• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.

作者信息

Sparaco M, Bonilla E, DiMauro S, Powers J M

机构信息

Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, New York 10032.

出版信息

J Neuropathol Exp Neurol. 1993 Jan;52(1):1-10. doi: 10.1097/00005072-199301000-00001.

DOI:10.1097/00005072-199301000-00001
PMID:8426185
Abstract
摘要

相似文献

1
Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.线粒体DNA缺陷所致线粒体脑肌病的神经病理学
J Neuropathol Exp Neurol. 1993 Jan;52(1):1-10. doi: 10.1097/00005072-199301000-00001.
2
MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.MERRF/MELAS 重叠综合征：线粒体 tRNA 基因的双重致病性突变。
J Med Genet. 2010 Oct;47(10):659-64. doi: 10.1136/jmg.2009.072058. Epub 2010 Jul 7.
3
Maternal inheritance and the evaluation of oxidative phosphorylation diseases.母系遗传与氧化磷酸化疾病的评估
Lancet. 1996 Nov 9;348(9037):1283-8. doi: 10.1016/S0140-6736(96)09138-6.
4
Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy.癫痫中的线粒体DNA突变与线粒体功能障碍
Epilepsia. 1999;40 Suppl 3:33-40. doi: 10.1111/j.1528-1157.1999.tb00897.x.
5
Neuropathological features of mitochondrial disorders.线粒体疾病的神经病理学特征。
Semin Cell Dev Biol. 2001 Dec;12(6):429-39. doi: 10.1006/scdb.2001.0280.
6
Mitochondrial dysfunction as a mechanism of CNS injury.
Res Publ Assoc Res Nerv Ment Dis. 1993;71:67-79.
7
Defects of mitochondrial DNA.线粒体DNA缺陷
Brain Pathol. 1992 Apr;2(2):121-32. doi: 10.1111/j.1750-3639.1992.tb00680.x.
8
[Genetic diagnosis of mitochondrial diseases].[线粒体疾病的基因诊断]
Nihon Ika Daigaku Zasshi. 1995 Oct;62(5):516-9. doi: 10.1272/jnms1923.62.516.
9
Abnormal excretion of urinary phospholipids and sulfatide in patients with mitochondrial encephalomyopathies.线粒体脑肌病患者尿中磷脂和硫脂的异常排泄。
Biochem Biophys Res Commun. 1993 Jul 15;194(1):266-73. doi: 10.1006/bbrc.1993.1814.
10
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanism.
Brain. 2000 Jan;123 ( Pt 1):93-104. doi: 10.1093/brain/123.1.93.

引用本文的文献

1
Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms.线粒体 DNA 缺失在 Kearns-Sayre 综合征中的细胞和分子反应：一些潜在的机制。
Mol Neurobiol. 2024 Aug;61(8):5665-5679. doi: 10.1007/s12035-024-03938-7.
2
Metabolic Determinants of Cerebellar Circuit Formation and Maintenance.代谢决定小脑回路的形成和维持。
Cerebellum. 2024 Aug;23(4):1626-1641. doi: 10.1007/s12311-023-01641-2. Epub 2023 Dec 20.
3
Experimental and Clinical Evidence of the Effectiveness of Riboflavin on Migraines.
核黄素治疗偏头痛的实验和临床证据。
Nutrients. 2021 Jul 29;13(8):2612. doi: 10.3390/nu13082612.
4
Mitochondrial Myopathy, Encephalopathy, Lactic acidosis and Stroke-Like Episodes Syndrome Presenting With Anton-Babinski Syndrome and Concurrent Occipital Lobe Seizures.线粒体肌病、脑病、乳酸性酸中毒和卒中样发作综合征伴安托万-巴宾斯基综合征及枕叶癫痫发作
Cureus. 2021 Jan 25;13(1):e12908. doi: 10.7759/cureus.12908.
5
Autopsied case with MERRF/MELAS overlap syndrome accompanied by stroke-like episodes localized to the precentral gyrus.尸检病例伴有 MERRF/MELAS 重叠综合征，并伴有局部在前中央回的类似中风发作。
Neuropathology. 2019 Jun;39(3):212-217. doi: 10.1111/neup.12551. Epub 2019 Apr 10.
6
A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging features.MELAS 中散发的小皮质病变簇：其独特的临床和神经影像学特征。
J Neurol. 2019 Jun;266(6):1459-1472. doi: 10.1007/s00415-019-09283-3. Epub 2019 Mar 19.
7
Impaired Bioenergetics in Mutant Mitochondrial DNA Determines Cell Fate During Seizure-Like Activity.突变线粒体 DNA 导致的生物能量障碍决定癫痫样活动期间的细胞命运。
Mol Neurobiol. 2019 Jan;56(1):321-334. doi: 10.1007/s12035-018-1078-9. Epub 2018 Apr 27.
8
Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy.线粒体DNA缺失会激活星形胶质细胞并导致海绵状脑病。
Nat Commun. 2018 Jan 4;9(1):70. doi: 10.1038/s41467-017-01859-9.
9
Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease.线粒体 DNA 损伤与神经退行性疾病中的活性氧
FEBS Lett. 2018 Mar;592(5):728-742. doi: 10.1002/1873-3468.12956. Epub 2018 Jan 9.
10
Inherited and acquired disorders of myelin: The underlying myelin pathology.髓鞘的遗传性和获得性疾病：潜在的髓鞘病理学
Exp Neurol. 2016 Sep;283(Pt B):452-75. doi: 10.1016/j.expneurol.2016.04.002. Epub 2016 Apr 9.