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    Results: 1 to 20 of 100

    1.

    The enhanced S-cone syndrome in children.

    Khan AO, Aldahmesh M, Meyer B.

    Br J Ophthalmol. 2007 Mar;91(3):394-6. No abstract available. PMID: 17322467 [PubMed - indexed for MEDLINE]Related articles

    2.

    High-definition optical coherence tomographic visualization of photoreceptor layer and retinal flecks in fundus albipunctatus associated with cone dystrophy.

    Querques G, Carrillo P, Querques L, Bux AV, Del Curatolo MV, Delle Noci N.

    Arch Ophthalmol. 2009 May;127(5):703-6. No abstract available. PMID: 19433727 [PubMed - indexed for MEDLINE]Related articles

    3.

    Double cone dystrophy and RPE degeneration in the retina of the zebrafish gnn mutant.

    Biehlmaier O, Neuhauss SC, Kohler K.

    Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1287-98.PMID: 12601061 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Ocular fundus images by scanning laser ophthalmoscopy in a patient with enhanced S-cone syndrome.

    Usui T, Ichibe M, Tanimoto N, Ueki S, Takagi M, Hasegawa S, Abe H, Miyagawa Y, Nakazawa M.

    Retina. 2004 Dec;24(6):946-52.PMID: 15579994 [PubMed - indexed for MEDLINE]Related articles

    5.

    Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

    Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC.

    Nat Genet. 2000 Feb;24(2):127-31.PMID: 10655056 [PubMed - indexed for MEDLINE]Related articles

    6.

    Phenotypic features of patients with NR2E3 mutations.

    Pachydaki SI, Klaver CC, Barbazetto IA, Roy MS, Gouras P, Allikmets R, Yannuzzi LA.

    Arch Ophthalmol. 2009 Jan;127(1):71-5.PMID: 19139342 [PubMed - indexed for MEDLINE]Related articles

    7.

    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

    8.

    Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.

    Hayashi T, Gekka T, Goto-Omoto S, Takeuchi T, Kubo A, Kitahara K.

    Ophthalmology. 2005 Dec;112(12):2115. Epub 2005 Oct 12.PMID: 16225923 [PubMed - indexed for MEDLINE]Related articles

    9.

    A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome.

    Corbo JC, Cepko CL.

    PLoS Genet. 2005 Aug;1(2):e11. Epub 2005 Aug 5. Erratum in: PLoS Genet. 2008 Jan;4(1):e18. PMID: 16110338 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Congenital hypertrophy of the retinal pigment epithelium in the macula.

    Nishikatsu H, Shiono T.

    Ophthalmologica. 1996;210(2):126-8.PMID: 8859490 [PubMed - indexed for MEDLINE]Related articles

    11.

    Histopathologic and immunohistochemical study of dominant cone degeneration.

    To K, Adamian M, Jakobiec FA, Berson EL.

    Am J Ophthalmol. 1998 Jul;126(1):140-2.PMID: 9683165 [PubMed - indexed for MEDLINE]Related articles

    12.

    Photopic ON- and OFF-pathway abnormalities in retinal dystrophies.

    Sieving PA.

    Trans Am Ophthalmol Soc. 1993;91:701-73. No abstract available. PMID: 8140708 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    [Increased lens opacity, retinal pigment epithelium degeneration and spontaneous retinal detachment in a family. Wagner syndrome]

    Meyer CH.

    Ophthalmologe. 2002 Aug;99(8):654-5. German. No abstract available. PMID: 12227281 [PubMed - indexed for MEDLINE]Related articles

    14.

    Retinal pigment epithelial window defect.

    Keno DD, Green WR.

    Arch Ophthalmol. 1978 May;96(5):854-6.PMID: 655923 [PubMed - indexed for MEDLINE]Related articles

    15.

    Histopathologic and immunohistochemical study of an autopsy eye with X-linked cone degeneration.

    To KW, Adamian M, Jakobiec FA, Berson EL.

    Arch Ophthalmol. 1998 Jan;116(1):100-3.PMID: 9445217 [PubMed - indexed for MEDLINE]Related articles

    16.

    Patterned anomalies of the retinal pigment epithelium: dystrophy or syndrome?

    Bastiaensen LA, Hoefnagels KL.

    Doc Ophthalmol. 1983 Feb 28;55(1-2):17-29.PMID: 6839931 [PubMed - indexed for MEDLINE]Related articles

    17.

    Bilateral retinal pigment epithelium changes associated with periorbital vitiligo and seizure disorders.

    Rosenbaum J, Bunke A, Cooperman E, Gombos GM.

    Ann Ophthalmol. 1979 Aug;11(8):1191-3. No abstract available. PMID: 556146 [PubMed - indexed for MEDLINE]Related articles

    18.

    Genetic ablation of cone photoreceptors eliminates retinal folds in the retinal degeneration 7 (rd7) mouse.

    Chen J, Nathans J.

    Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2799-805.PMID: 17525215 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    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

    20.

    Enhanced S cone syndrome: evidence for an abnormally large number of S cones.

    Hood DC, Cideciyan AV, Roman AJ, Jacobson SG.

    Vision Res. 1995 May;35(10):1473-81.PMID: 7645276 [PubMed - indexed for MEDLINE]Related articles

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