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- pseudonephritic retinitis 假肾炎性视网膜炎
- Two cases of central retinitis were recorded here. 例举中心性视网膜脉络膜炎验案两则以证之。
- The components of carrot correspond to Retin A. 胡萝卜中起主要作用的成分是维生素A。
- Ik denk het wordt geroepen retinitis pigmentosa. 我闻悉它某处。我接受提名为adminship 。
- Retinitis pigmentosa, or R.P, is a form of retinal degeneration. 视网膜炎或R.;P是视网膜变性的一种。
- The trio, who had lost almost all of their vision due to retinitis pigmentosa (RP). 他们由于患有色素性视网膜炎（rp）而几乎丧失了所有的视力。
- Abstract: This paper synthesized a kind of macromolecule retin yl schiff base salts. 文摘:合成了一种大分子视黄基席夫碱盐微波吸收剂。
- The trio,who had lost almost all of their vision due to retinitis pigmentosa (RP). 他们由于患有色素性视网膜炎（RP）而几乎丧失了所有的视力。
- Objective: To study the effects of rhodopsin (RHO) gene in autosomal dominant retinitis pigmentosa (adRP). 摘要目的：探讨视紫红质基因在视网膜色素变性疾病中的作用。
- Good at the treatment of virus keratitis, eyeground hemorrhage, centricity retinitis, vitreous body turbidness, etc. 并能充分发挥中医的优势治疗病毒性角膜炎、眼底出血、中心性视网膜炎、玻璃体混浊等疾病。
- 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。
- It changed the codon CGA for Arginine to a terminator codon TGA and causes retinitis pigmentosa in the two families. 它使该基因编码精氨酸的遗传密码CGA变为终止密码TGA,引起发病。
- The retinitis pigmentosa(RP)is an hereditary disease which causes visual deficiency leading to blindness. 视网膜色素变性是一种具有遗传性的致盲性眼病。
- RESULTS The parameter of EOG was lower in the patients with retinitis pigmentosa than in volunteers. 结果视网膜色素变性患者眼电图检测主要参数均低于对照组。
- CONCLUSION Detection of EOG may be available for evaluating condition of retinitis pigmentosa and bianzhengfenxing. 眼电图检测参数的主要特点是光峰电位下降 ( 5 5 67%25 )。 结论 眼电图检测可用于对视网膜色素变性患者病变程度评估和辨证分型。
- Objective To identify the disease locus in X-linked retinitis pigmentosa (RP) families using genetic linkage analysis. 目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析,定位其致病基因的所在位点。
- X-linked retinitis pigmentosa is the most devastating form of RP because of its severe clinical manifestations. 染色体连锁遗传RP作为其中的一种类型,具有发病早,损害最为严重等特点。
- Retinitis pigmentosa (RP) is a common genetic eye disease affecting about 1 in 3500 people the worldwide. 视网膜色素变性是一组常见的遗传性致盲眼病,患病率约为1／3500。
- Objective To identify the disease locus in X-linked retinitis pigmentosa(XLRP) families using genetic linkage analysis. 目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析,确定其致病基因的所在位点。
- Retinitis pigmentosa (RP) is a common genetic eye disease affecting about 1 in 3500 people worldwide with pan-ethnic occurrence. 视网膜色素变性(rp)是遗传性致盲眼病,其患病率约为1/3500。
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