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534 results

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Page 1
Unilateral BEST1-Associated Retinopathy.
Arora R, Khan K, Kasilian ML, Strauss RW, Holder GE, Robson AG, Thompson DA, Moore AT, Michaelides M. Arora R, et al. Among authors: thompson da. Am J Ophthalmol. 2016 Sep;169:24-32. doi: 10.1016/j.ajo.2016.05.024. Epub 2016 Jun 7. Am J Ophthalmol. 2016. PMID: 27287821 Free PMC article.
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.
Visual-evoked potential evidence of chiasmal hypoplasia.
Thompson DA, Kriss A, Chong K, Harris C, Russell-Eggitt I, Shawkat F, Neville BG, Aclimandos W, Taylor DS. Thompson DA, et al. Ophthalmology. 1999 Dec;106(12):2354-61. doi: 10.1016/S0161-6420(99)90539-0. Ophthalmology. 1999. PMID: 10599670
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. Among authors: thompson da. 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.
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. Among authors: thompson da. 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
Macular dystrophy in Kabuki syndrome: a new clinical feature?
Lindfield D, Griffiths MF, Thompson DA, Moore AT. Lindfield D, et al. Among authors: thompson da. J Pediatr Ophthalmol Strabismus. 2011 Jul 19;48 Online:e40-2. doi: 10.3928/01913913-20110712-04. J Pediatr Ophthalmol Strabismus. 2011. PMID: 21766738
Childhood-onset autosomal recessive bestrophinopathy.
Borman AD, Davidson AE, O'Sullivan J, Thompson DA, Robson AG, De Baere E, Black GC, Webster AR, Holder GE, Leroy BP, Manson FD, Moore AT. Borman AD, et al. Among authors: thompson da. Arch Ophthalmol. 2011 Aug;129(8):1088-93. doi: 10.1001/archophthalmol.2011.197. Arch Ophthalmol. 2011. PMID: 21825197 No abstract available.
534 results