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Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.

作者信息

Kobayashi M, Morishita H, Sugiyama N, Yokochi K, Nakano M, Wada Y, Hotta Y, Terauchi A, Nonaka I

出版信息

J Inherit Metab Dis. 1986;9(3):301-4. doi: 10.1007/BF01799670.

DOI:10.1007/BF01799670
PMID:3099078
Abstract
摘要

相似文献

1
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.线粒体肌病、脑病、乳酸酸中毒和卒中样发作综合征以及NADH-辅酶Q还原酶缺乏症。
J Inherit Metab Dis. 1986;9(3):301-4. doi: 10.1007/BF01799670.
2
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome.两例NADH-辅酶Q还原酶缺乏症：与线粒体脑肌病伴乳酸血症和卒中样发作综合征的关系
J Pediatr. 1987 Feb;110(2):223-7. doi: 10.1016/s0022-3476(87)80158-0.
3
Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathy.
Pediatr Res. 1989 Feb;25(2):194-201. doi: 10.1203/00006450-198902000-00023.
4
Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy.线粒体电子传递复合体I中还原型烟酰胺腺嘌呤二核苷酸脱氢酶成分缺乏。致命性婴儿乳酸酸中毒和伴有骨骼肌-心肌病及脑病的高代谢。
J Clin Invest. 1987 Jul;80(1):71-7. doi: 10.1172/JCI113066.
5
Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?线粒体肌病和脑病：三例报告——NADH-辅酶Q脱氢酶缺乏？
Neurology. 1983 Dec;33(12):1619-22. doi: 10.1212/wnl.33.12.1619.
6
Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.乳酸酸中毒和线粒体肌病与呼吸链复合体III的几种成分缺乏相关。
Pediatr Res. 1984 Oct;18(10):991-9. doi: 10.1203/00006450-198410000-00017.
7
[Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].
Neurologia. 1991 May;6(5):185-7.
8
Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.复合体I亚基缺乏与线粒体脑肌病
Ann Neurol. 1988 Mar;23(3):287-94. doi: 10.1002/ana.410230312.
9
[Neurological approach to mitochondrial abnormalities].[线粒体异常的神经学研究方法]
No To Hattatsu. 1987 Mar;19(2):118-24.
10
Impaired NADH-CoQ reductase activity in a child with moyamoya syndrome.烟雾病综合征患儿的NADH-辅酶Q还原酶活性受损。
Pediatr Neurol. 1988 Jul-Aug;4(4):241-4. doi: 10.1016/0887-8994(88)90038-0.

引用本文的文献

1
Surgical Trauma in Mice Modifies the Content of Circulating Extracellular Vesicles.小鼠手术创伤改变循环细胞外囊泡的内容物。
Front Immunol. 2022 Jan 18;12:824696. doi: 10.3389/fimmu.2021.824696. eCollection 2021.
2
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiography.线粒体肌病、脑病、乳酸酸中毒和卒中样发作（MELAS）患者经超声心动图评估显示左心室舒张功能降低。
Pediatr Cardiol. 1993 Jul;14(3):162-6. doi: 10.1007/BF00795646.
3
The biochemical basis of mitochondrial diseases.

本文引用的文献

1
A microspectrophotometric method for the determination of cytochrome oxidase.一种测定细胞色素氧化酶的显微分光光度法。
J Biol Chem. 1951 Apr;189(2):665-70.
2
An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study.与肝线粒体外膜相关的电子传递系统。一项生化与形态学研究。
J Cell Biol. 1967 Feb;32(2):415-38. doi: 10.1083/jcb.32.2.415.
3
Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver.进行性婴儿脊髓灰质炎。与肌肉和肝脏中丙酮酸氧化紊乱有关。
线粒体疾病的生化基础。
J Bioenerg Biomembr. 1988 Apr;20(2):161-91. doi: 10.1007/BF00768393.
Arch Neurol. 1981 Dec;38(12):767-72. doi: 10.1001/archneur.1981.00510120067011.
4
Different ketogenic response to medium-chain triglycerides and to long-chain triglycerides in a case of muscular carnitine palmitoyltransferase deficiency.一例肌肉肉碱棕榈酰转移酶缺乏症患者对中链甘油三酯和长链甘油三酯的不同生酮反应。
J Inherit Metab Dis. 1982;5(4):233-4. doi: 10.1007/BF02179151.
5
Neurologic deterioration with progressive CT changes in a child with Kearns-Shy syndrome.
Brain Dev. 1984;6(3):323-7. doi: 10.1016/s0387-7604(84)80046-7.
6
Mitochondrial myopathies. Clinical, morphological and biochemical aspects.线粒体肌病。临床、形态学及生化方面
Eur J Pediatr. 1984 Feb;141(4):192-207. doi: 10.1007/BF00572761.
7
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.线粒体肌病、脑病、乳酸酸中毒和卒中样发作：一种独特的临床综合征。
Ann Neurol. 1984 Oct;16(4):481-8. doi: 10.1002/ana.410160409.
8
Mitochondrial myopathies.线粒体肌病
Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602.
9
Pyruvate oxidation in rat and human skeletal muscle mitochondria.
Biochem Med. 1978 Dec;20(3):395-403. doi: 10.1016/0006-2944(78)90089-3.