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    Results: 1 to 20 of 490

    1.

    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

    2.

    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

    3.

    Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity.

    Robson AG, Egan CA, Luong VA, Bird AC, Holder GE, Fitzke FW.

    Invest Ophthalmol Vis Sci. 2004 Nov;45(11):4119-25.PMID: 15505064 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    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

    5.

    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.

    Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3544-50.PMID: 12882805 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa.

    Popović P, Jarc-Vidmar M, Hawlina M.

    Graefes Arch Clin Exp Ophthalmol. 2005 Oct;243(10):1018-27. Epub 2005 Oct 20.PMID: 15906064 [PubMed - indexed for MEDLINE]Related articles

    7.

    A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.

    Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT.

    Br J Ophthalmol. 2005 Feb;89(2):198-206.PMID: 15665353 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.

    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.

    Ophthalmology. 2002 Oct;109(10):1862-70.PMID: 12359607 [PubMed - indexed for MEDLINE]Related articles

    9.

    Phenotype in two families with RP3 associated with RPGR mutations.

    Lorenz B, Andrassi M, Kretschmann U.

    Ophthalmic Genet. 2003 Jun;24(2):89-101.PMID: 12789573 [PubMed - indexed for MEDLINE]Related articles

    10.

    Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data.

    Wegscheider E, Preising MN, Lorenz B.

    Graefes Arch Clin Exp Ophthalmol. 2004 Jun;242(6):501-11. Epub 2004 May 29.PMID: 15173948 [PubMed - indexed for MEDLINE]Related articles

    11.

    Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.

    Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.

    Invest Ophthalmol Vis Sci. 1997 Sep;38(10):1983-97.PMID: 9331262 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.

    Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL.

    Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1298-304.PMID: 17325176 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function.

    Kemp CM, Jacobson SG, Cideciyan AV, Kimura AE, Sheffield VC, Stone EM.

    Invest Ophthalmol Vis Sci. 1994 Jul;35(8):3154-62.PMID: 8045710 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.

    Ebenezer ND, Michaelides M, Jenkins SA, Audo I, Webster AR, Cheetham ME, Stockman A, Maher ER, Ainsworth JR, Yates JR, Bradshaw K, Holder GE, Moore AT, Hardcastle AJ.

    Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1891-8.PMID: 15914600 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.

    Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE.

    Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2355-60.PMID: 15223817 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Fundus autofluorescence in Stargardt macular dystrophy-fundus flavimaculatus.

    Lois N, Halfyard AS, Bird AC, Holder GE, Fitzke FW.

    Am J Ophthalmol. 2004 Jul;138(1):55-63.PMID: 15234282 [PubMed - indexed for MEDLINE]Related articles

    17.

    RP cone-rod degeneration.

    Heckenlively JR.

    Trans Am Ophthalmol Soc. 1987;85:438-70.PMID: 3447340 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.

    Duncan JL, Zhang Y, Gandhi J, Nakanishi C, Othman M, Branham KE, Swaroop A, Roorda A.

    Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3283-91.PMID: 17591900 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy.

    Birch DG, Anderson JL, Fish GE.

    Ophthalmology. 1999 Feb;106(2):258-68.PMID: 9951474 [PubMed - indexed for MEDLINE]Related articles

    20.

    A detailed phenotypic study of "cone dystrophy with supernormal rod ERG".

    Michaelides M, Holder GE, Webster AR, Hunt DM, Bird AC, Fitzke FW, Mollon JD, Moore AT.

    Br J Ophthalmol. 2005 Mar;89(3):332-9.PMID: 15722315 [PubMed - indexed for MEDLINE]Related articlesFree article

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