PubMed

Diagnostic and Therapeutic Challenges.

Santiago C, McBain VA, Lois N, Lotery AJ, Pulido JS.

Retina. 2009 Oct;29(9):1371-1374. No abstract available. PMID: 19934828 [PubMed - as supplied by publisher]

Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa.

Davidson AE, Millar ID, Urquhart JE, Burgess-Mullan R, Shweikh Y, Parry N, O'Sullivan J, Maher GJ, McKibbin M, Downes SM, Lotery AJ, Jacobson SG, Brown PD, Black GC, Manson FD.

Am J Hum Genet. 2009 Nov;85(5):581-92. Epub 2009 Oct 22.PMID: 19853238 [PubMed - in process]Related articles

Fibulin 5 forms a compact dimer in physiological solutions.

Jones RP, Wang MC, Jowitt TA, Ridley C, Mellody KT, Howard M, Wang T, Bishop PN, Lotery AJ, Kielty CM, Baldock C, Trump D.

J Biol Chem. 2009 Sep 18;284(38):25938-43. Epub 2009 Jul 17.PMID: 19617354 [PubMed - indexed for MEDLINE]Related articlesFree article

Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.

Thiadens AA, den Hollander AI, Roosing S, Nabuurs SB, Zekveld-Vroon RC, Collin RW, De Baere E, Koenekoop RK, van Schooneveld MJ, Strom TM, van Lith-Verhoeven JJ, Lotery AJ, van Moll-Ramirez N, Leroy BP, van den Born LI, Hoyng CB, Cremers FP, Klaver CC.

Am J Hum Genet. 2009 Aug;85(2):240-7. Epub 2009 Jul 16.PMID: 19615668 [PubMed - indexed for MEDLINE]Related articles

Localization of complement 1 inhibitor (C1INH/SERPING1) in human eyes with age-related macular degeneration.

Mullins RF, Faidley EA, Daggett HT, Jomary C, Lotery AJ, Stone EM.

Exp Eye Res. 2009 Nov;89(5):767-73. Epub 2009 Jul 14.PMID: 19607829 [PubMed - in process]Related articles

Support for the involvement of complement factor I in age-related macular degeneration.

Ennis S, Gibson J, Cree AJ, Collins A, Lotery AJ.

Eur J Hum Genet. 2009 Jul 15. [Epub ahead of print] No abstract available. PMID: 19603066 [PubMed - as supplied by publisher]Related articles

Novel software to self-monitor central serous retinopathy.

Turnbull AM, Abu-Ain MS, Lash SC, Murphy AS, Lotery AJ.

Eye (Lond). 2009 Feb 27. [Epub ahead of print] No abstract available. PMID: 19247387 [PubMed - as supplied by publisher]Related articles

Age-related macular degeneration is associated with the HLA-Cw*0701 Genotype and the natural killer cell receptor AA haplotype.

Goverdhan SV, Khakoo SI, Gaston H, Chen X, Lotery AJ.

Invest Ophthalmol Vis Sci. 2008 Nov;49(11):5077-82. Epub 2008 May 30.PMID: 18515573 [PubMed - indexed for MEDLINE]Related articlesFree article

Interleukin-8 promoter polymorphism -251A/T is a risk factor for age-related macular degeneration.

Goverdhan SV, Ennis S, Hannan SR, Madhusudhana KC, Cree AJ, Luff AJ, Lotery AJ.

Br J Ophthalmol. 2008 Apr;92(4):537-40. Epub 2008 Feb 29.PMID: 18310311 [PubMed - indexed for MEDLINE]Related articles

Autosomal dominant early onset aponeurotic ptosis and corneal limbal vascularization in a three-generation family.

Ismail AR, Cates CA, Mullins RF, Manners RM, Lotery AJ.

Ophthal Plast Reconstr Surg. 2007 Nov-Dec;23(6):484-6.PMID: 18030124 [PubMed - indexed for MEDLINE]Related articles

Idiopathic juxtafoveolar retinal telangiectasis in monozygotic twins.

Hannan SR, Madhusudhana KC, Rennie C, Lotery AJ.

