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Journal Abstract Search

156 related items for PubMed ID: 10463423

  • 21. Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
    Sharon D, Sandberg MA, Caruso RC, Berson EL, Dryja TP.
    Arch Ophthalmol; 2003 Sep; 121(9):1316-23. PubMed ID: 12963616
    [Abstract] [Full Text] [Related]

  • 22. Autosomal dominant vitreoretinochoroidopathy with normal electrooculogram in a German family.
    Kellner U, Jandeck C, Kraus H, Foerster MH.
    Graefes Arch Clin Exp Ophthalmol; 1998 Feb; 236(2):109-14. PubMed ID: 9498121
    [Abstract] [Full Text] [Related]

  • 23. Progressive generalized cone dysfunction.
    François J, de Rouck A, Verriest G, de Laey JJ, Cambie E.
    Ophthalmologica; 1974 Feb; 169(4):255-84. PubMed ID: 4547582
    [No Abstract] [Full Text] [Related]

  • 24. A new dominant progressive foveal dystrophy.
    Frank HR, Landers MB, Williams RJ, Sidbury JB.
    Am J Ophthalmol; 1974 Dec; 78(6):903-16. PubMed ID: 4440724
    [No Abstract] [Full Text] [Related]

  • 25. [Goldmann-Favre hyaloido-tapetoretinal degeneration].
    Fiore C, Ricci A.
    Arch Ophtalmol (Paris); 1976 Feb; 36(2):127-36. PubMed ID: 132917
    [Abstract] [Full Text] [Related]

  • 26. Relatively enhanced S cone function in the Goldmann-Favre syndrome.
    Jacobson SG, Román AJ, Román MI, Gass JD, Parker JA.
    Am J Ophthalmol; 1991 Apr 15; 111(4):446-53. PubMed ID: 2012146
    [Abstract] [Full Text] [Related]

  • 27. [Stargardt's disease (ERG, EOG and chromatic sense)].
    Pinckers A.
    Ann Ocul (Paris); 1971 Dec 15; 204(12):1331-46. PubMed ID: 5150321
    [No Abstract] [Full Text] [Related]

  • 28. Fundus flavimaculatus and Stargardt's disease.
    Hadden OB, Gass JD.
    Am J Ophthalmol; 1976 Oct 15; 82(4):527-39. PubMed ID: 1086060
    [Abstract] [Full Text] [Related]

  • 29. Golden tapetal-like fundus reflex and posterior hyaloid in a patient with x-linked juvenile retinoschisis.
    Miyake Y, Terasaki H.
    Retina; 1999 Oct 15; 19(1):84-6. PubMed ID: 10048383
    [No Abstract] [Full Text] [Related]

  • 30. Comparison of the Goldmann-Weekers dark adaptometer and LKC Technologies Scotopic Sensitivity tester-1.
    Peters AY, Locke KG, Birch DG.
    Doc Ophthalmol; 2000 Jul 15; 101(1):1-9. PubMed ID: 11128963
    [Abstract] [Full Text] [Related]

  • 31. Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.
    Dryja TP.
    Am J Ophthalmol; 2000 Nov 15; 130(5):547-63. PubMed ID: 11078833
    [Abstract] [Full Text] [Related]

  • 32. Pericentral retinal degeneration deteriorates during pregnancies.
    Hayasaka S, Ugomori S, Kanamori M, Setogawa T.
    Ophthalmologica; 1990 Nov 15; 200(2):72-6. PubMed ID: 2338988
    [Abstract] [Full Text] [Related]

  • 33. Progressive degeneration of the photopic system.
    Babel J, Stangos N.
    Am J Ophthalmol; 1973 Mar 15; 75(3):511-25. PubMed ID: 4540518
    [No Abstract] [Full Text] [Related]

  • 34. [Juvenile macular degenerations].
    François J.
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 Mar 15; 34(6-7):497-512. PubMed ID: 4142583
    [No Abstract] [Full Text] [Related]

  • 35. The diagnostic importance of functional electrooculography in some hereditary dystrophies of the eye fundus.
    François J.
    Ann Ophthalmol; 1971 Sep 15; 3(9):929-46. PubMed ID: 4950484
    [No Abstract] [Full Text] [Related]

  • 36. Annular fundus autofluorescence abnormality in a case of macular dystrophy.
    Poloschek CM, Hansen LL, Bach M.
    Doc Ophthalmol; 2008 Mar 15; 116(2):91-5. PubMed ID: 18008096
    [Abstract] [Full Text] [Related]

  • 37. The functional syndromes.
    François J.
    Ophthalmologica; 1974 Mar 15; 169(1-3):234-9. PubMed ID: 4547324
    [No Abstract] [Full Text] [Related]

  • 38. A teenager with nightblindness and cystic maculopathy: enhanced S cone syndrome (Goldmann-Favre syndrome).
    Marmor MF.
    Doc Ophthalmol; 2006 Nov 15; 113(3):213-5. PubMed ID: 17109156
    [Abstract] [Full Text] [Related]

  • 39. New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome.
    Kuniyoshi K, Hayashi T, Sakuramoto H, Mishima H, Tsuneoka H, Tsunoda K, Iwata T, Shimomura Y.
    Jpn J Ophthalmol; 2016 Nov 15; 60(6):476-485. PubMed ID: 27522502
    [Abstract] [Full Text] [Related]

  • 40. A case of erosive vitreoretinopathy.
    Kyung SE, Chang MH, Ji JY.
    Korean J Ophthalmol; 2002 Jun 15; 16(1):47-51. PubMed ID: 12162518
    [Abstract] [Full Text] [Related]

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