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182 related items for PubMed ID: 16612637

  • 21. Screening for BEST1 gene mutations in Chinese patients with bestrophinopathy.
    Tian R, Yang G, Wang J, Chen Y.
    Mol Vis; 2014; 20():1594-604. PubMed ID: 25489231
    [Abstract] [Full Text] [Related]

  • 22. Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy.
    Seddon JM, Afshari MA, Sharma S, Bernstein PS, Chong S, Hutchinson A, Petrukhin K, Allikmets R.
    Ophthalmology; 2001 Nov; 108(11):2060-7. PubMed ID: 11713080
    [Abstract] [Full Text] [Related]

  • 23. Near-infrared fundus autofluorescence in subclinical best vitelliform macular dystrophy.
    Parodi MB, Iacono P, Del Turco C, Bandello F.
    Am J Ophthalmol; 2014 Dec; 158(6):1247-1252.e2. PubMed ID: 25174897
    [Abstract] [Full Text] [Related]

  • 24. [Gene mutations and clinical features of adult vitelliform macular dystrophy in 5 patients].
    Xue Y, Zhang Y, Wang M, Liu W, Xu G.
    Zhonghua Yan Ke Za Zhi; 2014 Jul; 50(7):523-8. PubMed ID: 25312462
    [Abstract] [Full Text] [Related]

  • 25. Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.
    Iannaccone A, Kerr NC, Kinnick TR, Calzada JI, Stone EM.
    Arch Ophthalmol; 2011 Feb; 129(2):211-7. PubMed ID: 21320969
    [Abstract] [Full Text] [Related]

  • 26. A NOVEL P.ASP304GLY MUTATION IN BEST1 GENE ASSOCIATED WITH ATYPICAL BEST VITELLIFORM MACULAR DYSTROPHY PHENOTYPE AND HIGH INTRAFAMILIAL VARIABILITY.
    Peiretti E, Caminiti G, Forma G, Carboni G, Dhaenens CM, Querques L, Souied E, Querques G.
    Retina; 2016 Sep; 36(9):1733-40. PubMed ID: 26807628
    [Abstract] [Full Text] [Related]

  • 27. A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode.
    Bitner H, Mizrahi-Meissonnier L, Griefner G, Erdinest I, Sharon D, Banin E.
    Invest Ophthalmol Vis Sci; 2011 Jul 18; 52(8):5332-8. PubMed ID: 21467170
    [Abstract] [Full Text] [Related]

  • 28. 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 18; 32(2):83-96. PubMed ID: 21192766
    [Abstract] [Full Text] [Related]

  • 29. Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in Denmark.
    Bitner H, Schatz P, Mizrahi-Meissonnier L, Sharon D, Rosenberg T.
    Am J Ophthalmol; 2012 Aug 18; 154(2):403-412.e4. PubMed ID: 22633354
    [Abstract] [Full Text] [Related]

  • 30. Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy.
    Matson ME, Ly SV, Monarrez JL.
    Optom Vis Sci; 2015 Aug 18; 92(8):e180-9. PubMed ID: 26099059
    [Abstract] [Full Text] [Related]

  • 31. Mutation analysis of BEST1 in Japanese patients with Best's vitelliform macular dystrophy.
    Katagiri S, Hayashi T, Ohkuma Y, Sekiryu T, Takeuchi T, Gekka T, Kondo M, Iwata T, Tsuneoka H.
    Br J Ophthalmol; 2015 Nov 18; 99(11):1577-82. PubMed ID: 26201355
    [Abstract] [Full Text] [Related]

  • 32. Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization.
    Frennesson CI, Wadelius C, Nilsson SE.
    Acta Ophthalmol; 2014 May 18; 92(3):238-42. PubMed ID: 23617333
    [Abstract] [Full Text] [Related]

  • 33. 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 18; 29(3):139-44. PubMed ID: 18766995
    [Abstract] [Full Text] [Related]

  • 34. BEST1 sequence variants in Italian patients with vitelliform macular dystrophy.
    Sodi A, Passerini I, Murro V, Caputo R, Bacci GM, Bodoj M, Torricelli F, Menchini U.
    Mol Vis; 2012 Sep 18; 18():2736-48. PubMed ID: 23213274
    [Abstract] [Full Text] [Related]

  • 35. Novel and homozygous BEST1 mutations in Chinese patients with Best vitelliform macular dystrophy.
    Wong RL, Hou P, Choy KW, Chiang SW, Tam PO, Li H, Chan WM, Lam DS, Pang CP, Lai TY.
    Retina; 2010 May 18; 30(5):820-7. PubMed ID: 20057343
    [Abstract] [Full Text] [Related]

  • 36. New best1 mutations in autosomal recessive bestrophinopathy.
    Fung AT, Yzer S, Goldberg N, Wang H, Nissen M, Giovannini A, Merriam JE, Bukanova EN, Cai C, Yannuzzi LA, Tsang SH, Allikmets R.
    Retina; 2015 Apr 18; 35(4):773-82. PubMed ID: 25545482
    [Abstract] [Full Text] [Related]

  • 37. Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy.
    Qian CX, Charran D, Strong CR, Steffens TJ, Jayasundera T, Heckenlively JR.
    Ophthalmology; 2017 Apr 18; 124(4):456-463. PubMed ID: 28187978
    [Abstract] [Full Text] [Related]

  • 38. Clinical evaluation of two consanguineous families with homozygous mutations in BEST1.
    Piñeiro-Gallego T, Álvarez M, Pereiro I, Campos S, Sharon D, Schatz P, Valverde D.
    Mol Vis; 2011 Apr 18; 17():1607-17. PubMed ID: 21738390
    [Abstract] [Full Text] [Related]

  • 39. Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2.
    Schatz P, Klar J, Andréasson S, Ponjavic V, Dahl N.
    Ophthalmic Genet; 2006 Jun 18; 27(2):51-6. PubMed ID: 16754206
    [Abstract] [Full Text] [Related]

  • 40. BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene.
    Toto L, Boon CJ, Di Antonio L, Battaglia Parodi M, Mastropasqua R, Antonucci I, Stuppia L, Mastropasqua L.
    Retina; 2016 Aug 18; 36(8):1586-95. PubMed ID: 26716959
    [Abstract] [Full Text] [Related]

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