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Characteristic changes of macular microvascular structure in central retinal vein occlusion

Authors: Li Zefeng,  Zhou Xiyuan,  Liu Danning,  Zhou Jialin,  Ma Ning DOI: 10.3760/cma.j.cn115989-20200604-00396 Published 2022-07-10 Cite asChin J Exp Ophthalmol, ...
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Expert consensus on surgical technique for subretinal injection of gene therapy in China (2022)

Author: Fundus Disease Group of Chinese Medical Association Ophthalmology Branch,  Fundus Disease Committee of Chinese Medical Doctor Association Ophthalmology Branch ...
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Establishment of lens opacity model in Grx2 knockout mice based on CRISPR/cas9 system and the role of Grx2 in the pathogenesis of cataract

Authors: Guo Yong,  Guo Chenjun,  Zhang Jie,  Ning Xiaona,  Chen Xi,  Yan Hong DOI: 10.3760/cma.j.cn115989-20210308-00149 Published 2022-10-10 Cite asChin J ...
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Classification of adenoviral conjunctivitis based on sequencing and phylogenetic analysis of hexon and fiber

Authors: Wang Jing,  Zhu Jianfeng,  Lu Lina DOI: 10.3760/cma.j.cn115989-20200430-00300 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): 902-907. Abstract  ...
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Association between visual function and optic fiber layer thickness after gene therapy for Leber hereditary optic neuropathy

Authors: Yuan Jiajia,  Zhang Yong,  Chen Changzheng,  Yang Xueying,  Miao Qingmei,  Kai Yoon Fan,  Li Bin DOI: 10.3760/cma.j.cn115989-20210409-00242 Published 2022-10-10 ...
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Clinical and molecular genetics research of a Chinese Han family with Wagner syndrome

Authors: Cai Suping,  Zhang Daren,  Luo Xiaoling,  Huang Longxiang,  Wang Tingting,  Xu Tingting,  Liu Xuyang DOI: 10.3760/cma.j.cn115989-20210318-00184 Published 2022-10-10 Cite ...
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Genotypes and clinical phenotypes of Hermansky-Pudlak syndrome

Authors: Yang Shangying,  Cheng Wanyu,  Zhang Yan,  Sheng Xunlun DOI: 10.3760/cma.j.cn115989-20210728-00430 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): ...
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Screening of pathogenic mutation in a family with Axenfeld-Rieger syndrome by whole exome sequencing

Authors: Wang Qi,  Liu Xinna,  Shao Zhengbo,  Yuan Huiping DOI: 10.3760/cma.j.cn115989-20200802-00555 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): ...
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Identification of a COL2A1 mutation in a Chinese family with Stickler syndrome type 1 via whole exome sequencing

Authors: Deng Fang,  Cao Yingjie,  Xie Lijing,  Chen Shaowan,  Xiao Xiaoqiang,  Zhang Mingzhi DOI: 10.3760/cma.j.cn115989-20200612-00425 Published 2022-10-10 Cite asChin J ...
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Clinical and genetic characteristics of a Han Chinese family with autosomal recessive enhanced S-cone syndrome

Authors:Jiang Yongqiang,  Chen Kang,  Li Jie,  Guo Haoyi DOI: 10.3760/cma.j.cn115989-20210902-00490 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): 940-947 ...
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