Hutchinson A - Search Results

1

Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy.

Seddon JM, Afshari MA, Sharma S, Bernstein PS, Chong S, Hutchinson A, Petrukhin K, Allikmets R. Seddon JM, et al. Among authors: hutchinson a. Ophthalmology. 2001 Nov;108(11):2060-7. doi: 10.1016/s0161-6420(01)00777-1. Ophthalmology. 2001. PMID: 11713080

2

Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.

Allikmets R, Seddon JM, Bernstein PS, Hutchinson A, Atkinson A, Sharma S, Gerrard B, Li W, Metzker ML, Wadelius C, Caskey CT, Dean M, Petrukhin K. Allikmets R, et al. Among authors: hutchinson a. Hum Genet. 1999 Jun;104(6):449-53. doi: 10.1007/s004390050986. Hum Genet. 1999. PMID: 10453731

3

Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene.

Bernstein PS, Tammur J, Singh N, Hutchinson A, Dixon M, Pappas CM, Zabriskie NA, Zhang K, Petrukhin K, Leppert M, Allikmets R. Bernstein PS, et al. Among authors: hutchinson a. Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3331-6. Invest Ophthalmol Vis Sci. 2001. PMID: 11726641

4

Phenotype and genotype correlations in two best families.

Seddon JM, Sharma S, Chong S, Hutchinson A, Allikmets R, Adelman RA. Seddon JM, et al. Among authors: hutchinson a. Ophthalmology. 2003 Sep;110(9):1724-31. doi: 10.1016/S0161-6420(03)00575-X. Ophthalmology. 2003. PMID: 13129869

5

Macular pigment and visual acuity in Stargardt macular dystrophy.

Zhang X, Hargitai J, Tammur J, Hutchinson A, Allikmets R, Chang S, Gouras P. Zhang X, et al. Among authors: hutchinson a. Graefes Arch Clin Exp Ophthalmol. 2002 Oct;240(10):802-9. doi: 10.1007/s00417-002-0554-z. Epub 2002 Sep 14. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 12397427

6

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.

Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M. Allikmets R, et al. Among authors: hutchinson a. Science. 1997 Sep 19;277(5333):1805-7. doi: 10.1126/science.277.5333.1805. Science. 1997. PMID: 9295268

7

New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.

Simonelli F, Testa F, de Crecchio G, Rinaldi E, Hutchinson A, Atkinson A, Dean M, D'Urso M, Allikmets R. Simonelli F, et al. Among authors: hutchinson a. Invest Ophthalmol Vis Sci. 2000 Mar;41(3):892-7. Invest Ophthalmol Vis Sci. 2000. PMID: 10711710

8

Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration.

Sauer CG, White K, Stöhr H, Grimm T, Hutchinson A, Bernstein PS, Lewis RA, Simonelli F, Pauleikhoff D, Allikmets R, Weber BH. Sauer CG, et al. Among authors: hutchinson a. Br J Ophthalmol. 2001 Aug;85(8):969-75. doi: 10.1136/bjo.85.8.969. Br J Ophthalmol. 2001. PMID: 11466257 Free PMC article.

9

Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.

Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk LE, Seddon JM, Bernstein PS, Lewis RA, Tammur J, Yang Z, Li Y, Zhang H, Yashar BM, Liu J, Petrukhin K, Sieving PA, Allikmets R. Ayyagari R, et al. Among authors: hutchinson a. Ophthalmic Genet. 2001 Dec;22(4):233-9. doi: 10.1076/opge.22.4.233.2219. Ophthalmic Genet. 2001. PMID: 11803489

10

The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.

Zhang K, Kniazeva M, Hutchinson A, Han M, Dean M, Allikmets R. Zhang K, et al. Among authors: hutchinson a. Genomics. 1999 Sep 1;60(2):234-7. doi: 10.1006/geno.1999.5896. Genomics. 1999. PMID: 10486215 Free article.

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