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ATROPHIA GYRATA CHOROIDEAE ET RETINAE.

作者信息

Saebø J

机构信息

Norway.

出版信息

Br J Ophthalmol. 1948 Nov;32(11):824-47. doi: 10.1136/bjo.32.11.824.

DOI:10.1136/bjo.32.11.824
PMID:18170522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC510877/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/d12c72a0ad15/brjopthal00652-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/e30f45b40e9b/brjopthal00652-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/bb92ffca8531/brjopthal00652-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/7083f826f8f9/brjopthal00652-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/c6110a1ca178/brjopthal00652-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/d12c72a0ad15/brjopthal00652-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/e30f45b40e9b/brjopthal00652-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/bb92ffca8531/brjopthal00652-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/7083f826f8f9/brjopthal00652-0039-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/c6110a1ca178/brjopthal00652-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33e5/510877/d12c72a0ad15/brjopthal00652-0047-a.jpg

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1
ATROPHIA GYRATA CHOROIDEAE ET RETINAE.脉络膜视网膜回旋性萎缩
Br J Ophthalmol. 1948 Nov;32(11):824-47. doi: 10.1136/bjo.32.11.824.
2
[Apropos of gene carriers of Fuch's atrophia gyrata choroideae et retinae].[关于富克斯视网膜脉络膜回旋性萎缩的基因携带者]
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[On diffuse familial chorioretinal atrophies. (Cases of atrophia gyrata chorioideae et retinae complicated by calcareuous cataract)].[关于弥漫性家族性脉络膜视网膜萎缩。（回旋状脉络膜视网膜萎缩合并石灰样白内障病例）]
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[Atrophia gyrata choroideae et retinae and its syndromic relations].[脉络膜视网膜回旋性萎缩及其综合征关系]
Bull Soc Ophtalmol Fr. 1962 Mar;62:163-7.
6
[The conductors of the gene of Fuch's atrophia gyrata chorioideae et retinae (Alder's anomaly)].[富克斯视网膜脉络膜回旋性萎缩基因（阿尔德异常）的传导者]
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[Carrier of the gene of atrophia gyrata choroidae et retinae of Fuchs (Alder's anomaly)].
Bull Soc Belge Ophtalmol. 1959;122:367-82.
10
[Conductors of the gene of Fuchs' atrophia gyrata chorioideae et retinae (Alder's anomaly)].[富克斯视网膜脉络膜回旋性萎缩基因（阿尔德异常）的传导者]
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引用本文的文献

1
Multimodal imaging and genetic screening in Mexican patients with Gyrate atrophy: identification of novel OAT pathogenic variants.墨西哥回旋状萎缩患者的多模态成像与基因筛查：新型鸟氨酸氨基转移酶致病变异体的鉴定
Int Ophthalmol. 2024 Dec 7;45(1):1. doi: 10.1007/s10792-024-03260-0.
2
[Senile gyrate atrophy of the choroid and retina. Morphological and electroretinographic contribution].[脉络膜和视网膜老年性回旋状萎缩。形态学和视网膜电图的贡献]
Doc Ophthalmol. 1962;16:11-20. doi: 10.1007/BF00146716.
3
Choroideremia; clinical and genetic aspects.无脉络膜症；临床与遗传学方面
Br J Ophthalmol. 1952 Oct;36(10):547-81. doi: 10.1136/bjo.36.10.547.
4
[On nonretinal atrophia gyrata centralis choriodeae].关于中心性脉络膜视网膜萎缩性回旋状萎缩
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1966 Jul 15;170(2):117-22. doi: 10.1007/BF00419511.
5
[Clinical differential diagnosis of inflammatory and degenerative changes of the posterior pole of the eye].[眼后极部炎症性与退行性改变的临床鉴别诊断]
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1965 Dec 14;168(6):620-40. doi: 10.1007/BF02464827.
6
X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.影响眼睛的X染色体连锁疾病：杂合子女性的状况
Trans Am Ophthalmol Soc. 1969;67:535-608.
7
Genetic aspects in gyrate atrophy of the choroid and retina with hyperornithinaemia.伴有高鸟氨酸血症的脉络膜视网膜回旋性萎缩的遗传学方面。
Br J Ophthalmol. 1974 Nov;58(11):907-16. doi: 10.1136/bjo.58.11.907.