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Journal Abstract Search

286 related items for PubMed ID: 16799055

  • 21. Fundus autofluorescence imaging in Best's vitelliform dystrophy.
    Jarc-Vidmar M, Kraut A, Hawlina M.
    Klin Monbl Augenheilkd; 2003 Dec; 220(12):861-7. PubMed ID: 14704944
    [Abstract] [Full Text] [Related]

  • 22. Pseudo-vitelliform macular detachment and cuticular drusen: exclusion of 6 candidate genes.
    Barbazetto IA, Yannuzzi NA, Klais CM, Merriam JE, Zernant J, Peiretti E, Yannuzzi LA, Allikmets R.
    Ophthalmic Genet; 2007 Dec; 28(4):192-7. PubMed ID: 18161617
    [Abstract] [Full Text] [Related]

  • 23. Late onset is common in best macular dystrophy associated with VMD2 gene mutations.
    Renner AB, Tillack H, Kraus H, Krämer F, Mohr N, Weber BH, Foerster MH, Kellner U.
    Ophthalmology; 2005 Apr; 112(4):586-92. PubMed ID: 15808248
    [Abstract] [Full Text] [Related]

  • 24. Malattia leventinese/Doyne honeycomb retinal dystrophy in a chinese family with mutation of the EFEMP1 gene.
    Zhang T, Xie X, Cao G, Jiang H, Wu S, Su Z, Zhang K, Lu F.
    Retina; 2014 Dec; 34(12):2462-71. PubMed ID: 25111685
    [Abstract] [Full Text] [Related]

  • 25. Funduscopic and angiographic appearance in the neuronal ceroid lipofuscinoses.
    Hainsworth DP, Liu GT, Hamm CW, Katz ML.
    Retina; 2009 May; 29(5):657-68. PubMed ID: 19289983
    [Abstract] [Full Text] [Related]

  • 26. Autofluorescence imaging in age-related macular degeneration complicated by choroidal neovascularization: a prospective study.
    Vaclavik V, Vujosevic S, Dandekar SS, Bunce C, Peto T, Bird AC.
    Ophthalmology; 2008 Feb; 115(2):342-6. PubMed ID: 17599415
    [Abstract] [Full Text] [Related]

  • 27. Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).
    Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR.
    Ophthalmology; 2010 Jan; 117(1):120-127.e1. PubMed ID: 19818506
    [Abstract] [Full Text] [Related]

  • 28. The characterization of retinal phenotype in a family with C1QTNF5-related late-onset retinal degeneration.
    Vincent A, Munier FL, Vandenhoven CC, Wright T, Westall CA, Héon E.
    Retina; 2012 Sep; 32(8):1643-51. PubMed ID: 22277927
    [Abstract] [Full Text] [Related]

  • 29. Fifteen-year cumulative incidence of age-related macular degeneration: the Beaver Dam Eye Study.
    Klein R, Klein BE, Knudtson MD, Meuer SM, Swift M, Gangnon RE.
    Ophthalmology; 2007 Feb; 114(2):253-62. PubMed ID: 17270675
    [Abstract] [Full Text] [Related]

  • 30. [Optical coherence tomography in Malattia Leventinese].
    Gaillard MC, Wolfensberger TJ, Uffer S, Mantel I, Pournaras JA, Schorderet DF, Munier FL.
    Klin Monbl Augenheilkd; 2005 Mar; 222(3):180-5. PubMed ID: 15785976
    [Abstract] [Full Text] [Related]

  • 31. Functional aspects of drusen regression in age-related macular degeneration.
    Sallo FB, Rechtman E, Peto T, Stanescu-Segall D, Vogt G, Bird AC, Fitzke FW.
    Br J Ophthalmol; 2009 Oct; 93(10):1345-50. PubMed ID: 19535356
    [Abstract] [Full Text] [Related]

  • 32. Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.
    Atchaneeyasakul LO, Jinda W, Sakolsatayadorn N, Trinavarat A, Ruangvoravate N, Thanasombatskul N, Thongnoppakhun W, Limwongse C.
    Ophthalmic Genet; 2008 Sep; 29(3):139-44. PubMed ID: 18766995
    [Abstract] [Full Text] [Related]

  • 33. Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.
    Hamel CP, Meunier I, Arndt C, Ben Salah S, Lopez S, Bazalgette C, Bazalgette C, Zanlonghi X, Arnaud B, Defoort-Dellhemmes S, Puech B.
    Am J Ophthalmol; 2009 Apr; 147(4):609-20. PubMed ID: 19181301
    [Abstract] [Full Text] [Related]

  • 34. Optical coherent tomography features of malattia leventinese.
    Souied EH, Leveziel N, Letien V, Darmon J, Coscas G, Soubrane G.
    Am J Ophthalmol; 2006 Feb; 141(2):404-7. PubMed ID: 16458713
    [Abstract] [Full Text] [Related]

  • 35. Phenotypic variation in enhanced S-cone syndrome.
    Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE.
    Invest Ophthalmol Vis Sci; 2008 May; 49(5):2082-93. PubMed ID: 18436841
    [Abstract] [Full Text] [Related]

  • 36. [Fundus autofluorescence after selective RPE laser treatment].
    Framme C, Schüle G, Brinkmann R, Birngruber R, Roider J.
    Ophthalmologe; 2002 Nov; 99(11):854-60. PubMed ID: 12430038
    [Abstract] [Full Text] [Related]

  • 37. Spectral domain optical coherence tomography characteristics of cuticular drusen.
    Leng T, Rosenfeld PJ, Gregori G, Puliafito CA, Punjabi OS.
    Retina; 2009 Nov; 29(7):988-93. PubMed ID: 19584657
    [Abstract] [Full Text] [Related]

  • 38. Clinically detectable drusen domains in fibulin-5-associated age-related macular degeneration (AMD) : Drusen subdomains in fibulin-5 AMD.
    Kucukevcilioglu M, Patel CB, Stone EM, Russell SR.
    Int Ophthalmol; 2016 Aug; 36(4):569-75. PubMed ID: 26694911
    [Abstract] [Full Text] [Related]

  • 39. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
    Renner AB, Kellner U, Cropp E, Preising MN, MacDonald IM, van den Hurk JA, Cremers FP, Foerster MH.
    Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340
    [Abstract] [Full Text] [Related]

  • 40. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
    Neidhardt J, Barthelmes D, Farahmand F, Fleischhauer JC, Berger W.
    Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1630-5. PubMed ID: 16565402
    [Abstract] [Full Text] [Related]

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