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Journal Abstract Search

146 related items for PubMed ID: 8145394

  • 41. Variable expressivity of ocular associations of foveal hypoplasia in a family.
    Vincent A, Kemmanu V, Shetty R, Anandula V, Madhavarao B, Shetty B.
    Eye (Lond); 2009 Aug; 23(8):1735-9. PubMed ID: 19590516
    [Abstract] [Full Text] [Related]

  • 42. Impact of visual impairment on measures of cognitive function for children with congenital toxoplasmosis: implications for compensatory intervention strategies.
    Roizen N, Kasza K, Karrison T, Mets M, Noble AG, Boyer K, Swisher C, Meier P, Remington J, Jalbrzikowski J, McLeod R, Kipp M, Rabiah P, Chamot D, Estes R, Cezar S, Mack D, Pfiffner L, Stein M, Danis B, Patel D, Hopkins J, Holfels E, Stein L, Withers S, Cameron A, Perkins J, Heydemann P.
    Pediatrics; 2006 Aug; 118(2):e379-90. PubMed ID: 16864640
    [Abstract] [Full Text] [Related]

  • 43. Dystrophia retinae pigmentosa, fundus flavimaculatus and Stargardt's disease in one family.
    van Meel GJ, Winkelman JE.
    Ophthalmologica; 1982 Aug; 184(1):13-20. PubMed ID: 7054737
    [Abstract] [Full Text] [Related]

  • 44. Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses.
    Gerber S, Odent S, Postel-Vinay A, Janin N, Dufier JL, Munnich A, Frezal J, Kaplan J.
    J Med Genet; 1994 Mar; 31(3):222-3. PubMed ID: 8014971
    [Abstract] [Full Text] [Related]

  • 45. Retinal angiomatous proliferation: natural history and progression of visual loss.
    Viola F, Massacesi A, Orzalesi N, Ratiglia R, Staurenghi G.
    Retina; 2009 Jun; 29(6):732-9. PubMed ID: 19516115
    [Abstract] [Full Text] [Related]

  • 46. [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]

  • 47. Stargardt's type macular dystrophy associated with retinitis pigmentosa.
    Charney RE, Kraushar MF, Appel N.
    Ann Ophthalmol; 1982 Feb; 14(2):118-9. PubMed ID: 7092020
    [Abstract] [Full Text] [Related]

  • 48. Subfoveal exudative age-related macular degeneration: evidence for preoccult disease.
    Shah AR, Del Priore LV.
    Curr Opin Ophthalmol; 2009 May; 20(3):182-7. PubMed ID: 19367162
    [Abstract] [Full Text] [Related]

  • 49. Macular function impairment in eyes with early age-related macular degeneration.
    Midena E, Degli Angeli C, Blarzino MC, Valenti M, Segato T.
    Invest Ophthalmol Vis Sci; 1997 Feb; 38(2):469-77. PubMed ID: 9040480
    [Abstract] [Full Text] [Related]

  • 50. Transpupillary thermotherapy of occult subfoveal choroidal neovascularization in patients with age-related macular degeneration.
    Reichel E, Berrocal AM, Ip M, Kroll AJ, Desai V, Duker JS, Puliafito CA.
    Ophthalmology; 1999 Oct; 106(10):1908-14. PubMed ID: 10519584
    [Abstract] [Full Text] [Related]

  • 51. Sorsby's fundus dystrophy. A South African family with a point mutation on the tissue inhibitor of metalloproteinases-3 gene on chromosome 22.
    Peters AL, Greenberg J.
    Retina; 1995 Oct; 15(6):480-5. PubMed ID: 8747441
    [Abstract] [Full Text] [Related]

  • 52. Bilateral microphthalmos with poor visual acuity, high hyperopia, and papillomacular retinal folds in siblings.
    Kida Y, Kurome H, Hayasaka S.
    Jpn J Ophthalmol; 1995 Oct; 39(2):177-9. PubMed ID: 8538075
    [Abstract] [Full Text] [Related]

  • 53. A clinical review of Stargardt's disease and/or fundus flavimaculatus with follow-up.
    Gelisken O, De Laey JJ.
    Int Ophthalmol; 1985 Nov; 8(4):225-35. PubMed ID: 4086170
    [Abstract] [Full Text] [Related]

  • 54. Fundus flavimaculatus: polymorphic retinal change in siblings.
    Isashiki Y, Ohba N.
    Br J Ophthalmol; 1985 Jul; 69(7):522-4. PubMed ID: 4016047
    [Abstract] [Full Text] [Related]

  • 55. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
    [Abstract] [Full Text] [Related]

  • 56. [The clinical application of visual electro-oculography].
    Shan Y.
    Zhonghua Yan Ke Za Zhi; 1989 Nov; 25(6):337-9. PubMed ID: 2627855
    [Abstract] [Full Text] [Related]

  • 57. Adult-onset foveomacular vitelliform dystrophy.
    Do P, Ferrucci S.
    Optometry; 2006 Apr; 77(4):156-66. PubMed ID: 16567277
    [Abstract] [Full Text] [Related]

  • 58. [Stargardt's hereditary macular degeneration--report of 5 cases].
    Huang ZS.
    Zhonghua Yan Ke Za Zhi; 1985 Nov; 21(6):342-3. PubMed ID: 3939206
    [No Abstract] [Full Text] [Related]

  • 59. [Vitelliform dystrophy: study of 2 familial forms].
    Godard G, Bodard-Rickelman E, Laroche MA, Prepin F.
    J Fr Ophtalmol; 1986 Nov; 9(11):717-23. PubMed ID: 3571835
    [Abstract] [Full Text] [Related]

  • 60. Relationship between vision impairment and eye disease to vision-specific quality of life and function in rural India: the Aravind Comprehensive Eye Survey.
    Nirmalan PK, Tielsch JM, Katz J, Thulasiraj RD, Krishnadas R, Ramakrishnan R, Robin AL.
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2308-12. PubMed ID: 15980215
    [Abstract] [Full Text] [Related]

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