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Journal Abstract Search

95 related items for PubMed ID: 1513552

  • 1. Perimetric testing of tritan deficiency.
    Leinonen MT, Elenius V.
    Ophthalmologica; 1992; 204(4):204-9. PubMed ID: 1513552
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  • 2. Rod thresholds in dominantly inherited juvenile optic atrophy.
    Elenius V, Leinonen M, Airas K.
    Ophthalmologica; 1991; 202(4):208-12. PubMed ID: 1945301
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  • 3. Color vision in dominant optic atrophy.
    Mäntyjärvi MI, Nerdrum K, Tuppurainen K.
    J Clin Neuroophthalmol; 1992 Jun; 12(2):98-103. PubMed ID: 1629378
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  • 4. Electrophysiology and colour perimetry in dominant infantile optic atrophy.
    Berninger TA, Jaeger W, Krastel H.
    Br J Ophthalmol; 1991 Jan; 75(1):49-52. PubMed ID: 1991088
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  • 9. A new perimetric color vision analyzer.
    Iijima H, Satoh S.
    Jpn J Ophthalmol; 1988 Jan; 32(4):412-22. PubMed ID: 3266266
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  • 10. The assessment of acquired dyschromatopsia and clinical investigation of the acquired tritan defect in dominantly inherited juvenile atrophy.
    Smith DP.
    Am J Optom Arch Am Acad Optom; 1972 Jul; 49(7):574-88. PubMed ID: 4538241
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  • 13. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.
    Jacobson DM, Stone EM.
    J Clin Neuroophthalmol; 1991 Sep; 11(3):152-7. PubMed ID: 1836796
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  • 14. Dominant optic atrophy. The clinical profile.
    Kline LB, Glaser JS.
    Arch Ophthalmol; 1979 Sep; 97(9):1680-6. PubMed ID: 314284
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  • 15. Tritan pedigree without optic-nerve atrophy.
    Higgins KE, Brooks DN, Gottschalk G.
    Am J Optom Physiol Opt; 1983 Dec; 60(12):964-9. PubMed ID: 6606981
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  • 20. Chromatic discrimination losses in multiple sclerosis patients with and without optic neuritis using the Cambridge Colour Test.
    Moura AL, Teixeira RA, Oiwa NN, Costa MF, Feitosa-Santana C, Callegaro D, Hamer RD, Ventura DF.
    Vis Neurosci; 2008 Dec; 25(3):463-8. PubMed ID: 18598419
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