These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

172 related items for PubMed ID: 8145980

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.
    Shiono T, Hotta Y, Noro M, Sakuma T, Tamai M, Hayakawa M, Hashimoto T, Fujiki K, Kanai A, Nakajima A.
    Jpn J Ophthalmol; 1992; 36(1):69-75. PubMed ID: 1635298
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity.
    Robson AG, Egan CA, Luong VA, Bird AC, Holder GE, Fitzke FW.
    Invest Ophthalmol Vis Sci; 2004 Nov; 45(11):4119-25. PubMed ID: 15505064
    [Abstract] [Full Text] [Related]

  • 30. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
    Berson EL, Grimsby JL, Adams SM, McGee TL, Sweklo E, Pierce EA, Sandberg MA, Dryja TP.
    Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2217-24. PubMed ID: 11527933
    [Abstract] [Full Text] [Related]

  • 31. Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-up.
    Robson AG, Lenassi E, Saihan Z, Luong VA, Fitzke FW, Holder GE, Webster AR.
    Invest Ophthalmol Vis Sci; 2012 Sep 14; 53(10):6187-95. PubMed ID: 22899761
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa.
    Sandberg MA, Weigel-DiFranco C, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 1995 Aug 14; 36(9):1934-42. PubMed ID: 7635666
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Transient pupillary light reflex in relation to fundus autofluorescence and dark-adapted perimetry in typical retinitis pigmentosa.
    Liu Y, Liu DN, Meng XH, Yin ZQ.
    Ophthalmic Res; 2012 Aug 14; 47(3):113-21. PubMed ID: 21997281
    [Abstract] [Full Text] [Related]

  • 39. Dominant retinitis pigmentosa. A clinicopathologic correlation.
    Meyer KT, Heckenlively JR, Spitznas M, Foos RY.
    Ophthalmology; 1982 Dec 14; 89(12):1414-24. PubMed ID: 6984501
    [Abstract] [Full Text] [Related]

  • 40. Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin.
    Apfelstedt-Sylla E, Kunisch M, Horn M, Rüther K, Gal A, Zrenner E.
    Ger J Ophthalmol; 1992 Dec 14; 1(5):319-27. PubMed ID: 1477634
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.