Webster AR - Search Results

1

CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History.

de Guimaraes TAC, Robson AG, de Guimaraes IMC, Laich Y, Aychoua N, Wright G, Kalitzeos A, Mahroo OA, Webster AR, Michaelides M. de Guimaraes TAC, et al. Among authors: webster ar. Invest Ophthalmol Vis Sci. 2024 Jul 1;65(8):27. doi: 10.1167/iovs.65.8.27. Invest Ophthalmol Vis Sci. 2024. PMID: 39017633 Free PMC article.

2

Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, El-Amir A, Bailey C, Egan CA, Fitzke FW, Webster AR, Bird AC, Holder GE. Robson AG, et al. Among authors: webster ar. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3544-50. doi: 10.1167/iovs.02-1278. Invest Ophthalmol Vis Sci. 2003. PMID: 12882805

3

Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.

Kabanarou SA, Holder GE, Fitzke FW, Bird AC, Webster AR. Kabanarou SA, et al. Among authors: webster ar. Br J Ophthalmol. 2004 Aug;88(8):1018-22. doi: 10.1136/bjo.2003.033555. Br J Ophthalmol. 2004. PMID: 15258017 Free PMC article.

4

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: webster ar. Br J Ophthalmol. 2005 Mar;89(3):332-9. doi: 10.1136/bjo.2004.050567. Br J Ophthalmol. 2005. PMID: 15722315 Free PMC article.

5

Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.

Ebenezer ND, Michaelides M, Jenkins SA, Audo I, Webster AR, Cheetham ME, Stockman A, Maher ER, Ainsworth JR, Yates JR, Bradshaw K, Holder GE, Moore AT, Hardcastle AJ. Ebenezer ND, et al. Among authors: webster ar. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1891-8. doi: 10.1167/iovs.04-1482. Invest Ophthalmol Vis Sci. 2005. PMID: 15914600

6

Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.

Michaelides M, Wilkie SE, Jenkins S, Holder GE, Hunt DM, Moore AT, Webster AR. Michaelides M, et al. Among authors: webster ar. Ophthalmology. 2005 Aug;112(8):1442-7. doi: 10.1016/j.ophtha.2005.02.024. Ophthalmology. 2005. PMID: 15953638

7

Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, Saihan Z, Jenkins SA, Fitzke FW, Bird AC, Webster AR, Holder GE. Robson AG, et al. Among authors: webster ar. Br J Ophthalmol. 2006 Apr;90(4):472-9. doi: 10.1136/bjo.2005.082487. Br J Ophthalmol. 2006. PMID: 16547330 Free PMC article.

8

Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction.

Michaelides M, Jenkins SA, Brantley MA Jr, Andrews RM, Waseem N, Luong V, Gregory-Evans K, Bhattacharya SS, Fitzke FW, Webster AR. Michaelides M, et al. Among authors: webster ar. Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3085-97. doi: 10.1167/iovs.05-1600. Invest Ophthalmol Vis Sci. 2006. PMID: 16799055

9

Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.

Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, Jenkins SA, Mester V, Bird AC, Robson AG, Holder GE, Moore AT, Hunt DM, Webster AR. Wu H, et al. Among authors: webster ar. Am J Hum Genet. 2006 Sep;79(3):574-9. doi: 10.1086/507568. Epub 2006 Jul 24. Am J Hum Genet. 2006. PMID: 16909397 Free PMC article.

10

Autofluorescence findings in acute exudative polymorphous vitelliform maculopathy.

Vaclavik V, Ooi KG, Bird AC, Robson AG, Holder GE, Webster AR. Vaclavik V, et al. Among authors: webster ar. Arch Ophthalmol. 2007 Feb;125(2):274-7. doi: 10.1001/archopht.125.2.274. Arch Ophthalmol. 2007. PMID: 17296907 No abstract available.

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