Russell-Eggitt I - Search Results

1

An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy.

Henderson RH, Waseem N, Searle R, van der Spuy J, Russell-Eggitt I, Bhattacharya SS, Thompson DA, Holder GE, Cheetham ME, Webster AR, Moore AT. Henderson RH, et al. Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5684-9. doi: 10.1167/iovs.07-0207. Invest Ophthalmol Vis Sci. 2007. PMID: 18055820 Free article.

2

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

Henderson RH, Mackay DS, Li Z, Moradi P, Sergouniotis P, Russell-Eggitt I, Thompson DA, Robson AG, Holder GE, Webster AR, Moore AT. Henderson RH, et al. Br J Ophthalmol. 2011 Jun;95(6):811-7. doi: 10.1136/bjo.2010.186882. Epub 2010 Oct 17. Br J Ophthalmol. 2011. PMID: 20956273

3

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

Tan MH, Mackay DS, Cowing J, Tran HV, Smith AJ, Wright GA, Dev-Borman A, Henderson RH, Moradi P, Russell-Eggitt I, MacLaren RE, Robson AG, Cheetham ME, Thompson DA, Webster AR, Michaelides M, Ali RR, Moore AT. Tan MH, et al. PLoS One. 2012;7(3):e32330. doi: 10.1371/journal.pone.0032330. Epub 2012 Mar 6. PLoS One. 2012. PMID: 22412862 Free PMC article.

4

The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype.

Hull S, Arno G, Plagnol V, Chamney S, Russell-Eggitt I, Thompson D, Ramsden SC, Black GC, Robson AG, Holder GE, Moore AT, Webster AR. Hull S, et al. Invest Ophthalmol Vis Sci. 2014 Sep 30;55(10):6934-44. doi: 10.1167/iovs.14-14715. Invest Ophthalmol Vis Sci. 2014. PMID: 25270190

5

The optokinetic response differences between congenital profound and nonprofound unilateral visual deprivation.

Shawkat FS, Harris CM, Taylor DS, Thompson DA, Russell-Eggitt I, Kriss A. Shawkat FS, et al. Ophthalmology. 1995 Nov;102(11):1615-22. doi: 10.1016/s0161-6420(95)30819-6. Ophthalmology. 1995. PMID: 9098252

6

Incidence and patterns of detection and management of childhood-onset hereditary retinal disorders in the UK.

Hamblion EL, Moore AT, Rahi JS; British Childhood Onset Hereditary Retinal Disorders Network. Hamblion EL, et al. Br J Ophthalmol. 2012 Mar;96(3):360-5. doi: 10.1136/bjo.2010.201178. Epub 2011 Jun 7. Br J Ophthalmol. 2012. PMID: 21653210

7

A mutant connexin50 with enhanced hemichannel function leads to cell death.

Minogue PJ, Tong JJ, Arora A, Russell-Eggitt I, Hunt DM, Moore AT, Ebihara L, Beyer EC, Berthoud VM. Minogue PJ, et al. Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5837-45. doi: 10.1167/iovs.09-3759. Epub 2009 Aug 13. Invest Ophthalmol Vis Sci. 2009. PMID: 19684000 Free PMC article.

8

Visual acuity in unilateral cataract.

Thompson DA, Møller H, Russell-Eggitt I, Kriss A. Thompson DA, et al. Br J Ophthalmol. 1996 Sep;80(9):794-8. doi: 10.1136/bjo.80.9.794. Br J Ophthalmol. 1996. PMID: 8942375 Free PMC article. Clinical Trial.

9

Modulation of amblyopia therapy following early surgery for unilateral congenital cataracts.

Lloyd IC, Dowler JG, Kriss A, Speedwell L, Thompson DA, Russell-Eggitt I, Taylor D. Lloyd IC, et al. Br J Ophthalmol. 1995 Sep;79(9):802-6. doi: 10.1136/bjo.79.9.802. Br J Ophthalmol. 1995. PMID: 7488596 Free PMC article.

10

Retinal on-pathway deficit in congenital disorder of glycosylation due to phosphomannomutase deficiency.

Thompson DA, Lyons RJ, Liasis A, Russell-Eggitt I, Jägle H, Grünewald S. Thompson DA, et al. Arch Ophthalmol. 2012 Jun;130(6):712-9. doi: 10.1001/archophthalmol.2012.130. Arch Ophthalmol. 2012. PMID: 22801829

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