retinitis

retinitis

1. "Modulation of expression of retinal microRNAs may possibly represent a future therapeutic strategy for retinopathies such as retinitis pigmentosa.

"调制的表达视网膜小分子可能代表了未来的治疗策略，为视网膜病变，如视网膜色素变性" 。

2. actinic retinitis

[医] 光化性视网膜炎

3. retinitis punctata albescens

[医] 白点状视网膜炎

4. retinitis circumpapillaris retinitis

[视]乳头周视网膜炎

5. Keywords “Mingzhu Yin“;eye disease;central retinitis;

“明珠饮”;内眼病;中心性视网膜脉络膜炎;

6. 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

7. 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

8. She says there was a study which suggested that vitamin A helped some people with retinitis pigmentosa.But she notes that other investigators have disputed these findings.

一些研究显示维他命A有助于帮助一些人治疗视网膜炎，但她提醒到另一些调查人员对此发现有所争议。

9. 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

10. Linkage analysis of 8 chromosome in a Chinese family with autosomal dominant retinitis pigmentosa

中国人一个显性视网膜色素变性家系8号染色体连锁分析

11. toxic retinitis

中毒性视网膜炎

12. Laurence-Moon syndrome is a rare hereditary condition associated with retinitis pigmentosa, spastic paraplegia, hypogonadism and mental retardation.

什么是'劳伦斯文综合征-遗传综合征与精神发育迟滞和性腺机能减退'?

13. 6.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。

14. 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。

15. retinitis pseudoretinitis pigmentosa

假(性)色素性视网膜炎, 假(性)视网膜色素变性

16. retinitis pseudoalbuminurica

假蛋白尿性视网膜炎

17. congenital syphilitic retinitis

先天性梅毒性视网膜炎

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19. Keywords Retinitis pigmentosa/diagnosis;Vogt Koyanagi Harada syndrome/diagnosis;Fluorescein angiography;Indocyanine green/diagnostic use;

关键词视网膜炎;色素性/诊断;葡萄膜脑膜脑炎综合征/诊断;荧光素血管造影术;吲哚花青绿/诊断应用;

20. Keywords Retinitis pigmentosa;Chromosome abnormalities;Mutations;Polymerase chain reaction;Rhodopsin;DNA mutational analysis;

关键词视网膜炎;色素性;染色体异常;突变;聚合酶链反应;视紫红质;DNA突变分析;

21. Keywords retinitis pigmentosa;autosome dominant;linkage analysis;

关键词视网膜色素变性;显性遗传;连锁分析;

22. Keywords retinitis pigmentosa;linkage analysis;genome-wide screening;minimum critical region;

关键词视网膜色素变性;连锁分析;全基因组扫描;最小可能区域;

23. Patients with retinitis pigmentosa typically experience nyctalopia in adolescence or early adulthood because of primary degeneration of their rods.

其主要临床特征为夜盲、进行性视野缺损、眼底色素沉着和视网膜电图异常或无波等。

24. retinitis haemorrhagica

出血性视网膜炎

25. unilateral retinitis pigmentosa

单侧性视网膜色素变性

26. primary retinitis pigmentosa

原发性色素性视网膜炎

27. Keywords Retinitis pigmentosa;4+1 therapy;Retinal circulation;Visual function;

原发性视网膜色素变性;4+1疗法;视网膜循环;视功能;

28. 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

29. 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

30. Two patients presented with retinitis as the initial clinical manifestation of subacute sclerosing panencephalitis (SSPE), a delayed neurologic complication of measles.

双侧黄斑部视网膜炎作为亚急性硬化性全脑炎（SSPE）的表现特点：2例患者以视网膜炎为SSPE的初发临床表现，而神经病学并发症延迟。

31. RP Fighting Blindness (also known as the British Retinitis Pigmentosa Society) is a Medical Research Charity working to find a cure for RP.

反相战斗失明（也称为英国视网膜色素病变人士协会）是一个医学研究慈善工作，以找到治疗反相。

32. retin a micro question;

发表留言: equate;

33. It can be used to treat obdurate cerebrovascular disease, centrically retinitis, arteriosclerosis, coronary heart disease, pre-block syndrome, thrombophlebitis, etc.

可用于闭塞性脑血管病、中心性视网膜炎、动脉硬化、冠心病、梗塞前综合症、血栓性静脉炎等疾病。

34. Therefore, we believe that some of these drugs could be developed as potential treatments to delay or prevent blindness in rhodopsin retinitis pigmentosa patients.

因此，我们认为，这些药物可能发展成为潜在的治疗方法，延误或阻止失明的视紫红质视网膜色素变性病人。

35. The application of mesenchymal stem cells in the posterior eye mostly concentrates in seeking for the feasible treatment of retinitis pigmentosa.

在眼后节的应用重点集中于寻找治疗视网膜色素变性可行的治疗方法上。

36. There is ery little firm eidence that antimicrobial agents alter the natural history of toxoplasmic retinitis in otherwise non-immunocompromised patients.

在非免疫健全的患者中，很少有确实的证据证明抗微生物药改变弓形体性视网膜炎的自然病程。

37. * Foundation establishes partnership with Genable to develop gene therapy for dominant retinitis pigmentosa.

基金会建立夥伴关系，Genable开发基因治疗视网膜色素变性。

38. proliferating retinitis

增殖性视网膜炎

39. retinitis hemorrhagica externa

外层出血性视网膜炎, 寇茨(氏)病

40. external retinitis exudativa

外层渗出性视网膜炎

41. Keywords multifocal electroretinogram;first kernel response;primary retinitis pigmentosa;

多焦视网膜电图;一阶反应;原发性视网膜色素变性;

42. Keywords Multifocal visual evoked potential;Retinitis pigmentosa;Visual field;

多焦视诱发电位;视网膜色素变性;视野;

43. unilateral degenerative retinitis

奥尔德里奇氏综合征

44. retinitis gravidarum

妊娠性视网膜炎

45. 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。

46. sclopetaria retinitis

射伤性视网膜炎

47. The rare congenital condition of retinitis pigmentosa give rise to diffuse peripheral pigmentation with intervening pallor producing night, and later total, blindness.

