Sui R - Search Results

1

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. Among authors: sui r. Retina. 2019 Oct;39(10):2040-2052. doi: 10.1097/IAE.0000000000002242. Retina. 2019. PMID: 30134391

2

[Clinical application and observation of silicone oil in complicated retinal detachment].

Sui R, Dong F, Zhang C. Sui R, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1996 Oct;18(5):380-3. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1996. PMID: 9388966 Chinese.

3

Surgical management of macular epiretinal membranes.

Dong F, Sui R. Dong F, et al. Among authors: sui r. Yan Ke Xue Bao. 1996 Sep;12(3):140-4. Yan Ke Xue Bao. 1996. PMID: 9639840

4

R555W mutation of TGFbetaI related to granular corneal dystrophy in Chinese patients.

Hu L, Xu F, Ma WJ, Zhang H, Sui RF. Hu L, et al. Chin Med J (Engl). 2009 Nov 20;122(22):2691-4. Chin Med J (Engl). 2009. PMID: 19951597

5

Unique phenotype in a Chinese family pedigree: ectopia lentis with varicose great saphenous vein.

Shen W, Fu Q, Sui R, Wu J, Liu L. Shen W, et al. Among authors: sui r. Eye (Lond). 2010 Oct;24(10):1614-7. doi: 10.1038/eye.2010.82. Epub 2010 Jun 4. Eye (Lond). 2010. PMID: 20523356

6

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

7

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

8

[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.

9

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.

10

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.

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