• 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

Maternally inherited diabetes and deafness is a mitochondrial multiorgan disorder syndrome (MIMODS).

作者信息

Finsterer Josef, Frank Marlies

机构信息

Krankenanstalt Rudolfstiftung, Vienna, Austria.

First Medical Department, Krankenanstalt Rudolfstiftung, Vienna, Austria.

出版信息

Acta Diabetol. 2017 Oct;54(10):979-980. doi: 10.1007/s00592-017-1029-3. Epub 2017 Jul 29.

DOI:10.1007/s00592-017-1029-3
PMID:28756474
Abstract
摘要

相似文献

1
Maternally inherited diabetes and deafness is a mitochondrial multiorgan disorder syndrome (MIMODS).母系遗传糖尿病和耳聋是一种线粒体多器官功能障碍综合征(MIMODS)。
Acta Diabetol. 2017 Oct;54(10):979-980. doi: 10.1007/s00592-017-1029-3. Epub 2017 Jul 29.
2
Reply to Letter to the Editor "Maternally inherited diabetes and deafness is a mitochondrial multiorgan disorder syndrome (MIMODS)".
Acta Diabetol. 2017 Oct;54(10):981-982. doi: 10.1007/s00592-017-1030-x. Epub 2017 Aug 1.
3
Letter to the Editor: Maternally Inherited Diabetes and Deafness is Not Only Biorgan but Multiorgan.
Acta Med Port. 2017 Sep 29;30(9):665-666. doi: 10.20344/amp.9716.
4
A novel mutation in mitochondrial DNA in a patient with diabetes, deafness and proteinuria.一名患有糖尿病、耳聋和蛋白尿患者的线粒体DNA发生新型突变。
Neth J Med. 2016 Dec;74(10):455-457.
5
THE ROLE OF HETEROPLASMY IN THE DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS.异质性在母系遗传糖尿病和耳聋的诊断和管理中的作用。
Endocr Pract. 2020 Feb;26(2):241-246. doi: 10.4158/EP-2019-0270. Epub 2019 Nov 4.
6
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions.一位母系遗传糖尿病和耳聋患者,携带与多种线粒体缺失相关的 12S rRNA m.1555A>G 和 ND1 m.3308T>C 突变。
Biochem Biophys Res Commun. 2013 Feb 22;431(4):670-4. doi: 10.1016/j.bbrc.2013.01.063. Epub 2013 Jan 26.
7
Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G.线粒体DNA突变A3243G导致的家族表型异质性
Acta Med Port. 2017 Aug 31;30(7-8):581-585. doi: 10.20344/amp.8638.
8
Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.患有母系遗传糖尿病和耳聋(MIDD)及进行性肾病的患者线粒体DNA中携带tRNA(Leu)(UUR)突变的线粒体的功能和形态异常。
Diabetologia. 1999 Apr;42(4):485-92. doi: 10.1007/s001250051183.
9
A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.一个患有母系遗传糖尿病和耳聋的家族中,线粒体DNA发生了一个新的G3421A错义突变。
Mutat Res. 2006 Dec 1;602(1-2):26-33. doi: 10.1016/j.mrfmmm.2006.07.006. Epub 2006 Sep 1.
10
Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness.线粒体紊乱:母系遗传糖尿病和耳聋。
Adv Exp Med Biol. 2018;1085:163-165. doi: 10.1007/978-3-319-95046-4_31.

引用本文的文献

1
The Role of Lactate Exercise Test and Fasting Plasma C-Peptide Levels in the Diagnosis of Mitochondrial Diabetes: Analysis of Clinical Characteristics of 12 Patients With Mitochondrial Diabetes in a Single Center With Long-Term Follow-Up.乳酸运动试验和空腹血浆 C-肽水平在诊断线粒体糖尿病中的作用:单中心长期随访分析 12 例线粒体糖尿病患者的临床特征。
Front Endocrinol (Lausanne). 2022 Feb 21;13:835570. doi: 10.3389/fendo.2022.835570. eCollection 2022.
2
tRNA Biology in the Pathogenesis of Diabetes: Role of Genetic and Environmental Factors.tRNA 生物学在糖尿病发病机制中的作用:遗传和环境因素的作用。
Int J Mol Sci. 2021 Jan 6;22(2):496. doi: 10.3390/ijms22020496.