Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Michael Deng"'
Autor:
Tian-Hui Chen, Ai-Zhu Miao, Yu-Liang Wang, Min Zhang, Jia-Hui Chen, Jia-Lei Zheng, Michael Deng, Ying-Hong Ji, Yong-Xiang Jiang
Publikováno v:
International Journal of Ophthalmology, Vol 14, Iss 8, Pp 1218-1224 (2021)
AIM: To investigate whether the axial length (AL)/total corneal refractive power (TCRP) ratio is a sensitive and simple factor that can be used for the early diagnosis of Marfan's syndrome (MFS) in children. METHODS: The relationship between the AL/T
Externí odkaz:
https://doaj.org/article/7afbffdd652f4ee29f88c02233e2e0e7
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Marfan syndrome (MFS) is a hereditary disease with an incidence of 0.3% in the general population. Approximately 60% of MFS patients with FBN1 gene mutation will suffer ectopia lentis (EL) from the age of 3. With the development of EL, sever
Externí odkaz:
https://doaj.org/article/a89e528e80a74df1bf1e4dc27d23446d
Publikováno v:
Journal of Ophthalmology, Vol 2020 (2020)
Aims. To determine the characteristics of corneal biometrics in eyes from aniso-axial length cataract patients compared with eyes from non-aniso-axial length individuals. Methods. This is a retrospective case series. Cataract patients with preoperati
Externí odkaz:
https://doaj.org/article/a0338cda4ccb4c779eaae3d24c5df6b2
Publikováno v:
Journal of Ophthalmology, Vol 2019 (2019)
Purpose. To clarify the distribution of corneal spherical aberrations (SAs) in cataract patients with different corneal astigmatism and axial length. Setting. Department of Ophthalmology and Vision Science of the Eye and ENT Hospital of Fudan Univers
Externí odkaz:
https://doaj.org/article/098d3caefe1d446a8e2f4d88acdc2340
Autor:
Michael Deng, Zexu Chen, Jia-Lei Zheng, Li-Na Lan, Tianhui Chen, Jiahui Chen, Yongxiang Jiang, Min Zhang
Publikováno v:
Human Mutation. 42:1637-1647
Mutations of fibrillin-1 (FBN1) have been associated with Marfan syndrome and pleiotropic connective tissue disorders, collectively termed as "type I fibrillinopathy". However, few genotype-phenotype correlations are known in the ocular system. Patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d526c25f3f03433bf952ba035469c440
https://doi.org/10.1002/humu.24283
https://doi.org/10.1002/humu.24283
Autor:
Tianhui Chen, Li-Na Lan, Jiahui Chen, Yongxiang Jiang, Min Zhang, Michael Deng, Zexu Chen, Jia-Lei Zheng
Publikováno v:
British Journal of Ophthalmology. 106:1655-1661
AimsTo identify the mutation spectrum and genotype–phenotype correlations offibrillin-1(FBN1) mutations in a Chinese cohort with congenital ectopia lentis (EL).MethodsPatients clinically suspected of congenital zonulopathy were screened using panel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8254398ae67c6ef779abc5b713bc6fb1
https://doi.org/10.1136/bjophthalmol-2021-319084
https://doi.org/10.1136/bjophthalmol-2021-319084
Autor:
Zexu Chen, Yongxiang Jiang, Jiahui Chen, Min Zhang, Jia-Lei Zheng, Tianhui Chen, Michael Deng
Publikováno v:
European Journal of Ophthalmology. 32:924-932
Objective: To evaluate surgical outcomes of modified capsular tension ring (MCTR) and intraocular lens (IOL) implantation in eyes of Marfan syndrome (MFS). Methods: This retrospective case series included MFS patients receiving MCTR transscleral fixa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e41ec749edbbacd0e9615659e10709
https://doi.org/10.1177/11206721211012868
https://doi.org/10.1177/11206721211012868
Autor:
Jiahui Chen, Zexu Chen, Jia-Lei Zheng, Michael Deng, Yinghong Ji, Tianhui Chen, Yongxiang Jiang, Min Zhang
Publikováno v:
Ophthalmic Research. 64:811-819
Introduction: Marfan syndrome (MFS) is characterized by ectopia lentis (EL) and elongated axial length (AL). The characteristics of AL in young patients with MFS and bilateral EL before the lens surgery are not fully understood. Methods: This study r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a802589c293adc7cdf5a23624fc196f9
https://doi.org/10.1159/000517384
https://doi.org/10.1159/000517384
Autor:
Zexu Chen, Tianhui Chen, Min Zhang, Jiahui Chen, Michael Deng, Jialei Zheng, Li-Na Lan, Yongxiang Jiang
Publikováno v:
British Journal of Ophthalmology; Dec2022, Vol. 106 Issue 12, p1655-1661, 7p
Autor:
Jiahui Chen, Yongxiang Jiang, Min Zhang, Zexu Chen, Li-Na Lan, Tianhui Chen, Michael Deng, Jia-Lei Zheng
Publikováno v:
American journal of ophthalmology. 237
Purpose To evaluate the diagnostic yield of congenital ectopia lentis (EL) in a Chinese cohort by combining panel-based next-generation sequencing with clinical findings Design A cohort study. Methods In total, 175 patients with congenital EL and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6073e2fe9bb360f4abaa85bfa6412cba
https://pubmed.ncbi.nlm.nih.gov/34818515
https://pubmed.ncbi.nlm.nih.gov/34818515