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Journal Abstract Search

132 related items for PubMed ID: 6984501

  • 1. Dominant retinitis pigmentosa. A clinicopathologic correlation.
    Meyer KT, Heckenlively JR, Spitznas M, Foos RY.
    Ophthalmology; 1982 Dec; 89(12):1414-24. PubMed ID: 6984501
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  • 2. A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa.
    Grover S, Fishman GA, Stone EM.
    Ophthalmology; 2004 Oct; 111(10):1910-6. PubMed ID: 15465556
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  • 3. Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia.
    Lam BL, Judisch GF.
    Am J Ophthalmol; 1991 Apr 15; 111(4):454-6. PubMed ID: 2012147
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  • 4. Concentric retinitis pigmentosa: clinicopathologic correlations.
    Milam AH, De Castro EB, Smith JE, Tang WX, John SK, Gorin MB, Stone EM, Aguirre GD, Jacobson SG.
    Exp Eye Res; 2001 Oct 15; 73(4):493-508. PubMed ID: 11825021
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  • 6. Clinical and serum lipid findings in a large family with autosomal dominant retinitis pigmentosa.
    Newsome DA, Anderson RE, May JG, McKay TA, Maude M.
    Ophthalmology; 1988 Dec 15; 95(12):1691-5. PubMed ID: 3266001
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  • 7. Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.
    Bessant DA, Holder GE, Fitzke FW, Payne AM, Bhattacharya SS, Bird AC.
    Arch Ophthalmol; 2003 Jun 15; 121(6):793-802. PubMed ID: 12796249
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  • 8. Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8.
    Maubaret CG, Vaclavik V, Mukhopadhyay R, Waseem NH, Churchill A, Holder GE, Moore AT, Bhattacharya SS, Webster AR.
    Invest Ophthalmol Vis Sci; 2011 Dec 02; 52(13):9304-9. PubMed ID: 22039234
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  • 11. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
    Neidhardt J, Barthelmes D, Farahmand F, Fleischhauer JC, Berger W.
    Invest Ophthalmol Vis Sci; 2006 Apr 02; 47(4):1630-5. PubMed ID: 16565402
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  • 12. Clinical symptoms at different ages in autosomal dominant retinitis pigmentosa. A family study in three generations.
    Mäntyjärvi M, Tuppurainen K.
    Ophthalmologica; 1994 Apr 02; 208(1):23-8. PubMed ID: 8145980
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  • 13. Retinitis pigmentosa--an overview.
    Allard RE.
    J Am Optom Assoc; 1983 Sep 02; 54(9):793-800. PubMed ID: 6604745
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  • 14. Dominantly inherited retinitis pigmentosa. Ultrastructure and biochemical analysis.
    Rodrigues MM, Wiggert B, Hackett J, Lee L, Fletcher RT, Chader GJ.
    Ophthalmology; 1985 Aug 02; 92(8):1165-72. PubMed ID: 4047608
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  • 16. Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosa.
    Fishman GA, Stone EM, Gilbert LD, Sheffield VC.
    Arch Ophthalmol; 1992 May 02; 110(5):646-53. PubMed ID: 1580841
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  • 18. 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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  • 20. Familial occurrence of retinitis punctata albescens and congenital sensorineural deafness.
    Botelho PJ, Blinder KJ, Shahinfar S.
    Am J Ophthalmol; 1999 Aug 15; 128(2):246-7. PubMed ID: 10458190
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