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pigmentosa

网络色点；色素；眼点

pigmentosa

pigmentosa

pigmentosa

色点

彩绘笔的英文翻译 ... pigmentolysis 解除色素(作用) pigmentosa [植]色点 pigmy 矮人, 侏儒 ...

色素

大四上学期词汇-2... ... retinitis  视网膜炎 pigmentosa  色素 precocious …

眼点

社会工作专业英语词汇(P3) ... pigment spot 眼点 pigmentosa 眼点 pilot investigation 试点调查 ...

1

It is so far being used in people with retinitis pigmentosa , in which photoreceptor cells , which take in light, deteriorate .

目前人工视网膜被用于患有色素性视网膜炎的病人，他们的光感受器细胞退化了。

2

Retinitis pigmentosa is an inherited disorder that accounts for 11% of cases of blindness and has no medical treatment .

色素性视网膜炎是一种遗传性疾病，11%的病例中病人会完全失明并且没有治疗方法。

3

Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence of disease .

视网膜色素变性是一种遗传性致盲性眼病，发病率较高，危害性较大。

6

Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).

目的确定常染色体显性遗传视网膜色素变性家系的致病基因及其突变位点，并研究其临床表型。

9

Retinal diseases, such as retinitis pigmentosa (RP) or age-related macular degeneration (AMD) are leading causes of untreatable blindness .

视网膜疾病，例如视网膜色素变性或者老年性黄斑变性是导致不可治愈的失明的主要原因。

11

Two of them suffered from retinitis pigmentosa, while the third had a similar disease .

其中的两个患有视网膜炎色斑疾病，第三个患有类似的疾病。

12

The development of molecular biology has thrown new light on the treatment of retinitis pigmentosa .

分子生物学的发展为治疗视网膜色素变性带来了新的希望。

13

Analysis of the mutation of rhodopsin gene in an inbreeding family with autosomal recessive retinitis pigmentosa

常染色体隐性遗传视网膜色素变性家系视紫红质基因突变的检测分析

14

A recurrent rhodopsin gene missense mutation in a Chinese family with autosomal dominant retinitis pigmentosa

一个视网膜色素变性家系的视紫红质基因突变分析

16

Retinitis pigmentosa'characteristics for optical coherence tomography

视网膜色素变性的相干光断层成像

17

Advanced study of molecular biology and gene therapy in retinitis pigmentosa

视网膜色素变性的分子生物学及基因治疗研究进展

19

Intraocular lens implantation of patients with cataract complicated retinitis pigmentosa

视网膜色素变性合并白内障患者人工晶状体植入术

20

Screening Results of Rhodopsin Gene Mutations in Four Chinese Autosomal Dominant Retinitis Pigmentosa Families

视紫红质基因在显性视网膜色素变性家系的突变筛查

21

Study of relevant genes in the visual transduction of retinitis pigmentosa

视网膜色素变性光传递过程中相关基因研究

23

Screening of candidate genes in a family with autosomal dominant retinitis pigmentosa

常染色体显性遗传视网膜色素变性家系的基因筛查

24

Characteristics of retinitis pigmentosa for optical coherence tomography

视网膜色素变性患者视网膜光学相干断层扫描观察

27

28

The characteristics of retinitis pigmentosa with retinal vascular occlusion

原发性视网膜色素变性合并血管闭塞的临床特点分析

29

A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa

一个 X-连锁视网膜色素变性中国家系的 RPGR 基因的新突变

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