retinitis pigmentosa

In retinal degenerative diseases such as retinitis pigmentosa , cones stop providing vision before they die and can remain in a compromised state for several years .

在视网膜变性疾病，如色素性视网膜炎，视锥体停止提供视力死亡之前，可以在妥协的状态持续数年。

The intrinsic pathological features of retina tissue will be the detailed basis of clinical diagnosis and treatment , such as diabetic retinopathy , macular degeneration , retinitis pigmentosa .

眼科临床表明，研究视网膜组织的内部特征变化能够为眼底病变组织的临床诊断和治疗提供直观详细的依据，如糖尿病性视网膜病变、黄斑变性、色素性视网膜炎等。

The man from Brittany in France was diagnosed with retinitis pigmentosa 40 years ago .

通过利用藻类中首次发现的感光蛋白，一名完全失明男子的部分视力得到了恢复。40年前，这名来自法国布列塔尼的男子被诊断患有视网膜色素变性。

A study of clinical classification in primary retinitis pigmentosa

原发性视网膜色素变性临床分级方法初探

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

Gene diagnosis of X linked retinitis pigmentosa by linkage analysis

应用连锁分析方法对X连锁型视网膜色素变性进行基因诊断的研究

Genetics analysis and gene diagnosis of Chinese family with autosomal dominant retinitis pigmentosa

视网膜色素变性家系遗传分析及基因诊断

Haplotype analysis of two families with X - linked retinitis pigmentosa

两例疑为X连锁型视网膜色素变性家系的单倍型分析研究

Construction of a single copy probe library of retinitis pigmentosa type 3 gene locus

遗传性视网膜色素变性3型基因位点单拷贝探针库的构建

Study on Treatment of Retinitis Pigmentosa with Traditional Chinese Medicine by Flicker Electroretinogram

中医药治疗视网膜色素变性的闪烁光视网膜电图研究

Primary study of iontophoresis of zinc ion in treatment of retinitis pigmentosa

直流电锌离子导入治疗视网膜色素变性的初步报告

Clinical and hereditary study of a family with primary retinitis pigmentosa combined with myopia

视网膜色素变性合并近视家系的临床及遗传学研究

Investigation on genetic linkage analysis of X-linked retinitis pigmentosa using microsatellite markers

应用微卫星多态位点对X连锁型视网膜色素变性疾病进行遗传连锁分析的研究

Clinical Overview on the Treatment of Retinitis Pigmentosa With Acupuncture

针灸治疗视网膜色素变性的临床研究概况

The role of fundus fluorescence photography in evaluation of primary retinitis pigmentosa

眼底荧光影像对原发性视网膜色素变性病情严重性的评估作用

Progress in the research of mutation of genetic intron and retinitis pigmentosa

基因内含子突变与视网膜色素变性的研究进展

Linkage analysis of chromosome 3 in three Chinese families with autosomal dominant retinitis pigmentosa

视网膜色素变性显性遗传家系3号染色体连锁分析

Molecular study on rhodopsin gene point mutations in retinitis pigmentosa

RHO基因突变在视网膜色素变性中的分子遗传学分析

Color doppler imaging in the diagnosis of retinitis pigmentosa

视网膜色素变性的彩色超声多普勒应用

The Molecular Genetics Research of Two Retinitis Pigmentosa Pedigrees

两个视网膜色素变性家系的分子遗传学研究

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

Pigment epithelium layer The observation of ERG in patients with retinitis pigmentosa

视网膜色素变性患者视网膜电图观察

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。

Our laboratory found and has been establishing an inbred mouse model of retinitis pigmentosa .

我们实验室发现并建立了一种患有视网膜色素变性疾病的近交系小鼠（rdf小鼠，现已繁殖到F18代）。

A clinical analysis of photoreceptor cell degeneration in pri-mary retinitis pigmentosa

原发性视网膜色素变性光感受器细胞损害的临床分析

Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa

视网膜色素变性患者眼底异常自发荧光与视网膜功能的关系

Genetic linkage analysis of localizing an autosomal dominant retinitis pigmentosa gene in a family

遗传连锁分析法对一常染色体显性遗传性视网膜色素变性家系的基因定位研究

Objective To observe clinical features of Retinitis pigmentosa with retinal vascular occlusion and its prognosis .

目的探讨原发性视网膜色素变性（RP）合并视网膜血管闭塞患者的临床特点及预后。

The study of RDS gene mutation and clinical phenotype in a family with primary retinitis pigmentosa

原发性视网膜色素变性家系的RDS基因Pro216Leu突变及其表型研究

Treatment of retinitis pigmentosa by hyperbaric oxygenation and energetic complex

高压氧加能量合剂治疗视网膜色素变性