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1)  Mitochondrial encephalomypathies/diagnosis
线粒体脑肌病/诊断
2)  Mitochondrial encephalomyopathies
线粒体脑肌病
1.
Mitochondrial encephalomyopathies are a group of multisystemic disorders that caused by Mitochondrial DNA or nuclear mutations to result in disturbance of mitochondrial Structures and function, which involve central nervous system and muscle mainly.
线粒体脑肌病是一组以mtDNA或核DNA(nDNA)突变导致线粒体结构和功能异常,以中枢神经系统和肌肉组织病变为主要表现的多系统疾病。
3)  mitochondrial encephalomyopathy
线粒体脑肌病
1.
Clinical,imaging and pathological features of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(report of 1 case)
线粒体脑肌病伴高乳酸血症和脑卒中样发作的临床、影像学及病理学特点(附1例报告)
2.
Analysis of two mitochondrial encephalomyopathy cases on clinical、image and pathology
线粒体脑肌病2例临床、影像及病理分析
4)  Mitochondrial myopathy and encephalomyopathy
线粒体肌病/脑肌病
5)  Mitochondrial myopathies
线粒体肌病
6)  mitochondrial myopathy
线粒体肌病
1.
Chronic progressive external ophthalmoplegia type of mitochondrial myopathy(report of 3 families);
慢性进行性眼外肌瘫痪型线粒体肌病(附3个家系报告)
2.
Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy;
线粒体肌病患者线粒体DNA的突变分析
3.
Mitochondrial myopathy and mitochondrial encephalomyopathy;
线粒体肌病和脑肌病临床及预后的研究
补充资料:脑病性精神病


脑病性精神病


  即"脑器质性精神障碍"。
  
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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