视锥细胞退化 - Suppr

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超能文献

The cone degenerations.

作者信息

Krill A E, Deutman A F, Fishman M

出版信息

Doc Ophthalmol. 1973 Apr 16;35(1):1-80. doi: 10.1007/BF00234530.

DOI:10.1007/BF00234530

PMID:4573331

Abstract

摘要

相似文献

The cone degenerations.视锥细胞退化

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Progressive generalized cone dysfunction.进行性广泛性视锥功能障碍。

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A new dominant progressive foveal dystrophy.一种新的显性进行性黄斑营养不良。

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A new form of albinism.一种新型白化病。

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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。

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Visual functions in pericentral and central pigmentary retinopathy.

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[Cone dystrophies and dysfunctions].

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Peripheral cone disease.

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A retinal origin of nystagmus-a perspective.眼球震颤的视网膜起源——一种观点。

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Optical coherence tomography findings in unilateral peripheral cone dysfunction syndrome: a case report.单侧周边视锥细胞功能障碍综合征的光学相干断层扫描结果：一例报告

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Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy.进行性视锥细胞和视锥-视杆细胞营养不良：临床特征、分子遗传学及治疗前景

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Wearable Improved Vision System for Color Vision Deficiency Correction.用于纠正色觉缺陷的可穿戴视力改善系统。

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Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsia.两名兄弟姐妹眼部检查结果的差异：一名患有完全性色盲，另一名患有不完全性色盲。

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Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers.由始祖剪接位点突变c.828+3A>T导致的常染色体显性视网膜营养不良以及作为修饰因子的反式蛋白单倍型。

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Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene.由GUCA1A基因中的一种新突变（D100G）引起的常染色体显性锥体-杆体营养不良的疾病进展。

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Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration.两名患有迟发性视锥-视杆细胞营养不良且无明显黄斑变性的兄弟姐妹。

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本文引用的文献

[The minute structure of the macula region in connection with function tests in tapetoretinal degeneration].

AMA Arch Ophthalmol. 1951;151(5-6):476-99.

Tridione and the eye.三甲双酮与眼睛

Am J Ophthalmol. 1946 May;29:606. doi: 10.1016/0002-9394(46)91527-9.

Visual effects of tridione.三甲双酮的视觉效应。

Am J Ophthalmol. 1947 Nov;30(11):1387-1405. doi: 10.1016/0002-9394(47)90392-9.

THE DYSTROPHIES OF THE MACULA.黄斑营养不良

Br J Ophthalmol. 1940 Oct;24(10):469-484.25. doi: 10.1136/bjo.24.10.469.

[Contribution to the study of taped-to-retinian inheritances (family choriorinity degeneration with dominant hereditary; family coexistence of pigment degeneration of the retina and Stargardt disease)].[对视盘视网膜遗传的研究贡献（显性遗传性家族性脉络膜变性；视网膜色素变性与斯塔加特病的家族共存）]

Ophthalmologica. 1949 Jul;118(1):1-29. doi: 10.1159/000300704.

Cone electroretinography by flicker.闪烁光锥体细胞视网膜电图

Nature. 1951 Oct 27;168(4278):738. doi: 10.1038/168738a0.

Hereditary degeneration of the macula; occurring in five generations.黄斑遗传性变性；五代人发病。

Am J Ophthalmol. 1955 May;39(5):637-43. doi: 10.1016/0002-9394(55)90035-0.

CONE DYSFUNCTION SYNDROMES.视锥细胞功能障碍综合征

Arch Ophthalmol. 1963 Aug;70:214-31. doi: 10.1001/archopht.1963.00960050216013.

[Macular form of diffuse tapeto-retinal degeneration, with special reference to simultaneous color perception disorders].

Albrecht Von Graefes Arch Ophthalmol. 1962;165:227-45. doi: 10.1007/BF00682377.

The electroretinogram in central retinal degeneration.中心性视网膜变性的视网膜电图

Trans Am Acad Ophthalmol Otolaryngol. 1961 Jul-Aug;65:576-94.

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