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Si-quan Zhu

Showing results (1-10 of 30) with videos related to

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World Journal of Clinical Cases|October 30, 2023
Randomized controlled trial on the efficacy and safety of autologous serum eye drops in dry eye syndromeNa Zheng, Si-Quan Zhu
Molecular Vision|May 3, 2012
A novel p.F206I mutation in Cx46 associated with autosomal dominant congenital cataractKai Jie Wang, Si Quan Zhu
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|January 30, 2009
[Cortical plasticity in blind individual]Shu-zhen Wang, Si-quan Zhu
European Journal of Ophthalmology|December 8, 2009
Spontaneous dislocation of a Verisyse phakic intraocular lens with severe corneal endothelial cell lossKai-Jie Wang, Si-Quan Zhu
European Journal of Ophthalmology|November 15, 2018
Recurrent <i>PAX 6</i> mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardationDou-Dou Chen, Tao Yang, Si-Quan Zhu
Current Eye Research|March 25, 2014
A novel p.G112E mutation in BFSP2 associated with autosomal dominant pulverulent cataract with sutural opacitiesQing Liu, Kai Jie Wang, Si Quan Zhu
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|May 11, 2010
[Progress in pathogenic genes and their functions of congenital cataract]Kai-jie Wang, Si-quan Zhu, Jie Cheng
International Journal of Ophthalmology|October 20, 2022
Therapeutic potential of pupilloplasty combined with phacomulsification and intraocular lens implantation against uveitis-induced cataractHui Lu, Dou-Dou Chen, Si-Quan Zhu
Current Eye Research|December 31, 2014
Mutation analysis in Chinese families with autosomal dominant hereditary cataractsZhenfei Yang, Qian Li, Xu Ma, et al.
Current Eye Research|January 25, 2018
Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear CataractKai Jie Wang, Xu Zha, Dou Dou Chen, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
World Journal of Clinical Cases|October 30, 2023
Randomized controlled trial on the efficacy and safety of autologous serum eye drops in dry eye syndromeNa Zheng, Si-Quan Zhu
Molecular Vision|May 3, 2012
A novel p.F206I mutation in Cx46 associated with autosomal dominant congenital cataractKai Jie Wang, Si Quan Zhu
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|January 30, 2009
[Cortical plasticity in blind individual]Shu-zhen Wang, Si-quan Zhu
European Journal of Ophthalmology|December 8, 2009
Spontaneous dislocation of a Verisyse phakic intraocular lens with severe corneal endothelial cell lossKai-Jie Wang, Si-Quan Zhu
European Journal of Ophthalmology|November 15, 2018
Recurrent <i>PAX 6</i> mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardationDou-Dou Chen, Tao Yang, Si-Quan Zhu
Current Eye Research|March 25, 2014
A novel p.G112E mutation in BFSP2 associated with autosomal dominant pulverulent cataract with sutural opacitiesQing Liu, Kai Jie Wang, Si Quan Zhu
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|May 11, 2010
[Progress in pathogenic genes and their functions of congenital cataract]Kai-jie Wang, Si-quan Zhu, Jie Cheng
International Journal of Ophthalmology|October 20, 2022
Therapeutic potential of pupilloplasty combined with phacomulsification and intraocular lens implantation against uveitis-induced cataractHui Lu, Dou-Dou Chen, Si-Quan Zhu
Current Eye Research|December 31, 2014
Mutation analysis in Chinese families with autosomal dominant hereditary cataractsZhenfei Yang, Qian Li, Xu Ma, et al.
Current Eye Research|January 25, 2018
Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear CataractKai Jie Wang, Xu Zha, Dou Dou Chen, et al.
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