Ze-Xu Chen (Zexu Chen)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 6

Top Topics

Aortic Aneurysm

Optical Coherence Tomography

Patient Reported Outcomes

Top Venues

Journal of cataract and refractive surgery

This page only lists publications with an associated author ORCID identifier.

Publications

Ze-Xu Chen, Wannan Jia, Tianhui Chen, Xin Shen, Yalei Wang, Yang Sun, Yong-Xiang Jiang
Safety and efficacy of capsular tension ring and capsular hook implantation for managing ectopia lentis in Marfan syndrome: real-world study. Journal of cataract and refractive surgery 50 (7) (2024)
Ze-Xu Chen, Wannan Jia, Tianhui Chen, Xin Shen, Yalei Wang, Yang Sun, Yong-Xiang Jiang
Safety and efficacy of capsular tension ring and capsular hook implantation for managing ectopia lentis in Marfan syndrome: real-world study. Journal of cataract and refractive surgery 50 (7) (2024)
Ze-Xu Chen, Wannan Jia, Tianhui Chen, Xin Shen, Yalei Wang, Yang Sun, Yong-Xiang Jiang
Safety and Efficacy of Capsular Tension Ring and Capsular Hook Implantation for Managing Ectopia Lentis in Marfan Syndrome: A Real-World Study. Journal of cataract and refractive surgery (2024)
Ze-Xu Chen, Wan-Nan Jia, Yong Ma, Tian-Hui Chen, Jia-Hao Hong, Yang Sun, Yan Liu, Ling-Hao Song, Yong-Xiang Jiang
Predicting axial length in patients with Marfan syndrome and ectopia lentis after modified capsular tension ring and intraocular lens implantation. Journal of cataract and refractive surgery (2023)
Ze-Xu Chen, Wan-Nan Jia, Yong Ma, Tian-Hui Chen, Jia-Hao Hong, Yang Sun, Yan Liu, Ling-Hao Song, Yong-Xiang Jiang
Predicting axial length in patients with Marfan syndrome and ectopia lentis after modified capsular tension ring and intraocular lens implantation. Journal of cataract and refractive surgery (2023)
Ze-Xu Chen, Tian-Hui Chen, Min Zhang, Jia-Hui Chen, Li-Na Lan, Michael Deng, Jia-Lei Zheng, Yong-Xiang Jiang
Correlation between FBN1 mutations and ocular features with ectopia lentis in the setting of Marfan syndrome and related fibrillinopathies. Human mutation 42 (12) (2021)