PubMed

Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans.

Li Z, Sergouniotis PI, Michaelides M, Mackay DS, Wright GA, Devery S, Moore AT, Holder GE, Robson AG, Webster AR.

Am J Hum Genet. 2009 Nov;85(5):711-9. Epub 2009 Oct 29.PMID: 19878917 [PubMed - in process]Related articles

ISCEV standard for clinical visual evoked potentials (2009 update).

Odom JV, Bach M, Brigell M, Holder GE, McCulloch DL, Tormene AP, Vaegan.

Doc Ophthalmol. 2009 Oct 14. [Epub ahead of print]PMID: 19826847 [PubMed - as supplied by publisher]Related articles

Novel Mutations and Electrophysiologic Findings in RGS9- andR9AP-Associated Retinal Dysfunction (Bradyopsia).

Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR.

Ophthalmology. 2009 Oct 7. [Epub ahead of print]PMID: 19818506 [PubMed - as supplied by publisher]Related articles

Blue cone monochromacy: causative mutations and associated phenotypes.

Gardner JC, Michaelides M, Holder GE, Kanuga N, Webb TR, Mollon JD, Moore AT, Hardcastle AJ.

Mol Vis. 2009;15:876-84. Epub 2009 May 1.PMID: 19421413 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinicopathological case series of four patients with inherited macular disease.

Wickham L, Chen FK, Lewis GP, Uppal GS, Neveu MM, Wright GA, Robson AG, Webster AR, Grierson I, Hiscott P, Coffey PJ, Holder GE, Fisher SK, Da Cruz L.

Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3553-61. Epub 2009 Mar 11.PMID: 19279306 [PubMed - indexed for MEDLINE]Related articles

Electrodiagnostic assessment in optic nerve disease.

Holder GE, Gale RP, Acheson JF, Robson AG.

Curr Opin Neurol. 2009 Feb;22(1):3-10. Review.PMID: 19155758 [PubMed - indexed for MEDLINE]Related articles

ISCEV Standard for full-field clinical electroretinography (2008 update).

Marmor MF, Fulton AB, Holder GE, Miyake Y, Brigell M, Bach M; International Society for Clinical Electrophysiology of Vision.

Doc Ophthalmol. 2009 Feb;118(1):69-77. Epub 2008 Nov 22.PMID: 19030905 [PubMed - indexed for MEDLINE]Related articles

Haemorrhagic pituitary tumour presenting with unilateral paracentral visual disturbance.

Gore DM, Angunawela RI, Little BC, Holder GE.

Eye (Lond). 2009 Jul;23(7):1621-3. Epub 2008 Sep 19. No abstract available. PMID: 18806763 [PubMed - in process]Related articles

ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing.

Burgess R, MacLaren RE, Davidson AE, Urquhart JE, Holder GE, Robson AG, Moore AT, Keefe RO, Black GC, Manson FD.

J Med Genet. 2009 Sep;46(9):620-5. Epub 2008 Jul 8.PMID: 18611979 [PubMed - in process]Related articles

Differential changes in color and motion-onset visual evoked potentials from both eyes in early- and late-onset strabismic amblyopia.

Davis AR, Sloper JJ, Neveu MM, Hogg CR, Morgan MJ, Holder GE.

Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4418-26. Epub 2008 Jun 6.PMID: 18539945 [PubMed - indexed for MEDLINE]Related articlesFree article

Effect of gene therapy on visual function in Leber's congenital amaurosis.

Bainbridge JW, Smith AJ, Barker SS, Robbie S, Henderson R, Balaggan K, Viswanathan A, Holder GE, Stockman A, Tyler N, Petersen-Jones S, Bhattacharya SS, Thrasher AJ, Fitzke FW, Carter BJ, Rubin GS, Moore AT, Ali RR.

N Engl J Med. 2008 May 22;358(21):2231-9. Epub 2008 Apr 27.PMID: 18441371 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotypic variation in enhanced S-cone syndrome.

Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE.

Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93.PMID: 18436841 [PubMed - indexed for MEDLINE]Related articlesFree article

The loss of the PDE6 deactivating enzyme, RGS9, results in precocious light adaptation at low light levels.