Br J Ophthalmol. 2007 Dec;91(12):1729-30. No abstract available. PMID: 18024833 [PubMed - indexed for MEDLINE]Related articles

Intravitreal bevacizumab (Avastin) for the treatment of choroidal neovascularization in age-related macular degeneration: results from 118 cases.

Madhusudhana KC, Hannan SR, Williams CP, Goverdhan SV, Rennie C, Lotery AJ, Luff AJ, Newsom RS.

Br J Ophthalmol. 2007 Dec;91(12):1716-7. No abstract available. PMID: 18024821 [PubMed - indexed for MEDLINE]Related articles

Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus.

Self JE, Shawkat F, Malpas CT, Thomas NS, Harris CM, Hodgkins PR, Chen X, Trump D, Lotery AJ.

Arch Ophthalmol. 2007 Sep;125(9):1255-63.PMID: 17846367 [PubMed - indexed for MEDLINE]Related articlesFree article

Retinal pigment epithelial tear following intravitreal bevacizumab for choroidal neovascular membrane due to age-related macular degeneration.

Hannan SR, Madhusudhana KC, Lotery AJ, Newsom RS.

Br J Ophthalmol. 2007 Jul;91(7):977-8. No abstract available. PMID: 17576713 [PubMed - indexed for MEDLINE]Related articles

An analysis of the CFH Y402H genotype in AMD patients and controls from the UK, and response to PDT treatment.

Goverdhan SV, Hannan S, Newsom RB, Luff AJ, Griffiths H, Lotery AJ.

Eye (Lond). 2008 Jun;22(6):849-54. Epub 2007 Apr 27.PMID: 17464302 [PubMed - indexed for MEDLINE]Related articles

Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.

Self JE, Ennis S, Collins A, Shawkat F, Harris CM, Mackey DA, Hodgkins PR, Temple IK, Chen X, Lotery AJ.

Mol Vis. 2006 Oct 18;12:1211-6.PMID: 17102799 [PubMed - indexed for MEDLINE]Related articlesFree article

Complement factor H Y402H gene polymorphism in coronary artery disease and atherosclerosis.

Goverdhan SV, Lotery AJ, Cree AJ, Ye S.

Atherosclerosis. 2006 Sep;188(1):213-4. Epub 2006 May 30. No abstract available. PMID: 16730735 [PubMed - indexed for MEDLINE]Related articles

Case of Stargardt disease caused by uniparental isodisomy.

Fingert JH, Eliason DA, Phillips NC, Lotery AJ, Sheffield VC, Stone EM.

Arch Ophthalmol. 2006 May;124(5):744-5. No abstract available. PMID: 16682602 [PubMed - indexed for MEDLINE]Related articles

Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxa.

Lotery AJ, Baas D, Ridley C, Jones RP, Klaver CC, Stone E, Nakamura T, Luff A, Griffiths H, Wang T, Bergen AA, Trump D.

Hum Mutat. 2006 Jun;27(6):568-74.PMID: 16652333 [PubMed - indexed for MEDLINE]Related articlesFree article

HLA and eye disease: a synopsis.

Goverdhan SV, Lotery AJ, Howell WM.

Int J Immunogenet. 2005 Dec;32(6):333-42. Review.PMID: 16313296 [PubMed - indexed for MEDLINE]Related articles

Macular degeneration associated with a novel Treacher Collins tcof1 mutation and evaluation of this mutation in age related macular degeneration.

Goverdhan SV, Temple IK, Self J, Lotery AJ, Dixon MJ, Evans AR.

Br J Ophthalmol. 2005 Aug;89(8):1063-4. No abstract available. PMID: 16024866 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of HLA class I and class II polymorphisms with age-related macular degeneration.

Goverdhan SV, Howell MW, Mullins RF, Osmond C, Hodgkins PR, Self J, Avery K, Lotery AJ.

Invest Ophthalmol Vis Sci. 2005 May;46(5):1726-34.PMID: 15851575 [PubMed - indexed for MEDLINE]Related articlesFree article

Glutamate excitotoxicity in glaucoma: truth or fiction?

Lotery AJ.

Eye (Lond). 2005 Apr;19(4):369-70. No abstract available. PMID: 15806116 [PubMed - indexed for MEDLINE]Related articles

Radiotherapy for age-related macular degeneration: no more pilot studies please.

