Liu Xing
In this database
8
2016 โ 2025
DB Citations
102
across indexed articles
h-index
โ
Not available
Total Citations
โ
Not available
8 articles in Glaucoma Journal Club
Visual field defect classification in the Zhongshan Ophthalmic Center-Brien Holden Vision Institute High Myopia Registry Study.
A proposed combined visual field classification for high myopia and glaucoma demonstrates acceptable intergrader agreement.
Novel BEST1 mutations and special clinical characteristics of autosomal recessive bestrophinopathy in Chinese patients.
The six novel mutations and high frequency of p.R255W suggest ethnical differences in the BEST1 mutation spectrum among Chinese patients.
Laser in Glaucoma and Ocular Hypertension Trial (LIGHT) in China - A Randomized Controlled Trial: Design and Baseline Characteristics.
Compared with participants in the LiGHT UK trial, participants in this trial were younger, more myopic and had more severe visual field defects.
Corneal Configurations and High-order Aberrations in Primary Congenital Glaucoma.
Abnormal corneal irregularity and HOAs are common in PCG eyes, even in those with limited optic nerve damage. These abnormalities relate to compromised visual outcomes.
Microcatheter-Assisted Circumferential Trabeculotomy After Failed Glaucoma Surgeries in Childhood Glaucoma.
MAT can effectively manage PCG, JOAG, and SCG after failed surgeries, providing successful outcomes and no serious complications.
Comparison of the Choroid in Primary Open Angle and Angle Closure Glaucoma Using Optical Coherence Tomography.
The CVI of POAG and PACG eyes was significantly lower than that of normal eyes.
Visual Outcomes of Children With Primary Congenital Glaucoma Receiving Different Refractive Corrections: The CLEVR-PCG Randomized Clinical Trial.
These findings suggest that RGPCLs provided superior visual acuity and contrast sensitivity improvement vs continued spectacle wear for children after PCG surgery.
Clinical features of patients with mutations in genes for nanophthalmos.
Totally, 67 patients from 63 families harboured 57 P/LP variants in the four genes, including 30 in(47.6%), 23 in(36.5%), 5 in(7.9%) and 5 in(7.9%).