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Journal Abstract Search

607 related items for PubMed ID: 24845635

  • 21. "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
    Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, Hunt DM, Moore AT, Holder GE.
    Retina; 2010 Jan; 30(1):51-62. PubMed ID: 19952985
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  • 22. High-resolution retinal imaging of cone-rod dystrophy.
    Wolfing JI, Chung M, Carroll J, Roorda A, Williams DR.
    Ophthalmology; 2006 Jun; 113(6):1019.e1. PubMed ID: 16650474
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  • 23. DISCREPANCY BETWEEN FUNDUS AUTOFLUORESCENCE ABNORMALITY AND VISUAL FIELD LOSS IN BIETTI CRYSTALLINE DYSTROPHY.
    Sakai D, Maeda T, Maeda A, Yamamoto M, Yokota S, Hirami Y, Nakamura M, Takahashi M, Mandai M, Kurimoto Y.
    Retina; 2024 Aug 01; 44(8):1394-1402. PubMed ID: 39047130
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  • 24. Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations.
    Manes G, Mamouni S, Hérald E, Richard AC, Sénéchal A, Aouad K, Bocquet B, Meunier I, Hamel CP.
    Mol Vis; 2017 Aug 01; 23():198-209. PubMed ID: 28442884
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  • 25. Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.
    Robson AG, Saihan Z, Jenkins SA, Fitzke FW, Bird AC, Webster AR, Holder GE.
    Br J Ophthalmol; 2006 Apr 01; 90(4):472-9. PubMed ID: 16547330
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  • 26. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
    Boon CJ, van den Born LI, Visser L, Keunen JE, Bergen AA, Booij JC, Riemslag FC, Florijn RJ, van Schooneveld MJ.
    Ophthalmology; 2013 Apr 01; 120(4):809-20. PubMed ID: 23290749
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  • 27. 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 01; 131(10):1314-23. PubMed ID: 23929416
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  • 28. Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.
    Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW.
    Br J Ophthalmol; 2008 Jan 01; 92(1):95-102. PubMed ID: 17962389
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  • 29. High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.
    Duncan JL, Zhang Y, Gandhi J, Nakanishi C, Othman M, Branham KE, Swaroop A, Roorda A.
    Invest Ophthalmol Vis Sci; 2007 Jul 01; 48(7):3283-91. PubMed ID: 17591900
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  • 30. Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.
    Cho SC, Woo SJ, Park KH, Hwang JM.
    Korean J Ophthalmol; 2013 Feb 01; 27(1):19-27. PubMed ID: 23372375
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  • 31. Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.
    Talib M, van Schooneveld MJ, van Genderen MM, Wijnholds J, Florijn RJ, Ten Brink JB, Schalij-Delfos NE, Dagnelie G, Cremers FPM, Wolterbeek R, Fiocco M, Thiadens AA, Hoyng CB, Klaver CC, Bergen AA, Boon CJF.
    Ophthalmology; 2017 Jun 01; 124(6):884-895. PubMed ID: 28341475
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  • 32. SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa.
    Matsui R, McGuigan Iii DB, Gruzensky ML, Aleman TS, Schwartz SB, Sumaroka A, Koenekoop RK, Cideciyan AV, Jacobson SG.
    Ophthalmic Genet; 2016 Sep 01; 37(3):333-8. PubMed ID: 26854980
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  • 33. RP cone-rod degeneration.
    Heckenlively JR.
    Trans Am Ophthalmol Soc; 1987 Sep 01; 85():438-70. PubMed ID: 3447340
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  • 34. Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.
    Scheidecker S, Hull S, Perdomo Y, Studer F, Pelletier V, Muller J, Stoetzel C, Schaefer E, Defoort-Dhellemmes S, Drumare I, Holder GE, Hamel CP, Webster AR, Moore AT, Puech B, Dollfus HJ.
    Am J Ophthalmol; 2015 Aug 01; 160(2):364-372.e1. PubMed ID: 25982971
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  • 35. Ultra-wide-field fundus autofluorescence in multiple evanescent white dot syndrome.
    Hashimoto H, Kishi S.
    Am J Ophthalmol; 2015 Apr 01; 159(4):698-706. PubMed ID: 25634532
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  • 36. Intra-familial Similarity of Wide-Field Fundus Autofluorescence in Inherited Retinal Dystrophy.
    Furutani Y, Ogino K, Oishi A, Gotoh N, Makiyama Y, Oishi M, Kurimoto M, Yoshimura N.
    Adv Exp Med Biol; 2016 Apr 01; 854():299-305. PubMed ID: 26427425
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  • 37. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.
    Ophthalmology; 2002 Oct 01; 109(10):1862-70. PubMed ID: 12359607
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  • 38. High-resolution photoreceptor imaging in idiopathic macular telangiectasia type 2 using adaptive optics scanning laser ophthalmoscopy.
    Ooto S, Hangai M, Takayama K, Arakawa N, Tsujikawa A, Koizumi H, Oshima S, Yoshimura N.
    Invest Ophthalmol Vis Sci; 2011 Jul 25; 52(8):5541-50. PubMed ID: 21642620
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  • 39. Near-infrared fundus autofluorescence in subclinical best vitelliform macular dystrophy.
    Parodi MB, Iacono P, Del Turco C, Bandello F.
    Am J Ophthalmol; 2014 Dec 25; 158(6):1247-1252.e2. PubMed ID: 25174897
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  • 40. Electrophysiological testing as a method of cone-rod and cone dystrophy diagnoses and prediction of disease progression.
    Langwińska-Wośko E, Szulborski K, Zaleska-Żmijewska A, Szaflik J.
    Doc Ophthalmol; 2015 Apr 25; 130(2):103-9. PubMed ID: 25603773
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