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Journal Abstract Search

160 related items for PubMed ID: 5449911

  • 1. [Wagner's syndrome: electro-oculography and color sense].
    Pinckers A.
    Ann Ocul (Paris); 1970 Jun; 203(6):569-78. PubMed ID: 5449911
    [No Abstract] [Full Text] [Related]

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

  • 3. [Degenerative ocular retinal albinism in a girl ten years old (author's transl)].
    Franceschetti A, Fiore C, Korol S, Klein D.
    Klin Monbl Augenheilkd; 1978 Apr; 172(4):484-7. PubMed ID: 651216
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary hyaloido-retinal degeneration (Wagner's disease)].
    Eremenko NS.
    Vestn Oftalmol; 1970 Apr; 4():75-6. PubMed ID: 5502580
    [No Abstract] [Full Text] [Related]

  • 5. [Bio-electric tests in tapeto-retinal peripheral degeneration].
    François J, De Rouck A.
    Bull Soc Belge Ophtalmol; 1974 Apr; 166(2):504-16. PubMed ID: 4433950
    [No Abstract] [Full Text] [Related]

  • 6. [Familial annular pigmented retinal degeneration].
    Toussaint D, Ohrn-Deguelder C.
    Bull Soc Belge Ophtalmol; 1979 Feb 17; 184():157-74. PubMed ID: 553699
    [No Abstract] [Full Text] [Related]

  • 7. [Wagner's hyaloido-retinal degeneration].
    Guillaumat L, Rouchy JP, Arrata M.
    Bull Soc Ophtalmol Fr; 1970 Feb 17; 70(7):809-15. PubMed ID: 5526306
    [No Abstract] [Full Text] [Related]

  • 8. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
    Auslender N, Sharon D, Abbasi AH, Garzozi HJ, Banin E, Ben-Yosef T.
    Invest Ophthalmol Vis Sci; 2007 Dec 17; 48(12):5431-8. PubMed ID: 18055789
    [Abstract] [Full Text] [Related]

  • 9. [Wagner's disease].
    Mozhaĭtsev BN.
    Vestn Oftalmol; 1968 Dec 17; 81(3):69-70. PubMed ID: 5742538
    [No Abstract] [Full Text] [Related]

  • 10. Wagner's hereditary vitreoretinal degeneration and retinal detachment.
    Hirose T, Lee KY, Schepens CL.
    Arch Ophthalmol; 1973 Mar 17; 89(3):176-85. PubMed ID: 4691317
    [No Abstract] [Full Text] [Related]

  • 11. [Differential diagnosis of early onset tapetoretinal degenerations using retinal functional diagnosis].
    Schneider T, Zrenner E.
    Fortschr Ophthalmol; 1987 Mar 17; 84(3):292-7. PubMed ID: 3623382
    [No Abstract] [Full Text] [Related]

  • 12. [Electroretinographic study of hereditary vitreo-retinal degeneration].
    Dehon P, Comhaire-Poutchinian Y, Watillon M.
    Bull Soc Belge Ophtalmol; 1977 Mar 17; (176):58-81. PubMed ID: 614088
    [No Abstract] [Full Text] [Related]

  • 13. [Wagner's dystrophia hyaloideoretinalis].
    Zygulska-Machowa H, Osterczy-Sliwińska H.
    Klin Oczna; 1972 Mar 17; 42(5):1263-5. PubMed ID: 4637339
    [No Abstract] [Full Text] [Related]

  • 14. The vitreo-tapeto-retinal degenerations.
    Carr RE, Siegel IM.
    Arch Ophthalmol; 1970 Oct 17; 84(4):436-41 passim. PubMed ID: 5312812
    [No Abstract] [Full Text] [Related]

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  • 19. 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 17; 112(8):1442-7. PubMed ID: 15953638
    [Abstract] [Full Text] [Related]

  • 20. Choroideremia (progressive chorioretinal degeneration).
    Francois J.
    Int Ophthalmol Clin; 1968 Aug 17; 8(4):949-64. PubMed ID: 5741530
    [No Abstract] [Full Text] [Related]

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