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Photothermal Ring Integrated Intraocular Lens for High‐Efficient Eye Disease Treatment

Advanced materials (Weinheim), 2017-09, Vol.29 (34), p.n/a

2017

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Therapeutic potential of pupilloplasty combined with phacomulsification and intraocular lens implantation against uveitis-induced cataract

International journal of ophthalmology, 2022-10, Vol.15 (10), p.1598-1603

2022

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Spaceflight-associated neuro-ocular syndrome: a review of potential pathogenesis and intervention

International journal of ophthalmology, 2022-02, Vol.15 (2), p.336-341

2022

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Recurrent PAX 6 mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardation

European journal of ophthalmology, 2020-01, Vol.30 (1), p.181-188

2020

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A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract

Chinese medical journal, 2007-05, Vol.120 (9), p.820-824

2007

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Characterization of a p.R76H mutation in Cx50 identified in a Chinese family with congenital nuclear cataract

Journal of the Formosan Medical Association, 2020-01, Vol.119 (1), p.144-149

2020

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Retinal necrosis and apoptosis changes in mice under simulated microgravity

Guo ji yan ke za zhi, 2022-11, Vol.22 (11), p.1765-1770

2022

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Quantitative assessment of choroidal vascular sublayers in patients with pre-eclampsia compared to healthy pregnant women

Guo ji yan ke za zhi, 2021-04, Vol.21 (4), p.580-584

2021

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Analysis of the Related Risk Factors of Cerebral AVM Hemorrhage and the Relationship Between EPCs and SDF-1 in Brain AVM

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2020-07, Vol.51 (4), p.556-561

2020

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Randomized controlled trial on the efficacy and safety of autologous serum eye drops in dry eye syndrome

World journal of clinical cases, 2023-10, Vol.11 (28), p.6774-6781

2023

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A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts

Molecular vision, 2008-10, Vol.14, p.1906-1911

2008

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Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts

Molecular vision, 2008-04, Vol.14, p.750-755

2008

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Spontaneous Dislocation of a Verisyse Phakic Intraocular Lens with Severe Corneal Endothelial Cell Loss

European journal of ophthalmology, 2010-05, Vol.20 (3), p.601-603

2010

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Mutation analysis of a family affected with congenital aniridia and congenital cataract

Guo ji yan ke za zhi, 2019-08, Vol.19 (8), p.1396-1399

2019

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Progress in pathogenic genes and their functions of congenital cataract

Chung-hua yen k'o tsa chih, 2010-03, Vol.46 (3), p.280

2010

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Clinical analysis of dry eye and tear film stability in pterygium patients after autologous conjunctival flap transplantation

Guo ji yan ke za zhi, 2020-04, Vol.20 (4), p.680-683

2020

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先天性无虹膜合并先天性白内障家系致病基因突变分析

国际眼科杂志, 2019-08, Vol.19 (8), p.1396-1399

2019

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Research progress on the relationship between dry eye and sleep deprivation

Guo ji yan ke za zhi, 2021-05, Vol.21 (5), p.814-817

2021

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Detection of differentially expressed lumican gene mRNA level in scleral tissue in human eye

Zhong hua yi xue za zhi, 2012-03, Vol.92 (9), p.608-611

2012

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Cortical plasticity in blind individual

Chung-hua yen k'o tsa chih, 2008-10, Vol.44 (10), p.956

2008

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Evaluation of intraocular lens power after keratorefractive surgery by IOLMaster

Chung-hua yen k'o tsa chih, 2010-11, Vol.46 (11), p.989

2010

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带角膜缘干细胞的自体结膜瓣移植术对翼状胬肉患者泪膜稳定性的影响

国际眼科杂志, 2020-04, Vol.20 (4), p.680-683

2020

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Quality of vision in patients with aspherical diffractive multifocal intraocular lens implantation

Zhong hua yi xue za zhi, 2009-08, Vol.89 (31), p.2175-2178

2009

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干眼与睡眠障碍关系的研究进展

国际眼科杂志, 2021-05, Vol.21 (5), p.814-817

2021

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novel mutation in CRYBB1 associated with congenital cataract-microcornea syndrome: the p.Ser129Arg mutation destabilizes the βB1/βA3-crystallin heteromer but not the βB1-crystallin homomer

Human mutation, 2011-03, Vol.32 (3), p.E2050-E2060

2011

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Photothermal Ring Integrated Intraocular Lens for High‐Efficient Eye Disease Treatment

Therapeutic potential of pupilloplasty combined with phacomulsification and intraocular lens implantation against uveitis-induced cataract

Spaceflight-associated neuro-ocular syndrome: a review of potential pathogenesis and intervention

Recurrent PAX 6 mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardation

A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract

Characterization of a p.R76H mutation in Cx50 identified in a Chinese family with congenital nuclear cataract

Retinal necrosis and apoptosis changes in mice under simulated microgravity

Quantitative assessment of choroidal vascular sublayers in patients with pre-eclampsia compared to healthy pregnant women

Analysis of the Related Risk Factors of Cerebral AVM Hemorrhage and the Relationship Between EPCs and SDF-1 in Brain AVM

Randomized controlled trial on the efficacy and safety of autologous serum eye drops in dry eye syndrome

A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts

Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts

Spontaneous Dislocation of a Verisyse Phakic Intraocular Lens with Severe Corneal Endothelial Cell Loss

Mutation analysis of a family affected with congenital aniridia and congenital cataract

Progress in pathogenic genes and their functions of congenital cataract

Clinical analysis of dry eye and tear film stability in pterygium patients after autologous conjunctival flap transplantation

先天性无虹膜合并先天性白内障家系致病基因突变分析

Research progress on the relationship between dry eye and sleep deprivation

Detection of differentially expressed lumican gene mRNA level in scleral tissue in human eye

Cortical plasticity in blind individual

Evaluation of intraocular lens power after keratorefractive surgery by IOLMaster

带角膜缘干细胞的自体结膜瓣移植术对翼状胬肉患者泪膜稳定性的影响

Quality of vision in patients with aspherical diffractive multifocal intraocular lens implantation

干眼与睡眠障碍关系的研究进展

novel mutation in CRYBB1 associated with congenital cataract-microcornea syndrome: the p.Ser129Arg mutation destabilizes the βB1/βA3-crystallin heteromer but not the βB1-crystallin homomer

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