少见的先天性色素性视网膜病变引起周边部位呈弥漫性色素沉着并杂以灰白色沉着于其间，而产生夜盲，到晚期导致全盲，即失明。

48. uremic retinitis

尿毒性视网膜炎

49. cytomegalovirus retinitis (CMVR)

巨细胞病毒性视网膜炎

50. Cytomegalovirus retinitis in patients with acquired immunodeficiency syndrome

巨细胞病毒性视网膜炎与获得性免疫缺陷综合征

51. Bright's retinitis

布赖特(氏)视网膜炎, 肾性视网膜病

52. Bright retinitis

布赖特视网膜炎

53. autosomal dominant retinitis pigmentosa

常染色体显性色素性视网膜炎

54. Analysis of NRL gene in patients with retinitis pigmentosa

常染色体显性视网膜色素变性NRL基因的突变研究

55. The Study of Loca lization of Autosomal Dominant Retinitis Pigmentosa Gene and Detection of Mutation on Rhodopsin Gene

常染色体显性视网膜色素变性基因定位的研究与视紫红质基因突变的检测

56. Genetic linkage and mutation analysis of the candidate genes in a big family with autosomal dominant retinitis pigmentosa

常染色体显性视网膜色素变性家系的基因连锁定位和候选基因的序列分析

57. Analysis of the mutations of rhodopsin gene in autosomal dominant retinitis pigmentosa family

常染色体显性视网膜色素变性家系视紫红质基因突变的检测分析

58. Mutation analysis of rhodopsin gene in Chinese with autosomal dominant retinitis pigmentosa

常染色体显性遗传RP患者视紫红质基因突变的检测分析

59. 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

60. 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。

61. diffuse syphilitic retinitis

弥散性梅毒性视网膜炎

62. When the patient gets weak such as after radio, chemotherapy, the toxin gets active again, the patient then will get pneumonia, Retinitis, Hepatitis B and etc. and finally even death.

当病人免疫力变弱，如接受化疗、电疗时，病毒便有机可乘，严重者可引致肺炎、视网膜炎、肝炎等，最后更可能致命。

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65. Ik denk het wordt geroepen retinitis pigmentosa.

我闻悉它某处。我接受提名为adminship 。

66. Juxtapapillary focal retinitis and retinochoroiditis

接近视乳头的病灶性视网膜炎和视网膜脉络膜炎

67. Abstract： OBJECTIVE To detect of parameter of electro-oculogram(EOG) in the patients with retinitis pigmentosa and its relation with bianzhengfenxing(辨证分型).

摘 要： 目的探讨视网膜色素变性患者眼电图变化及其与辨证分型的关系。

68. Purpose: To report a rare case of enophthalmos associated with the absence of the greater sphenoid wing simultaneous with retinitis pigmentose (RP).

摘要目的：报告一罕见病例，病患因蝶骨大翼缺损而导致眼球内陷，且合并有视网膜色素变性。

69. 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。

70. METHODS Parameter of EOG in 97 patients with retinitis pigmentosa and 47 volunteers by YD-1 visual elector physiology apparatus.

方法应用YD-1型眼电图仪对97例视网膜色素变性患者和正常对照组的47例志愿受试者的眼电图各参数进行检测。

71. pigmentosa sine pigmento retinitis

无色素性视网膜色素变性

72. hemeralopia atypical pigmentosa retinitis and chronic polyneuritis syndrome

昼盲非典型色素视网膜炎及慢性多发性神经炎综合征

73. The crystal glass and retin of combining operation applying complexity detached retina with high myopia

晶状体玻璃体视网膜联合手术治疗高度近视复杂性视网膜脱离疗效分析

74. More about retinitis pigmentosa and current research threads can be found in the "About RP" and "Research" sections of this site.

更多关于视网膜色素变性和目前的研究线索中可以找到“关于反相”和“研究”节本网站。

75. The characteristics of scotopic ERG in 76 patients(151 eyes)with retinitis pigmentosa were studied. All of them showed abnormal patterns, 84.8% extinguished and 15.2% subnormal.

本文总结76例151只眼视网膜色素变性的暗视视网膜电图的特性,全部病例都呈现异常的病理改变,其中84.8%为熄灭型,15.2%为降低型,证实熄灭型为本病主要电生理特征。

76. Wereport on a patient with enophthalmos caused by the greater sphenoid wing dyspiasia with simultaneous retinitis pigmentosa, but without stogmata or family history of neurofibromatosis.

本病例普未发现有第一型神经纤维瘤病的临床表徵或家族史，但发现有双眼视网膜色素变性。

77. Conclusion The crystal glass and retin of combining operation was safety at the same time treat the detached retina, cataract and correct refractive errors.

术后屈光度均为轻度近视或低度远视(硅油填充眼)结论联合手术安全可行,可同时治疗视网膜脱离、内障并纠正屈光不正。

78. Conclusion The crystal glass and retin of combining operation was safety at the same time treat the detached retina ,cataract and correct refractive errors.

术后屈光度均为轻度近视或低度远视(非硅油填充眼)。结论联合手术安全可行,可同时治疗视网膜脱离、白内障并纠正屈光不正。

79. 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。

80. embolic retinitis

栓子性视网膜炎