The significance of autoantibodies against nodal and paranodal proteins in autoimmune nodopathies
Author:
Affiliation:
1. Department of Neurology, Kyushu University Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/63/11/63_cn-001878/_pdf
Reference52 articles.
1. 1) 「慢性炎症性脱髄性多発根ニューロパチー，多巣性運動ニューロパチー診療ガイドライン」作成委員会編．慢性炎症性脱髄性多発根ニューロパチー，多巣性運動ニューロパチー診療ガイドライン2013．東京：南江堂；2011.
2. 2) Latov N, Sherman WH, Nemni R, et al. Plasma-cell dyscrasia and peripheral neuropathy with a monoclonal antibody to peripheral-nerve myelin. N Engl J Med 1980;303:618-621.
3. 3) Joint Task Force of the EFNS and the PNS. European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of multifocal motor neuropathy. Report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society-first revision. J Peripher Nerv Syst 2010;15:295-301.
4. 4) Van den Bergh PYK, van Doorn PA, Hadden RDM, et al. 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. J Peripher Nerv Syst 2021;26:242-268.
5. 5) Bunschoten C, Jacobs BC, Van den Bergh PYK, et al. Progress in diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy. Lancet Neurol 2019;18:784-794.
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