期刊文献+

散发性包涵体肌炎研究进展 被引量:3

下载PDF
导出
摘要 最近的研究提示散发性包涵体肌炎的发病机制可能与免疫炎性反应、细胞变性、异常蛋白聚集、线粒体异常等有关,对于包涵体肌炎的诊断主要依赖病理诊断,免疫调节治疗可能有效。本文就包涵体肌炎发病机制的研究、临床表现及治疗等有关方面的最新进展进行了简要综述。
作者 李珂 蒲传强
出处 《国际神经病学神经外科学杂志》 2009年第6期514-518,共5页 Journal of International Neurology and Neurosurgery
  • 相关文献

参考文献29

  • 1Chou SM. Myxovirus-like structures in a case of human chronic polymyositis. Science, 1967, 158 ( 807 ) : 1453- 1455.
  • 2Yunis E J, Samaha FJ. Inclusion body myositis. Lab Invest, 1971, 25(3) : 240-248.
  • 3Carpenter S, Karpati G, HeIler I, et al. Inclusion body myosiris: a distinct variety of idiopathic inflammatory myopathy. Neurology, 1978, 28(1) : 8-17.
  • 4Shamim EA, Rider LG, Pandey JP, et al. Differences in idiopathic inflammatory myopathy phenotypes and genotypes between Mesoamerican Mestizos and North American caucasians: ethnogeographic infl uences in the genetics and clinical expression of myositis. Arthritis Rheum, 2002, 46 ( 7 ) : 1885- 1893.
  • 5Felice KJ, North WA. Inclusion body myositis in Connecticut: observations in 35 patients during an 8-year period. Medicine, 2001, 80(5): 320-327.
  • 6Dalakas MC. Inflammatory, immune, and viral aspects of inclusion-body myositis. Neurology, 2006, 66 (2 Suppl 1 ) : S33 -S38.
  • 7Askanas V, Engel WK. Inclusion-body myositis, a multifactorial muscle disease associated with aging: current concepts of pathogenesis. Curr Opin Rheumatol, 2007, 19 ( 6 ) : 550- 559.
  • 8Delaunay A, Bromberg KD, Hayashi Y, et al. The ER- bound RING finger protein 5 ( RNF5/RMA 1 ) causes degenerative myopathy in transgenic mice and is deregulated in in- clusion body myositis. PLoS ONE, 2008 , 3 (2) : e1609.
  • 9Fidzianska A, Rowinska- Marcinska K, Hausmanowa- Petrusewicz I. Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology. Acta Neuropathol, 2004, 107(3) : 197-203.
  • 10Chou SM. Myxovims-like structures and accompanying nuclear changes in chronic polymyositis. Arch Pathol, 1968, 86 (6) : 649-658.

二级参考文献13

共引文献12

同被引文献15

  • 1王敏,笪宇威,卢岩,徐敏,刘璐,贾建平.散发性包涵体肌炎临床病理分析[J].脑与神经疾病杂志,2011,19(5):389-392. 被引量:2
  • 2吕海东,张三军,李增富,秦东香,钱琪,韩凯,马晓丽,宋学云,杨斌.包涵体肌炎的临床与病理特点(附2例报告)[J].临床神经病学杂志,2007,20(3):188-190. 被引量:4
  • 3Nakanishi H, Koike H, Matsuo K, et al. Demographic lea tures of Japanese patients with sporadic inclusion body myosi tis: a single-center referral experienee[J]. Intern Med, 2013 52(3) :333-337.
  • 4Cortese A, Machado P, Morrow J, et al. Longitudinal obser- vational study of sporadic inclusion body myositis: implications for clinical trials[J]. Neuromuscul Disord, 2013, 23 (5) : 404- 412.
  • 5Clerici AM,Bono G,Delodovici ML,et al. A rare association of early-onset inclusion body myositis, rheumatoid arthritis and autoimmune thyroiditis: a case report and literature review [J]. Funct Neurol, 2013, 28(2) :127-132.
  • 6Lindberg C, Oldfors A, Hedstrom A. Inclusion body myositis: peripheral nerve involvement. Combined morphological and electrophysiological studies on peripheral nerves [J]. J Neurol Sci, 1990, 99(2/3): 327-338.
  • 7Allenbaeh Y, Benveniste O, Decostre V, et al. Quadriceps strength is a sensitive marker of disease progression in sporadic inclusion body myositis[J]. Neuromuscul Disord, 2012, 22 (11) :980-986.
  • 8Finsterer J, Stollberger C, Kovacs GG. Asymptomatic hyper creatine-kinase-emia as sole manifestation of inclusion body myositis[J]. NeuroI Int, 2013, 5(2): 34-36.
  • 9Greenberg SA, Pinkus JL, Amato AA. Nuclear membrane proteins are present with in rimmed vacuoles in inclusion body myositis[J]. Muscle Nerve, 2006, 34 (4): 406-416.
  • 10Breithaupt M, Schmidt J. Update on treatment of inclusion body myositis[J]. Curr RheumatolRep, 2013, 15(5) :329.

引证文献3

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