Detalhe da pesquisa
1.
Chinese Guideline on the Management of Polypoidal Choroidal Vasculopathy (2022).
Chin Med Sci J
; 38(2): 77-93, 2023 Jun 30.
Artigo
Inglês
| MEDLINE | ID: mdl-37263796
2.
Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses.
BMC Ophthalmol
; 20(1): 212, 2020 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32487042
3.
Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa.
Ophthalmology
; 126(11): 1549-1556, 2019 11.
Artigo
Inglês
| MEDLINE | ID: mdl-31054281
4.
Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy.
Mol Vis
; 23: 605-613, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28867931
5.
Generation and characterization of immortalized rat retinal microglial cell lines.
J Neurosci Res
; 92(4): 424-31, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24452530
6.
CCR2 overexpression promotes the efficient recruitment of retinal microglia in vitro.
Mol Vis
; 18: 2982-92, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-23288990
7.
[Photodynamic therapy for treatment of chronic or recurrent central serous chorioretinopathy].
Zhonghua Yan Ke Za Zhi
; 48(2): 106-13, 2012 Feb.
Artigo
Chinês
| MEDLINE | ID: mdl-22490944
8.
Mutation Analysis of the RPGR Gene in a Chinese Cohort.
Front Genet
; 13: 850122, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35432464
9.
Genotypic spectrum and phenotype correlations of EYS-associated disease in a Chinese cohort.
Eye (Lond)
; 36(11): 2122-2129, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34689181
10.
The electrotonic architecture of the retinal microvasculature: modulation by angiotensin II.
J Physiol
; 589(Pt 9): 2383-99, 2011 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21486796
11.
Erythropoietin receptor positive circulating progenitor cells and endothelial progenitor cells in patients with different stages of diabetic retinopathy.
Chin Med Sci J
; 26(2): 69-76, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21703113
12.
A simple new technique for the induction of residual posterior vitreous cortex removal and membrane peeling.
Int J Ophthalmol
; 14(4): 622-625, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33875957
13.
Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population.
Orphanet J Rare Dis
; 16(1): 174, 2021 04 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33952291
14.
Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China.
Acta Ophthalmol
; 99(4): e470-e479, 2021 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-33124204
15.
Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease.
Br J Ophthalmol
; 105(1): 87-92, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32188678
16.
[Clinical observations of macular hole with and without retinal detachment in high myopic eyes].
Zhonghua Yan Ke Za Zhi
; 46(6): 508-12, 2010 Jun.
Artigo
Chinês
| MEDLINE | ID: mdl-21055195
17.
Association of adjuvant aromatase inhibitor with cataract risk in postmenopausal women with breast cancer.
Ann Transl Med
; 8(6): 342, 2020 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-32355786
18.
Interaction of two functional genetic variants LOXL1 rs1048661 and VEGFA rs3025039 on the risk of age-related macular degeneration in Chinese women.
Ann Transl Med
; 8(13): 818, 2020 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-32793663
19.
Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy.
Br J Ophthalmol
; 104(6): 846-851, 2020 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31519547
20.
Clinical and Genetic Characteristics of Chinese Patients with Occult Macular Dystrophy.
Invest Ophthalmol Vis Sci
; 61(3): 10, 2020 03 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32176261