线粒体病

  • 网络mitochondrial disease;Mitochondrial disorders;mitochondrial genetic disorders;mitochondriopathy
线粒体病线粒体病
  1. 成人线粒体病:一种监测进展与治疗的量表

    Mitochondrial disease in adults : A scale to monitor progression and treatment

  2. 目的探讨神经肌肉系统线粒体病的发病机制、临床与病理特征及诊断。

    Objective To investigate the pathogenesis , diagnosis , clinical and pathological features of the mitochondrial disease of neuromuscular system .

  3. 对表现为多系统受累的患者,如果同时合并高乳酸血症,就应考虑线粒体病的可能,应进行线粒体DNA突变的检查以明确诊断。

    Mitochondrial diseases should be considered in patients with multiple organ involvement and elevated serum lactic acid mtDNA mutation examination is necessary for the diagnosis of mitochondrial diseases .

  4. 结论成人型Leigh综合征属于线粒体病,是由于线粒体基因缺陷所致的致死性遗传性神经病。

    Conclusion Adult Leigh syndrome is a fatal inherited neuropathy which is caused by the defect of mitochondria gene .

  5. 中国味道的国际大家庭线粒体病的母系遗传

    The international family in Chinses style Maternal inheritance of mitochondrial diseases

  6. 线粒体病和其他肌病患者短期非缺血性前臂训练后的乳酸生成

    Lactate production upon short-term non-ischemic forearm exercise in mitochondrial disorders and other myopathies

  7. 本文综述了线粒体病的特点,并对线粒体病的母系遗传方式进行了分析。

    This review summarized some characteristics of mitochondrial diseases , and analysed the pattern of maternal inheritance about mitochondrial diseases .

  8. 遗传病是影响人口素质的重要因素,也是出生缺陷的主要原因。遗传病包括染色体病、单基因病、多基因病和线粒体病。

    The genetic disease is an important factor affecting the quality of the population and the main cause of birth defects , including chromosomal diseases , single gene disorders , polygenic disease , and mitochondrial disease .

  9. 介绍了如何用FLASHMX制作线粒体遗传病的网络课件,以及其中制作的技巧。

    This paper discusses how to make Web-based courseware of Mitochondrial Inherited Disease with Flash MX and how to use the technique .

  10. 由营养缺乏或环境损伤等因素引起的氧化损伤所导致的线粒体衰退是帕金森病的早期事件。

    Mitochondrial decay due to oxidative damage by environmental insults or nutrient deficient is a key contributor to Parkinson 's disease ( PD ) .

  11. 有关线粒体DNA(mtDNA)的突变与人类疾病和衰老乃至肿瘤的关系日益受到人们的关注,研究表明,mtDNA突变的积累与氧化损伤是人类线粒体遗传病与各种退行性疾病的分子基础。

    Studies show that the accumulation of mutation and oxidative damage of mitochondrial DNA ( mtDNA ) are the molecular mechanism of mitochondrial heredopathia and degenerative diseases .