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    Results: 1 to 20 of 109

    1.

    Oligocone trichromacy: a rare and unusual cone dysfunction syndrome.

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

    Br J Ophthalmol. 2004 Apr;88(4):497-500.PMID: 15031164 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    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

    3.

    ["Oligocone" trichromasy, a rare form of incomplete achromatopsia]

    Ehlich P, Sadowski B, Zrenner E.

    Ophthalmologe. 1997 Nov;94(11):801-6. German. PMID: 9465713 [PubMed - indexed for MEDLINE]Related articles

    4.

    Oligocone trichromacy: Clinical and molecular genetic investigations.

    Andersen M, Christoffersen N, Sander B, Edmund C, Larsen M, Grau T, Wissinger B, Kohl S, Rosenberg T.

    Invest Ophthalmol Vis Sci. 2009 Sep 24. [Epub ahead of print]PMID: 19797231 [PubMed - as supplied by publisher]Related articles

    5.

    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

    6.

    Progressive cone dystrophy associated with mutation in CNGB3.

    Michaelides M, Aligianis IA, Ainsworth JR, Good P, Mollon JD, Maher ER, Moore AT, Hunt DM.

    Invest Ophthalmol Vis Sci. 2004 Jun;45(6):1975-82.PMID: 15161866 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.

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

    Eye (Lond). 2005 Jan;19(1):2-10.PMID: 15094734 [PubMed - indexed for MEDLINE]Related articles

    8.

    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.

    Br J Ophthalmol. 2003 Nov;87(11):1317-20. Erratum in: Br J Ophthalmol. 2004 Feb;88(2):314. PMID: 14609822 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    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

    10.

    The cone dysfunction syndromes.

    Michaelides M, Hunt DM, Moore AT.

    Br J Ophthalmol. 2004 Feb;88(2):291-7. Review.PMID: 14736794 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Foveal cone dysfunction syndrome.

    ten Hove MW, Siatkowski RM, Smith JL.

    J Neuroophthalmol. 1998 Mar;18(1):9-14.PMID: 9532531 [PubMed - indexed for MEDLINE]Related articles

    12.

    Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.

    Michaelides M, Wilkie SE, Jenkins S, Holder GE, Hunt DM, Moore AT, Webster AR.

    Ophthalmology. 2005 Aug;112(8):1442-7.PMID: 15953638 [PubMed - indexed for MEDLINE]Related articles

    13.

    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

    14.

    Clinical heterogeneity between two Japanese siblings with congenital achromatopsia.

    Hayashi T, Kozaki K, Kitahara K, Kubo A, Nishio Y, Omoto S, Nakamura Y, Watanabe A, Toda K, Ueoka Y.

    Vis Neurosci. 2004 May-Jun;21(3):413-20.PMID: 15518223 [PubMed - indexed for MEDLINE]Related articles

    15.

    Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).

    Nakamura Y, Hayashi T, Kozaki K, Kubo A, Omoto S, Watanabe A, Toda K, Takeuchi T, Gekka T, Kitahara K.

    Acta Ophthalmol Scand. 2004 Oct;82(5):616-22.PMID: 15453866 [PubMed - indexed for MEDLINE]Related articles

    16.

    Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

    Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.

    Invest Ophthalmol Vis Sci. 2008 Feb;49(2):751-7.PMID: 18235024 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.

    Kondo M, Miyake Y, Kondo N, Ueno S, Takakuwa H, Terasaki H.

    Ophthalmology. 2004 Apr;111(4):732-9.PMID: 15051206 [PubMed - indexed for MEDLINE]Related articles

    18.

    [Molecular genetic findings in patients with congenital cone dysfunction. Mutations in the CNGA3, CNGB3, or GNAT2 genes]

    Kellner U, Wissinger B, Kohl S, Kraus H, Foerster MH.

    Ophthalmologe. 2004 Aug;101(8):830-5. German. PMID: 15459792 [PubMed - indexed for MEDLINE]Related articles

    19.

    Color vision defects in pigmentary retinal dystrophy.

    Okajima O, Tanino T, Okamoto M.

    Jpn J Ophthalmol. 1982;26(3):292-301.PMID: 6984101 [PubMed - indexed for MEDLINE]Related articles

    20.

    Progressive cone dystrophy with deutan genotype and phenotype.

    Scholl HP, Kremers J, Besch D, Zrenner E, Jägle H.

    Graefes Arch Clin Exp Ophthalmol. 2006 Feb;244(2):183-91. Epub 2005 Aug 5.PMID: 16082559 [PubMed - indexed for MEDLINE]Related articles

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