Holder GE - Search Results

1

Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3).

Arno G, Holder GE, Chakarova C, Kohl S, Pontikos N, Fiorentino A, Plagnol V, Cheetham ME, Hardcastle AJ, Webster AR, Michaelides M; UK Inherited Retinal Disease Consortium. Arno G, et al. Among authors: holder ge. JAMA Ophthalmol. 2016 Aug 1;134(8):924-7. doi: 10.1001/jamaophthalmol.2016.1543. JAMA Ophthalmol. 2016. PMID: 27281386

2

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.

Gregory-Evans K, Kelsell RE, Gregory-Evans CY, Downes SM, Fitzke FW, Holder GE, Simunovic M, Mollon JD, Taylor R, Hunt DM, Bird AC, Moore AT. Gregory-Evans K, et al. Among authors: holder ge. Ophthalmology. 2000 Jan;107(1):55-61. doi: 10.1016/s0161-6420(99)00038-x. Ophthalmology. 2000. PMID: 10647719

3

Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1.

Downes SM, Holder GE, Fitzke FW, Payne AM, Warren MJ, Bhattacharya SS, Bird AC. Downes SM, et al. Among authors: holder ge. Arch Ophthalmol. 2001 Jan;119(1):96-105. Arch Ophthalmol. 2001. PMID: 11146732

4

Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 gene.

Stanga PE, Chong NH, Reck AC, Hardcastle AJ, Holder GE. Stanga PE, et al. Among authors: holder ge. Retina. 2001;21(1):78-80. doi: 10.1097/00006982-200102000-00019. Retina. 2001. PMID: 11217940 No abstract available.

5

An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.

Michaelides M, Johnson S, Tekriwal AK, Holder GE, Bellmann C, Kinning E, Woodruff G, Trembath RC, Hunt DM, Moore AT. Michaelides M, et al. Among authors: holder ge. Invest Ophthalmol Vis Sci. 2003 May;44(5):2178-83. doi: 10.1167/iovs.02-1094. Invest Ophthalmol Vis Sci. 2003. PMID: 12714659

6

Isolated foveal retinoschisis as a cause of visual loss in young females.

Kabanarou SA, Holder GE, Bird AC, Webster AR, Stanga PE, Vickers S, Harney BA. Kabanarou SA, et al. Among authors: holder ge. Br J Ophthalmol. 2003 Jun;87(6):801-3. doi: 10.1136/bjo.87.6.801. Br J Ophthalmol. 2003. PMID: 12770998 Free PMC article. No abstract available.

7

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: holder ge. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3544-50. doi: 10.1167/iovs.02-1278. Invest Ophthalmol Vis Sci. 2003. PMID: 12882805

8

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections.

Zito I, Downes SM, Patel RJ, Cheetham ME, Ebenezer ND, Jenkins SA, Bhattacharya SS, Webster AR, Holder GE, Bird AC, Bamiou DE, Hardcastle AJ. Zito I, et al. Among authors: holder ge. J Med Genet. 2003 Aug;40(8):609-15. doi: 10.1136/jmg.40.8.609. J Med Genet. 2003. PMID: 12920075 Free PMC article. No abstract available.

9

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2).

Michaelides M, Aligianis IA, Holder GE, Simunovic M, Mollon JD, Maher ER, Hunt DM, Moore AT. Michaelides M, et al. Among authors: holder ge. Br J Ophthalmol. 2003 Nov;87(11):1317-20. doi: 10.1136/bjo.87.11.1317. Br J Ophthalmol. 2003. PMID: 14609822 Free PMC article.

10

Oligocone trichromacy: a rare and unusual cone dysfunction syndrome.

Michaelides M, Holder GE, Bradshaw K, Hunt DM, Mollon JD, Moore AT. Michaelides M, et al. Among authors: holder ge. Br J Ophthalmol. 2004 Apr;88(4):497-500. doi: 10.1136/bjo.2003.028142. Br J Ophthalmol. 2004. PMID: 15031164 Free PMC article.

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