Myopathy with mitochondrial changes presenting as respiratory failure in two brothers.

Lemos AB; Mosquera J; Mate A; Sirvent J

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Myopathy with mitochondrial changes presenting as respiratory failure in two brothers.

机译：患有线粒体变化的肌病表现为两个兄弟的呼吸衰竭。

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来源
《Pediatric Pulmonology》 |1999年第3期|共5页
作者
Lemos AB; Mosquera J; Mate A; Sirvent J;
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正文语种 eng
中图分类儿科学;呼吸系及胸部疾病;
关键词
Lung Diseases; Interstitial; Mitochondrial Myopathies; Respiratory Insufficiency; 肺疾病; 间质性; 线粒体肌病; 呼吸功能不全;

机译：Lung Diseases;Interstitial;Mitochondrial Myopathies;Respiratory Insufficiency;肺疾病;间质性;线粒体肌病;呼吸功能不全;
入库时间 2022-08-18 15:42:27

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专利

1. Myopathy with mitochondrial changes presenting as respiratory failure in two brothers. [J] . Lemos AB, Mosquera J, Mate A, Pediatric Pulmonology . 1999,第3期

机译：患有线粒体变化的肌病表现为两个兄弟的呼吸衰竭。
2. Diagnostic value of the activity of mitochondrial respiratory chain complex for mitochondrial myopathies [J] . Lebrato-Hernandez L., Rivas-Infante E., Cortes-Rodriguez A., Neuromuscular disorders: NMD . 2016,第Suppla2期

机译：线粒体呼吸链复合物活性对线粒体肌病的诊断价值
3. The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment. [J] . Ronchi D, Virgilio R, Bordoni A, Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2010,第1a2期

机译：线粒体tRNA Leu（CUN）基因中的m.12316G> A突变与线粒体肌病和呼吸障碍有关。
4. NIR spectroscopic investigation of m. vastus lateralis in patients with mitochondrial myopathies as detected by respirometric investigation of mitochondrial function in skinned fibers [C] . Frank N. Gellerich, Martin-Luther-Univ. Halle-Wittenberg, Halle, Conference on photon propagation in tissues . 1998

机译：近红外光谱研究通过呼吸法研究皮肤纤维线粒体功能检测线粒体肌病患者的股外侧肌
5. Exercise training as therapy for mitochondrial myopathies: Physiological, biochemical and genetic effects [D] . Taivassalo, Tanja. 2001

机译：运动训练作为线粒体肌病的疗法：生理，生化和遗传作用
6. Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy encephalopathy lactic acidosis and strokelike episodes. [O] . M P King, Y Koga, M Davidson, 1992

机译：线粒体蛋白合成和呼吸链活性的缺陷与与线粒体肌病脑病乳酸性酸中毒和中风样发作相关的tRNA（Leu（UUR））突变分离。
7. Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies [O] . Bentlage H.A.C.M., Janssen A.J.M., Chomyn A., 1995

机译：肽和亚基特异性抗体在线粒体肌病中检测到呼吸NADH脱氢酶的线粒体DNA和核编码亚基的多个缺陷

Myopathy with mitochondrial changes presenting as respiratory failure in two brothers.

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