进行性广泛性视锥功能障碍。 - Suppr

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超能文献

Progressive generalized cone dysfunction.

作者信息

François J, de Rouck A, Verriest G, de Laey J J, Cambie E

出版信息

Ophthalmologica. 1974;169(4):255-84. doi: 10.1159/000307127.

DOI:10.1159/000307127

PMID:4547582

Abstract

摘要

相似文献

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

Ophthalmologica. 1974;169(4):255-84. doi: 10.1159/000307127.

[Achromatopsia congenita combined with sectoral pigment-degeneration of the retina].先天性全色盲合并视网膜扇形色素变性

Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1972;183(4):310-6. doi: 10.1007/BF00496158.

The cone degenerations.视锥细胞退化

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

Cone dystrophies: clinical and electrophysiological findings.视锥细胞营养不良：临床及电生理检查结果

Ger J Ophthalmol. 1992;1(2):105-9.

[Juvenile macular degenerations].[青少年黄斑变性]

Arch Ophtalmol Rev Gen Ophtalmol. 1974 Jun-Jul;34(6-7):497-512.

Recovery of the human early receptor potential during dark adaptation in hereditary retinal disease.

Vision Res. 1970 Mar;10(3):219-26. doi: 10.1016/0042-6989(70)90127-6.

[Congenital achromatopsia].[先天性全色盲]

Ann Ocul (Paris). 1972 Jul;205(7):821-34.

[Cone dystrophies and dysfunctions].

Vestn Oftalmol. 2001 Jul-Aug;117(4):48-52.

Familiary bilateral segmental retinopathia pigmentosa.

Ophthalmologica. 1973;166(5):327-41. doi: 10.1159/000306862.

The functional syndromes.功能性综合征

Ophthalmologica. 1974;169(1-3):234-9. doi: 10.1159/000307125.

引用本文的文献

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。

Clin Ophthalmol. 2013;7:1703-11. doi: 10.2147/OPTH.S48723. Epub 2013 Aug 28.

Is there a dysfunction in the visual system of depressed patients?抑郁症患者的视觉系统是否存在功能障碍？

Ann Gen Psychiatry. 2005 Mar 29;4(1):7. doi: 10.1186/1744-859X-4-7.

Photopic ON- and OFF-pathway abnormalities in retinal dystrophies.视网膜营养不良中明视觉开通路和关通路异常

Trans Am Ophthalmol Soc. 1993;91:701-73.

The inverse electro-oculogram.逆向眼电图

Br J Ophthalmol. 1982 Jun;66(6):379-81. doi: 10.1136/bjo.66.6.379.

Supernormal scotopic ERG in cone dystrophy.圆锥角膜营养不良中的超常暗视视网膜电图。

Br J Ophthalmol. 1984 Feb;68(2):69-78. doi: 10.1136/bjo.68.2.69.

A clinical review of Stargardt's disease and/or fundus flavimaculatus with follow-up.

Int Ophthalmol. 1985 Nov;8(4):225-35. doi: 10.1007/BF00137651.

Temporal aspects of the electroretinogram in cone-rod dystrophy.视锥-视杆营养不良患者视网膜电图的时间特征

Doc Ophthalmol. 1985 Aug 30;60(2):219-27. doi: 10.1007/BF00158038.

Progressive cone dystrophy.进行性圆锥角膜营养不良

Trans Am Ophthalmol Soc. 1987;85:82-100.

Juvenile atrophy of pigment epithelium and choriocapillaris.

Graefes Arch Clin Exp Ophthalmol. 1992;230(3):230-2. doi: 10.1007/BF00176294.

Differential diagnosis of typical and atypical congenital achromatopsia. Analysis of a progressive foveal dystrophy and a nonprogressive oligo-cone trichromasy (general cone dysfunction without achromatopsia), both of which at first had been diagnosed as achromatopsia.典型与非典型先天性全色盲的鉴别诊断。对一种进行性黄斑营养不良和一种非进行性少视锥三色视觉（无全色盲的一般性视锥功能障碍）的分析，这两种情况最初都被诊断为全色盲。

Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1978 Dec 8;209(1):19-28. doi: 10.1007/BF00419159.

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