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Scientific Reports|October 14, 2015
SPP2 Mutations Cause Autosomal Dominant Retinitis PigmentosaYuan Liu, Xue Chen, Qihua Xu, et al.
Frontiers in Public Health|March 16, 2023
Cost-effectiveness analysis of myopia management: A systematic reviewSylvia Agyekum, Poemen P Chan, Yuzhou Zhang, et al.
Investigative Ophthalmology & Visual Science|November 6, 2025
Accelerated Biological Aging and Genetic Pleiotropy in Age-Related Eye Diseases: A Population-Based Cohort and Integrative Genetic AnalysisYuelan Gao, Yuyao Wang, Yuzhou Zhang, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 8, 2023
Effects of firsthand tobacco smoking on retinal vessel caliber: a systematic review and meta-analysisVincent L Yuen, Xiu Juan Zhang, Xiangtian Ling, et al.
The British Journal of Ophthalmology|February 14, 2018
Association of the <i>PAX6</i> gene with extreme myopia rather than lower grade myopiasShu Min Tang, Li Ma, Shi Yao Lu, et al.
Investigative Ophthalmology & Visual Science|April 12, 2016
Identification of PGF as a New Gene for Neovascular Age-Related Macular Degeneration in a Chinese PopulationLi Jia Chen, Li Ma, Wai Kit Chu, et al.
Investigative Ophthalmology & Visual Science|November 26, 2009
Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese populationYaping Yang, Xin Zhang, Li Jia Chen, et al.
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