Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Zhilan Yuan"'
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background The purpose of this study is to identify the proteomic differences between the aqueous humour of diabetes patients with cataracts and that of non-diabetic sufferers of cataracts in a clinical setting. Methods Patients were divided
Externí odkaz:
https://doaj.org/article/c83b086470a24cb69cab34d231bb9cd8
Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background To evaluate the efficacy and safety of modified suture-assisted canaloplasty in Asians with primary open-angle glaucoma (POAG). Methods A prospective, consecutive cases study, evaluating a modified canaloplasty by twisted 6/0 sutu
Externí odkaz:
https://doaj.org/article/b619c1e0761343baafd0eee3bc46ae2f
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0284618 (2023)
BackgroundTo investigate the inhibitory effect of a hyaluronic acid hydrogel loaded with hydroxycamptothecin (HCPT) on scar formation after filtration surgery in a rabbit model.MethodsScleral fibroblasts were isolated and extracted from rabbits' eyes
Externí odkaz:
https://doaj.org/article/508ed8c034ea4fc6944f261e2ea7f50a
Publikováno v:
Heliyon, Vol 8, Iss 12, Pp e12543- (2022)
Objecive: To describe the clinical and genetic findings of an Axenfeld-Rieger syndrome (ARS) family with a new PITX2 splicing mutation. Methods: A Chinese ARS family with five affected individuals was recruited. Exome sequencing was performed on the
Externí odkaz:
https://doaj.org/article/6f24104e40f54a7791c6a5abc71ade8c
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background To compare the efficacy and safety of focused ultrasound cycloplasty (UCP) and transscleral cyclophotocoagulation (TSCP) in the treatment of refractory glaucoma in a Chinese population. Methods We retrospectively compared twenty-e
Externí odkaz:
https://doaj.org/article/698c9f01cbb4472f9fc5681b684d27b5
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 23
Introduction: Diabetic retinopathy (DR) is a major complication of diabetes and a leading cause of visual loss. This study aimed to explore biomarkers for DR that may provide additional reference to DR pathogenesis and development. Methods: The diffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41656813b97da9a8e81333a25c700a43
https://doi.org/10.2174/1871530323666230419081351
https://doi.org/10.2174/1871530323666230419081351
Publikováno v:
Irish Journal of Medical Science (1971 -). 191:865-876
Mutations in mitochondrial DNA (mtDNA) are the most important causes for Leber’s hereditary optic neuropathy (LHON). Of these, three primary mtDNA mutations account for more than 90% cases of this disease. However, to date, little is known regardin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09eab88a7ad36bb294bf7b675871c44f
https://doi.org/10.1007/s11845-021-02656-6
https://doi.org/10.1007/s11845-021-02656-6
Publikováno v:
BMC ophthalmology. 22(1)
Background To evaluate the efficacy and safety of modified suture-assisted canaloplasty in Asians with primary open-angle glaucoma (POAG). Methods A prospective, consecutive cases study, evaluating a modified canaloplasty by twisted 6/0 suture was pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c484bb102f011b2ccec986d49379503
https://pubmed.ncbi.nlm.nih.gov/35509003
https://pubmed.ncbi.nlm.nih.gov/35509003
Publikováno v:
International Journal of Medical Sciences
To evaluate the efficacy of Ahmed glaucoma valve (AGV) implantation in treating neovascular glaucoma (NVG) and analyze the factors influencing the surgical success rate, a retrospective investigation of 59 NVG patients (66 eyes) who underwent AGV imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35dd48166116ea3d5e51646626e4b370
https://doi.org/10.7150/ijms.35267
https://doi.org/10.7150/ijms.35267
Publikováno v:
J Biomed Res
Complete congenital achromatopsia is a devastating hereditary visual disorder. Mutations in the CNGB3 gene account for more than 50% of all known cases of achromatopsia. This work investigated the efficiency of subretinal (SR) delivered AAV8 (Y447, 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f32de162422cf9d7cfd54f0994aa5ca
https://pubmed.ncbi.nlm.nih.gov/32305965
https://pubmed.ncbi.nlm.nih.gov/32305965