Bird AC - Search Results

1

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.

Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, Bhattacharya SS, Bird AC, Kaplan J, Maumenee IH. Dharmaraj S, et al. Among authors: bird ac. Arch Ophthalmol. 2004 Jul;122(7):1029-37. doi: 10.1001/archopht.122.7.1029. Arch Ophthalmol. 2004. PMID: 15249368

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

Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families.

Downes SM, Fitzke FW, Holder GE, Payne AM, Bessant DA, Bhattacharya SS, Bird AC. Downes SM, et al. Among authors: bird ac. Arch Ophthalmol. 1999 Oct;117(10):1373-83. doi: 10.1001/archopht.117.10.1373. Arch Ophthalmol. 1999. PMID: 10532447

4

Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1.

Downes SM, Holder GE, Fitzke FW, Payne AM, Warren MJ, Bhattacharya SS, Bird AC. Downes SM, et al. Among authors: bird ac. Arch Ophthalmol. 2001 Jan;119(1):96-105. Arch Ophthalmol. 2001. PMID: 11146732

5

Fundus autofluorescence in patients with leber congenital amaurosis.

Scholl HP, Chong NH, Robson AG, Holder GE, Moore AT, Bird AC. Scholl HP, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2747-52. doi: 10.1167/iovs.03-1208. Invest Ophthalmol Vis Sci. 2004. PMID: 15277500

6

Novel phenotypic and genotypic findings in X-linked retinoschisis.

Tsang SH, Vaclavik V, Bird AC, Robson AG, Holder GE. Tsang SH, et al. Among authors: bird ac. Arch Ophthalmol. 2007 Feb;125(2):259-67. doi: 10.1001/archopht.125.2.259. Arch Ophthalmol. 2007. PMID: 17296904 Free PMC article.

7

Clinical variations in assessment of bull's-eye maculopathy.

Kurz-Levin MM, Halfyard AS, Bunce C, Bird AC, Holder GE. Kurz-Levin MM, et al. Among authors: bird ac. Arch Ophthalmol. 2002 May;120(5):567-75. doi: 10.1001/archopht.120.5.567. Arch Ophthalmol. 2002. PMID: 12003605

8

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.

Lois N, Holder GE, Bunce C, Fitzke FW, Bird AC. Lois N, et al. Among authors: bird ac. Arch Ophthalmol. 2001 Mar;119(3):359-69. doi: 10.1001/archopht.119.3.359. Arch Ophthalmol. 2001. PMID: 11231769

9

Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1.

Downes SM, Payne AM, Kelsell RE, Fitzke FW, Holder GE, Hunt DM, Moore AT, Bird AC. Downes SM, et al. Among authors: bird ac. Arch Ophthalmol. 2001 Nov;119(11):1667-73. doi: 10.1001/archopht.119.11.1667. Arch Ophthalmol. 2001. PMID: 11709018

10

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

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