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Journal Abstract Search

286 related items for PubMed ID: 16799055

  • 41. Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus.
    Lois N, Holder GE, Fitzke FW, Plant C, Bird AC.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2668-75. PubMed ID: 10509664
    [Abstract] [Full Text] [Related]

  • 42. Comparison of nonmydriatic digital retinal imaging versus dilated ophthalmic examination for nondiabetic eye disease in persons with diabetes.
    Chow SP, Aiello LM, Cavallerano JD, Katalinic P, Hock K, Tolson A, Kirby R, Bursell SE, Aiello LP.
    Ophthalmology; 2006 May; 113(5):833-40. PubMed ID: 16650680
    [Abstract] [Full Text] [Related]

  • 43. EFEMP1 is not associated with sporadic early onset drusen.
    Sauer CG, White K, Kellner U, Rudolph G, Jurklies B, Pauleikhoff D, Weber BH.
    Ophthalmic Genet; 2001 Mar; 22(1):27-34. PubMed ID: 11262647
    [Abstract] [Full Text] [Related]

  • 44. Laser clearance of drusen deposit in patients with autosomal dominant drusen (p.Arg345Trp in EFEMP1).
    Lenassi E, Troeger E, Wilke R, Tufail A, Hawlina M, Jeffery G, Webster AR.
    Am J Ophthalmol; 2013 Jan; 155(1):190-8. PubMed ID: 23036572
    [Abstract] [Full Text] [Related]

  • 45. Distribution of cathepsin D in human eyes with or without age-related maculopathy.
    Rakoczy PE, Sarks SH, Daw N, Constable IJ.
    Exp Eye Res; 1999 Oct; 69(4):367-74. PubMed ID: 10504270
    [Abstract] [Full Text] [Related]

  • 46. Autologous translocation of the choroid and retinal pigment epithelium in age-related macular degeneration.
    Joussen AM, Heussen FM, Joeres S, Llacer H, Prinz B, Rohrschneider K, Maaijwee KJ, van Meurs J, Kirchhof B.
    Am J Ophthalmol; 2006 Jul; 142(1):17-30. PubMed ID: 16815247
    [Abstract] [Full Text] [Related]

  • 47. Autologous transplantation of retinal pigment epithelium-Bruch's membrane complex for hemorrhagic age-related macular degeneration.
    Ma Z, Han L, Wang C, Dou H, Hu Y, Feng X, Xu Y, Wang Z, Yin Z, Liu Y.
    Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2975-81. PubMed ID: 19117919
    [Abstract] [Full Text] [Related]

  • 48. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
    Auslender N, Sharon D, Abbasi AH, Garzozi HJ, Banin E, Ben-Yosef T.
    Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5431-8. PubMed ID: 18055789
    [Abstract] [Full Text] [Related]

  • 49. Clinical findings in a carrier of a new mutation in the choroideremia gene.
    Potter MJ, Wong E, Szabo SM, McTaggart KE.
    Ophthalmology; 2004 Oct; 111(10):1905-9. PubMed ID: 15465555
    [Abstract] [Full Text] [Related]

  • 50. Fundus changes in central retinal artery occlusion.
    Hayreh SS, Zimmerman MB.
    Retina; 2007 Mar; 27(3):276-89. PubMed ID: 17460582
    [Abstract] [Full Text] [Related]

  • 51. [Solitary albinotic spot of the retinal pigment epithelium: a functional and imaging study].
    Barbazetto IA, Maris PJ, Greenstein VC.
    Klin Monbl Augenheilkd; 2008 Apr; 225(4):295-7. PubMed ID: 18401797
    [Abstract] [Full Text] [Related]

  • 52. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
    Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2008 Feb; 49(2):751-7. PubMed ID: 18235024
    [Abstract] [Full Text] [Related]

  • 53. Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.
    Seeliger MW, Biesalski HK, Wissinger B, Gollnick H, Gielen S, Frank J, Beck S, Zrenner E.
    Invest Ophthalmol Vis Sci; 1999 Jan; 40(1):3-11. PubMed ID: 9888420
    [Abstract] [Full Text] [Related]

  • 54. Characteristics of highly myopic eyes: the Beijing Eye Study.
    Xu L, Li Y, Wang S, Wang Y, Wang Y, Jonas JB.
    Ophthalmology; 2007 Jan; 114(1):121-6. PubMed ID: 17070594
    [Abstract] [Full Text] [Related]

  • 55. Autologous translocation of the choroid and retinal pigment epithelium in patients with geographic atrophy.
    Joussen AM, Joeres S, Fawzy N, Heussen FM, Llacer H, van Meurs JC, Kirchhof B.
    Ophthalmology; 2007 Mar; 114(3):551-60. PubMed ID: 17324697
    [Abstract] [Full Text] [Related]

  • 56. Correlation between the area of increased autofluorescence surrounding geographic atrophy and disease progression in patients with AMD.
    Schmitz-Valckenberg S, Bindewald-Wittich A, Dolar-Szczasny J, Dreyhaupt J, Wolf S, Scholl HP, Holz FG, Fundus Autofluorescence in Age-Related Macular Degeneration Study Group.
    Invest Ophthalmol Vis Sci; 2006 Jun; 47(6):2648-54. PubMed ID: 16723482
    [Abstract] [Full Text] [Related]

  • 57. Angiography features of early onset drusen.
    Guigui B, Leveziel N, Martinet V, Massamba N, Sterkers M, Coscas G, Souied EH.
    Br J Ophthalmol; 2011 Feb; 95(2):238-44. PubMed ID: 20610475
    [Abstract] [Full Text] [Related]

  • 58. Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?
    Audo I, Vanakker OM, Smith A, Leroy BP, Robson AG, Jenkins SA, Coucke PJ, Bird AC, De Paepe A, Holder GE, Webster AR.
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4250-6. PubMed ID: 17724214
    [Abstract] [Full Text] [Related]

  • 59. Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.
    Mantel I, Brantley MA, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT.
    Klin Monbl Augenheilkd; 2004 May; 221(5):427-30. PubMed ID: 15162299
    [Abstract] [Full Text] [Related]

  • 60. Association of EFEMP1 with malattia leventinese and age-related macular degeneration: a mini-review.
    Marmorstein L.
    Ophthalmic Genet; 2004 Sep; 25(3):219-26. PubMed ID: 15512998
    [Abstract] [Full Text] [Related]

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