Dong F - 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: dong f. Retina. 2019 Oct;39(10):2040-2052. doi: 10.1097/IAE.0000000000002242. Retina. 2019. PMID: 30134391

2

[Relationship between the classification of diabetic macular edema and its related factors].

Liu LY, Dong FT, Li H. Liu LY, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007 Dec;29(6):797-802. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007. PMID: 18595262 Chinese.

3

Surgical management of epiretinal membrane in combined hamartomas of the retina and retinal pigment epithelium.

Zhang X, Dong F, Dai R, Yu W. Zhang X, et al. Among authors: dong f. Retina. 2010 Feb;30(2):305-9. Retina. 2010. PMID: 20175272

4

[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.

5

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: dong f. Doc Ophthalmol. 2011 Aug;123(1):21-7. doi: 10.1007/s10633-011-9278-x. Epub 2011 Jun 24. Doc Ophthalmol. 2011. PMID: 21701876

6

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: dong f. Ophthalmic Genet. 2012 Jun;33(2):77-82. doi: 10.3109/13816810.2011.628359. Epub 2011 Dec 15. Ophthalmic Genet. 2012. PMID: 22171610

7

[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.

8

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: dong f. Mol Vis. 2012;18:309-16. Epub 2012 Feb 3. Mol Vis. 2012. PMID: 22355242 Free PMC article.

9

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: dong q, dong f. Mol Vis. 2012;18:744-50. Epub 2012 Mar 28. Mol Vis. 2012. PMID: 22509104 Free PMC article.

10

Sequential bilateral central retinal artery occlusion as the primary manifestation of systemic lupus erythematosus.

Zou X, Zhuang Y, Dong FT, Zhang F, Chen YX. Zou X, et al. Among authors: dong ft. Chin Med J (Engl). 2012 Apr;125(8):1517-9. Chin Med J (Engl). 2012. PMID: 22613664

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