期刊文献+

水通道蛋白4与视神经脊髓炎的发病机制 被引量:2

原文传递
导出
摘要 视神经脊髓炎(neuromyelitisoptica,NMO)是视神经和脊髓主要受累的中枢神经系统脱髓鞘疾病。特异性NMO—IgG抗体[也称抗水通道蛋白4(AQP4)抗体]的发现支持NMO是一独立疾病,而非多发性硬化(multiple sclerosis,MS)的亚型,开辟了NMO研究的新领域。NMO—IgG诊断NMO的敏感度为50%-91%,特异度85%~99%,2006年已被纳入NMO修订的诊断标准。
出处 《中华神经科杂志》 CAS CSCD 北大核心 2010年第4期296-298,共3页 Chinese Journal of Neurology
  • 相关文献

参考文献1

共引文献19

同被引文献49

  • 1刘红,张本恕,张天林.视神经脊髓炎一家系二例[J].中华神经科杂志,2006,39(8):535-535. 被引量:3
  • 2Lennon VA, Wingerchuk DM, Kryzer TJ, et al. A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet, 2004, 364: 2106-2112.
  • 3Lennon VA, Kryzer TJ, Pittock SJ, et al. IgG marker of opticspinal multiple sclerosis binds to the aquaporin-4 water channel. J Exp Med, 2005, 202: 473-477..
  • 4Fujihara K. Neuromyelitis optica and astrocytic damage in its pathogenesis. J Neurol Sci, 2011, 306: 183-187.
  • 5Mata S, Lolli F. Neuromyelitis optica: an update. J Neurol Sci, 2011, 303: 13-21.
  • 6Misu T, Takahashi T, Nishiyama S, et al. New insights into thepathogenesis of neuromyelitis optica. Brain Nerve, 2010, 62: 921-931.
  • 7Kira J. Neuromyelitis optica and opticospinal multiple sclerosis: Mechanisms and pathogenesis. Pathophysiology, 2011, 18: 69- 79.
  • 8Lim BC, Hwang H, Kim KJ, et al. Relapsing demyelinating CNS disease in a Korean pediatric population: multiple sclerosis versus neuromyelitis optica. Muh Scler, 2011, 17: 67-73.
  • 9Jarius S, Paul F, Franciotta D, et al. Cerebrospinal fluid findings in aquaporin-4 antibody positive neuromyelitis optica : Results from 211 lumbar punctures. J Neurol Sci, 2011,306: 82-90.
  • 10Matsushita T, Isobe N, Piao H, et al. Reappraisal of brain MRI features in patients with multiple sclerosis and neuromyelitis optica according to anti-aquaporin-4 antibody status. J Neurol Sci, 2010, 291 : 37-43.

引证文献2

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部