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Journal Abstract Search

391 related items for PubMed ID: 7943119

  • 1. Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epithelium.
    van den Born LI, van Soest S, van Schooneveld MJ, Riemslag FC, de Jong PT, Bleeker-Wagemakers EM.
    Am J Ophthalmol; 1994 Oct 15; 118(4):430-9. PubMed ID: 7943119
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  • 4. Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.
    Heckenlively JR.
    Br J Ophthalmol; 1982 Jan 15; 66(1):26-30. PubMed ID: 7055539
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  • 6. Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.
    Heckenlively JR.
    Birth Defects Orig Artic Ser; 1982 Jan 15; 18(6):193-6. PubMed ID: 7171755
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  • 7. CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservation.
    Lotery AJ, Malik A, Shami SA, Sindhi M, Chohan B, Maqbool C, Moore PA, Denton MJ, Stone EM.
    Ophthalmic Genet; 2001 Sep 15; 22(3):163-9. PubMed ID: 11559858
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  • 14. Retinal fluorescein leakage in retinitis pigmentosa.
    Newsome DA.
    Am J Ophthalmol; 1986 Mar 15; 101(3):354-60. PubMed ID: 3953729
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  • 15. Bull's-eye macular dystrophy associated with peripheral involvement.
    Suzuki R, Hirose T.
    Ophthalmologica; 1998 Mar 15; 212(4):260-7. PubMed ID: 9672216
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  • 17. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
    den Hollander AI, ten Brink JB, de Kok YJ, van Soest S, van den Born LI, van Driel MA, van de Pol DJ, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, Heckenlively JR, Cremers FP, Bergen AA.
    Nat Genet; 1999 Oct 15; 23(2):217-21. PubMed ID: 10508521
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  • 19. Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N.
    Tsui I, Chou CL, Palmer N, Lin CS, Tsang SH.
    Curr Eye Res; 2008 Nov 15; 33(11):1014-22. PubMed ID: 19085385
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