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1.
PSCs Reveal PUFA-Provoked Mitochondrial Stress as a Central Node Potentiating RPE Degeneration in Bietti's Crystalline Dystrophy.
Mol Ther
; 28(12): 2642-2661, 2020 12 02.
Article
in English
| MEDLINE | ID: mdl-32755565
2.
RETINAL AND CHOROIDAL BLOOD PERFUSION IN PATIENTS WITH BIETTI CRYSTALLINE DYSTROPHY.
Retina
; 41(11): 2351-2360, 2021 Nov 01.
Article
in English
| MEDLINE | ID: mdl-33840785
3.
Ocular abnormalities in a large patient cohort with retinitis pigmentosa in Western China.
BMC Ophthalmol
; 21(1): 43, 2021 Jan 18.
Article
in English
| MEDLINE | ID: mdl-33461530
4.
Clinical and genetic characteristics of Stargardt disease in a large Western China cohort: Report 1.
Am J Med Genet C Semin Med Genet
; 184(3): 694-707, 2020 09.
Article
in English
| MEDLINE | ID: mdl-32845068
5.
Oguchi disease caused by a homozygous novel SAG splicing alteration associated with the multiple evanescent white dot syndrome: A 15-month follow-up.
Doc Ophthalmol
; 141(3): 217-226, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32333190
6.
Neovascular glaucoma in a pediatric patient with neurofibromatosis type 1: a case report.
BMC Ophthalmol
; 20(1): 168, 2020 Apr 28.
Article
in English
| MEDLINE | ID: mdl-32345252
7.
[Contributions of human rods and cones pathway to different components of oscillatory potentials in time and frequency domain].
Zhonghua Yan Ke Za Zhi
; 51(5): 369-73, 2015 May.
Article
in Zh
| MEDLINE | ID: mdl-26311699
8.
Application effect of diversified health-promoting models on rehabilitation exercises for cervical spondylotic myelopathy.
Technol Health Care
; 32(2): 705-718, 2024.
Article
in English
| MEDLINE | ID: mdl-37483032
9.
Clinical manifestation and long-term follow-up of presumed ocular tuberculosis in China.
J Clin Tuberc Other Mycobact Dis
; 34: 100413, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38259975
10.
Construction and optimization of a polygenic risk model for venous thromboembolism in the Chinese population.
J Vasc Surg Venous Lymphat Disord
; 12(1): 101666, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-37619711
11.
Comprehensive analysis of UGT1A1 genetic polymorphisms in Chinese Tibetan and Han populations.
Biochem Genet
; 50(11-12): 967-77, 2012 Dec.
Article
in English
| MEDLINE | ID: mdl-22983686
12.
Effect of Alginate Gelatin Hydrogel Composited with Nano-Zinc on Cesarean Section Wound Healing.
J Biomed Nanotechnol
; 18(2): 600-606, 2022 Feb 01.
Article
in English
| MEDLINE | ID: mdl-35484735
13.
Ocular Characteristics of Patients With Bardet-Biedl Syndrome Caused by Pathogenic BBS Gene Variation in a Chinese Cohort.
Front Cell Dev Biol
; 9: 635216, 2021.
Article
in English
| MEDLINE | ID: mdl-33777945
14.
Molecular genetics with clinical characteristics of Leber congenital amaurosis in the Han population of western China.
Ophthalmic Genet
; 42(4): 392-401, 2021 08.
Article
in English
| MEDLINE | ID: mdl-33970760
15.
Online survey on healthcare skin reactions for wearing medical-grade protective equipment against COVID-19 in Hubei Province, China.
PLoS One
; 16(4): e0250869, 2021.
Article
in English
| MEDLINE | ID: mdl-33914813
16.
Comparative Study of a Modified Sub-Tenon's Capsule Injection of Triamcinolone Acetonide and the Intravenous Infusion of Umbilical Cord Mesenchymal Stem Cells in Retinitis Pigmentosa Combined With Macular Edema.
Front Pharmacol
; 12: 694225, 2021.
Article
in English
| MEDLINE | ID: mdl-34646129
17.
Quantitative assessment of visual pathway function in blind retinitis pigmentosa patients.
Clin Neurophysiol
; 132(2): 392-403, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33450562
18.
Ocular Characteristics of Patients with Leber Congenital Amaurosis 6 Caused by Pathogenic RPGRIP1 Gene Variation in a Chinese Cohort.
J Ophthalmol
; 2021: 9966427, 2021.
Article
in English
| MEDLINE | ID: mdl-34796026
19.
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.
Cell Prolif
; 54(9): e13100, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34347352
20.
Long-term follow-up of a Chinese patient with KCNV2-retinopathy.
Ophthalmic Genet
; 42(2): 144-149, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33372566