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Journal Abstract Search

167 related items for PubMed ID: 16340543

  • 1. Disappearance of puncta after uveitis in an eye with fundus albipunctatus.
    Imaizumi M, Tatewaki SY, Kimoto K, Takaki Y, Nakatsuka K, Furushima M, Matsumoto CS, Choshi T.
    Retina; 2005 Dec; 25(8):1096-8. PubMed ID: 16340543
    [No Abstract] [Full Text] [Related]

  • 2. Spectral-domain optical coherence tomography and fundus autofluorescence characteristics in patients with fundus albipunctatus and retinitis punctata albescens.
    Genead MA, Fishman GA, Lindeman M.
    Ophthalmic Genet; 2010 Jun; 31(2):66-72. PubMed ID: 20450307
    [Abstract] [Full Text] [Related]

  • 3. Fundus albipunctatus and other flecked retina syndromes.
    Flynn MF, Bohnert D.
    J Am Optom Assoc; 1999 Sep; 70(9):571-80. PubMed ID: 10547972
    [Abstract] [Full Text] [Related]

  • 4. Retinal findings in a patient of French ancestry with CABP4-related retinal disease.
    Smirnov VM, Zeitz C, Soumittra N, Audo I, Defoort-Dhellemmes S.
    Doc Ophthalmol; 2018 Apr; 136(2):135-143. PubMed ID: 29525873
    [Abstract] [Full Text] [Related]

  • 5. Macular dystrophy in a 9-year-old boy with fundus albipunctatus.
    Nakamura M, Miyake Y.
    Am J Ophthalmol; 2002 Feb; 133(2):278-80. PubMed ID: 11812441
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  • 8. A frequent 1085delC/insGAAG mutation in the RDH5 gene in Japanese patients with fundus albipunctatus.
    Wada Y, Abe T, Fuse N, Tamai M.
    Invest Ophthalmol Vis Sci; 2000 Jun; 41(7):1894-7. PubMed ID: 10845614
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  • 11. Variable expressivity in fundus albipunctatus.
    Margolis S, Siegel IM, Ripps H.
    Ophthalmology; 1987 Nov; 94(11):1416-22. PubMed ID: 3500444
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  • 12. A novel RDH5 gene mutation in a patient with fundus albipunctatus presenting with macular atrophy and fading white dots.
    Yamamoto H, Yakushijin K, Kusuhara S, Escaño MF, Nagai A, Negi A.
    Am J Ophthalmol; 2003 Sep; 136(3):572-4. PubMed ID: 12967826
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  • 13. Spontaneous regression of juvenile retinoschisis.
    Boucher MC.
    Can J Ophthalmol; 1997 Oct; 32(6):392-5. PubMed ID: 9363344
    [No Abstract] [Full Text] [Related]

  • 14. A family with crystalline retinopathy demonstrating an autosomal dominant inheritance pattern.
    Miyauchi O, Murayama K, Adachi-Usami E.
    Retina; 1999 Oct; 19(6):573-4. PubMed ID: 10606466
    [No Abstract] [Full Text] [Related]

  • 15. Clinical and molecular characterization of enhanced S-cone syndrome in children.
    Hull S, Arno G, Sergouniotis PI, Tiffin P, Borman AD, Chandra A, Robson AG, Holder GE, Webster AR, Moore AT.
    JAMA Ophthalmol; 2014 Nov; 132(11):1341-9. PubMed ID: 25079116
    [Abstract] [Full Text] [Related]

  • 16. Clinical course of HTLV-I-associated uveitis.
    Nakao K, Ohba N, Nakagawa M, Osame M.
    Jpn J Ophthalmol; 1999 Nov; 43(5):404-9. PubMed ID: 10580663
    [Abstract] [Full Text] [Related]

  • 17. A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene.
    Nakamura M, Hotta Y, Tanikawa A, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):3925-32. PubMed ID: 11053295
    [Abstract] [Full Text] [Related]

  • 18. Clinical features of human T lymphotropic virus type 1-associated uveitis in Hokkaido, Japan.
    Kase S, Namba K, Kitaichi N, Iwata D, Ohno S, Ishida S.
    Jpn J Ophthalmol; 2013 Jul; 57(4):379-84. PubMed ID: 23608951
    [Abstract] [Full Text] [Related]

  • 19. Young monozygotic twin sisters with fundus albipunctatus and cone dystrophy.
    Nakamura M, Lin J, Miyake Y.
    Arch Ophthalmol; 2004 Aug; 122(8):1203-7. PubMed ID: 15302662
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  • 20. Mutations in the 11-cis retinol dehydrogenase gene in Japanese patients with Fundus albipunctatus.
    Hirose E, Inoue Y, Morimura H, Okamoto N, Fukuda M, Yamamoto S, Fujikado T, Tano Y.
    Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):3933-5. PubMed ID: 11053296
    [Abstract] [Full Text] [Related]

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