• 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

Fundus autofluorescence: the key in the diagnosis of maternally inherited diabetes and deafness.

作者信息

Esteban Olivia, Mateo Javier, Peiro Carlos, Del Buey Maria Ángeles, Ascaso Francisco J

机构信息

Department of Ophthalmology, Lozano Blesa University Clinic Hospital, Zaragoza, Spain.

出版信息

Clin Exp Optom. 2018 Jul;101(4):604-606. doi: 10.1111/cxo.12549. Epub 2017 Jul 11.

DOI:10.1111/cxo.12549
PMID:28696040
Abstract
摘要

相似文献

1
Fundus autofluorescence: the key in the diagnosis of maternally inherited diabetes and deafness.眼底自发荧光:母系遗传糖尿病和耳聋诊断的关键
Clin Exp Optom. 2018 Jul;101(4):604-606. doi: 10.1111/cxo.12549. Epub 2017 Jul 11.
2
Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy.一位患有母系遗传糖尿病伴耳聋(MIDD)相关黄斑营养不良患者的光学相干断层扫描显示的黄斑囊样改变。
Ophthalmic Genet. 2017 Sep-Oct;38(5):467-472. doi: 10.1080/13816810.2016.1253106. Epub 2017 Jan 31.
3
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.由线粒体DNA 3243 tRNA(Leu)A到G突变引起的色素性视网膜营养不良以及母系遗传糖尿病和耳聋综合征。
Ophthalmology. 1999 Jun;106(6):1101-8. doi: 10.1016/S0161-6420(99)90244-0.
4
Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation.携带 m.3243A>G 突变的母系遗传性糖尿病和耳聋(MIDD)患者的黄斑营养不良的多模态影像学分析。
Ophthalmic Genet. 2021 Jun;42(3):304-311. doi: 10.1080/13816810.2021.1881978. Epub 2021 Feb 5.
5
Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature.与线粒体 DNA A3243G 突变相关的黄斑营养不良:中心旁色素沉积还是萎缩?两例报告及文献复习。
BMC Ophthalmol. 2014 Jun 6;14:77. doi: 10.1186/1471-2415-14-77.
6
[Optical coherence tomography, angiography and conventional multimodal imaging findings in a case of maternally inherited diabetes and deafness].
J Fr Ophtalmol. 2020 Dec;43(10):e405-e408. doi: 10.1016/j.jfo.2020.02.005. Epub 2020 Sep 16.
7
Outer retinal tubulations in maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy.母系遗传糖尿病和耳聋(MIDD)相关黄斑营养不良中的外层视网膜管状结构。
Graefes Arch Clin Exp Ophthalmol. 2013 Sep;251(9):2265-7. doi: 10.1007/s00417-012-2217-z. Epub 2013 Jan 12.
8
Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group.母系遗传糖尿病和耳聋中黄斑图案营养不良的患病率。GEDIAM研究小组。
Ophthalmology. 1999 Sep;106(9):1821-7. doi: 10.1016/s0161-6420(99)90356-1.
9
Progression of Retinopathy Secondary to Maternally Inherited Diabetes and Deafness - Evaluation of Predicting Parameters.由母系遗传性糖尿病和耳聋引发的视网膜病变的进展-预测参数的评估。
Am J Ophthalmol. 2020 May;213:134-144. doi: 10.1016/j.ajo.2020.01.013. Epub 2020 Jan 24.
10
Structural Features Associated With the Development and Progression of RORA Secondary to Maternally Inherited Diabetes and Deafness.母系遗传糖尿病和耳聋继发 RORA 结构特征与发育和进展相关。
Am J Ophthalmol. 2020 Oct;218:136-147. doi: 10.1016/j.ajo.2020.05.023. Epub 2020 May 22.

引用本文的文献

1
Multimodal analysis in symptomatic MIDD-associated retinopathy. A case report and literature review.症状性线粒体糖尿病相关视网膜病变的多模态分析。病例报告及文献综述。
GMS Ophthalmol Cases. 2023 Dec 12;13:Doc23. doi: 10.3205/oc000231. eCollection 2023.