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Journal Abstract Search

159 related items for PubMed ID: 7847373

  • 41. X-shaped macular dystrophy with flavimaculatus flecks.
    Puech B, Hache JC, Turut P, François P.
    Ophthalmologica; 1989; 199(4):146-57. PubMed ID: 2640291
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  • 42.
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  • 43. A new locus for dominant drusen and macular degeneration maps to chromosome 6q14.
    Kniazeva M, Traboulsi EI, Yu Z, Stefko ST, Gorin MB, Shugart YY, O'Connell JR, Blaschak CJ, Cutting G, Han M, Zhang K.
    Am J Ophthalmol; 2000 Aug; 130(2):197-202. PubMed ID: 11004294
    [Abstract] [Full Text] [Related]

  • 44. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.
    Cremers FP, van de Pol DJ, van Driel M, den Hollander AI, van Haren FJ, Knoers NV, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Deutman AF, Hoyng CB.
    Hum Mol Genet; 1998 Mar; 7(3):355-62. PubMed ID: 9466990
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  • 45.
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  • 46. Sorsby's fundus dystrophy.
    Hamilton WK, Ewing CC, Ives EJ, Carruthers JD.
    Ophthalmology; 1989 Dec; 96(12):1755-62. PubMed ID: 2695876
    [Abstract] [Full Text] [Related]

  • 47. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
    Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.
    Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2458-65. PubMed ID: 11581183
    [Abstract] [Full Text] [Related]

  • 48. Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.
    Hull S, Arno G, Robson AG, Broadgate S, Plagnol V, McKibbin M, Halford S, Michaelides M, Holder GE, Moore AT, Khan KN, Webster AR.
    JAMA Ophthalmol; 2016 Sep 01; 134(9):992-1000. PubMed ID: 27386845
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  • 49. Stargardt's disease and fundus flavimaculatus.
    Noble KG, Carr RE.
    Arch Ophthalmol; 1979 Jul 01; 97(7):1281-5. PubMed ID: 454263
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  • 51. Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.
    Khaliq S, Hameed A, Ismail M, Anwar K, Leroy BP, Mehdi SQ, Payne AM, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2000 Nov 01; 41(12):3709-12. PubMed ID: 11053266
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  • 52.
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  • 53. Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter.
    Weber BH, Vogt G, Wolz W, Ives EJ, Ewing CC.
    Nat Genet; 1994 Jun 01; 7(2):158-61. PubMed ID: 7920634
    [Abstract] [Full Text] [Related]

  • 54. Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21.
    Héon E, Piguet B, Munier F, Sneed SR, Morgan CM, Forni S, Pescia G, Schorderet D, Taylor CM, Streb LM, Wiles CD, Nishimura DY, Sheffield VC, Stone EM.
    Arch Ophthalmol; 1996 Feb 01; 114(2):193-8. PubMed ID: 8573024
    [Abstract] [Full Text] [Related]

  • 55. Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography.
    Querques G, Leveziel N, Benhamou N, Voigt M, Soubrane G, Souied EH.
    Br J Ophthalmol; 2006 Sep 01; 90(9):1157-62. PubMed ID: 16754647
    [Abstract] [Full Text] [Related]

  • 56. Linkage studies of Best's macular dystrophy.
    Yoder FE, Cross HE, Chase GA, Fine SL, Freidhoff L, Machan CH, Bias WB.
    Clin Genet; 1988 Jul 01; 34(1):26-30. PubMed ID: 3165727
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  • 57. [From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa].
    Cremers FP, Maugeri A, Klevering BJ, Hoefsloot LH, Hoyng CB.
    Ned Tijdschr Geneeskd; 2002 Aug 24; 146(34):1581-4. PubMed ID: 12224481
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  • 58. Dominant slowly progressive macular dystrophy.
    Singerman LJ, Berkow JW, Patz A.
    Am J Ophthalmol; 1977 May 24; 83(5):680-93. PubMed ID: 868967
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  • 59. [Fundus autofluorescence imaging in patients with Stargardt dystrophy and fundus flavimaculatus].
    Dolar-Szczasny J, Mackiewicz J, Biziorek B, Zagórski Z.
    Klin Oczna; 2007 May 24; 109(4-6):176-8. PubMed ID: 17725280
    [Abstract] [Full Text] [Related]

  • 60. Long-term follow-up of Stargardt's disease and fundus flavimaculatus.
    Armstrong JD, Meyer D, Xu S, Elfervig JL.
    Ophthalmology; 1998 Mar 24; 105(3):448-57; discussion 457-8. PubMed ID: 9499775
    [Abstract] [Full Text] [Related]

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