Goverdhan SV, Gibbs FA, Lotery AJ.

Eye (Lond). 2005 Nov;19(11):1137-41. Review. No abstract available. PMID: 15543181 [PubMed - indexed for MEDLINE]Related articles

Missense variations in the fibulin 5 gene and age-related macular degeneration.

Stone EM, Braun TA, Russell SR, Kuehn MH, Lotery AJ, Moore PA, Eastman CG, Casavant TL, Sheffield VC.

N Engl J Med. 2004 Jul 22;351(4):346-53.PMID: 15269314 [PubMed - indexed for MEDLINE]Related articlesFree article

Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retina.

Lotery AJ, Yang GS, Mullins RF, Russell SR, Schmidt M, Stone EM, Lindbloom JD, Chiorini JA, Kotin RM, Davidson BL.

Hum Gene Ther. 2003 Nov 20;14(17):1663-71.PMID: 14633408 [PubMed - indexed for MEDLINE]Related articles

Characterization of rabbit myocilin: Implications for human myocilin glycosylation and signal peptide usage.

Shepard AR, Jacobson N, Sui R, Steely HT, Lotery AJ, Stone EM, Clark AF.

BMC Genet. 2003 Apr 2;4:5.PMID: 12697062 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetics update of macular diseases.

Chung M, Lotery AJ.

Ophthalmol Clin North Am. 2002 Dec;15(4):459-65. Review.PMID: 12515078 [PubMed - indexed for MEDLINE]Related articles

Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations.

Koenekoop RK, Fishman GA, Iannaccone A, Ezzeldin H, Ciccarelli ML, Baldi A, Sunness JS, Lotery AJ, Jablonski MM, Pittler SJ, Maumenee I.

Arch Ophthalmol. 2002 Oct;120(10):1325-30.PMID: 12365911 [PubMed - indexed for MEDLINE]Related articles

Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectors.

Lotery AJ, Derksen TA, Russell SR, Mullins RF, Sauter S, Affatigato LM, Stone EM, Davidson BL.

Hum Gene Ther. 2002 Apr 10;13(6):689-96.PMID: 11936968 [PubMed - indexed for MEDLINE]Related articles

CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservation.

Lotery AJ, Malik A, Shami SA, Sindhi M, Chohan B, Maqbool C, Moore PA, Denton MJ, Stone EM.

Ophthalmic Genet. 2001 Sep;22(3):163-9.PMID: 11559858 [PubMed - indexed for MEDLINE]Related articles

Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degeneration.

Guymer RH, Héon E, Lotery AJ, Munier FL, Schorderet DF, Baird PN, McNeil RJ, Haines H, Sheffield VC, Stone EM.

Arch Ophthalmol. 2001 May;119(5):745-51.PMID: 11346402 [PubMed - indexed for MEDLINE]Related articlesFree article

An analysis of allelic variation in the ABCA4 gene.

Webster AR, Héon E, Lotery AJ, Vandenburgh K, Casavant TL, Oh KT, Beck G, Fishman GA, Lam BL, Levin A, Heckenlively JR, Jacobson SG, Weleber RG, Sheffield VC, Stone EM.

Invest Ophthalmol Vis Sci. 2001 May;42(6):1179-89.PMID: 11328725 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in the CRB1 gene cause Leber congenital amaurosis.

Lotery AJ, Jacobson SG, Fishman GA, Weleber RG, Fulton AB, Namperumalsamy P, Héon E, Levin AV, Grover S, Rosenow JR, Kopp KK, Sheffield VC, Stone EM.

Arch Ophthalmol. 2001 Mar;119(3):415-20.PMID: 11231775 [PubMed - indexed for MEDLINE]Related articlesFree article

Correctable visual impairment in stroke rehabilitation patients.

Lotery AJ, Wiggam MI, Jackson AJ, Refson K, Fullerton KJ, Gilmore DH, Beringer TR.

Age Ageing. 2000 May;29(3):221-2.PMID: 10855903 [PubMed - indexed for MEDLINE]Related articlesFree article

Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.

