Bird A - Search Results

1

Complement factor H deficiency in aged mice causes retinal abnormalities and visual dysfunction.

Coffey PJ, Gias C, McDermott CJ, Lundh P, Pickering MC, Sethi C, Bird A, Fitzke FW, Maass A, Chen LL, Holder GE, Luthert PJ, Salt TE, Moss SE, Greenwood J. Coffey PJ, et al. Among authors: bird a. Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16651-6. doi: 10.1073/pnas.0705079104. Epub 2007 Oct 5. Proc Natl Acad Sci U S A. 2007. PMID: 17921253 Free PMC article.

2

Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.

Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE. Bellmann C, et al. Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2355-60. doi: 10.1167/iovs.03-1090. Invest Ophthalmol Vis Sci. 2004. PMID: 15223817

3

Pathological and electrophysiological features of a canine cone-rod dystrophy in the miniature longhaired dachshund.

Turney C, Chong NH, Alexander RA, Hogg CR, Fleming L, Flack D, Barnett KC, Bird AC, Holder GE, Luthert PJ. Turney C, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4240-9. doi: 10.1167/iovs.04-0737. Invest Ophthalmol Vis Sci. 2007. PMID: 17724213

4

Macular and retinal dysfunction of unknown origin in adults with normal fundi: evidence for an autoimmune pathophysiology.

Mantel I, Ramchand KV, Holder GE, Ohbayashi M, Morohoshi K, Patel N, Toda M, Fitzke FW, Bird AC, Ono SJ. Mantel I, et al. Exp Mol Pathol. 2008 Apr;84(2):90-101. doi: 10.1016/j.yexmp.2007.10.006. Epub 2007 Nov 9. Exp Mol Pathol. 2008. PMID: 18255057

5

Correlation of functional impairment and morphological alterations in patients with group 2A idiopathic juxtafoveal retinal telangiectasia.

Schmitz-Valckenberg S, Fan K, Nugent A, Rubin GS, Peto T, Tufail A, Egan C, Bird AC, Fitzke FW. Schmitz-Valckenberg S, et al. Among authors: bird ac. Arch Ophthalmol. 2008 Mar;126(3):330-5. doi: 10.1001/archopht.126.3.330. Arch Ophthalmol. 2008. PMID: 18332311

6

Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope.

von Rückmann A, Fitzke FW, Bird AC. von Rückmann A, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 1997 Feb;38(2):478-86. Invest Ophthalmol Vis Sci. 1997. PMID: 9040481

7

A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.

Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT. Michaelides M, et al. Among authors: bird ac. Br J Ophthalmol. 2005 Feb;89(2):198-206. doi: 10.1136/bjo.2004.050773. Br J Ophthalmol. 2005. PMID: 15665353 Free PMC article.

8

A detailed phenotypic study of "cone dystrophy with supernormal rod ERG".

Michaelides M, Holder GE, Webster AR, Hunt DM, Bird AC, Fitzke FW, Mollon JD, Moore AT. Michaelides M, et al. Among authors: bird ac. Br J Ophthalmol. 2005 Mar;89(3):332-9. doi: 10.1136/bjo.2004.050567. Br J Ophthalmol. 2005. PMID: 15722315 Free PMC article.

9

Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry.

Robson AG, Moreland JD, Pauleikhoff D, Morrissey T, Holder GE, Fitzke FW, Bird AC, van Kuijk FJ. Robson AG, et al. Vision Res. 2003 Jul;43(16):1765-75. doi: 10.1016/s0042-6989(03)00280-3. Vision Res. 2003. PMID: 12818346 Free article.

10

Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa.

Robson AG, Egan C, Holder GE, Bird AC, Fitzke FW. Robson AG, et al. Adv Exp Med Biol. 2003;533:41-7. doi: 10.1007/978-1-4615-0067-4_6. Adv Exp Med Biol. 2003. PMID: 15180246 No abstract available.

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