Research & Literature
Explore the leading researchers and institutions driving advances in this area, and dive into the full body of literature that informs this resource.
Top Authors
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Yale University
New Haven, United States
University College London
London, United Kingdom
Xenon Pharmaceuticals (Canada)
Burnaby, Canada
University of Oxford
Oxford, United Kingdom
Pfizer (United Kingdom)
Tadworth, United Kingdom
Maastricht University
Maastricht, The Netherlands
Maastricht University Medical Centre
Maastricht, The Netherlands
University of Edinburgh
Edinburgh, United Kingdom
University of Arizona
Tucson, United States
Mayo Clinic in Arizona
Scottsdale, United States
References
References (44)
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Annales de dermatologie et de venereologie 2015; (142(8-9)):513-8.
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Primary erythromelalgia: a review.
Tang Z, Chen Z, Tang B, Jiang H
Orphanet journal of rare diseases 2015; (10()):127 doi:10.1186/s13023-015-0347-1.
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Inherited erythromelalgia due to mutations in SCN9A: natural history, clinical phenotype and somatosensory profile.
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Brain : a journal of neurology 2016; (139(Pt 4)):1052-65 doi:10.1093/brain/aww007.
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Clinical features and management of erythromelalgia: long term follow-up of 46 cases.
Parker LK, Ponte C, Howell KJ, et al.
Clinical and experimental rheumatology 2017; (35(1)):80-84.
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Spinal Cord Stimulation for Treatment of Neuropathic Pain Associated With Erythromelalgia.
Matzke LL, Lamer TJ, Gazelka HM
Regional anesthesia and pain medicine 2016; (41(5)):619-20 doi:10.1097/AAP.0000000000000457.
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[Erythromelalgia: Diagnosis and therapeutic approach].
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Reverse pharmacogenomics: carbamazepine normalizes activation and attenuates thermal hyperexcitability of sensory neurons due to Nav 1.7 mutation I234T.
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British journal of pharmacology 2018; (175(12)):2261-2271 doi:10.1111/bph.13935.
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How a Simple Ankle Sprain Turned Into Neuropathic Pain: Complex Reflex Sympathetic Dystrophy Versus Erythromelalgia.
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Secondary erythromelalgia: a tryptophan dietary supplement-induced case associated with elevated 5-hydroxyindoleacetic acid (5HIAA) urinary levels.
Michelerio A, Derlino F, Brazzelli V, Vassallo C
International journal of dermatology 2018; (57(1)):83-85 doi:10.1111/ijd.13760.
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Reduction in pain following treatment with ranolazine in primary erythromelalgia: a case report.
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The British journal of dermatology 2018; (179(3)):783-784 doi:10.1111/bjd.16654.
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Erythromelalgia: a cutaneous manifestation of neuropathy?
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Chemical lumbar sympathectomy in the treatment of recalcitrant erythromelalgia.
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Journal of vascular surgery 2018; (68(6)):1897-1905 doi:10.1016/j.jvs.2018.05.226.
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Insensitivity to Pain upon Adult-Onset Deletion of Nav1.7 or Its Blockade with Selective Inhibitors.
Shields SD, Deng L, Reese RM, et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2018; (38(47)):10180-10201 doi:10.1523/JNEUROSCI.1049-18.2018.
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Pediatric Erythromelalgia and SCN9A Mutations: Systematic Review and Single-Center Case Series.
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The Journal of pediatrics 2019; (206()):217-224.e9 doi:10.1016/j.jpeds.2018.10.024.
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Review of primary and secondary erythromelalgia.
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Clinical and experimental dermatology 2019; (44(5)):477-482 doi:10.1111/ced.13891.
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Cureus 2018; (10(10)):e3506 doi:10.7759/cureus.3506.
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Pediatric erythromelalgia treated with epidural ropivacaine infusion.
Lee CE, Paulk K, Garvie K, et al.
JAAD case reports 2019; (5(4)):306-308 doi:10.1016/j.jdcr.2019.01.029.
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Sporadic Erythromelalgia Associated with a Homozygous Carrier of Common Missense Polymorphism in SCN9A Gene Coding for NaV1.7 Voltage-gated Sodium Channel.
Janicki PK, Ruiz-Velasco V, Adhikary S
Cureus 2019; (11(5)):e4587 doi:10.7759/cureus.4587.
PMID: 31309012 - 20
Erythromelalgia Caused by Polycythemia Vera Combined with Primary Aldosteronism.
Suzuki M, Watari T
European journal of case reports in internal medicine 2020; (7(11)):001852 doi:10.12890/2020_001852.
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Dorsal Root Ganglion Stimulation for Erythromelalgia Related Foot Pain: A Case Report and Review of the Literature.
Hagedorn JM, Canzanello N, Lamer TJ
Pain practice : the official journal of World Institute of Pain 2021; (21(6)):698-702 doi:10.1111/papr.12998.
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Painful, reappearing eruption in a medically complex 4-year-old.
