中国现代神经疾病杂志 ›› 2014, Vol. 14 ›› Issue (5): 382-385. doi: 10.3969/j.issn.1672-6731.2014.05.004

• 专题综述 • 上一篇    下一篇

2 神经肌肉病研究新亮点

张成   

  1. 510080 广州，中山大学附属第一医院神经科
  • 出版日期:2014-05-25 发布日期:2014-05-27
  • 通讯作者: 张成 (Email: zhangch6@mail.sysu.edu.cn)
  • 基金资助:

    国家自然科学基金-广东省联合基金重点资助项目（项目编号：U1032004）；国家自然科学基金资助项目（项目编号：30870851）；国家自然科学基金资助项目（项目编号：81271401）；国家科技支撑计划项目（项目编号：2012BAI09B04）；国家科技重大专项课题-重大新药创制（项目编号：2011ZX09307-001）；广东省科技计划项目（项目编号：2011A030400006）；广东省人口和计划生育委员会科技项目（项目编号：2009208）；广东省人口和计划生育委员会重点项目（项目编号：2010102）

Research highlights of partial neuromuscular disorders

ZHANG Cheng   

  1. Department of Neurology, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, Guangdong, China
  • Online:2014-05-25 Published:2014-05-27
  • Contact: ZHANG Cheng (Email: zhangch6@mail.sysu.edu.cn)
  • Supported by:

    This study was supported by Joint Fund of National Natural Science Foundation of China and Natural Science Foundation of Guangdong Province of China (No. U1032004), National Natural Science Foundation of China (No. 30870851, 81271401), Supporting Program for Science and Technology Research of China (No. 2012BAI09B04), Major New Drugs Innovation and Development of Important National Science & Technology Specific Projects (No. 2011ZX09307-001), Technology Plan Project of Guangdong Province (No. 2011A030400006), Science and Technology Project of Population and Family Planning Commission of Guangdong Province (No. 2009208), and Key Project of Population and Family Planning Commission of Guangdong Province (No. 2010102).

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摘要： 为方便临床医师了解神经肌肉病的最新进展，笔者对2013 年1 月-2014 年2 月美国国立医学图书馆（PubMed）收录的神经肌肉病相关文章进行筛选并整理，从临床诊断和治疗角度提纲挈领地介绍糖原贮积病Ⅱ型、Duchenne 型肌营养不良症、肌萎缩侧索硬化症和脊髓性肌萎缩症的研究背景和最新研究亮点，并附相应参考文献供读者参考。

关键词: 糖原贮积病Ⅱ型, 肌营养不良, 杜氏, 肌萎缩侧索硬化, 肌萎缩, 脊髓性, 综述

Abstract: In order to understand the latest progression on neuromuscular disorders for clinicians, this review screened and systemized the papers on neuromuscular disorders which were collected by PubMed from January 2013 to February 2014. This review also introduced the clinical diagnosis and treatment hightlights on glycogen storage disease type Ⅱ (GSD Ⅱ), Duchenne muscular dystrophy (DMD), amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). The important references will be useful for clinicians.

Key words: Glycogen storage disease type Ⅱ, Muscular dystrophy, Duchenne, Amyotrophic lateral sclerosis, Muscular atrophy, spinal, Review

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