Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Yang-shun Gu"'
Autor:
Dong-Yu Guo, Yuan-Yuan Shen, Miao-Miao Zhu, Yang-Yang Zhan, Xia-Wei Wang, Jian-Hua Xia, Bo Jiang, Yang-Shun Gu, Yan Long
Publikováno v:
International Journal of Ophthalmology, Vol 15, Iss 7, Pp 1116-1121 (2022)
AIM: To evaluate the effects of virtual reality (VR) training on different parameters of vision. METHODS: Sixty individuals ranged 18-60 years old with asthenopia were randomly divided into short-term (n=40) and long-term (n=20) treatment groups. The
Externí odkaz:
https://doaj.org/article/2cf976d21bb047879e9a6accb19c15c2
Publikováno v:
International Journal of Ophthalmology, Vol 13, Iss 3, Pp 481-487 (2020)
AIM: To compare the outcomes of four adjuvants used for internal limiting membrane (ILM) peeling in macular hole surgery, including indocyanine green (ICG), brilliant blue G (BBG), triamcinolone (TA) and trypan blue (TB), through systematic review an
Externí odkaz:
https://doaj.org/article/bf908fb9031a46b585d6a01fc92a0e51
Publikováno v:
International Journal of Ophthalmology, Vol 10, Iss 8, Pp 1331-1333 (2017)
Letter to the editor
Externí odkaz:
https://doaj.org/article/cc2f2d7bcfd54a63a4eae1edce2ad8cc
Autor:
Bo Jiang, Maurice K H Yap, Kim Hung Leung, Po Wah Ng, Wai Yan Fung, Wai Wa Lam, Yang-Shun Gu, Shea Ping Yip
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19587 (2011)
The paired box 6 (PAX6) gene is considered as a master gene for eye development. Linkage of myopia to the PAX6 region on chromosome 11p13 was shown in several studies, but the results for association between myopia and PAX6 were inconsistent so far.W
Externí odkaz:
https://doaj.org/article/8a9bde2655b347a48ef28e90b8401104
Publikováno v:
Seminars in Ophthalmology. 35:170-173
Consumer-grade virtual reality (VR) headset is being used with increasing frequency nowadays, however, the effect on visual function is not clear.We here investigate whether using VR headset changes adults' visual function and take into account the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebd1fa7f22a60b21023c8e0634051fd0
https://doi.org/10.1080/08820538.2020.1776342
https://doi.org/10.1080/08820538.2020.1776342
Publikováno v:
Journal of Zhejiang University-SCIENCE B. 18:421-429
Background: Leber congenital amaurosis (LCA) is a group of clinically and genetically heterogeneous retinal dystrophy. To date, 22 genes are known to be responsible for LCA, and some specific phenotypic features could provide significant prognostic i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c41e072f42ea0c43fd29af718de7d3
https://doi.org/10.1631/jzus.b1600156
https://doi.org/10.1631/jzus.b1600156
Publikováno v:
Experimental Eye Research. 145:456-467
Age-related macular degeneration (AMD) is the leading cause of blindness in the aged people. The latest systemic review of epidemiological investigations revealed that excessive light exposure increases the risk of AMD. With the drastically increasin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::528e3402d9c2e0cb254d519210370330
https://doi.org/10.1016/j.exer.2015.09.016
https://doi.org/10.1016/j.exer.2015.09.016
Autor:
Xin Li, Jian-lian Deng, Chen Xie, Yue-qing Yang, Yang-shun Gu, Hui Huang, Ming Qi, Yan-hua Chen, Nan Hong, Ying-ping Huang, Bai-sheng Xu
Publikováno v:
Journal of Zhejiang University-SCIENCE B. 15:727-734
Objective: Nance-Horan syndrome (NHS) is a rare X-linked disorder characterized by congenital nuclear cataracts, dental anomalies, and craniofacial dysmorphisms. Mental retardation was present in about 30% of the reported cases. The purpose of this s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6544ff99252a9de60fad6dcfa53e69d
https://doi.org/10.1631/jzus.b1300321
https://doi.org/10.1631/jzus.b1300321
Publikováno v:
International Journal of Ophthalmology.
To analyze the influences of different genotypes (After a systematic literature search, all relevant studies evaluating the association between the three primary mutations of LHON and visual prognosis were included. All statistical tests were calcula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::122b83d7597ddb310de08a9c652c66bc
https://doi.org/10.18240/ijo.2016.10.21
https://doi.org/10.18240/ijo.2016.10.21
Publikováno v:
Genetic Testing. 12:421-425
The aim of this study was to conduct clinical, genetic, and molecular analysis of Chinese patients with granular corneal dystrophy type I (CDGG1). Two large unrelated Chinese families with CDGG1 were clinically and genetically evaluated. Molecular ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::840376707393130a0d5fbd77cbe23c7f
https://doi.org/10.1089/gte.2008.0005
https://doi.org/10.1089/gte.2008.0005