Stockman A, Smithson HE, Webster AR, Holder GE, Rana NA, Ripamonti C, Sharpe LT.

J Vis. 2008 Jan 17;8(1):10.1-10.PMID: 18318613 [PubMed - indexed for MEDLINE]Related articlesFree article

Electrophysiological monitoring in a patient with an optic nerve glioma.

Moradi P, Robson AG, Rose GE, Holder GE.

Doc Ophthalmol. 2008 Sep;117(2):171-4. Epub 2008 Feb 27.PMID: 18301934 [PubMed - indexed for MEDLINE]Related articles

Macular and retinal dysfunction of unknown origin in adults with normal fundi: evidence for an autoimmune pathophysiology.

Mantel I, Ramchand KV, Holder GE, Ohbayashi M, Morohoshi K, Patel N, Toda M, Fitzke FW, Bird AC, Ono SJ.

Exp Mol Pathol. 2008 Apr;84(2):90-101. Epub 2007 Nov 9. Erratum in: Exp Mol Pathol. 2009 Oct;87(2):166. PMID: 18255057 [PubMed - indexed for MEDLINE]Related articles

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.

Bakrania P, Efthymiou M, Klein JC, Salt A, Bunyan DJ, Wyatt A, Ponting CP, Martin A, Williams S, Lindley V, Gilmore J, Restori M, Robson AG, Neveu MM, Holder GE, Collin JR, Robinson DO, Farndon P, Johansen-Berg H, Gerrelli D, Ragge NK.

Am J Hum Genet. 2008 Feb;82(2):304-19. Epub 2008 Jan 31.PMID: 18252212 [PubMed - indexed for MEDLINE]Related articlesFree article

Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance.

Vaclavik V, Chakarova C, Bhattacharya SS, Robson AG, Holder GE, Bird AC, Webster AR.

Br J Ophthalmol. 2008 Feb;92(2):299-300. No abstract available. PMID: 18227217 [PubMed - indexed for MEDLINE]Related articles

The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction.

Audo I, Robson AG, Holder GE, Moore AT.

Surv Ophthalmol. 2008 Jan-Feb;53(1):16-40. Review.PMID: 18191655 [PubMed - indexed for MEDLINE]Related articles

Biallelic mutation of BEST1 causes a distinct retinopathy in humans.

Burgess R, Millar ID, Leroy BP, Urquhart JE, Fearon IM, De Baere E, Brown PD, Robson AG, Wright GA, Kestelyn P, Holder GE, Webster AR, Manson FD, Black GC.

Am J Hum Genet. 2008 Jan;82(1):19-31.PMID: 18179881 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5684-9.PMID: 18055820 [PubMed - indexed for MEDLINE]Related articlesFree article

ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy.

Michaelides M, Chen LL, Brantley MA Jr, Andorf JL, Isaak EM, Jenkins SA, Holder GE, Bird AC, Stone EM, Webster AR.

Br J Ophthalmol. 2007 Dec;91(12):1650-5.PMID: 18024811 [PubMed - indexed for MEDLINE]Related articles

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Robson AG, Michaelides M, Saihan Z, Bird AC, Webster AR, Moore AT, Fitzke FW, Holder GE.

Doc Ophthalmol. 2008 Mar;116(2):79-89. Epub 2007 Nov 6. Review.PMID: 17985165 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.

Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW.

Br J Ophthalmol. 2008 Jan;92(1):95-102. Epub 2007 Oct 25.PMID: 17962389 [PubMed - indexed for MEDLINE]Related articles

Complement factor H deficiency in aged mice causes retinal abnormalities and visual dysfunction.

Coffey PJ, Gias C, McDermott CJ, Lundh P, Pickering MC, Sethi C, Bird A, Fitzke FW, Maass A, Chen LL, Holder GE, Luthert PJ, Salt TE, Moss SE, Greenwood J.

Proc Natl Acad Sci U S A. 2007 Oct 16;104(42):16651-6. Epub 2007 Oct 5.PMID: 17921253 [PubMed - indexed for MEDLINE]Related articlesFree article

Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?

Audo I, Vanakker OM, Smith A, Leroy BP, Robson AG, Jenkins SA, Coucke PJ, Bird AC, De Paepe A, Holder GE, Webster AR.

Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4250-6.PMID: 17724214 [PubMed - indexed for MEDLINE]Related articlesFree article

Pathological and electrophysiological features of a canine cone-rod dystrophy in the miniature longhaired dachshund.

Turney C, Chong NH, Alexander RA, Hogg CR, Fleming L, Flack D, Barnett KC, Bird AC, Holder GE, Luthert PJ.

Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4240-9.PMID: 17724213 [PubMed - indexed for MEDLINE]Related articlesFree article

Autofluorescence imaging in a case of benign familial fleck retina.

Audo I, Tsang SH, Fu AD, Barnes JA, Holder GE, Moore AT.

Arch Ophthalmol. 2007 May;125(5):714-5. No abstract available. PMID: 17502520 [PubMed - indexed for MEDLINE]Related articles

ISCEV standard for clinical pattern electroretinography--2007 update.

Holder GE, Brigell MG, Hawlina M, Meigen T, Vaegan, Bach M; International Society for Clinical Electrophysiology of Vision.

Doc Ophthalmol. 2007 May;114(3):111-6. Epub 2007 Apr 14.PMID: 17435967 [PubMed - indexed for MEDLINE]Related articlesFree article

Autofluorescence findings in acute exudative polymorphous vitelliform maculopathy.

Vaclavik V, Ooi KG, Bird AC, Robson AG, Holder GE, Webster AR.

Arch Ophthalmol. 2007 Feb;125(2):274-7. No abstract available. PMID: 17296907 [PubMed - indexed for MEDLINE]Related articles

Novel phenotypic and genotypic findings in X-linked retinoschisis.

Tsang SH, Vaclavik V, Bird AC, Robson AG, Holder GE.

Arch Ophthalmol. 2007 Feb;125(2):259-67.PMID: 17296904 [PubMed - indexed for MEDLINE]Related articlesFree article

Assessment of patients with suspected non-organic visual loss using pattern appearance visual evoked potentials.

McBain VA, Robson AG, Hogg CR, Holder GE.

Graefes Arch Clin Exp Ophthalmol. 2007 Apr;245(4):502-10. Epub 2006 Nov 17.PMID: 17111152 [PubMed - indexed for MEDLINE]Related articles

Differential changes of magnocellular and parvocellular visual function in early- and late-onset strabismic amblyopia.

Davis AR, Sloper JJ, Neveu MM, Hogg CR, Morgan MJ, Holder GE.

Invest Ophthalmol Vis Sci. 2006 Nov;47(11):4836-41.PMID: 17065495 [PubMed - indexed for MEDLINE]Related articlesFree article

A comparison of pattern and multifocal electroretinography in the evaluation of age-related macular degeneration and its treatment with photodynamic therapy.

Neveu MM, Tufail A, Dowler JG, Holder GE.

Doc Ophthalmol. 2006 Sep;113(2):71-81. Epub 2006 Sep 14.PMID: 16972084 [PubMed - indexed for MEDLINE]Related articles

A randomised controlled trial investigating the effect of n-3 long-chain polyunsaturated fatty acid supplementation on cognitive and retinal function in cognitively healthy older people: the Older People And n-3 Long-chain polyunsaturated fatty acids (OPAL) study protocol [ISRCTN72331636].

Dangour AD, Clemens F, Elbourne D, Fasey N, Fletcher AE, Hardy P, Holder GE, Huppert FA, Knight R, Letley L, Richards M, Truesdale A, Vickers M, Uauy R.

Nutr J. 2006 Aug 31;5:20.PMID: 16945130 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Am J Hum Genet. 2006 Sep;79(3):574-9. Epub 2006 Jul 24.PMID: 16909397 [PubMed - indexed for MEDLINE]Related articlesFree article

Early midline interactions are important in mouse optic chiasm formation but are not critical in man: a significant distinction between man and mouse.

Neveu MM, Holder GE, Ragge NK, Sloper JJ, Collin JR, Jeffery G.

Eur J Neurosci. 2006 Jun;23(11):3034-42.PMID: 16819992 [PubMed - indexed for MEDLINE]Related articles

Batten disease: features to facilitate early diagnosis.

Collins J, Holder GE, Herbert H, Adams GG.

