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Journal Abstract Search

119 related items for PubMed ID: 18844018

  • 41. Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1.
    Schatz P, Bitner H, Sander B, Holfort S, Andreasson S, Larsen M, Sharon D.
    Invest Ophthalmol Vis Sci; 2010 Sep; 51(9):4754-65. PubMed ID: 20375334
    [Abstract] [Full Text] [Related]

  • 42. 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; 92(3):238-42. PubMed ID: 23617333
    [Abstract] [Full Text] [Related]

  • 43. Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
    Kubota D, Gocho K, Akeo K, Kikuchi S, Sugahara M, Matsumoto CS, Shinoda K, Mizota A, Yamaki K, Takahashi H, Kameya S.
    Doc Ophthalmol; 2016 Jun; 132(3):233-43. PubMed ID: 27071392
    [Abstract] [Full Text] [Related]

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

  • 45. Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy.
    Lin Y, Li T, Gao H, Lian Y, Chen C, Zhu Y, Li Y, Liu B, Zhou W, Jiang H, Liu X, Zhao X, Liang X, Jin C, Huang X, Lu L.
    Mol Med Rep; 2017 Oct; 16(4):4751-4755. PubMed ID: 28791410
    [Abstract] [Full Text] [Related]

  • 46. Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration.
    Krämer F, White K, Pauleikhoff D, Gehrig A, Passmore L, Rivera A, Rudolph G, Kellner U, Andrassi M, Lorenz B, Rohrschneider K, Blankenagel A, Jurklies B, Schilling H, Schütt F, Holz FG, Weber BH.
    Eur J Hum Genet; 2000 Apr; 8(4):286-92. PubMed ID: 10854112
    [Abstract] [Full Text] [Related]

  • 47. Bilateral macular holes and a new onset vitelliform lesion in Best disease.
    Liu J, Xuan Y, Zhang Y, Liu W, Xu G.
    Ophthalmic Genet; 2017 Apr; 38(1):79-82. PubMed ID: 27031371
    [Abstract] [Full Text] [Related]

  • 48. Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and loci.
    Umeda S, Ayyagari R, Allikmets R, Suzuki MT, Karoukis AJ, Ambasudhan R, Zernant J, Okamoto H, Ono F, Terao K, Mizota A, Yoshikawa Y, Tanaka Y, Iwata T.
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):683-91. PubMed ID: 15671300
    [Abstract] [Full Text] [Related]

  • 49. 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; 27(2):51-6. PubMed ID: 16754206
    [Abstract] [Full Text] [Related]

  • 50. Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies.
    Nowomiejska K, Nasser F, Stingl K, Schimpf-Linzenbold S, Biskup S, Brzozowska A, Rejdak R, Kohl S, Zrenner E.
    Acta Ophthalmol; 2022 May; 100(3):e847-e858. PubMed ID: 34327816
    [Abstract] [Full Text] [Related]

  • 51. Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families.
    Chibani Z, Abid IZ, Molbaek A, Söderkvist P, Feki J, Hmani-Aifa M.
    Clin Exp Ophthalmol; 2019 Nov; 47(8):1063-1073. PubMed ID: 31254423
    [Abstract] [Full Text] [Related]

  • 52. 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 Nov; 18():2736-48. PubMed ID: 23213274
    [Abstract] [Full Text] [Related]

  • 53. [Clinical features of Best vitelliform macular dystrophy].
    Ouyang YL, Zhang YJ, Xu GZ, Liu W, Huang X, Jiang CH, Wang L, Qian YS, Li L, Chen Q.
    Zhonghua Yan Ke Za Zhi; 2007 Dec; 43(12):1089-92. PubMed ID: 18331678
    [Abstract] [Full Text] [Related]

  • 54. NOVEL BEST1 MUTATIONS DETECTED BY NEXT-GENERATION SEQUENCING IN A CHINESE POPULATION WITH VITELLIFORM MACULAR DYSTROPHY.
    Guo J, Gao F, Tang W, Qi Y, Xuan Y, Liu W, Li L, Ye X, Xu G, Wu J, Zhang Y.
    Retina; 2019 Aug; 39(8):1613-1622. PubMed ID: 29781975
    [Abstract] [Full Text] [Related]

  • 55. 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]

  • 56. 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; 36(8):1586-95. PubMed ID: 26716959
    [Abstract] [Full Text] [Related]

  • 57. Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1.
    Kellner S, Stöhr H, Fiebig B, Weinitz S, Farmand G, Kellner U, Weber BH.
    Ophthalmic Genet; 2016 Jun; 37(2):201-8. PubMed ID: 26771239
    [Abstract] [Full Text] [Related]

  • 58. Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisons.
    Wang Y, Jiang Y, Li X, Xiao X, Li S, Sun W, Wang P, Zhang Q.
    Exp Eye Res; 2022 Oct; 223():109217. PubMed ID: 35973442
    [Abstract] [Full Text] [Related]

  • 59. 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]

  • 60. Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.
    Crowley C, Paterson R, Lamey T, McLaren T, De Roach J, Chelva E, Khan J.
    Doc Ophthalmol; 2014 Aug; 129(1):57-63. PubMed ID: 24859690
    [Abstract] [Full Text] [Related]

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