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Journal Abstract Search

173 related items for PubMed ID: 11431457

  • 21.
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  • 22. Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa.
    Jacobson SG, Cideciyan AV, Iannaccone A, Weleber RG, Fishman GA, Maguire AM, Affatigato LM, Bennett J, Pierce EA, Danciger M, Farber DB, Stone EM.
    Invest Ophthalmol Vis Sci; 2000 Jun; 41(7):1898-908. PubMed ID: 10845615
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  • 23. Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in the C1QTNF5 gene.
    De Zaeytijd J, Coppieters F, De Bruyne M, Van Royen J, Roels D, Six R, Van Cauwenbergh C, De Baere E, Leroy BP.
    Ophthalmic Genet; 2021 Oct; 42(5):521-532. PubMed ID: 33949280
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  • 27. Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy.
    Bonilha VL, Hollyfield JG, Grover S, Fishman GA.
    Ophthalmic Genet; 2005 Jun; 26(2):69-76. PubMed ID: 16020309
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  • 28. Abnormal dark adaptation and rhodopsin kinetics in Sorsby's fundus dystrophy.
    Steinmetz RL, Polkinghorne PC, Fitzke FW, Kemp CM, Bird AC.
    Invest Ophthalmol Vis Sci; 1992 Apr; 33(5):1633-6. PubMed ID: 1559761
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  • 29. Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.
    Evans K, Duvall-Young J, Fitzke FW, Arden GB, Bhattacharya SS, Bird AC.
    Arch Ophthalmol; 1995 Feb; 113(2):195-201. PubMed ID: 7864751
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  • 30. Hereditary macular dystrophy. A clinical and genetic study of two specific forms.
    Pearce WG.
    Can J Ophthalmol; 1975 Jul; 10(3):319-25. PubMed ID: 1148903
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  • 33. Pattern dystrophy of the retinal pigment epithelium and geographic atrophy of the macula.
    Marmor MF, McNamara JA.
    Am J Ophthalmol; 1996 Sep; 122(3):382-92. PubMed ID: 8794711
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  • 34.
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  • 35. Aging and cone dark adaptation.
    Gaffney AJ, Binns AM, Margrain TH.
    Optom Vis Sci; 2012 Aug; 89(8):1219-24. PubMed ID: 22773176
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  • 36. Progressive cone dystrophy.
    Ripps H, Noble KG, Greenstein VC, Siegel IM, Carr RE.
    Trans Am Ophthalmol Soc; 1987 Aug; 85():82-100. PubMed ID: 3502298
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  • 39. Retinal functions in dominant cystoid macular dystrophy (DCMD).
    Pinckers A, Deutman AF, Notting JG.
    Acta Ophthalmol (Copenh); 1976 Oct; 54(5):579-90. PubMed ID: 990013
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  • 40. X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon.
    Heckenlively JR, Weleber RG.
    Arch Ophthalmol; 1986 Sep; 104(9):1322-8. PubMed ID: 3489456
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