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肌萎缩侧索硬化患者的呼吸功能评价进展 被引量：4

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摘要 肌萎缩侧索硬化（amyotrophic lateral sclerosis，ALS）是一种选择性侵犯脊髓前角细胞、脑干运动神经元、皮质锥体细胞及锥体束的神经系统变性病，最早由Charcot于1869年发现并报道，平均生存期仅3—5年，迄今尚无有效治愈方法，因此对呼吸困难、延髓性麻痹等并发症的治疗显得尤为重要。
作者 杜宝新 郑瑜 张成
机构地区 广州中医药大学第一临床医学院神经四科 中山大学附属第一医院神经内科
出处 《中华神经科杂志》 CAS CSCD 北大核心 2010年第6期447-449,共3页 Chinese Journal of Neurology
基金 广东省中医药局资助课题（2008325）
关键词 肌萎缩侧索硬化 呼吸功能 神经系统变性病 患者 脊髓前角细胞 运动神经元 平均生存期 延髓性麻痹
分类号 R744 [医药卫生—神经病学与精神病学]
  • 相关文献

参考文献30

  • 1Andersen PM,Borasio GD,Dengler R,et al.EFNS task force on management of amyotrophic lateral sclerosis:guidelines for diagnosing and clinical care of patients and relatives.Eur J Neurol,2005,12:921-938.
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  • 3Kurian KM,Forbes RB,Colville S,et al.Cause of death and clinical grading criteria in a cohort of aniyotrophic lateral sclerosis cases undergoing autopsy from the Scottish Motor Neurone Disease Register.J Neurol Neurosurg Psychiatry,2009,80:84-87.
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二级参考文献27

  • 1康德瑄,樊东升.胸锁乳突肌肌电图在鉴别肌萎缩侧索硬化与颈椎病性脊髓病的研究[J].中国神经精神疾病杂志,1994,20(1):5-7. 被引量：47
  • 2刘明生,崔丽英,汤晓芙,李本红,杜华.运动神经元病162例的节段性运动神经传导测定分析[J].中华神经科杂志,2005,38(11):694-696. 被引量：13
  • 3陈文族,赵振华,吴志英.家族性肌萎缩侧索硬化致病基因的研究进展[J].中华神经科杂志,2007,40(6):425-428. 被引量：5
  • 4Brooks BR, Miller RG, Swash M, et al. El Escorial revisited revised criteria for the diagnosis of amyotrophic lateral sclerosis Amyotroph Lateral Scler Other Motor Neuron Disord, 2000, 1:293-299.
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  • 10Zhang Y, Zhang H, Fu Y, et al. VEGF C2578A polymorphism does not contribute to amyotrophic lateral sclerosis susceptibility in sporadic Chinese patients. Amyotroph Lateral Scler, 2006, 7: 119-122.

共引文献13

同被引文献50

  • 1赵立军,李强.实用肺功能临床解读手册[M].上海:第二军医大学出版社,2010:13-20.
  • 2中华医学会神经病学分会肌电图与临床神经电生理学组,中华医学会神经病学分会神经肌肉病学组.中国肌萎缩侧索硬化诊断和治疗指南[J].中华神经科杂志,2012, 45:531-533.
  • 3Hardiman O,van den Berg LH,Kiernan MC.Clinical diagnosis and management of amyotrophic lateral sclerosis[J].Nat Rev Neuro1,2011,7(11):639-649.
  • 4Gautier G,Verschueren A,Monnier A,et a1.ALS with respiratory onset:clinical features and effects of non-invasive ventilation on the prognosis[J].Amyotroph Lateral Scler,2010,11(4):379-382.
  • 5Del Aguila MA,Longstreth WT,McGuire V,et a1.Prognosis in amyotrophic lateral sclerosis:apopulation-based study[J].Neurology,2003,60(5):813-819.
  • 6Magnus T,Beck M,Giess R,et a1.Disease progression in amyotrophic lateral sclerosis:predictors of survival[J].Muscle Nerve,2002,25(5):709-714.
  • 7Ferguson KA,Strong MJ,Ahmad D,et a1.Sleep disordered breathing in amyotrophic lateral sclerosis[J].Chest,1996,110(3):664-669.
  • 8Stewart H,Eisen A,Road J,et al.Electromyography of respiratory muscles in amyotrophic lateral sclerosis[J].J Neural Sci,200l,191(1-2):67-73.
  • 9Tsara V,Serasli E,Steiropoulos P,et a1.Respiratory function in amyotrophic lateral sclerosis patients.The role of sleep studies[J].Hippokratia,2010,14(1):33-36.
  • 10Schmidt EP,Drachman DB,Wiener CM,et a1.Pulmonary predictors of survival in amyotrophic lateral sclerosis:use in clinical trial design[J].Muscle Nerve,2006,33(1):127-132.

引证文献4

二级引证文献21

中华神经科杂志
2010年 第6期

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