Lotery AJ, Munier FL, Fishman GA, Weleber RG, Jacobson SG, Affatigato LM, Nichols BE, Schorderet DF, Sheffield VC, Stone EM.

Invest Ophthalmol Vis Sci. 2000 May;41(6):1291-6.PMID: 10798642 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation analysis of 3 genes in patients with Leber congenital amaurosis.

Lotery AJ, Namperumalsamy P, Jacobson SG, Weleber RG, Fishman GA, Musarella MA, Hoyt CS, Héon E, Levin A, Jan J, Lam B, Carr RE, Franklin A, Radha S, Andorf JL, Sheffield VC, Stone EM.

Arch Ophthalmol. 2000 Apr;118(4):538-43.PMID: 10766140 [PubMed - indexed for MEDLINE]Related articlesFree article

Electrophysiology findings in a large family with central areolar choroidal dystrophy.

Lotery AJ, Silvestri G, Collins AD.

Doc Ophthalmol. 1998-1999;97(2):103-19.PMID: 10765965 [PubMed - indexed for MEDLINE]Related articles

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.

Stone EM, Lotery AJ, Munier FL, Héon E, Piguet B, Guymer RH, Vandenburgh K, Cousin P, Nishimura D, Swiderski RE, Silvestri G, Mackey DA, Hageman GS, Bird AC, Sheffield VC, Schorderet DF.

Nat Genet. 1999 Jun;22(2):199-202.PMID: 10369267 [PubMed - indexed for MEDLINE]Related articles

Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration.

Stone EM, Webster AR, Vandenburgh K, Streb LM, Hockey RR, Lotery AJ, Sheffield VC.

Nat Genet. 1998 Dec;20(4):328-9. No abstract available. PMID: 9843201 [PubMed - indexed for MEDLINE]Related articles

Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.

Hughes AE, Lotery AJ, Silvestri G.

J Med Genet. 1998 Sep;35(9):770-2.PMID: 9733038 [PubMed - indexed for MEDLINE]Related articlesFree article

Familial deafness associated with iris degeneration and glaucoma.

Rundle P, Lotery AJ, Archer DB, McGinnity FG.

Eye (Lond). 1997;11 ( Pt 4):476-8.PMID: 9425410 [PubMed - indexed for MEDLINE]Related articles

Localisation of a gene for central areolar choroidal dystrophy to chromosome 17p.

Lotery AJ, Ennis KT, Silvestri G, Nicholl S, McGibbon D, Collins AD, Hughes AE.

Hum Mol Genet. 1996 May;5(5):705-8.PMID: 8733141 [PubMed - indexed for MEDLINE]Related articlesFree article

Pseudoretinitis pigmentosa due to sub-optimal treatment of neurosyphilis.

Lotery AJ, McBride MO, Larkin C, Sharkey JA.

Eye (Lond). 1996;10 ( Pt 6):759-60. No abstract available. PMID: 9091384 [PubMed - indexed for MEDLINE]Related articles

Iatrogenic acute angle closure glaucoma masked by general anaesthesia and intensive care.

Lotery AJ, Frazer DG.

Ulster Med J. 1995 Oct;64(2):178-80. No abstract available. PMID: 8533185 [PubMed - indexed for MEDLINE]Related articlesFree article

Proliferation of lens epithelial remnants after Nd-YAG laser capsulotomy.

Lotery AJ, Sharkey JA.

Br J Ophthalmol. 1995 Oct;79(10):964. No abstract available. PMID: 7488590 [PubMed - indexed for MEDLINE]Related articlesFree article

Treatment and long-term follow up of a capillary angioma of the optic disc.

Johnston PB, Lotery AJ, Logan WC.

Int Ophthalmol. 1995;19(2):129-32.PMID: 8586497 [PubMed - indexed for MEDLINE]Related articles

Fungal keratitis caused by Scopulariopsis brevicaulis: successful treatment with topical amphotericin B and chloramphenicol without the need for surgical debridement.

Lotery AJ, Kerr JR, Page BA.

Br J Ophthalmol. 1994 Sep;78(9):730. No abstract available. PMID: 7947559 [PubMed - indexed for MEDLINE]Related articlesFree article