Bird AC - Search Results

1

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

Moore AT, Fitzke FW, Kemp CM, Arden GB, Keen TJ, Inglehearn CF, Bhattacharya SS, Bird AC. Moore AT, et al. Among authors: bird ac. Br J Ophthalmol. 1992 Aug;76(8):465-9. doi: 10.1136/bjo.76.8.465. Br J Ophthalmol. 1992. PMID: 1390527 Free PMC article.

2

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

Chakarova CF, Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS. Chakarova CF, et al. Among authors: bird ac. Hum Mol Genet. 2002 Jan 1;11(1):87-92. doi: 10.1093/hmg/11.1.87. Hum Mol Genet. 2002. PMID: 11773002

3

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

4

Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy.

Steinmetz RL, Polkinghorne PC, Fitzke FW, Kemp CM, Bird AC. Steinmetz RL, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 1992 Apr;33(5):1633-6. Invest Ophthalmol Vis Sci. 1992. PMID: 1559761

5

Long-term effect of acetazolamide in a patient with retinitis pigmentosa.

Chen JC, Fitzke FW, Bird AC. Chen JC, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 1990 Sep;31(9):1914-8. Invest Ophthalmol Vis Sci. 1990. PMID: 2211037

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

A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa.

Lyness AL, Ernst W, Quinlan MP, Clover GM, Arden GB, Carter RM, Bird AC, Parker JA. Lyness AL, et al. Among authors: bird ac. Br J Ophthalmol. 1985 May;69(5):326-39. doi: 10.1136/bjo.69.5.326. Br J Ophthalmol. 1985. PMID: 3873253 Free PMC article.

8

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.

9

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

10

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

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