Publications by authors named "Xiao-Hong Meng"

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The first Chinese case with LCAEOD syndrome caused by mutation of gene.
Yan-Ling Long, Xiao Liu, Gang Wang, Bo Liu, Xiao-Hong Meng

Int J Ophthalmol· April 2025

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Application effect of diversified health-promoting models on rehabilitation exercises for cervical spondylotic myelopathy.
Bi-Hua Lin, Gui-Qin Zhong, Xiao-Hong Meng, Hai-E Han, Xue-Qin Hu

Technol Health Care· March 2024

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A phase I clinical trial of human embryonic stem cell-derived retinal pigment epithelial cells for early-stage Stargardt macular degeneration: 5-years' follow-up.
Shi-Ying Li, Yong Liu, Lei Wang, Fang Wang, Tong-Tao Zhao, Xiao-Hong Meng

Cell Prolif· September 2021

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Intravitreally injected ranibizumab versus photodynamic therapy for CNV secondary to choroidal osteoma: a 7-year follow-up case report.
Li-Yuan Rong, Li Ran, Shi-Ying Li, Xiao-Hong Meng, Yan-Ling Long

Int J Ophthalmol· June 2021

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Novel mutations in in Bietti corneoretinal crystalline dystrophy: Next-generation sequencing technology and genotype-phenotype correlations.
Xiao Hong Meng, Yan He, Tong Tao Zhao, Shi Ying Li, Yong Liu

Mol Vis· April 2020

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Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing.
Ling-Hui Qu, Xin Jin, Yan-Ling Long, Jia-Yun Ren, Chuang-Huang Weng, Xiao-Hong Meng

Biosci Rep· January 2020

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Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients.
Yong Liu, Shao Jun Chen, Shi Ying Li, Ling Hui Qu, Xiao Hong Meng

Stem Cell Res Ther· September 2017

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Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family.
Xin Jin, Ling-Hui Qu, Bao-Ke Hou, Hai-Wei Xu, Xiao-Hong Meng

Biosci Rep· October 2016

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Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti's crystalline corneoretinal dystrophy.
Xiao Hong Meng, Hong Guo, Hai Wei Xu, Qi You Li, Xin Jin

Mol Vis· December 2015

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Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology.
Xin Jin, Ling Hui Qu, Xiao Hong Meng, Hai Wei Xu, Zheng Qin Yin

Mol Vis· September 2014

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Spectral-domain optical coherence tomography in patients with congenital nystagmus.
Hong Yang, Tao Yu, Cheng Sun, Xiao-Hong Meng, Yan-Ji Yu

Int J Ophthalmol· August 2012

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Transient pupillary light reflex in relation to fundus autofluorescence and dark-adapted perimetry in typical retinitis pigmentosa.
Yong Liu, Dan Ning Liu, Xiao Hong Meng, Zheng Qin Yin

Ophthalmic Res· May 2012

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The characterization of functional disturbances in Chinese patients with Bietti's crystalline dystrophy at different fundus stages.
Dan Ning Liu, Yong Liu, Xiao Hong Meng, Zheng Qin Yin

Graefes Arch Clin Exp Ophthalmol· February 2012

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A complete screen for mutations of the rhodopsin gene in a panel of Chinese patients with autosomal dominant retinitis pigmentosa.
Xiao-li Zhang, Ming Liu, Xiao-hong Meng, Wei-ling Fu, Zheng-qin Yin

Chin Med Sci J· March 2005

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[Study on exons 3 and 4 of alpha-synuclein gene in Chinese familial Parkinson disease patients].
Xi Chen, Yue-ting Liu, Jin-ru Li, Ling Chen, Yan-ming Xu, Xiao-hong Meng

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· December 2003

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