Dong F - Search Results

1

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.

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

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

4

Locally produced insulin-like growth factor-1 by orbital fibroblasts as implicative pathogenic factor rather than systemically circulated IGF-1 for patients with thyroid-associated ophthalmopathy.

Song D, Wang R, Zhong Y, Li W, Li H, Dong F. Song D, et al. Among authors: dong f. Graefes Arch Clin Exp Ophthalmol. 2012 Mar;250(3):433-40. doi: 10.1007/s00417-011-1876-5. Epub 2011 Dec 9. Graefes Arch Clin Exp Ophthalmol. 2012. PMID: 22159761

5

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

6

[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.

7

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.

8

A novel splice site mutation in the COL4A5 gene in a Chinese female patient with rare ocular abnormalities.

Zhao C, Wang F, Zhang Y, Wen Y, Su Y, Zhang C, Sui R, Xu F, Ding J, Dong F. Zhao C, et al. Among authors: dong f. Mol Vis. 2012;18:2205-12. Epub 2012 Aug 8. Mol Vis. 2012. PMID: 22919268 Free PMC article.

9

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: dong f. Mol Vis. 2012;18:3021-xxx. Epub 2012 Dec 14. Mol Vis. 2012. PMID: 23288994 Free PMC article.

10

[Progress in the studies of molecular genetics in Bietti crystalline corneoretinal dystrophy].

Xu F, Sui RF, Dong FT. Xu F, et al. Among authors: dong ft. Zhonghua Yan Ke Za Zhi. 2012 Oct;48(10):948-51. Zhonghua Yan Ke Za Zhi. 2012. PMID: 23302251 Review. Chinese.

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