pigmentosa相关论文
The Evaluation of Vision Related Quality of Life in Patients with Retinitis Pigmentosa after Suprach
<strong>Background:</strong> The aim of this study was to evaluate vision related quality of life (VRQoL) in patients wi......
Retinal neovascularization induced by mutant Vldlr gene inhibited in an inherited retinitis pigmento
AIM:To explore whether the retinal neovascularization(NV)in a genetic mutant mice model could be ameliorated in an inher......
Congenital hepatic fibrosis is part of many different malformation syndromes, of which oculo-encephalohepato-renal syndr......
·AIM: To identify the pathogenic mutations in a Chinese pedigree affected with Usher syndrome type II(USH2).· METHODS:......
目的探讨视网膜色素变性(RP)患者脉络膜厚度变化及对视功能的影响。方法选取RP患者37例62只患眼和健康志愿者30例60只眼作为对照组......
目的 探讨细胞因子Ⅱ(calpain Ⅱ)在视网膜色素变性过程中表达的变化,以此窥视遗传性视网膜色素变性的转基因小鼠(rds小鼠)发病的......
我们报告4例双眼特发性黄斑囊样水肿(CME)的临床表现、眼底血管荧光造影和干涉光断层扫描(OCT)检查结果。患者均为男性,年龄30 ～52......
目的采用光学相干断层扫描(optical coherence tomography,OCT)和多焦视网膜电图(multifocal electroretinography,mfERG),观察视......
An in vivo Study of Basic Fibroblast Growth Factor on Activation and Proliferation of Retinal Progen
Purpose: To investigate the effect of intravitreal injection of basic fibroblast growth factor(bFGF) on activation and p......
Gene therapy is a potentially effective treatment for retinal degenerative diseases.Clustered regularly interspaced shor......
感光细胞(Photoreceptors)退化是年龄相关性黄斑变性(Age-related macular degeneration,AMD)和视网膜色素变性(Retinitis pigment......
Systemic mastocytosis (SM) is a rare disease with abnormal proliferation and infiltration of mast cells in the skin, bon......
AChinese family with autosomal dominant retinitis pigmentosa and a pro 347 Leur hodopsin gene mutati
ｅｔｉｎｉｔｉｓｐｉｇｍｅｎｔｏｓａ (ＲＰ )ｉｓａｃｌｉｎｉｃａｌｌｙａｎｄｇｅｎｅｔｉｃａｌｌｙｈｅｔｅｒｏｇｅｎｅｏｕｓｇｒｏｕｐｏｆｒｅｔｉｎａｌｄｅｇｅｎｅｒａｔｉｏｎｓｔｈａｔａｒｅｃｈａｒａｃｔｅｒｉｚｅｄｂｙｌｏｓｓｏｆｐｈｏｔｏｒｅｃｅｐ
etinitispigmentosa (RP) isaclinically and geneticallyheterogeneousgroupofretinaldegenerationsthatarecharacterizedb......
Aim:To investigate the effect of jujuboside A(JuA)on modulating gene expres-sion in the hippocampus.Methods:The spontan......
AIM:To determine the location of c-jun protein,dynamic changes in c-jun mRNA and protein expression,and ultrastructure c......
Neurotrophin-3 (NT-3) can promote the repair of central nervous system and retinal damage. In previous reports, NT-3 has......
视网膜色素变性是以视网膜的进行性变性伴有夜盲、视野缺损为特征的一种遗传性疾病。1857年由Donder命名为“色素性视网膜炎”(re......
视网膜色素变性(retinitis pigmentosa,RP)是一组变性性的视网膜病变,其临床表现和病情进展个体差异较大,典型者包括:(1)夜盲症;(......
Coats型视网膜色素变性(Coats-type retinitis pigmentosa,简称Coats型RP),即视网膜毛细血管扩张症和/或渗出性视网膜脱离。本病......
Retinitis pigmentosa is a common ophthalmological monogenic-inheritance disease. It has been confirmed that the patterns......
Macrophages in Human Epiretinal and Vitreal Membranes in Patients with Proliferative Intraocular Dis
Purpose: Macrophages are versatile cells and have been known as a cellular component of epiretinal membranes of prolife......
目的:对国人视网膜色素变性(retinitis pigmentosa RP)患者中视紫红质基因不同突变与临床表型相关性进行初步研究。方法:对经异源......
Purpose: To investigate the expression status of p53, Fas and bcl-2 in the developmentof retinal degeneration in C3H, r......
Purpose: To test the feasibility of recording rod multifocal electroretinograms(ERG) in humans and observe appropriate ......
SCREENING FOR MUTATIONS IN A NOVEL RETINA-SPECIFIC GENE AMONG CHINESE PATIENTS WITH RETINITIS PIGMEN
To identify and evaluate mutations in the RPl gene among Chinese patients with retinitis pigmen-tosa (RP).Methods. Leuko......
目的 研究中国视网膜色素变性 (retinitis pigmentosa,RP)患者 RP1基因的突变频率、特征及其在 RP发病机理中所起的作用。方法 ......
视网膜色素变性 (retinitis pigmentosa,RP)是一组进行性、可致盲的单基因遗传性视网膜疾病 ,以视网膜光感受器和色素上皮功能进行......
视网膜色素变性是视网膜感光细胞和色素上皮细胞变性导致夜盲和进行性视野缺损的一类眼底遗传病。常染色体显性遗传视网膜色素变性......
目的了解常染色体隐性遗传视网膜色素变性(autosomal recessive retinitis pigmentosa,ARRP)致病基因磷酸二酯酶β亚单位(phosphod......
Purpose: To investigate the clinical characteristics of juvenile macular hole without trauma and hypermyopia, and resear......
Objective To evaluate the prevalence of rhodopsin (RHO) mutations and the genotype-phenotype relationships in Chinese pa......
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。方法 对一个常染色体显性遗传视网膜......
Objective To investigate the properties of proliferation and differentiation of neonatal rat retinal progenitor cells (R......
先证者(Ⅴ6) 女,32岁.3岁开始发现夜晚不能辨别物体,渐进性视力下降20多年,自述生第2个孩子后发现视力严重下降.1年前入院检查,发......
报告1例色素性荨麻疹.患者男,43岁.躯干及四肢色素沉着斑伴瘙痒5年.躯干及四肢广泛分布大量色素性斑片、少量红斑及抓痕.皮损组织......
目的:分析视网膜色素变性的中西医结合治疗效果,评价其有效性和临床实用性。方法:全面检索计算机数据库及手工检索,对关于中西医结......
患者男,30岁.全身网状黑褐色色素沉着20余年.面颈、躯干及四肢可见网状黑褐色色素沉着,尤以颈部、躯干及上肢为重,头部毛发稀疏,发......
患者女,20岁.背部红色丘疹伴剧烈瘙痒,并消退后遗留褐色网状色素沉着3年.皮损组织病理示:角化过度,毛孔角栓,棘层轻度水肿,真皮浅......
Does Stem Cell Implantation Have an Effect on Severity of Retinitis Pigmentosa: Evaluation with a Cl
<strong>Background:</strong> Cell replacement therapies have been evaluated in recent years as an alternative for variou......
目的遗传性脊髓小脑共济失调 7型( SCA7)是 SCA系列中首个确定累及视网膜的疾病,该研究探讨中国 SCA7的临床特点.方法对一个表现为......
目的:寻找遗传性视网膜色素变性动物模型rds小鼠发病时差异表达的基因.方法:采用差异显示技术比较25d rds小鼠和正常对照小鼠的视......
