Zou X - Search Results

1

Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2.

Yang L, Joo K, Tsunoda K, Kondo M, Fujinami-Yokokawa Y, Arno G, Pontikos N, Liu X, Nakamura N, Kurihara T, Tsubota K, Iwata T, Li H, Zou X, Wu S, Sun Z, Ahn SJ, Kim MS, Mun YS, Park KH, Robson AG, Miyake Y, Woo SJ, Sui R, Fujinami K; East Asia Inherited Retinal Disease Society Study Group. Yang L, et al. Among authors: zou x. Am J Ophthalmol. 2021 Jan;221:169-180. doi: 10.1016/j.ajo.2020.07.025. Epub 2020 Jul 21. Am J Ophthalmol. 2021. PMID: 32707201 Free article.

2

[Correlation between photoreceptor layer and visual acuity in eyes with persistent cystoid macular edema secondary to branch retinal vein occlusion].

Zou X, Dai RP, Dong FT. Zou X, et al. Zhonghua Yan Ke Za Zhi. 2010 Nov;46(11):1006-10. Zhonghua Yan Ke Za Zhi. 2010. PMID: 21211297 Chinese.

3

[The development in the studies of AAV-mediated gene therapy in retina].

Zou X, Sui RF, Dong FT. Zou X, et al. Zhonghua Yan Ke Za Zhi. 2011 Nov;47(11):1049-52. Zhonghua Yan Ke Za Zhi. 2011. PMID: 22336072 Review. Chinese.

4

Transthyretin Ala36Pro mutation in a Chinese pedigree of familial transthyretin amyloidosis with elevated vitreous and serum vascular endothelial growth factor.

Zou X, Dong F, Zhang S, Tian R, Sui R. Zou X, et al. Exp Eye Res. 2013 May;110:44-9. doi: 10.1016/j.exer.2013.02.005. Epub 2013 Feb 21. Exp Eye Res. 2013. PMID: 23438977

5

De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients.

Zou X, Yao F, Liang X, Xu F, Li H, Sui R, Dong F. Zou X, et al. Ophthalmic Genet. 2015 Mar;36(1):21-6. doi: 10.3109/13816810.2013.827219. Epub 2013 Sep 3. Ophthalmic Genet. 2015. PMID: 24001014

6

Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort.

Wang H, Wang X, Zou X, Xu S, Li H, Soens ZT, Wang K, Li Y, Dong F, Chen R, Sui R. Wang H, et al. Among authors: zou x. Invest Ophthalmol Vis Sci. 2015 Jun;56(6):3642-55. doi: 10.1167/iovs.14-15972. Invest Ophthalmol Vis Sci. 2015. PMID: 26047050 Free PMC article.

7

Improved Diagnosis of Inherited Retinal Dystrophies by High-Fidelity PCR of ORF15 followed by Next-Generation Sequencing.

Li J, Tang J, Feng Y, Xu M, Chen R, Zou X, Sui R, Chang EY, Lewis RA, Zhang VW, Wang J, Wong LC. Li J, et al. Among authors: zou x. J Mol Diagn. 2016 Nov;18(6):817-824. doi: 10.1016/j.jmoldx.2016.06.007. Epub 2016 Sep 10. J Mol Diagn. 2016. PMID: 27620828 Free article.

8

Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinism.

Zou X, Li H, Yang L, Sun Z, Yuan Z, Li H, Sui R. Zou X, et al. Sci Rep. 2017 Feb 17;7:33713. doi: 10.1038/srep33713. Sci Rep. 2017. PMID: 28211458 Free PMC article.

9

PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY.

Zou X, Fu Q, Fang S, Li H, Ge Z, Yang L, Xu M, Sun Z, Li H, Li Y, Dong F, Chen R, Sui R. Zou X, et al. Retina. 2019 Oct;39(10):2040-2052. doi: 10.1097/IAE.0000000000002242. Retina. 2019. PMID: 30134391

10

Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake Disease): East Asia Occult Macular Dystrophy Studies Report Number 1.

Fujinami K, Yang L, Joo K, Tsunoda K, Kameya S, Hanazono G, Fujinami-Yokokawa Y, Arno G, Kondo M, Nakamura N, Kurihara T, Tsubota K, Zou X, Li H, Park KH, Iwata T, Miyake Y, Woo SJ, Sui R; East Asia Inherited Retinal Disease Society study group. Fujinami K, et al. Among authors: zou x. Ophthalmology. 2019 Oct;126(10):1432-1444. doi: 10.1016/j.ophtha.2019.04.032. Epub 2019 Apr 25. Ophthalmology. 2019. PMID: 31028767 Free article.

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