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Mitochondrial cytopathy.

作者信息

Ito T, Hattori K, Tanaka M, Sugiyama S, Ozawa T

机构信息

Department of Internal Medicine, Faculty of Medicine, University of Nagoya, Japan.

出版信息

Jpn Circ J. 1990 Sep;54(9):1214-20. doi: 10.1253/jcj.54.1214.

DOI:10.1253/jcj.54.1214
PMID:2266580
Abstract
摘要

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Mitochondrial cytopathy.线粒体细胞病
Jpn Circ J. 1990 Sep;54(9):1214-20. doi: 10.1253/jcj.54.1214.
2
[Familial cases of mitochondrial cytopathy].
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Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.患有卡恩斯-塞尔综合征和线粒体脑肌病伴乳酸血症和卒中样发作综合征综合特征患者的线粒体DNA缺失
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Mitochondrial encephalomyopathies.
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[Mitochondrial encephalomyopathy].
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[Molecular biology of defects in the mitochondrial electron-transfer complexes].
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Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.
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Cardiovascular magnetic resonance imaging (CMR) reveals characteristic pattern of myocardial damage in patients with mitochondrial myopathy.心血管磁共振成像（CMR）显示线粒体肌病患者心肌损伤的特征模式。
Clin Res Cardiol. 2012 Apr;101(4):255-61. doi: 10.1007/s00392-011-0387-z. Epub 2011 Dec 6.
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A follow up study of myocardial involvement in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）患者心肌受累的随访研究。
Heart. 1998 Sep;80(3):292-5. doi: 10.1136/hrt.80.3.292.
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Mitochondrial DNA deletion in human myocardium.人类心肌中的线粒体DNA缺失
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