Spectral-domain optical coherence tomography in mitochondrial encephalopathy, lactic acidosis, and strokelike episodes

Navajas Eduardo V.; Xu Kunyong

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Spectral-domain optical coherence tomography in mitochondrial encephalopathy, lactic acidosis, and strokelike episodes

机译：线粒体脑病，乳酸性酸中毒和中风样发作的光谱域光学相干断层扫描

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来源
《Canadian journal of ophthalmology》 |2015年第6期|共3页
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Navajas Eduardo V.; Xu Kunyong;
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中图分类眼科学;
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入库时间 2022-08-18 09:14:54

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专利

1. Spectral-domain optical coherence tomography in mitochondrial encephalopathy, lactic acidosis, and strokelike episodes [J] . Navajas Eduardo V., Xu Kunyong Canadian journal of ophthalmology . 2015,第6期

机译：线粒体脑病，乳酸性酸中毒和中风样发作的光谱域光学相干断层扫描
2. Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes) [J] . Annette Bakker, Cyrille Barthélémy, Paule Frachon, Pediatric Research . 2000,第2期

机译：携带与MELAS综合征相关的线粒体DNA突变的线粒体细胞中的功能性线粒体异质性（线粒体脑病，乳酸性酸中毒和中风样发作）
3. Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. [J] . Mita S, Tokunaga M, Kumamoto T, Muscle and Nerve . 1995,第Suppla期

机译：线粒体肌病，脑病，乳酸性酸中毒和中风样发作的线粒体DNA突变和肌肉病理。
4. Quantitative comparison of phase retardation measured, by polarization-sensitive spectral-domain optical, coherence tomography and scanning laser tomography [C] . Yamanari, M., Miura, Lasers and Electro-Optics, 2007 Pacific Rim Conference on . 2007

机译：偏振敏感光谱域光学，相干层析成像和扫描激光层析成像对相位延迟的定量比较
5. Estimation of papilledema severity using spectral-domain optical coherence tomography. [D] . Wang, Jui-Kai. 2016

机译：使用光谱域光学相干断层扫描估计乳头状浮肿的严重程度。
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. Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes) [O] . Annette Bakker, Cyrille Barthélémy, Paule Frachon, 2000

机译：携带与Melas综合征（线粒体脑病，乳酸中医和跨细胞剧集相关的线粒体DNA突变的外质细胞的功能性线粒体异质性

Spectral-domain optical coherence tomography in mitochondrial encephalopathy, lactic acidosis, and strokelike episodes

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