Br J Ophthalmol. 2006 Sep;90(9):1119-24. Epub 2006 Jun 5.PMID: 16754648 [PubMed - indexed for MEDLINE]Related articlesFree article

Progressive retinal dysfunction in diffuse unilateral subacute neuroretinitis.

Audo I, Webster AR, Bird AC, Holder GE, Kidd MN.

Br J Ophthalmol. 2006 Jun;90(6):793-4. No abstract available. PMID: 16714269 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.

Tschernutter M, Jenkins SA, Waseem NH, Saihan Z, Holder GE, Bird AC, Bhattacharya SS, Ali RR, Webster AR.

Br J Ophthalmol. 2006 Jun;90(6):718-23.PMID: 16714263 [PubMed - indexed for MEDLINE]Related articlesFree article

Chromatic VEP assessment of human macular pigment: comparison with minimum motion and minimum flicker profiles.

Robson AG, Holder GE, Moreland JD, Kulikowski JJ.

Vis Neurosci. 2006 Mar-Apr;23(2):275-83.PMID: 16638178 [PubMed - indexed for MEDLINE]Related articles

A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of disease.

Abu-Safieh L, Vithana EN, Mantel I, Holder GE, Pelosini L, Bird AC, Bhattacharya SS.

Mol Vis. 2006 Apr 18;12:384-8.PMID: 16636657 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Br J Ophthalmol. 2006 Apr;90(4):472-9.PMID: 16547330 [PubMed - indexed for MEDLINE]Related articlesFree article

Didanosine-induced retinopathy in adults can be reversible.

Fernando AI, Anderson OA, Holder GE, Mitchell SM.

Eye (Lond). 2006 Dec;20(12):1435-7. Epub 2006 Mar 10. No abstract available. PMID: 16531973 [PubMed - indexed for MEDLINE]Related articles

Evidence of genetic heterogeneity in MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome.

Michaelides M, Urquhart J, Holder GE, Restori M, Kayali N, Manson FD, Black GC.

Am J Ophthalmol. 2006 Feb;141(2):418-20.PMID: 16458719 [PubMed - indexed for MEDLINE]Related articles

Functional observations in vitamin A deficiency: diagnosis and time course of recovery.

McBain VA, Egan CA, Pieris SJ, Supramaniam G, Webster AR, Bird AC, Holder GE.

Eye (Lond). 2007 Mar;21(3):367-76. Epub 2005 Dec 9.PMID: 16341129 [PubMed - indexed for MEDLINE]Related articles

Unilateral electronegative ERG of non-vascular aetiology.

Robson AG, Richardson EC, Koh AH, Pavesio CE, Hykin PG, Calcagni A, Graham EM, Holder GE.

Br J Ophthalmol. 2005 Dec;89(12):1620-6.PMID: 16299143 [PubMed - indexed for MEDLINE]Related articlesFree article

Optic chiasm formation in humans is independent of foveal development.

Neveu MM, Holder GE, Sloper JJ, Jeffery G.

Eur J Neurosci. 2005 Oct;22(7):1825-9.PMID: 16197526 [PubMed - indexed for MEDLINE]Related articles

Comparison of fundus autofluorescence and minimum-motion measurements of macular pigment distribution profiles derived from identical retinal areas.

Robson AG, Harding G, van Kuijk FJ, Pauleikhoff D, Holder GE, Bird AC, Fitzke FW, Moreland JD.

Perception. 2005;34(8):1029-34.PMID: 16178159 [PubMed - indexed for MEDLINE]Related articles

Cone-rod dystrophy, intrafamilial variability, and incomplete penetrance associated with the R172W mutation in the peripherin/RDS gene.

Michaelides M, Holder GE, Bradshaw K, Hunt DM, Moore AT.

Ophthalmology. 2005 Sep;112(9):1592-8.PMID: 16019073 [PubMed - indexed for MEDLINE]Related articles

X-linked cone dysfunction syndrome with myopia and protanopia.

Michaelides M, Johnson S, Bradshaw K, Holder GE, Simunovic MP, Mollon JD, Moore AT, Hunt DM.

Ophthalmology. 2005 Aug;112(8):1448-54.PMID: 15953640 [PubMed - indexed for MEDLINE]Related articles