Bird A - Search Results

1

An analysis of ABCR mutations in British patients with recessive retinal dystrophies.

Papaioannou M, Ocaka L, Bessant D, Lois N, Bird A, Payne A, Bhattacharya S. Papaioannou M, et al. Among authors: bird a. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):16-9. Invest Ophthalmol Vis Sci. 2000. PMID: 10634594 Free article.

2

Mutations in the gene coding for the pre-mRNA splicing factor, PRPF31, in patients with autosomal dominant retinitis pigmentosa.

Waseem NH, Vaclavik V, Webster A, Jenkins SA, Bird AC, Bhattacharya SS. Waseem NH, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1330-4. doi: 10.1167/iovs.06-0963. Invest Ophthalmol Vis Sci. 2007. PMID: 17325180

3

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies.

Payne AM, Downes SM, Bessant DA, Plant C, Moore T, Bird AC, Bhattacharya SS. Payne AM, et al. Among authors: bird ac. J Med Genet. 1999 Sep;36(9):691-3. J Med Genet. 1999. PMID: 10507726 Free PMC article.

4

NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies.

Bessant DA, Payne AM, Plant C, Bird AC, Swaroop A, Bhattacharya SS. Bessant DA, et al. Among authors: bird ac. Eur J Hum Genet. 2000 Oct;8(10):783-7. doi: 10.1038/sj.ejhg.5200538. Eur J Hum Genet. 2000. PMID: 11039579

5

RP1 protein truncating mutations predominate at the RP1 adRP locus.

Payne A, Vithana E, Khaliq S, Hameed A, Deller J, Abu-Safieh L, Kermani S, Leroy BP, Mehdi SQ, Moore AT, Bird AC, Bhattacharya SS. Payne A, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 2000 Dec;41(13):4069-73. Invest Ophthalmol Vis Sci. 2000. PMID: 11095597

6

Spectrum of mutations in USH2A in British patients with Usher syndrome type II.

Leroy BP, Aragon-Martin JA, Weston MD, Bessant DA, Willis C, Webster AR, Bird AC, Kimberling WJ, Payne AM, Bhattacharya SS. Leroy BP, et al. Among authors: bird ac. Exp Eye Res. 2001 May;72(5):503-9. doi: 10.1006/exer.2000.0978. Exp Eye Res. 2001. PMID: 11311042

7

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

8

Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?

Vithana EN, Abu-Safieh L, Pelosini L, Winchester E, Hornan D, Bird AC, Hunt DM, Bustin SA, Bhattacharya SS. Vithana EN, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4204-9. doi: 10.1167/iovs.03-0253. Invest Ophthalmol Vis Sci. 2003. PMID: 14507862

9

The role of molecular genetics in the prenatal diagnosis of retinal dystrophies.

Evans K, Gregory CY, Fryer A, Whittaker J, Duvall-Young J, Bird AC, Jay MR, Bhattacharya SS. Evans K, et al. Among authors: bird ac. Eye (Lond). 1995;9 ( Pt 1):24-8. doi: 10.1038/eye.1995.3. Eye (Lond). 1995. PMID: 7713246

10

Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy.

Holz FG, Evans K, Gregory CY, Bhattacharya S, Bird AC. Holz FG, et al. Among authors: bird ac. Arch Ophthalmol. 1995 Feb;113(2):178-84. doi: 10.1001/archopht.1995.01100020062029. Arch Ophthalmol. 1995. PMID: 7864750

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