Sui R - Search Results

1

Genotype-Phenotype Associations in an X-Linked Retinoschisis Patient Cohort: The Molecular Dynamic Insight and a Promising SD-OCT Indicator.

Wei X, Li H, Zhu T, Sun Z, Sui R. Wei X, et al. Among authors: sui r. Invest Ophthalmol Vis Sci. 2024 Feb 1;65(2):17. doi: 10.1167/iovs.65.2.17. Invest Ophthalmol Vis Sci. 2024. PMID: 38324300 Free PMC article.

2

Phenotypic expression of X-linked retinoschisis in Chinese families with mutations in the RS1 gene.

Xu F, Xiang H, Jiang R, Dong F, Sui R. Xu F, et al. Among authors: sui r. Doc Ophthalmol. 2011 Aug;123(1):21-7. doi: 10.1007/s10633-011-9278-x. Epub 2011 Jun 24. Doc Ophthalmol. 2011. PMID: 21701876

3

Thirty-two years follow-up of X-linked juvenile retinoschisis in a Chinese patient with RS1 mutation.

Xu F, Sui R, Dong F. Xu F, et al. Among authors: sui r. Ophthalmic Genet. 2012 Jun;33(2):77-82. doi: 10.3109/13816810.2011.628359. Epub 2011 Dec 15. Ophthalmic Genet. 2012. PMID: 22171610

4

[Analysis of optical coherence tomography in early stage of optic neuritis in multiple sclerosis patients].

Cheng GW, Zhao JL, Liang Z, Zhong Y, Zhang H, Ma JM, Sui RF, Mao J. Cheng GW, et al. Zhonghua Yan Ke Za Zhi. 2011 Oct;47(10):913-9. Zhonghua Yan Ke Za Zhi. 2011. PMID: 22321502 Chinese.

5

Genetic and phenotypic characteristics of three Mainland Chinese families with choroideremia.

Zhou Q, Liu L, Xu F, Li H, Sergeev Y, Dong F, Jiang R, MacDonald I, Sui R. Zhou Q, et al. Among authors: sui r. Mol Vis. 2012;18:309-16. Epub 2012 Feb 3. Mol Vis. 2012. PMID: 22355242 Free PMC article.

6

Novel RPE65 mutations associated with Leber congenital amaurosis in Chinese patients.

Xu F, Dong Q, Liu L, Li H, Liang X, Jiang R, Sui R, Dong F. Xu F, et al. Among authors: sui r. Mol Vis. 2012;18:744-50. Epub 2012 Mar 28. Mol Vis. 2012. PMID: 22509104 Free PMC article.

7

Delayed visual recovery in pregnancy-associated thrombotic thrombocytopenic purpura with bilateral serous retinal detachment.

Zhao C, Qu Y, Sui R, Feng J, Gao J, Ma J, Jiang R, Li H. Zhao C, et al. Among authors: sui r. Doc Ophthalmol. 2013 Apr;126(2):163-9. doi: 10.1007/s10633-012-9365-7. Epub 2012 Dec 4. Doc Ophthalmol. 2013. PMID: 23208746

8

Novel PRPF31 mutations associated with Chinese autosomal dominant retinitis pigmentosa patients.

Xu F, Sui R, Liang X, Li H, Jiang R, Dong F. Xu F, et al. Among authors: sui r. Mol Vis. 2012;18:3021-xxx. Epub 2012 Dec 14. Mol Vis. 2012. PMID: 23288994 Free PMC article.

9

[Clinical features of congenital stationary night blindness].

Li H, Liu LY, Xu HY, Xu F, Jiang RX, Sui RF. Li H, et al. Zhonghua Yi Xue Za Zhi. 2012 Oct 23;92(39):2756-9. Zhonghua Yi Xue Za Zhi. 2012. PMID: 23290162 Chinese.

10

Phenotypic characterization of a Chinese family with autosomal dominant cone-rod dystrophy related to GUCY2D.

Xu F, Dong F, Li H, Li X, Jiang R, Sui R. Xu F, et al. Among authors: sui r. Doc Ophthalmol. 2013 Jun;126(3):233-40. doi: 10.1007/s10633-013-9383-0. Epub 2013 May 21. Doc Ophthalmol. 2013. PMID: 23686677

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