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Journal Abstract Search

142 related items for PubMed ID: 2356700

  • 1.
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  • 4. Rod and cone dysfunction in carriers of X-linked retinitis pigmentosa.
    Peachey NS, Fishman GA, Derlacki DJ, Alexander KR.
    Ophthalmology; 1988 May; 95(5):677-85. PubMed ID: 3174027
    [Abstract] [Full Text] [Related]

  • 5. A genetic linkage study of a kindred with X-linked retinitis pigmentosa.
    Bhattacharya SS, Clayton JF, Harper PS, Hoare GW, Jay MR, Lyness AL, Wright AF.
    Br J Ophthalmol; 1985 May; 69(5):340-7. PubMed ID: 3994951
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  • 6. Electroretinographic findings in retinitis pigmentosa.
    Berson EL.
    Jpn J Ophthalmol; 1987 May; 31(3):327-48. PubMed ID: 2448510
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  • 7. A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa.
    Grover S, Fishman GA, Anderson RJ, Lindeman M.
    Ophthalmology; 2000 Feb; 107(2):386-96. PubMed ID: 10690843
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  • 8. A modified ERG technique and the results obtained in X-linked retinitis pigmentosa.
    Arden GB, Carter RM, Hogg CR, Powell DJ, Ernst WJ, Clover GM, Lyness AL, Quinlan MP.
    Br J Ophthalmol; 1983 Jul; 67(7):419-30. PubMed ID: 6860609
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  • 9. Retinitis pigmentosa and allied diseases: applications of electroretinographic testing.
    Berson EL.
    Int Ophthalmol; 1981 Aug; 4(1-2):7-22. PubMed ID: 7028651
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  • 10. Carrier detection in X-linked retinitis pigmentosa.
    Gurvitz A, Leigh DA, Halliday F, Lai LY, McDonald BL.
    Aust N Z J Ophthalmol; 1994 May; 22(2):111-3. PubMed ID: 7917263
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  • 11. Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.
    Andréasson S, Ponjavic V, Abrahamson M, Ehinger B, Wu W, Fujita R, Buraczynska M, Swaroop A.
    Am J Ophthalmol; 1997 Jul; 124(1):95-102. PubMed ID: 9222238
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  • 12. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
    Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A.
    Ophthalmology; 1998 Dec; 105(12):2286-96. PubMed ID: 9855162
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  • 13. [Molecular genetic diagnosis in X chromosome-linked retinitis pigmentosa].
    Hogenkamp T, Wienker TF, Majewski F, Gal A.
    Klin Monbl Augenheilkd; 1987 Oct; 191(4):307-9. PubMed ID: 2891868
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  • 14. [X-linked retinitis pigmentosa].
    Ignaczak R, Sobolewski P.
    Klin Oczna; 1992 Oct; 94(2-3):78-9. PubMed ID: 1640690
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  • 15. Visual Function in Carriers of X-Linked Retinitis Pigmentosa.
    Comander J, Weigel-DiFranco C, Sandberg MA, Berson EL.
    Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542
    [Abstract] [Full Text] [Related]

  • 16. X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGR.
    Weleber RG, Butler NS, Murphey WH, Sheffield VC, Stone EM.
    Arch Ophthalmol; 1997 Nov; 115(11):1429-35. PubMed ID: 9366675
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  • 17. Detection using the multifocal electroretinogram of mosaic retinal dysfunction in carriers of X-linked retinitis pigmentosa.
    Vajaranant TS, Seiple W, Szlyk JP, Fishman GA.
    Ophthalmology; 2002 Mar; 109(3):560-8. PubMed ID: 11874762
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  • 18. Dependence of cone b-wave implicit time on rod amplitude in retinitis pigmentosa.
    Birch DG, Sandberg MA.
    Vision Res; 1987 Mar; 27(7):1105-12. PubMed ID: 3660664
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  • 19. The electroretinogram in retinitis pigmentosa.
    Marmor MF.
    Arch Ophthalmol; 1979 Jul; 97(7):1300-4. PubMed ID: 454267
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  • 20. Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation.
    Rosenfeld PJ, Hahn LB, Sandberg MA, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 1995 Oct; 36(11):2186-92. PubMed ID: 7558711
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