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Journal Abstract Search

383 related items for PubMed ID: 21436275

  • 21. ATTENUATION OUTER RETINAL BANDS ON OPTICAL COHERENCE TOMOGRAPHY FOLLOWING MACULAR EDEMA: A Possible Manifestation of Photoreceptor Misalignment.
    Paques M, Rossant F, Finocchio L, Grieve K, Sahel JA, Pedinielli A, Mrejen S.
    Retina; 2020 Nov; 40(11):2232-2239. PubMed ID: 31922497
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  • 22. Macular cone abnormalities in retinitis pigmentosa with preserved central vision using adaptive optics scanning laser ophthalmoscopy.
    Makiyama Y, Ooto S, Hangai M, Takayama K, Uji A, Oishi A, Ogino K, Nakagawa S, Yoshimura N.
    PLoS One; 2013 Nov; 8(11):e79447. PubMed ID: 24260224
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  • 23. Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsia.
    Ueno S, Nakanishi A, Sayo A, Kominami T, Ito Y, Hayashi T, Tsunoda K, Iwata T, Terasaki H.
    Doc Ophthalmol; 2017 Apr; 134(2):141-147. PubMed ID: 28197754
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  • 24. High-resolution adaptive optics retinal imaging of cellular structure in choroideremia.
    Morgan JI, Han G, Klinman E, Maguire WM, Chung DC, Maguire AM, Bennett J.
    Invest Ophthalmol Vis Sci; 2014 Sep 04; 55(10):6381-97. PubMed ID: 25190651
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  • 25. Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.
    Langlo CS, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Erker LR, Parker M, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Wilson DJ, Pennesi ME, Lam BL, Chiang J, Chulay JD, Dubra A, Hauswirth WW, Carroll J, ACHM-001 Study Group.
    Invest Ophthalmol Vis Sci; 2016 Aug 01; 57(10):3984-95. PubMed ID: 27479814
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  • 26. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.
    Duncan JL, Ratnam K, Birch DG, Sundquist SM, Lucero AS, Zhang Y, Meltzer M, Smaoui N, Roorda A.
    Invest Ophthalmol Vis Sci; 2011 Dec 20; 52(13):9614-23. PubMed ID: 22110067
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  • 27. Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.
    Ratnam K, Västinsalo H, Roorda A, Sankila EM, Duncan JL.
    JAMA Ophthalmol; 2013 Jan 20; 131(1):67-74. PubMed ID: 22964989
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  • 28. Selective cone photoreceptor injury in acute macular neuroretinopathy.
    Hansen SO, Cooper RF, Dubra A, Carroll J, Weinberg DV.
    Retina; 2013 Sep 20; 33(8):1650-8. PubMed ID: 23615345
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  • 29. Characterization of Retinal Structure in ATF6-Associated Achromatopsia.
    Mastey RR, Georgiou M, Langlo CS, Kalitzeos A, Patterson EJ, Kane T, Singh N, Vincent A, Moore AT, Tsang SH, Lin JH, Young MP, Hartnett ME, Héon E, Kohl S, Michaelides M, Carroll J.
    Invest Ophthalmol Vis Sci; 2019 Jun 03; 60(7):2631-2640. PubMed ID: 31237654
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  • 30. Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders.
    Vincent A, Wright T, Billingsley G, Westall C, Héon E.
    Ophthalmic Genet; 2011 Jun 03; 32(2):107-13. PubMed ID: 21268679
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  • 31. Cone structure in retinal degeneration associated with mutations in the peripherin/RDS gene.
    Duncan JL, Talcott KE, Ratnam K, Sundquist SM, Lucero AS, Day S, Zhang Y, Roorda A.
    Invest Ophthalmol Vis Sci; 2011 Mar 01; 52(3):1557-66. PubMed ID: 21071739
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  • 32. Photoreceptor Degeneration is Correlated With the Deterioration of Macular Retinal Sensitivity in High Myopia.
    Wang Y, Ye J, Shen M, Yao A, Xue A, Fan Y, Huang S, Wang J, Lu F, Shao Y.
    Invest Ophthalmol Vis Sci; 2019 Jul 01; 60(8):2800-2810. PubMed ID: 31266057
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  • 33. Persistent Dark Cones in Oligocone Trichromacy Revealed by Multimodal Adaptive Optics Ophthalmoscopy.
    Li J, Liu T, Flynn OJ, Turriff A, Liu Z, Ullah E, Liu J, Dubra A, Johnson MA, Brooks BP, Hufnagel RB, Hammer DX, Huryn LA, Jeffrey BG, Tam J.
    Front Aging Neurosci; 2021 Jul 01; 13():629214. PubMed ID: 33767618
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  • 34. LONGITUDINAL ADAPTIVE OPTICS SCANNING LASER OPHTHALMOSCOPY REVEALS REGIONAL VARIATION IN CONE AND ROD PHOTORECEPTOR LOSS IN STARGARDT DISEASE.
    Song H, Hang H, Li K, Rossi EA, Zhang J.
    Retina; 2024 Aug 01; 44(8):1403-1412. PubMed ID: 38484106
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  • 35. Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency.
    Patterson EJ, Wilk M, Langlo CS, Kasilian M, Ring M, Hufnagel RB, Dubis AM, Tee JJ, Kalitzeos A, Gardner JC, Ahmed ZM, Sisk RA, Larsen M, Sjoberg S, Connor TB, Dubra A, Neitz J, Hardcastle AJ, Neitz M, Michaelides M, Carroll J.
    Invest Ophthalmol Vis Sci; 2016 Jul 01; 57(8):3853-63. PubMed ID: 27447086
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  • 36. High-resolution retinal imaging of cone-rod dystrophy.
    Wolfing JI, Chung M, Carroll J, Roorda A, Williams DR.
    Ophthalmology; 2006 Jun 01; 113(6):1019.e1. PubMed ID: 16650474
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  • 37. The Cone Photoreceptor Mosaic in Aniridia: Within-Family Phenotype-Genotype Discordance.
    Pedersen HR, Neitz M, Gilson SJ, Landsend ECS, Utheim ØA, Utheim TP, Baraas RC.
    Ophthalmol Retina; 2019 Jun 01; 3(6):523-534. PubMed ID: 31174676
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  • 38. High-resolution optical coherence tomography imaging in KCNV2 retinopathy.
    Sergouniotis PI, Holder GE, Robson AG, Michaelides M, Webster AR, Moore AT.
    Br J Ophthalmol; 2012 Feb 01; 96(2):213-7. PubMed ID: 21558291
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  • 39. The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.
    Carroll J, Dubra A, Gardner JC, Mizrahi-Meissonnier L, Cooper RF, Dubis AM, Nordgren R, Genead M, Connor TB, Stepien KE, Sharon D, Hunt DM, Banin E, Hardcastle AJ, Moore AT, Williams DR, Fishman G, Neitz J, Neitz M, Michaelides M.
    Invest Ophthalmol Vis Sci; 2012 Dec 05; 53(13):8006-15. PubMed ID: 23139274
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  • 40. Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).
    Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR.
    Ophthalmology; 2010 Jan 05; 117(1):120-127.e1. PubMed ID: 19818506
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