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Journal Abstract Search

132 related items for PubMed ID: 6984501

  • 21. Mathematical models of retinitis pigmentosa: a study of the rate of progress in the different genetic forms.
    Pearlman JT.
    Trans Am Ophthalmol Soc; 1979; 77():643-56. PubMed ID: 317544
    [No Abstract] [Full Text] [Related]

  • 22. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1298-304. PubMed ID: 17325176
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  • 23. Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19q.
    Nakazawa M, Xu S, Gal A, Wada Y, Tamai M.
    Arch Ophthalmol; 1996 Mar; 114(3):318-22. PubMed ID: 8600893
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  • 24. Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.
    Owens SL, Fitzke FW, Inglehearn CF, Jay M, Keen TJ, Arden GB, Bhattacharya SS, Bird AC.
    Br J Ophthalmol; 1994 May; 78(5):353-8. PubMed ID: 8025068
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  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Arrestin gene mutations in autosomal recessive retinitis pigmentosa.
    Nakazawa M, Wada Y, Tamai M.
    Arch Ophthalmol; 1998 Apr; 116(4):498-501. PubMed ID: 9565049
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  • 31. Retinitis pigmentosa in the Navajo.
    Heckenlively J, Friederich R, Farson C, Pabalis G.
    Metab Pediatr Ophthalmol; 1981 Apr; 5(3-4):201-6. PubMed ID: 7311662
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  • 32. Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype.
    Farber MD, Fishman GA, Weiss RA.
    Arch Ophthalmol; 1985 Apr; 103(4):524-8. PubMed ID: 3985831
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  • 33. Retinitis pigmentosa: accelerated course of visual loss secondary to exogenous thyroid administration.
    Pearlman JT, Saxton J, Van Herle A.
    Adv Exp Med Biol; 1977 Apr; 77():223-32. PubMed ID: 300551
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  • 34. Statistical evaluation of visual functions in dominant and recessive autosomal pigmentary retinopathy.
    De Rouck A, de Bie S, Kayembe D.
    Doc Ophthalmol; 1986 Mar 31; 62(3):265-80. PubMed ID: 3698795
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  • 35. Retinitis pigmentosa.
    Hamel C.
    Orphanet J Rare Dis; 2006 Oct 11; 1():40. PubMed ID: 17032466
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