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Journal Abstract Search

119 related items for PubMed ID: 18844018

  • 61. Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1).
    Small KW, Jampol LM, Bakall B, Small L, Wiggins R, Agemy S, Udar N, Avetisjan J, Vincent A, Shaya FS.
    Ophthalmic Genet; 2021 Dec 13; ():1-11. PubMed ID: 34895015
    [Abstract] [Full Text] [Related]

  • 62. Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).
    Marquardt A, Stöhr H, Passmore LA, Krämer F, Rivera A, Weber BH.
    Hum Mol Genet; 1998 Sep 13; 7(9):1517-25. PubMed ID: 9700209
    [Abstract] [Full Text] [Related]

  • 63. VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.
    White K, Marquardt A, Weber BH.
    Hum Mutat; 2000 Sep 13; 15(4):301-8. PubMed ID: 10737974
    [Abstract] [Full Text] [Related]

  • 64. Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2.
    Subash M, Rotsos T, Wright GA, Devery S, Holder GE, Robson AG, Pal B, Tufail A, Webster AR, Moore AT, Michaelides M.
    Br J Ophthalmol; 2012 May 13; 96(5):719-22. PubMed ID: 22174098
    [Abstract] [Full Text] [Related]

  • 65. Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.
    Caldwell GM, Kakuk LE, Griesinger IB, Simpson SA, Nowak NJ, Small KW, Maumenee IH, Rosenfeld PJ, Sieving PA, Shows TB, Ayyagari R.
    Genomics; 1999 May 15; 58(1):98-101. PubMed ID: 10331951
    [Abstract] [Full Text] [Related]

  • 66. Association of Clinical and Genetic Heterogeneity With BEST1 Sequence Variations.
    Shah M, Broadgate S, Shanks M, Clouston P, Yu J, MacLaren RE, Németh AH, Halford S, Downes SM.
    JAMA Ophthalmol; 2020 May 01; 138(5):544-551. PubMed ID: 32239196
    [Abstract] [Full Text] [Related]

  • 67. [Congenital dystrophy: unilateral involvement in vitelliform retinal dystrophy or Best disease].
    Meunier I, Ben Salah S, Arndt C, Hamel C.
    J Fr Ophtalmol; 2008 Jun 01; 31(6 Pt 1):640-1. PubMed ID: 18772821
    [No Abstract] [Full Text] [Related]

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  • 70. Multimodal imaging and genetic analysis of adult-onset best vitelliform macular dystrophy in Chinese patients.
    Lin Y, Li T, Liu B, Lyu C, Lian Y, Li J, Huang Y, Li H, Wu Q, Jin C, Lu L.
    Exp Ther Med; 2021 Sep 01; 22(3):1034. PubMed ID: 34373720
    [Abstract] [Full Text] [Related]

  • 71. Novel Presenting Phenotype in a Child With Autosomal Dominant Best's Vitelliform Macular Dystrophy.
    Abdalla YF, De Salvo G, Elsahn A, Self JE.
    Ophthalmic Surg Lasers Imaging Retina; 2017 Jul 01; 48(7):580-585. PubMed ID: 28728185
    [Abstract] [Full Text] [Related]

  • 72. Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.
    Wittström E, Ekvall S, Schatz P, Bondeson ML, Ponjavic V, Andréasson S.
    Ophthalmic Genet; 2011 Jun 01; 32(2):83-96. PubMed ID: 21192766
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  • 74. Chloride channel activity of bestrophin mutants associated with mild or late-onset macular degeneration.
    Yu K, Qu Z, Cui Y, Hartzell HC.
    Invest Ophthalmol Vis Sci; 2007 Oct 01; 48(10):4694-705. PubMed ID: 17898294
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  • 75. High-definition optical coherence tomography features in vitelliform macular dystrophy.
    Querques G, Regenbogen M, Quijano C, Delphin N, Soubrane G, Souied EH.
    Am J Ophthalmol; 2008 Oct 01; 146(4):501-507. PubMed ID: 18619572
    [Abstract] [Full Text] [Related]

  • 76. Deep learning to distinguish Best vitelliform macular dystrophy (BVMD) from adult-onset vitelliform macular degeneration (AVMD).
    Crincoli E, Zhao Z, Querques G, Sacconi R, Carlà MM, Giannuzzi F, Ferrara S, Ribarich N, L'Abbate G, Rizzo S, Souied EH, Miere A.
    Sci Rep; 2022 Jul 26; 12(1):12745. PubMed ID: 35882966
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  • 78. Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.
    Booij JC, Boon CJ, van Schooneveld MJ, ten Brink JB, Bakker A, de Jong PT, Hoyng CB, Bergen AA, Klaver CC.
    Ophthalmology; 2010 Jul 26; 117(7):1415-22. PubMed ID: 20381869
    [Abstract] [Full Text] [Related]

  • 79. Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.
    Allikmets R, Seddon JM, Bernstein PS, Hutchinson A, Atkinson A, Sharma S, Gerrard B, Li W, Metzker ML, Wadelius C, Caskey CT, Dean M, Petrukhin K.
    Hum Genet; 1999 Jun 26; 104(6):449-53. PubMed ID: 10453731
    [Abstract] [Full Text] [Related]

  • 80. Peripherin/RDS and VMD2 mutations in macular dystrophies with adult-onset vitelliform lesion.
    Zhuk SA, Edwards AO.
    Mol Vis; 2006 Jul 24; 12():811-5. PubMed ID: 16885924
    [Abstract] [Full Text] [Related]

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