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Journal Abstract Search

107 related items for PubMed ID: 1148903

  • 21. Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy.
    Holz FG, Evans K, Gregory CY, Bhattacharya S, Bird AC.
    Arch Ophthalmol; 1995 Feb; 113(2):178-84. PubMed ID: 7864750
    [Abstract] [Full Text] [Related]

  • 22. Dominant cone-rod dystrophy.
    Hittner HM, Murphree AL, Garcia CA, Justice J, Chokshi DB.
    Doc Ophthalmol; 1975 Nov 21; 39(1):29-52. PubMed ID: 1201699
    [Abstract] [Full Text] [Related]

  • 23. [Hereditary macular degenerations].
    Jaeger W, Alexandridis E, Kraus E, Tenner A, Käfer O.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975 Nov 21; (73):695-735. PubMed ID: 1106398
    [No Abstract] [Full Text] [Related]

  • 24. The diagnostic importance of functional electrooculography in some hereditary dystrophies of the eye fundus.
    François J.
    Ann Ophthalmol; 1971 Sep 21; 3(9):929-46. PubMed ID: 4950484
    [No Abstract] [Full Text] [Related]

  • 25. Stargardt's disease and fundus flavimaculatus.
    Noble KG, Carr RE.
    Arch Ophthalmol; 1979 Jul 21; 97(7):1281-5. PubMed ID: 454263
    [Abstract] [Full Text] [Related]

  • 26. A normal electrooculogram in a patient with a typical vitelliform macular lesion.
    Birndorf LA, Dawson WW.
    Invest Ophthalmol; 1973 Nov 21; 12(11):830-3. PubMed ID: 4752921
    [No Abstract] [Full Text] [Related]

  • 27. [Stargardt's macular degeneration of macular type of diffuse tapeto-retinal degeneration?].
    Schmidt JG, Deom M.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1974 Nov 21; 72():235-42. PubMed ID: 4480199
    [No Abstract] [Full Text] [Related]

  • 28. Diagnostic features of the Favre-Goldmann syndrome.
    Fishman GA, Jampol LM, Goldberg MF.
    Br J Ophthalmol; 1976 May 21; 60(5):345-53. PubMed ID: 1085161
    [Abstract] [Full Text] [Related]

  • 29. Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy.
    Jacobson SG, Cideciyan AV, Bennett J, Kingsley RM, Sheffield VC, Stone EM.
    Arch Ophthalmol; 2002 Mar 21; 120(3):376-9. PubMed ID: 11879143
    [Abstract] [Full Text] [Related]

  • 30. Bilateral macular dysplasia ('colobomata') and congenital retinal dystrophy.
    Moore AT, Taylor DS, Harden A.
    Br J Ophthalmol; 1985 Sep 21; 69(9):691-9. PubMed ID: 4041416
    [Abstract] [Full Text] [Related]

  • 31. [Visual function in Stargardt's disease. Physiopathologic deductions].
    Bessiére E, Verin P, Rougier-Houssin J, Le Rebeller MJ.
    Arch Ophtalmol Rev Gen Ophtalmol; 1969 Sep 21; 29(6):463-77. PubMed ID: 4242349
    [No Abstract] [Full Text] [Related]

  • 32. [Stargardt's disease and fundus flavimaculatus].
    François P, Turut P, Puech B, Hache JC.
    Arch Ophtalmol Rev Gen Ophtalmol; 1975 Nov 21; 35(11):817-46. PubMed ID: 131535
    [Abstract] [Full Text] [Related]

  • 33. [Stargardt's disease (ERG, EOG and chromatic sense)].
    Pinckers A.
    Ann Ocul (Paris); 1971 Dec 21; 204(12):1331-46. PubMed ID: 5150321
    [No Abstract] [Full Text] [Related]

  • 34. The various categories of juvenile macular degeneration.
    Krill AE, Deutman AF.
    Trans Am Ophthalmol Soc; 1972 Dec 21; 70():220-45. PubMed ID: 4541358
    [No Abstract] [Full Text] [Related]

  • 35. [Significance of a macular lesion of undetermined origin in the father for the genetic prognosis of his son, who has infantile macular degeneration (Stargardt's syndrome)].
    Klein D.
    J Genet Hum; 1973 Sep 21; 21(3):229-30. PubMed ID: 4805912
    [No Abstract] [Full Text] [Related]

  • 36. Multifocal electroretinogram (mfERG) in a family with occult macular dystrophy (OMD).
    Wildberger H, Niemeyer G, Junghardt A.
    Klin Monbl Augenheilkd; 2003 Mar 21; 220(3):111-5. PubMed ID: 12664360
    [Abstract] [Full Text] [Related]

  • 37. Macular degeneration of undetermined type: probable autosomal recessive inheritance.
    Goldberg MF, Nissim J.
    Birth Defects Orig Artic Ser; 1971 Mar 21; 7(3):193-5. PubMed ID: 5173142
    [No Abstract] [Full Text] [Related]

  • 38. Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy.
    Arno G, Hull S, Robson AG, Holder GE, Cheetham ME, Webster AR, Plagnol V, Moore AT.
    Invest Ophthalmol Vis Sci; 2015 Apr 21; 56(4):2358-65. PubMed ID: 25766589
    [Abstract] [Full Text] [Related]

  • 39. [Stargardt's disease and its intrafamilial variability].
    Lansel N, Niemeyer G, Thölen A.
    Klin Monbl Augenheilkd; 2000 May 21; 216(5):342-5. PubMed ID: 10863711
    [Abstract] [Full Text] [Related]

  • 40. [Butterfly-shaped dystrophy of the macula (author's transl)].
    Starzycka M, Bryk E.
    Klin Monbl Augenheilkd; 1976 Oct 21; 169(4):454-8. PubMed ID: 994401
    [Abstract] [Full Text] [Related]

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