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    Results: 1 to 20 of 143

    1.

    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

    2.

    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

    3.

    Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene cluster.

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

    Graefes Arch Clin Exp Ophthalmol. 2004 Sep;242(9):729-35.PMID: 15069569 [PubMed - indexed for MEDLINE]Related articles

    4.

    The cone dystrophies.

    Simunovic MP, Moore AT.

    Eye (Lond). 1998;12 ( Pt 3b):553-65. Review.PMID: 9775217 [PubMed - indexed for MEDLINE]Related articles

    5.

    ["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

    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.

    [Genetic causes of hereditary cone and cone-rod dystrophies]

    Kohl S.

    Ophthalmologe. 2009 Feb;106(2):109-15. Review. German. PMID: 19184602 [PubMed - indexed for MEDLINE]Related articles

    8.

    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

    9.

    The genetics of inherited macular dystrophies.

    Michaelides M, Hunt DM, Moore AT.

    J Med Genet. 2003 Sep;40(9):641-50. Review.PMID: 12960208 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Association of acquired color vision defects in blue cone monochromatism.

    Terasaki H, Miyake Y.

    Jpn J Ophthalmol. 1995;39(1):55-9.PMID: 7643484 [PubMed - indexed for MEDLINE]Related articles

    11.

    [Genetics of congenital color vision defects. II. Rare types of color blindness]

    Krawczyński MR.

    Klin Oczna. 1995 Jan-Feb;97(1-2):39-43. Review. Polish. PMID: 7637312 [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.

    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

    14.

    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

    15.

    Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations.

    Rosenberg T, Baumann B, Kohl S, Zrenner E, Jorgensen AL, Wissinger B.

    Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4256-62.PMID: 15557429 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.

    Nishiguchi KM, Sandberg MA, Gorji N, Berson EL, Dryja TP.

    Hum Mutat. 2005 Mar;25(3):248-58.PMID: 15712225 [PubMed - indexed for MEDLINE]Related articles

    17.

    Differential diagnosis of typical and atypical congenital achromatopsia. Analysis of a progressive foveal dystrophy and a nonprogressive oligo-cone trichromasy (general cone dysfunction without achromatopsia), both of which at first had been diagnosed as achromatopsia.

    Neuhann T, Krastel H, Jaeger W.

    Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1978 Dec 8;209(1):19-28.PMID: 311163 [PubMed - indexed for MEDLINE]Related articles

    18.

    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

    19.

    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

    20.

    Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2.

    Chang B, Dacey MS, Hawes NL, Hitchcock PF, Milam AH, Atmaca-Sonmez P, Nusinowitz S, Heckenlively JR.

    Invest Ophthalmol Vis Sci. 2006 Nov;47(11):5017-21.PMID: 17065522 [PubMed - indexed for MEDLINE]Related articlesFree article

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