• 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

Acute peripheral neuropathy, rhabdomyolysis, and severe lactic acidosis associated with 3243 A to G mitochondrial DNA mutation.

作者信息

Hara H, Wakayama Y, Kouno Y, Yamada H, Tanaka M, Ozawa T

出版信息

J Neurol Neurosurg Psychiatry. 1994 Dec;57(12):1545-6. doi: 10.1136/jnnp.57.12.1545-a.

DOI:10.1136/jnnp.57.12.1545-a
PMID:7798993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1073245/
Abstract
摘要

相似文献

1
Acute peripheral neuropathy, rhabdomyolysis, and severe lactic acidosis associated with 3243 A to G mitochondrial DNA mutation.与线粒体DNA 3243A到G突变相关的急性周围神经病、横纹肌溶解症和严重乳酸酸中毒。
J Neurol Neurosurg Psychiatry. 1994 Dec;57(12):1545-6. doi: 10.1136/jnnp.57.12.1545-a.
2
Exertional rhabdomyolysis, profound lactic acidosis, and acute kidney injury in a young boy: Questions.一名小男孩出现劳力性横纹肌溶解、严重乳酸酸中毒和急性肾损伤：问题探讨。
Pediatr Nephrol. 2016 Oct;31(10):1605-6. doi: 10.1007/s00467-015-3152-0. Epub 2015 Jul 9.
3
[Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease].线粒体 trifunctional 蛋白缺乏症：一名病情进展与夏科-马里-图思病相似的成年患者
Rinsho Shinkeigaku. 2017 Feb 25;57(2):82-87. doi: 10.5692/clinicalneurol.cn-000976. Epub 2017 Jan 28.
4
Persistent Profound Lactic Acidosis: an Unusual Case.持续性严重乳酸酸中毒：一例罕见病例。
Am J Med. 2018 Aug;131(8):e335-e336. doi: 10.1016/j.amjmed.2018.03.006. Epub 2018 Mar 23.
5
Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adults.成人线粒体三功能蛋白缺陷症以感觉神经元病为主要临床特征。
Rev Neurol (Paris). 2020 May;176(5):380-386. doi: 10.1016/j.neurol.2019.11.011. Epub 2020 Apr 3.
6
Continuous venovenous hemodiafiltration for life-threatening mitochondrial myopathy with lactic acidosis and rhabdomyolysis.连续性静脉-静脉血液透析滤过治疗伴乳酸酸中毒和横纹肌溶解的危及生命的线粒体肌病
J Intensive Care Med. 2007 Jul-Aug;22(4):240-4. doi: 10.1177/0885066607301343.
7
High-output heart failure in mitochondrial myopathy: a fulminant form with severe lactic acidosis and rhabdomyolysis.线粒体肌病中的高输出量心力衰竭：一种伴有严重乳酸酸中毒和横纹肌溶解的暴发性形式。
Intern Med. 1993 Oct;32(10):798-801. doi: 10.2169/internalmedicine.32.798.
8
Severe lactic acidosis secondary to minocycline in a teenager with infectious mononucleosis and mitochondrial myopathy.
Clin Neurol Neurosurg. 2008 Jun;110(6):627-30. doi: 10.1016/j.clineuro.2008.03.006. Epub 2008 Apr 28.
9
Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene.一例罕见的肌病、乳酸酸中毒和严重横纹肌溶解症，由铁氧化还原蛋白-2（FDX2）基因的纯合突变引起。
Am J Med Genet A. 2023 Dec;191(12):2843-2849. doi: 10.1002/ajmg.a.63368. Epub 2023 Aug 11.
10
Leptospire-induced acute rhabdomyolysis in a patient with previously undiagnosed mitochondrial myopathy.
Ir Med J. 2000 Sep;93(6):182-3.

引用本文的文献

1
[Characteristics of anesthesia in patients with MELAS syndrome: Case report of anesthesia in video-assisted thoracoscopy].[线粒体脑肌病伴乳酸血症和卒中样发作综合征患者的麻醉特点：电视辅助胸腔镜手术麻醉病例报告]
Anaesthesist. 2015 Oct;64(10):747-53. doi: 10.1007/s00101-015-0075-x. Epub 2015 Aug 28.
2
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation.散发性患者中新型线粒体 DNA tRNA（Ile）突变导致的复发性肌红蛋白尿。
J Neurol Sci. 2011 Apr 15;303(1-2):39-42. doi: 10.1016/j.jns.2011.01.018. Epub 2011 Feb 15.
3
[Rhabdomyolysis and myoglobinuria].[横纹肌溶解症与肌红蛋白尿]
Nervenarzt. 2003 Jun;74(6):505-15. doi: 10.1007/s00115-003-1518-1. Epub 2003 May 14.

本文引用的文献

1
Neuropathy and mitochondrial myopathy.神经病变和线粒体肌病。
Ann Neurol. 1980 Mar;7(3):262-8. doi: 10.1002/ana.410070310.
2
Pathological findings of the sural nerve in mitochondrial encephalomyopathy.
Jpn J Psychiatry Neurol. 1988 Jun;42(2):307-13. doi: 10.1111/j.1440-1819.1988.tb01981.x.
3
Peripheral neuropathy associated with mitochondrial myopathy.与线粒体肌病相关的周围神经病变
Ann Neurol. 1986 Aug;20(2):249-57. doi: 10.1002/ana.410200211.
4
Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Biochem Biophys Res Commun. 1991 Jan 31;174(2):861-8. doi: 10.1016/0006-291x(91)91497-z.
5
Lactic acidemia, mitochondrial myopathy, and basal ganglia calcification.乳酸性酸中毒、线粒体肌病和基底节钙化。
Neurology. 1979 Jul;29(7):1057-60. doi: 10.1212/wnl.29.7.1057.