Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ze-xu Chen"'
Autor:
Xing-Yang Liu, Ke Wang, Xian-Hua Deng, Yi-Hua Wei, Rui Guo, Sui-Feng Liu, Yi-Fan Zhu, Jia-Jun Zhong, Jing-Yuan Zheng, Meng-Dan Wang, Qiu-Hong Ye, Jian-Quan He, Kai-Hang Guo, Jun-Rong Zhu, Shu-Qiong Huang, Ze-Xu Chen, Chong-Shan Lv, Lei Wen
Publikováno v:
Cell & Bioscience, Vol 13, Iss 1, Pp 1-20 (2023)
Abstract Background Olfactory dysfunction is among the earliest non-motor symptoms of Parkinson’s disease (PD). As the foremost pathological hallmark, α-synuclein initiates the pathology in the olfactory pathway at the early stage of PD, particula
Externí odkaz:
https://doaj.org/article/c34f41dbf0de4dbf91248e78e67e5a0c
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Isolated sulfite oxidase deficiency (ISOD) caused by sulfite oxidase gene (SUOX) mutations is a rare neurometabolic disease associated with ectopia lentis (EL). However, few genotype–phenotype correlations have been established
Externí odkaz:
https://doaj.org/article/8090aba5f44c40309fd47351d5dd848a
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Marfan syndrome (MFS, OMIM: 154700) is a heritable multisystemic disease characterized by a wide range of clinical manifestations. The underlying molecular defect is caused by variants in the FBN1. Meanwhile, FBN1 variants are also detected in a spec
Externí odkaz:
https://doaj.org/article/829888f284274e609754adc82bfcbaf1
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
ObjectiveThe aim of this study was to examine the biometric ocular manifestations and structural ocular features of anterior megalophthalmos (AM).MethodsFifteen patients with AM (30 eyes) from the Eye & ENT Hospital of Fudan University were included.
Externí odkaz:
https://doaj.org/article/924bdd9f577e44149f92a571961369b0
Autor:
Ze-Xu Chen, Zhen-Nan Zhao, Yang Sun, Wan-Nan Jia, Jia-Lei Zheng, Jia-Hui Chen, Tian-Hui Chen, Li-Na Lan, Yong-Xiang Jiang
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundMicrospherophakia (MSP) is a rare ocular condition, the lens surgery of which is complicated by both insufficient zonules and undersized capsule.MethodsThis study included MSP eyes managed with phacoemulsification combined with supra-capsul
Externí odkaz:
https://doaj.org/article/b225bc2178f74427a67dfd543efeecda
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Aims: To investigate the lens biometric parameters in congenital lens deformities, using a novel technique of swept-source anterior segment optical coherence tomography (SS-ASOCT).Methods: This prospective study included patients with microspherophak
Externí odkaz:
https://doaj.org/article/44ffb5b5a8e04d70b37e326592dab69b
Publikováno v:
American Journal of Ophthalmology. 251:24-31
Autor:
Ze-Xu Chen, Wan-Nan Jia, Yong Ma, Tian-Hui Chen, Jia-Hao Hong, Yang Sun, Yan Liu, Ling-Hao Song, Yong-Xiang Jiang
Publikováno v:
Journal of Cataract and Refractive Surgery. 49:571-577
Autor:
Ze‐Xu Chen, Wan‐Nan Jia, Yang Sun, Tian‐Hui Chen, Zhen‐Nan Zhao, Li‐Na Lan, Yan Liu, Ling‐Hao Song, Yong‐Xiang Jiang
Publikováno v:
Human mutationREFERENCES. 43(12)
ADAMTSL4 variants are one of the common causes of congenital ectopia lentis (EL), reported ocular comorbidities of which include iris anomalies, cataract, and glaucoma. However, a genotype-phenotype correlation has not been established. Potentially p
Publikováno v:
Ophthalmic research.
Introduction: This is a cross-sectional cohort study focused on assessing the influence of ocular biometric parameters of different camera devices for accurately predicting the intraocular lens (IOL) power in the congenital ectopia lentis (EL) patien