6.Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.
目研究兔角膜穿孔伤后血-屏改变及川芎嗪对环丙沙星在兔角膜穿孔伤内渗透性响。
7.Conclusions The major manifestion of ocular posterior segment syphilis is chorioretinitis.
结论 梅毒在后段主要表现是脉络膜视网膜炎;
8.Ovary of female flower 2(or 3)-locular, densely yellow-brown pubescent.
10.Ocular infections with helminthic parasites are uncommon and have been well described previously.
结论:寄生虫感染相当少见,但陆续都有病例被报告。
11.Ovary 1-3(or 4)-locular, with 1 or 2 ovules per locule;
子房1-3(或4)室,每室具1或2胚珠;
12.Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.
球外肌是维持球正常运动及形成正常视觉关键因素,其病变表现为斜视及球运动碍。
13.The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.
致盲和致低视力病均以白内位,其次为角膜病、青光、底病等。
14.ocular secretion and conjunctival hyperemia.,papillary hyperplasia in palpebral conjunctiva,follicles are full of upper and lower fornical conjunctiva.
分泌物增多,结膜充血,睑结膜乳头增生,上下穹窿部结膜布满滤泡。
15.Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
16.To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.
目:探讨球穿通伤角巩膜伤口修补同时行超声乳化白内吸除加后房型人工晶体植入手术效果。
17.Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.
目:探讨球穿通伤角巩膜伤口修补同时行超声乳化白内吸除加后房型人工晶体植入手术效果。
18.Researches are mature on mesenchymal stem cells as seed cells acting on damaged tissue in ocular repairs and regeneration.But its oncogenicity and the security are waiting for further solving.
间充质干细胞作为种子细胞参与部受损组织修复与再生研究趋于成熟,但其致瘤性及安全性还有待进一步解决。
19.Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.