot‐Marie‐Tooth disease7
ABSTRACT7
Proximal weakness involvement in the first Italian case of Charcot‐Marie‐Tooth 2CC harboring a novel frameshift variant in NEFH6
Variations within Toll‐like receptor (TLR) and TLR signaling pathway‐related genes and their synergistic effects on the risk of Guillain‐Barré syndrome6
Focal chronic inflammatory demyelinating polyradiculoneuropathy: Onset, course, and distinct features6
Early onset demyelinating Charcot‐Marie‐Tooth disease caused by a novel in‐frame isoleucine deletion in peripheral myelin protein 26
Severe distinct dysautonomia in RFC1‐related disease associated with Parkinsonism6
Frequency dependent, reversible focused ultrasound suppression of evoked potentials in the reflex arc in an anesthetized animal6
Feasibility of assessing progression of transthyretin amyloid polyneuropathy using nerve conduction studies: Findings from the Transthyretin Amyloidosis Outcomes Survey (THAOS)5
The epidemiology of Guillain‐Barré syndrome in Thailand over 13 years (2005‐2017): A nationwide population‐based retrospective cohort study5
Diagnosis of Guillain‐Barré syndrome and validation of the Brighton criteria in Malaysia5
Description of a patient cohort with Hereditary Sensory Neuropathy type 1 without retinal disease Macular Telangiectasia type 2 ‐ implications for retinal screening in HSN15
Autoimmune nodo‐paranodopathies 10 years later: Clinical features, pathophysiology and treatment5
Validation of the Italian version of the Charcot‐Marie‐Tooth disease Pediatric Scale5
Comorbidities, anthropometric, demographic, and lifestyle risk factors for ulnar neuropathy at the elbow: A case control study5
Neutrophil‐lymphocyte ratio in Guillain‐Barré syndrome: A prognostic biomarker of severe disease and mechanical ventilation in Bangladesh5
Comparing neuropathy in multiple myeloma and AL amyloidosis5
Riveting hammer vibration damages mechanosensory nerve endings5
Wearables, sensors, and smart devices for the detection and monitoring of chemotherapy‐induced peripheral neurotoxicity: Systematic review and directions for future research5
Vitamin B6 levels do not correlate with severity of neuropathy in chronic idiopathic axonal polyneuropathy5
A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?5
Vibratory testing with the 64 Hz Rydel‐Seiffer tuning fork and its relation to the sural nerve action potential5
Oxaliplatin rechallenge in metastatic colorectal cancer patients with clinically significant oxaliplatin‐induced peripheral neurotoxicity5
Expanding the spectrum of SPTLC1‐related disorders beyond hereditary sensory and autonomic neuropathies: A novel case of the distinct “S331 syndrome”5
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy5
European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain–Barré syndrome5
0.021718978881836