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Journal Abstract Search

154 related items for PubMed ID: 20069340

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  • 2. Fundus autofluorescence in cone dystrophy.
    Wang NK, Chou CL, Lima LH, Cella W, Tosi J, Yannuzzi LA, Tsang SH.
    Doc Ophthalmol; 2009 Oct; 119(2):141-4. PubMed ID: 19340470
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  • 3. Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.
    Kondo M, Miyake Y, Kondo N, Ueno S, Takakuwa H, Terasaki H.
    Ophthalmology; 2004 Apr; 111(4):732-9. PubMed ID: 15051206
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  • 8. A rare case of RGR/CDHR1 haplotype identified in Bulgarian patient with cone-rod dystrophy.
    Mermeklieva E, Kamenarova K, Mihova K, Shakola F, Kaneva R.
    Ophthalmic Genet; 2021 Dec; 42(6):747-752. PubMed ID: 34229535
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  • 11. Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy.
    Mäntyjärvi M, Nurmenniemi P, Partanen J, Myöhänen T, Peippo M, Alitalo T.
    Acta Ophthalmol Scand; 2001 Aug; 79(4):359-65. PubMed ID: 11453854
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  • 17. Clinical study of a large family with autosomal dominant progressive cone degeneration.
    Small KW, Gehrs K.
    Am J Ophthalmol; 1996 Jan; 121(1):1-12. PubMed ID: 8554074
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  • 18. Foveal cavitation as an optical coherence tomography finding in central cone dysfunction.
    Leng T, Marmor MF, Kellner U, Thompson DA, Renner AB, Moore W, Sowden JC.
    Retina; 2012 Jul; 32(7):1411-9. PubMed ID: 22466470
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