Bird AC - Search Results

1

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: bird ac. Ophthalmology. 2000 Jan;107(1):55-61. doi: 10.1016/s0161-6420(99)00038-x. Ophthalmology. 2000. PMID: 10647719

2

Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.

Bessant DA, Holder GE, Fitzke FW, Payne AM, Bhattacharya SS, Bird AC. Bessant DA, et al. Among authors: bird ac. Arch Ophthalmol. 2003 Jun;121(6):793-802. doi: 10.1001/archopht.121.6.793. Arch Ophthalmol. 2003. PMID: 12796249

3

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: bird ac. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3544-50. doi: 10.1167/iovs.02-1278. Invest Ophthalmol Vis Sci. 2003. PMID: 12882805

4

Phenotypic variation in enhanced S-cone syndrome.

Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE. Audo I, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93. doi: 10.1167/iovs.05-1629. Invest Ophthalmol Vis Sci. 2008. PMID: 18436841

5

Acute macular neuroretinopathy.

Miller MH, Spalton DJ, Fitzke FW, Bird AC. Miller MH, et al. Among authors: bird ac. Ophthalmology. 1989 Feb;96(2):265-9. doi: 10.1016/s0161-6420(89)32906-x. Ophthalmology. 1989. PMID: 2704546

6

The dark choroid in posterior retinal dystrophies.

Uliss AE, Moore AT, Bird AC. Uliss AE, et al. Among authors: bird ac. Ophthalmology. 1987 Nov;94(11):1423-7. doi: 10.1016/s0161-6420(87)33270-1. Ophthalmology. 1987. PMID: 3684216

7

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.

Evans K, al-Maghtheh M, Fitzke FW, Moore AT, Jay M, Inglehearn CF, Arden GB, Bird AC. Evans K, et al. Among authors: bird ac. Br J Ophthalmol. 1995 Sep;79(9):841-6. doi: 10.1136/bjo.79.9.841. Br J Ophthalmol. 1995. PMID: 7488604 Free PMC article.

8

Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS gene.

Kim RY, Dollfus H, Keen TJ, Fitzke FW, Arden GB, Bhattacharya SS, Bird AC. Kim RY, et al. Among authors: bird ac. Arch Ophthalmol. 1995 Apr;113(4):451-5. doi: 10.1001/archopht.1995.01100040067029. Arch Ophthalmol. 1995. PMID: 7710395

9

Cutaneous melanoma-associated retinopathy.

Kim RY, Retsas S, Fitzke FW, Arden GB, Bird AC. Kim RY, et al. Among authors: bird ac. Ophthalmology. 1994 Nov;101(11):1837-43. doi: 10.1016/s0161-6420(94)31092-x. Ophthalmology. 1994. PMID: 7800366

10

Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.

Evans K, Duvall-Young J, Fitzke FW, Arden GB, Bhattacharya SS, Bird AC. Evans K, et al. Among authors: bird ac. Arch Ophthalmol. 1995 Feb;113(2):195-201. doi: 10.1001/archopht.1995.01100020079033. Arch Ophthalmol. 1995. PMID: 7864751

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