• 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

Congenital stationary nightblindness.

作者信息

Carr R E

出版信息

Trans Am Ophthalmol Soc. 1974;72:448-87.

PMID:4376877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1311408/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/1311408/843dc529aadc/taos00027-0477-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/1311408/cc5707a0e72c/taos00027-0476-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/1311408/843dc529aadc/taos00027-0477-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/1311408/cc5707a0e72c/taos00027-0476-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/1311408/843dc529aadc/taos00027-0477-a.jpg

相似文献

1
Congenital stationary nightblindness.先天性静止性夜盲
Trans Am Ophthalmol Soc. 1974;72:448-87.
2
Photopic abnormalities in congenital stationary nightblindness.先天性静止性夜盲症中的明视觉异常。
Invest Ophthalmol. 1971 Aug;10(8):625-36.
3
Fleck retina.
Am J Ophthalmol. 1972 May;73(5):673-85. doi: 10.1016/0002-9394(72)90385-6.
4
Vitreous fluorophotometry in congenital stationary nightblindness.先天性静止性夜盲症的玻璃体荧光光度测定
Arch Ophthalmol. 1983 Apr;101(4):574-6. doi: 10.1001/archopht.1983.01040010574008.
5
Fundus reflectometry.眼底反射测量法
Ophthalmologica. 1974;169(1-3):30-7. doi: 10.1159/000307108.
6
Rod densitometry in night blindness: a review and two puzzling cases. Rod densitometry in night blindness.
Doc Ophthalmol. 1988 Mar-Apr;68(3-4):375-87. doi: 10.1007/BF00156443.
7
Congenital stationary night blindness with myopia: a clinico-pathologic study.
Doc Ophthalmol. 1986 Jun 16;63(1):55-62. doi: 10.1007/BF00153012.
8
A rod-cone dysfunction syndrome with separate clinical entity: incomplete-type congenital stationary night blindness (Miyake).一种具有独立临床实体的视杆-视锥功能障碍综合征：不完全型先天性静止性夜盲（三宅型）
Prog Clin Biol Res. 1987;247:137-45.
9
[Seven cases of congenital hemeralopia].[七例先天性昼盲症]
Nippon Ganka Gakkai Zasshi. 1972 Apr;76(4):179-83.
10
The diagnostic importance of functional electrooculography in some hereditary dystrophies of the eye fundus.功能性眼电图在某些遗传性眼底营养不良中的诊断重要性。
Ann Ophthalmol. 1971 Sep;3(9):929-46.

引用本文的文献

1
Introduction and Discovery of Retinitis Pigmentosa.视网膜色素变性的介绍与发现
Methods Mol Biol. 2023;2560:1-14. doi: 10.1007/978-1-0716-2651-1_1.
2
A Systematic Review of Optogenetic Vision Restoration: History, Challenges, and New Inventions from Bench to Bedside.光遗传学视觉修复的系统评价：从实验室到临床的历史、挑战和新发明。
Cold Spring Harb Perspect Med. 2023 Jun 1;13(6):a041304. doi: 10.1101/cshperspect.a041304.
3
Novel variants in the RDH5 Gene in a Chinese Han family with fundus albipunctatus.一个中国汉族眼底白点病家系中 RDH5 基因的新变异。

本文引用的文献

1
CAROTENOIDS AND THE VISUAL CYCLE.类胡萝卜素与视觉周期。
J Gen Physiol. 1935 Nov 20;19(2):351-71. doi: 10.1085/jgp.19.2.351.
2
VITAMIN A DEFICIENCY AND NIGHT BLINDNESS.维生素A缺乏与夜盲症。
Proc Natl Acad Sci U S A. 1958 Jul 15;44(7):648-61. doi: 10.1073/pnas.44.7.648.
3
[Analysis of the human electroretinogram].[人类视网膜电图分析]
BMC Ophthalmol. 2022 Feb 11;22(1):69. doi: 10.1186/s12886-022-02301-5.
4
Correlations Between Dark-Adapted Rod Threshold Elevations and ERG Response Deficits in Duchenne Muscular Dystrophy.Duchenne 型肌营养不良症的暗适应杆状阈值升高与 ERG 反应缺陷之间的相关性。
Invest Ophthalmol Vis Sci. 2021 Apr 1;62(4):29. doi: 10.1167/iovs.62.4.29.
5
Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.新型腺相关病毒载体玻璃体内注射靶向视锥双极细胞并恢复完全性先天性静止性夜盲小鼠模型的视觉功能。
Hum Mol Genet. 2015 Nov 1;24(21):6229-39. doi: 10.1093/hmg/ddv341. Epub 2015 Aug 26.
6
Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness.中国X连锁先天性静止性夜盲症家系中的两个新的NYX基因突变
Sci Rep. 2015 Aug 3;5:12679. doi: 10.1038/srep12679.
7
Genetic disruption of the On visual pathway affects cortical orientation selectivity and contrast sensitivity in mice.视觉通路中的基因缺失会影响小鼠大脑皮层的方位选择性和对比敏感度。
J Neurophysiol. 2014 Jun 1;111(11):2276-86. doi: 10.1152/jn.00558.2013. Epub 2014 Mar 5.
8
Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.两种先天性静止性夜盲症 2 型小鼠模型中的光感受器变性。
PLoS One. 2014 Jan 21;9(1):e86769. doi: 10.1371/journal.pone.0086769. eCollection 2014.
9
Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease.评估完全性先天性静止性夜盲症和 Oguchi 病的视网膜结构。
Am J Ophthalmol. 2012 Dec;154(6):987-1001.e1. doi: 10.1016/j.ajo.2012.06.003. Epub 2012 Sep 7.
10
TRPM1 mutations are associated with the complete form of congenital stationary night blindness.瞬时受体电位阳离子通道蛋白1（TRPM1）突变与完全型先天性静止性夜盲症相关。
Mol Vis. 2010 Mar 12;16:425-37.
Ophthalmologica. 1952 Jun;123(6):396-413. doi: 10.1159/000301211.
4
[Fundus albipunctatus with hemeralopia of 49 years' duration].[病程49年的白点状眼底伴昼盲]
Ophthalmologica. 1951 Apr;121(4):185-93. doi: 10.1159/000301006.
5
Retinitis punctata albescens. A functional evaluation of an unusual case.白点状视网膜病变。一例罕见病例的功能评估。
Am J Ophthalmol. 1962 Mar;53:450-5.
6
LIGHT-INDUCED DC RESPONSES OF MONKEY RETINA BEFORE AND AFTER CENTRAL RETINAL ARTERY INTERRUPTION.视网膜中央动脉阻断前后猴视网膜的光诱导直流反应
Invest Ophthalmol. 1965 Jun;4:310-7.
7
SOME PROPERTIES OF COMPONENTS OF THE CAT ELECTRORETINOGRAM REVEALED BY LOCAL RECORDING UNDER OIL.油下局部记录所揭示的猫视网膜电图成分的一些特性
J Physiol. 1965 Feb;176(3):429-61. doi: 10.1113/jphysiol.1965.sp007560.
8
ANALYSIS OF FOVEAL DENSITOMETRY.
Nature. 1965 Jan 2;205:52-6. doi: 10.1038/205052a0.
9
OGUCHI'S DISEASE.小口氏病
Arch Ophthalmol. 1965 May;73:646-56. doi: 10.1001/archopht.1965.00970030648010.
10
ELECTROPHYSIOLOGIC ASPECTS OF SEVERAL RETINAL DISEASES.几种视网膜疾病的电生理方面
Am J Ophthalmol. 1964 Jul;58:95-107.