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Journal Abstract Search


172 related items for PubMed ID: 8145980

  • 1. Clinical symptoms at different ages in autosomal dominant retinitis pigmentosa. A family study in three generations.
    Mäntyjärvi M, Tuppurainen K.
    Ophthalmologica; 1994; 208(1):23-8. PubMed ID: 8145980
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  • 2. 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; 73(4):493-508. PubMed ID: 11825021
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  • 3. Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene.
    Kozma P, Hughbanks-Wheaton DK, Locke KG, Fish GE, Gire AI, Spellicy CJ, Sullivan LS, Bowne SJ, Daiger SP, Birch DG.
    Am J Ophthalmol; 2005 Nov; 140(5):858-867. PubMed ID: 16214101
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  • 6. 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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  • 11. 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; 121(6):793-802. PubMed ID: 12796249
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  • 14. Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study.
    Rosas DJ, Roman AJ, Weissbrod P, Macke JP, Nathans J.
    Invest Ophthalmol Vis Sci; 1994 Jul; 35(8):3134-44. PubMed ID: 8045708
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  • 16. Sector retinitis pigmentosa. Electrophysiological and psychophysical study of the visual system.
    Abraham FA.
    Doc Ophthalmol; 1975 Nov 21; 39(1):13-28. PubMed ID: 1201696
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  • 18. Vision change after sheet transplant of fetal retina with retinal pigment epithelium to a patient with retinitis pigmentosa.
    Radtke ND, Aramant RB, Seiler MJ, Petry HM, Pidwell D.
    Arch Ophthalmol; 2004 Aug 21; 122(8):1159-65. PubMed ID: 15302656
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  • 19. Clinical and electrophysiological observations on genetic carriers of retinitis pigmentosa in a family (pedigree Tt) showing sex-linked inheritance.
    Imaizumi K, Takahashi R, Tazawa Y, Yamada K, Mita K.
    Adv Exp Med Biol; 1972 Aug 21; 24(0):301-7. PubMed ID: 4671885
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  • 20. 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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