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

128 related items for PubMed ID: 6966889

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Retinitis pigmentosa. Visual loss.
    Fishman GA.
    Arch Ophthalmol; 1978 Jul; 96(7):1185-8. PubMed ID: 307377
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers.
    Fishman GA, Weinberg AB, McMahon TT.
    Arch Ophthalmol; 1986 Sep; 104(9):1329-35. PubMed ID: 3753283
    [Abstract] [Full Text] [Related]

  • 6. Electroretinographic testing as an aid in detection of carriers of X-chromosome-linked retinitis pigmentosa.
    Berson EL, Rosen JB, Simonoff EA.
    Am J Ophthalmol; 1979 Apr; 87(4):460-8. PubMed ID: 443310
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Assessing the risk of retinitis pigmentosa with age-of-onset data.
    Seiff SR, Heckenlively JR, Pearlman JT.
    Am J Ophthalmol; 1982 Jul; 94(1):38-43. PubMed ID: 6979936
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Mathematical models of retinitis pigmentosa: a study of the rate of progress in the different genetic forms.
    Pearlman JT.
    Trans Am Ophthalmol Soc; 1979 Apr 15; 77():643-56. PubMed ID: 317544
    [No Abstract] [Full Text] [Related]

  • 11. Retinitis pigmentosa: problems associated with genetic classification.
    Haim M.
    Clin Genet; 1993 Aug 15; 44(2):62-70. PubMed ID: 8275561
    [Abstract] [Full Text] [Related]

  • 12. Novel compound heterozygous TULP1 mutations in a family with severe early-onset retinitis pigmentosa.
    den Hollander AI, van Lith-Verhoeven JJ, Arends ML, Strom TM, Cremers FP, Hoyng CB.
    Arch Ophthalmol; 2007 Jul 15; 125(7):932-5. PubMed ID: 17620573
    [Abstract] [Full Text] [Related]

  • 13. A survey of hereditary aspects of pigmentary retinal dystrophies.
    Dickinson P, Mulhall L.
    Aust N Z J Ophthalmol; 1989 Aug 15; 17(3):247-56. PubMed ID: 2803770
    [Abstract] [Full Text] [Related]

  • 14. Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
    Wada Y, Sandberg MA, McGee TL, Stillberger MA, Berson EL, Dryja TP.
    Invest Ophthalmol Vis Sci; 2005 May 15; 46(5):1735-41. PubMed ID: 15851576
    [Abstract] [Full Text] [Related]

  • 15. Severity of familial isolated retinitis pigmentosa across different inheritance patterns among an Asian Indian cohort.
    Bende P, Natarajan K, Marudhamuthu T, Madhavan J.
    J Pediatr Ophthalmol Strabismus; 2013 May 15; 50(1):34-6. PubMed ID: 23463886
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Retinitis pigmentosa in South Africa.
    Oswald AH, Goldblatt J, Sampson G, Clokie R, Beighton P.
    S Afr Med J; 1985 Dec 07; 68(12):863-6. PubMed ID: 4071341
    [Abstract] [Full Text] [Related]

  • 19. On the heredity of retinitis pigmentosa.
    Jay M.
    Br J Ophthalmol; 1982 Jul 07; 66(7):405-16. PubMed ID: 7093178
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.