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Journal Abstract Search

328 related items for PubMed ID: 22084217

  • 21. Full-field ERG as a predictor of the natural course of ABCA4-associated retinal degenerations.
    Schroeder M, Kjellström U.
    Mol Vis; 2018; 24():1-16. PubMed ID: 29386879
    [Abstract] [Full Text] [Related]

  • 22. Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene.
    van Huet RA, Estrada-Cuzcano A, Banin E, Rotenstreich Y, Hipp S, Kohl S, Hoyng CB, den Hollander AI, Collin RW, Klevering BJ.
    Invest Ophthalmol Vis Sci; 2013 Jul 12; 54(7):4683-90. PubMed ID: 23788369
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  • 23. Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2D.
    Stunkel ML, Brodie SE, Cideciyan AV, Pfeifer WL, Kennedy EL, Stone EM, Jacobson SG, Drack AV.
    Am J Ophthalmol; 2018 Jun 12; 190():58-68. PubMed ID: 29559409
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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 12; 125(5):725-734. PubMed ID: 29276052
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  • 25. Phenotype in two families with RP3 associated with RPGR mutations.
    Lorenz B, Andrassi M, Kretschmann U.
    Ophthalmic Genet; 2003 Jun 12; 24(2):89-101. PubMed ID: 12789573
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  • 28. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.
    Invest Ophthalmol Vis Sci; 1997 Sep 12; 38(10):1983-97. PubMed ID: 9331262
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  • 29. Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation.
    Reinis A, Golovleva I, Köhn L, Sandgren O.
    Acta Ophthalmol; 2013 May 12; 91(3):259-66. PubMed ID: 22405330
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  • 31. 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 May 12; 27():78-94. PubMed ID: 33688152
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  • 32. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
    van Huet RA, Collin RW, Siemiatkowska AM, Klaver CC, Hoyng CB, Simonelli F, Khan MI, Qamar R, Banin E, Cremers FP, Theelen T, den Hollander AI, van den Born LI, Klevering BJ.
    Invest Ophthalmol Vis Sci; 2014 May 29; 55(6):3939-53. PubMed ID: 24876279
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  • 35. Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 Years.
    Cideciyan AV, Charng J, Roman AJ, Sheplock R, Garafalo AV, Heon E, Jacobson SG.
    Invest Ophthalmol Vis Sci; 2018 Sep 04; 59(11):4558-4566. PubMed ID: 30208424
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  • 38. Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene.
    Vaclavik V, Gaillard MC, Tiab L, Schorderet DF, Munier FL.
    Mol Vis; 2010 Mar 19; 16():467-75. PubMed ID: 20309403
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  • 39. Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa.
    Abdulridha-Aboud W, Kjellström U, Andréasson S, Ponjavic V.
    Mol Vis; 2016 Mar 19; 22():362-73. PubMed ID: 27212874
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  • 40. Low-frequency damped electroretinographic wavelets in young asymptomatic patients with dominant retinitis pigmentosa: a new electroretinographic finding.
    Lam BL, Liu M, Hamasaki DI.
    Ophthalmology; 1999 Jun 19; 106(6):1109-13. PubMed ID: 10366078
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