Publications by authors named "Longhao Kuang"

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Case Report: Post-LASIK exacerbation of granular corneal dystrophy type 2: a familial case with mutation.
Longhao Kuang, Xuanjun Zhang, Yufang Wang, Qing Zhan, Jingjing Su

Front Med (Lausanne)· December 2025

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Myopia Control Efficacy of Asymmetric Multipoint Defocus Technique Spectacle Lenses: One-Year Double-Masked Randomized Controlled Trial.
Mengyi Wang, Runting Ma, Longhao Kuang, Xiaoqin Chen, Stephen J Vincent

Ophthalmology· September 2025

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WITHDRAWN: Retinal Phenotypes and Single-cell Sequencing Analysis of Ush2a Knockout Mice.
Yudie Ning, Longhao Kuang, Tao Huang, JunFeng Lv, Xiaohe Yan

Exp Eye Res· January 2025

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A novel compound heterozygous variant of MYO7A in Usher syndrome type 1.
Wenchao Cao, Longhao Kuang, Run Gan, Tao Huang, Xiaohe Yan

Exp Eye Res· October 2024

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The Role of OCTA in Evaluating Diabetic Retinopathy Progression: A Meta-Analysis.
Lei Xi, Minfang Fan, Longhao Kuang, Feng Zhao

Altern Ther Health Med· August 2024

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Effect of COVID-19 home confinement on the efficacy of orthokeratology, 0.01% atropine and combined treatment.
Shengsong Xu, Jinyun Jiang, Mengting Yu, Jiajia Gao, Mengyi Wang, Longhao Kuang

Acta Ophthalmol· June 2024

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-associated retinal degeneration caused by a homozygous pathogenic variant of 146C>T and literature review.
Jin Li, Yi-Qun Hu, Hong-Bo Cheng, Ting Wang, Long-Hao Kuang

Int J Ophthalmol· February 2024

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The molecular genetics of anterior segment dysgenesis.
Longhao Kuang, Min Zhang, Ting Wang, Tao Huang, Jin Li

Exp Eye Res· September 2023

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Association between prediabetes/hyperglycemia and retinal diseases: A meta-analysis.
Ting Wang, Longhao Kuang, Xue Yao, Run Gan, Qingshan Chen

Eur J Ophthalmol· July 2023

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Latest progress in the study of nanoparticle-based delivery of the CRISPR/Cas9 system.
Mingyu Yu, Xiaowen Liu, Hongbo Cheng, Longhao Kuang, Shaochong Zhang

Methods· October 2021

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New compound heterozygous CYP4V2 mutations in bietti crystalline corneoretinal dystrophy.
Ting Wang, Qingshan Chen, Xue Yao, Longhao Kuang, Run Gan

Gene· July 2021

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New compound heterozygous USH2A mutations in Usher syndrome.
Longhao Kuang, Qingshan Chen, Run Gan, Xiaohe Yan

Acta Ophthalmol· February 2020

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