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Journal Abstract Search

1148 related items for PubMed ID: 24876279

  • 21. Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.
    Bessant DA, Holder GE, Fitzke FW, Payne AM, Bhattacharya SS, Bird AC.
    Arch Ophthalmol; 2003 Jun; 121(6):793-802. PubMed ID: 12796249
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  • 22. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1298-304. PubMed ID: 17325176
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  • 23. Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History.
    Georgiou M, Grewal PS, Narayan A, Alser M, Ali N, Fujinami K, Webster AR, Michaelides M.
    Am J Ophthalmol; 2021 Jan; 221():299-310. PubMed ID: 32795431
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  • 24. Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.
    Kimchi A, Khateb S, Wen R, Guan Z, Obolensky A, Beryozkin A, Kurtzman S, Blumenfeld A, Pras E, Jacobson SG, Ben-Yosef T, Newman H, Sharon D, Banin E.
    Ophthalmology; 2018 May; 125(5):725-734. PubMed ID: 29276052
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  • 25. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.
    Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT.
    Br J Ophthalmol; 2005 Feb; 89(2):198-206. PubMed ID: 15665353
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  • 26. Long-term clinical course of 2 Japanese patients with PRPF31-related retinitis pigmentosa.
    Kurata K, Hosono K, Hotta Y.
    Jpn J Ophthalmol; 2018 Mar; 62(2):186-193. PubMed ID: 29305715
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  • 27. Clinical and genetic findings in Italian patients with sector retinitis pigmentosa.
    Verdina T, Greenstein VC, Tsang SH, Murro V, Mucciolo DP, Passerini I, Mastropasqua R, Cavallini GM, Virgili G, Giansanti F, Sodi A.
    Mol Vis; 2021 Mar; 27():78-94. PubMed ID: 33688152
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  • 32. Correlation between macular morphology and sensitivity in patients with retinitis pigmentosa and hyperautofluorescent ring.
    Lenassi E, Troeger E, Wilke R, Hawlina M.
    Invest Ophthalmol Vis Sci; 2012 Jan 03; 53(1):47-52. PubMed ID: 22110079
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  • 33. Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma.
    Pierrache LHM, Kimchi A, Ratnapriya R, Roberts L, Astuti GDN, Obolensky A, Beryozkin A, Tjon-Fo-Sang MJH, Schuil J, Klaver CCW, Bongers EMHF, Haer-Wigman L, Schalij N, Breuning MH, Fischer GM, Banin E, Ramesar RS, Swaroop A, van den Born LI, Sharon D, Cremers FPM.
    Ophthalmology; 2017 Jul 03; 124(7):992-1003. PubMed ID: 28412069
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  • 36. Correlation of fundus autofluorescence with photoreceptor morphology and functional changes in eyes with retinitis pigmentosa.
    Wakabayashi T, Sawa M, Gomi F, Tsujikawa M.
    Acta Ophthalmol; 2010 Aug 03; 88(5):e177-83. PubMed ID: 20491687
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  • 39. Fundus autofluorescence imaging in Best's vitelliform dystrophy.
    Jarc-Vidmar M, Kraut A, Hawlina M.
    Klin Monbl Augenheilkd; 2003 Dec 03; 220(12):861-7. PubMed ID: 14704944
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  • 40. Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1.
    Dessalces E, Bocquet B, Bourien J, Zanlonghi X, Verdet R, Meunier I, Hamel CP.
    JAMA Ophthalmol; 2013 Oct 03; 131(10):1314-23. PubMed ID: 23929416
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