Reply to: Myopathy in Myasthenia Positive for Antibodies Against MuSK, Lrp4, and Titin.
作者信息
Yamashita Rika, Okuno Tatsusada, Mochizuki Hideki
机构信息
Department of Neurology, Osaka University Hospital, Japan.
出版信息
Intern Med. 2021 May 1;60(9):1487. doi: 10.2169/internalmedicine.6377-20. Epub 2020 Dec 7.
Abstract
摘要
相似文献
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Reply to: Myopathy in Myasthenia Positive for Antibodies Against MuSK, Lrp4, and Titin.回复：抗MuSK、Lrp4和肌联蛋白抗体阳性的重症肌无力患者中的肌病
Intern Med. 2021 May 1;60(9):1487. doi: 10.2169/internalmedicine.6377-20. Epub 2020 Dec 7.
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Myopathy or Myasthenia Positive for Antibodies Against MuSK, Lrp4, and Titin.抗肌肉特异性激酶（MuSK）、低密度脂蛋白受体相关蛋白4（Lrp4）和肌联蛋白抗体阳性的肌病或重症肌无力
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Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis.筛查脂蛋白受体相关蛋白4、聚集蛋白和肌联蛋白抗体并探索重症肌无力的自身免疫谱。
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Anti-AChR, MuSK, and LRP4 antibodies coexistence: A rare and distinct subtype of myasthenia gravis from Indian subcontinent.乙酰胆碱受体抗体、肌肉特异性酪氨酸激酶抗体和低密度脂蛋白受体相关蛋白 4 抗体共存：来自印度次大陆的一种罕见且独特的重症肌无力亚型。
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Multiple antibody detection in 'seronegative' myasthenia gravis patients.“血清反应阴性”重症肌无力患者的多种抗体检测
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A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis.抗 LRP4 抗体在重症肌无力中的流行病学和临床特征的综合分析。
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Electrophysiological findings in patients with low density lipoprotein receptor related protein 4 positive myasthenia gravis.载脂蛋白脂蛋白受体 4 阳性重症肌无力患者的电生理发现。
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MuSK myasthenia gravis IgG4 disrupts the interaction of LRP4 with MuSK but both IgG4 and IgG1-3 can disperse preformed agrin-independent AChR clusters.肌肉特异性激酶（MuSK）型重症肌无力免疫球蛋白G4（IgG4）会破坏低密度脂蛋白受体相关蛋白4（LRP4）与MuSK之间的相互作用，但IgG4和IgG1 - 3均可使预先形成的不依赖聚集蛋白的乙酰胆碱受体（AChR）簇分散。
PLoS One. 2013 Nov 7;8(11):e80695. doi: 10.1371/journal.pone.0080695. eCollection 2013.
本文引用的文献
1
Anti-MuSK Positive Myasthenia Gravis with Anti-Lrp4 and Anti-titin Antibodies.抗 MuSK 阳性重症肌无力伴抗 Lrp4 和抗titin 抗体。
Intern Med. 2021 Jan 1;60(1):137-140. doi: 10.2169/internalmedicine.4957-20. Epub 2020 Aug 22.
2
Repetitive Nerve Stimulation in MuSK-Antibody-Positive Myasthenia Gravis.肌肉特异性激酶抗体阳性重症肌无力的重复神经刺激
J Clin Neurol. 2017 Jul;13(3):287-292. doi: 10.3988/jcn.2017.13.3.287. Epub 2017 May 15.
3
Myopathic changes detected by quantitative electromyography in patients with MuSK and AChR positive myasthenia gravis.通过定量肌电图在MuSK和乙酰胆碱受体阳性重症肌无力患者中检测到的肌病性改变。
J Clin Neurosci. 2016 May;27:126-9. doi: 10.1016/j.jocn.2015.08.041. Epub 2016 Jan 5.
4
Quantitative EMG of facial muscles in myasthenia patients with MuSK antibodies.抗肌肉特异性激酶（MuSK）抗体的重症肌无力患者面部肌肉的定量肌电图
Clin Neurophysiol. 2007 Feb;118(2):269-77. doi: 10.1016/j.clinph.2006.10.004. Epub 2006 Dec 8.
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