EY10539/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1995	4
1996	3
1997	6
1998	1
1999	3
2000	2
2001	8
2004	3
2008	1
2009	1
2024	0

1

Molecular genetics of age-related macular degeneration.

Stone EM, Sheffield VC, Hageman GS. Stone EM, et al. Hum Mol Genet. 2001 Oct 1;10(20):2285-92. doi: 10.1093/hmg/10.20.2285. Hum Mol Genet. 2001. PMID: 11673412 Review.

2

Pediatric canalicular tear repairs--revisiting the pigtail probe.

Forbes BJ, Katowitz WR, Binenbaum G. Forbes BJ, et al. J AAPOS. 2008 Oct;12(5):518-20. doi: 10.1016/j.jaapos.2008.05.006. Epub 2008 Jul 14. J AAPOS. 2008. PMID: 18620879 Free PMC article.

3

Fluctuating vision in Best disease.

Park DW, Polk TD, Stone EM. Park DW, et al. Arch Ophthalmol. 1997 Nov;115(11):1469-70. doi: 10.1001/archopht.1997.01100160639022. Arch Ophthalmol. 1997. PMID: 9366684 No abstract available.

4

An analysis of allelic variation in the ABCA4 gene.

Webster AR, Héon E, Lotery AJ, Vandenburgh K, Casavant TL, Oh KT, Beck G, Fishman GA, Lam BL, Levin A, Heckenlively JR, Jacobson SG, Weleber RG, Sheffield VC, Stone EM. Webster AR, et al. Invest Ophthalmol Vis Sci. 2001 May;42(6):1179-89. Invest Ophthalmol Vis Sci. 2001. PMID: 11328725

5

Congenital trigemino-abducens synkinesis in a neonate.

Ghodasra DH, Nallasamy S, Binenbaum G. Ghodasra DH, et al. J AAPOS. 2009 Aug;13(4):417-8. doi: 10.1016/j.jaapos.2009.04.005. J AAPOS. 2009. PMID: 19683197

6

Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene.

Piguet B, Héon E, Munier FL, Grounauer PA, Niemeyer G, Butler N, Schorderet DF, Sheffield VC, Stone EM. Piguet B, et al. Ophthalmic Genet. 1996 Dec;17(4):175-86. doi: 10.3109/13816819609057891. Ophthalmic Genet. 1996. PMID: 9010868

7

Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14.

Brown DM, Graemiger RA, Hergersberg M, Schinzel A, Messmer EP, Niemeyer G, Schneeberger SA, Streb LM, Taylor CM, Kimura AE, et al. Brown DM, et al. Arch Ophthalmol. 1995 May;113(5):671-5. doi: 10.1001/archopht.1995.01100050139045. Arch Ophthalmol. 1995. PMID: 7748141

8

Clinical phenotype as a prognostic factor in Stargardt disease.

Oh KT, Weleber RG, Oh DM, Billingslea AM, Rosenow J, Stone EM. Oh KT, et al. Retina. 2004 Apr;24(2):254-62. doi: 10.1097/00006982-200404000-00011. Retina. 2004. PMID: 15097887

9

Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.

Swain PK, Chen S, Wang QL, Affatigato LM, Coats CL, Brady KD, Fishman GA, Jacobson SG, Swaroop A, Stone E, Sieving PA, Zack DJ. Swain PK, et al. Neuron. 1997 Dec;19(6):1329-36. doi: 10.1016/s0896-6273(00)80423-7. Neuron. 1997. PMID: 9427255 Free article.

10

Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1).

Brown J Jr, Fingert JH, Taylor CM, Lake M, Sheffield VC, Stone EM. Brown J Jr, et al. Arch Ophthalmol. 1997 Jan;115(1):95-9. doi: 10.1001/archopht.1997.01100150097016. Arch Ophthalmol. 1997. PMID: 9006432

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