Holder GE - Search Results

1

Clinical Features of a Retinopathy Associated With a Dominant Allele of the RGR Gene.

Ba-Abbad R, Leys M, Wang X, Chakarova C, Waseem N, Carss KJ, Raymond FL, Bujakowska KM, Pierce EA, Mahroo OA, Mohamed MD, Holder GE, Hummel M, Arno G, Webster AR. Ba-Abbad R, et al. Among authors: holder ge. Invest Ophthalmol Vis Sci. 2018 Oct 1;59(12):4812-4820. doi: 10.1167/iovs.18-25061. Invest Ophthalmol Vis Sci. 2018. PMID: 30347075 Free PMC article.

2

Visual loss from central serous retinopathy in systemic lupus erythematosus.

Eckstein MB, Spalton DJ, Holder G. Eckstein MB, et al. Br J Ophthalmol. 1993 Sep;77(9):607-9. doi: 10.1136/bjo.77.9.607. Br J Ophthalmol. 1993. PMID: 8218067 Free PMC article. No abstract available.

3

Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus.

Lois N, Holder GE, Fitzke FW, Plant C, Bird AC. Lois N, et al. Among authors: holder ge. Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2668-75. Invest Ophthalmol Vis Sci. 1999. PMID: 10509664

4

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.

Gregory-Evans K, Kelsell RE, Gregory-Evans CY, Downes SM, Fitzke FW, Holder GE, Simunovic M, Mollon JD, Taylor R, Hunt DM, Bird AC, Moore AT. Gregory-Evans K, et al. Among authors: holder ge. Ophthalmology. 2000 Jan;107(1):55-61. doi: 10.1016/s0161-6420(99)00038-x. Ophthalmology. 2000. PMID: 10647719

5

Electrophysiological and psychophysical differences between early- and late-onset strabismic amblyopia.

Davis AR, Sloper JJ, Neveu MM, Hogg CR, Morgan MJ, Holder GE. Davis AR, et al. Among authors: holder ge. Invest Ophthalmol Vis Sci. 2003 Feb;44(2):610-7. doi: 10.1167/iovs.02-0240. Invest Ophthalmol Vis Sci. 2003. PMID: 12556390

6

An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.

Michaelides M, Johnson S, Tekriwal AK, Holder GE, Bellmann C, Kinning E, Woodruff G, Trembath RC, Hunt DM, Moore AT. Michaelides M, et al. Among authors: holder ge. Invest Ophthalmol Vis Sci. 2003 May;44(5):2178-83. doi: 10.1167/iovs.02-1094. Invest Ophthalmol Vis Sci. 2003. PMID: 12714659

7

Isolated foveal retinoschisis as a cause of visual loss in young females.

Kabanarou SA, Holder GE, Bird AC, Webster AR, Stanga PE, Vickers S, Harney BA. Kabanarou SA, et al. Among authors: holder ge. Br J Ophthalmol. 2003 Jun;87(6):801-3. doi: 10.1136/bjo.87.6.801. Br J Ophthalmol. 2003. PMID: 12770998 Free PMC article. No abstract available.

8

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss.

Francis PJ, Johnson S, Edmunds B, Kelsell RE, Sheridan E, Garrett C, Holder GE, Hunt DM, Moore AT. Francis PJ, et al. Among authors: holder ge. Br J Ophthalmol. 2003 Jul;87(7):893-8. doi: 10.1136/bjo.87.7.893. Br J Ophthalmol. 2003. PMID: 12812894 Free PMC article.

9

Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, El-Amir A, Bailey C, Egan CA, Fitzke FW, Webster AR, Bird AC, Holder GE. Robson AG, et al. Among authors: holder ge. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3544-50. doi: 10.1167/iovs.02-1278. Invest Ophthalmol Vis Sci. 2003. PMID: 12882805

10

An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene.

Dandekar SS, Ebenezer ND, Grayson C, Chapple JP, Egan CA, Holder GE, Jenkins SA, Fitzke FW, Cheetham ME, Webster AR, Hardcastle AJ. Dandekar SS, et al. Among authors: holder ge. Br J Ophthalmol. 2004 Apr;88(4):528-32. doi: 10.1136/bjo.2003.027979. Br J Ophthalmol. 2004. PMID: 15031171 Free PMC article.

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