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BMJ case reports 2021; (14(2)) doi:10.1136/bcr-2020-239310.
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Erythromelalgia: A Child With V400M Mutation in the SCN9A Gene.
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Neurology. Genetics 2021; (7(2)):e570 doi:10.1212/NXG.0000000000000570.
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Erythromelalgia: Pain and Redness of the Feet after Warm Water Exposure.
Fukui S, Tamaki H, Okada M
Internal medicine (Tokyo, Japan) 2022; (61(2)):279 doi:10.2169/internalmedicine.8038-21.
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High frequency dorsal column spinal cord stimulation for management of erythromelalgia.
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BMJ case reports 2021; (14(8)) doi:10.1136/bcr-2021-244758.
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KCNQ variants and pain modulation: a missense variant in Kv7.3 contributes to pain resilience.
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Eltrombopag-associated erythromelalgia in idiopathic thrombocytopenic purpura.
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The British journal of dermatology 2022; (186(3)):585-586 doi:10.1111/bjd.20829.
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Life-threatening hypothermia in a child with primary erythromelalgia.
Matarneh B, Witman P
Pediatric dermatology 2022; (39(1)):135-136 doi:10.1111/pde.14866.
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A Case of Pediatric Auricular Erythromelalgia.
Reese A, DiNardo L, Powers K, Carr MM
Cureus 2022; (14(1)):e21088 doi:10.7759/cureus.21088.
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Pain triangle phenomenon in possible association with SCN9A: A case report.
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Molecular genetics & genomic medicine 2022; (10(10)):e2026 doi:10.1002/mgg3.2026.
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Erythromelalgia in an Adolescent Female.
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Mediterranean journal of rheumatology 2022; (33(2)):256-258 doi:10.31138/mjr.33.2.256.
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Primary Erythromelalgia Treated With 10% Capsaicin Cream: A Case Report and a 10-Year Follow-Up.
Tolley JA, Walsh LE
Cureus 2022; (14(8)):e28342 doi:10.7759/cureus.28342.
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Erythromelalgia successfully treated with low-dose gabapentin in a pediatric patient.
Phong CH, Birmingham SW, Rojek NW
SAGE open medical case reports 2022; (10()):2050313X221136768 doi:10.1177/2050313X221136768.
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Erythromelalgia: A Review of Medical Management Options and Our Approach to Management.
Ma JE, Lee JUJ, Sartori-Valinotti JC, et al.
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A severe case of primary erythromelalgia presenting as small fiber neuropathy with a novel SCN9A mutation.
Watabe D, Tominaga M, Toyama S, et al.
The Journal of dermatology 2023; (50(7)):938-941 doi:10.1111/1346-8138.16754.
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Endoscopic lumbar sympathectomy as a treatment option for primary erythromelalgia - case report and review.
Loureiro MP, Novais PM, Paulin JAN, et al.
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Efficacy and safety of acupuncture therapy for neuropsychiatric symptoms among patients with Parkinson's disease: A systematic review and meta-analysis.
Tan W, Xie F, Zhou J, et al.
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Procedural interventions for erythromelalgia: A narrative review.
Lee JU, Ma JE, Sartori Valinotti JC, et al.
Vascular medicine (London, England) 2024; (29(6)):723-732 doi:10.1177/1358863X241279427.
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Severe Pediatric Erythromelalgia: A Case Report on Multimodal Pain Management and the Role of Regional Anesthesia.
Zyani A, El Moutawakil El Alami M, Alkouh R, et al.
Cureus 2024; (16(10)):e71351 doi:10.7759/cureus.71351.
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The Cutaneous Pathology of Erythromelalgia and Its Role in Establishing Critical Clues Regarding Pathogenesis.
Magro C, Kalomeris T, Guo L
The American Journal of dermatopathology 2025; (47(3)):184-190 doi:10.1097/DAD.0000000000002912.
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Genetic Variants in the SCN9A Gene are Detected in a Minority of Erythromelalgia Patients.
Skystad Kvernebo M, Grayson C, Stylianou IM, et al.
Acta dermato-venereologica 2025; (105()):adv42022 doi:10.2340/actadv.v105.42022.
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Severe Erythromelalgia Pain Attack in a Young Lebanese Woman Leading to Hospitalization: A Case Report and Literature Review.
Assaad W, El Tarras O, Al Osta S, Kallassy C
Cureus 2025; (17(9)):e91530 doi:10.7759/cureus.91530.
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Genetic and Clinical Insights into Inherited Erythromelalgia: A Comprehensive Review of Cases from China and Worldwide.
Li Y, He Z, Liu Y, et al.
The Journal of investigative dermatology 2025; doi:10.1016/j.jid.2025.07.034.
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[A clinical case of erythromelalgia in a patient comorbid with antiphospholipid syndrome].
Kudrjavtseva AA, Meladze AV, Trapeznikova ES, et al.
Terapevticheskii arkhiv 2026; (97(12)):1018-1022 doi:10.26442/00403660.2025.12.203468.
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