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Items: 1 to 20 of 178

1.

Foveal cavitation as an optical coherence tomography finding in central cone dysfunction.

Leng T, Marmor MF, Kellner U, Thompson DA, Renner AB, Moore W, Sowden JC.

Retina. 2012 Jul;32(7):1411-9. doi: 10.1097/IAE.0b013e318236e4ea.

PMID:
22466470
2.

Oligocone trichromacy: clinical and molecular genetic investigations.

Andersen MK, Christoffersen NL, Sander B, Edmund C, Larsen M, Grau T, Wissinger B, Kohl S, Rosenberg T.

Invest Ophthalmol Vis Sci. 2010 Jan;51(1):89-95. doi: 10.1167/iovs.09-3988. Epub 2009 Sep 24.

PMID:
19797231
3.
4.

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;27(1):19-27. doi: 10.3341/kjo.2013.27.1.19. Epub 2013 Jan 15.

5.

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 1;57(10):3984-95. doi: 10.1167/iovs.16-19313.

6.

Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsia.

Greenberg JP, Sherman J, Zweifel SA, Chen RW, Duncker T, Kohl S, Baumann B, Wissinger B, Yannuzzi LA, Tsang SH.

JAMA Ophthalmol. 2014 Apr 1;132(4):437-45. doi: 10.1001/jamaophthalmol.2013.7987.

7.

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;131(10):1314-23. doi: 10.1001/jamaophthalmol.2013.4476.

PMID:
23929416
8.

Diagnostic fundus autofluorescence patterns in achromatopsia.

Fahim AT, Khan NW, Zahid S, Schachar IH, Branham K, Kohl S, Wissinger B, Elner VM, Heckenlively JR, Jayasundera T.

Am J Ophthalmol. 2013 Dec;156(6):1211-1219.e2. doi: 10.1016/j.ajo.2013.06.033. Epub 2013 Aug 20.

PMID:
23972307
9.

Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.

Chen Y, Ratnam K, Sundquist SM, Lujan B, Ayyagari R, Gudiseva VH, Roorda A, Duncan JL.

Invest Ophthalmol Vis Sci. 2011 May 17;52(6):3281-92. doi: 10.1167/iovs.10-6538.

10.

Integrity of the cone photoreceptor mosaic in oligocone trichromacy.

Michaelides M, Rha J, Dees EW, Baraas RC, Wagner-Schuman ML, Mollon JD, Dubis AM, Andersen MK, Rosenberg T, Larsen M, Moore AT, Carroll J.

Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4757-64. doi: 10.1167/iovs.10-6659.

11.

Multimodal imaging of foveal cavitation in retinal dystrophies.

Parodi MB, Cicinelli MV, Iacono P, Bolognesi G, Bandello F.

Graefes Arch Clin Exp Ophthalmol. 2017 Feb;255(2):271-279. doi: 10.1007/s00417-016-3450-7. Epub 2016 Aug 5.

PMID:
27491512
12.

Foveal sparing in Stargardt disease.

van Huet RA, Bax NM, Westeneng-Van Haaften SC, Muhamad M, Zonneveld-Vrieling MN, Hoefsloot LH, Cremers FP, Boon CJ, Klevering BJ, Hoyng CB.

Invest Ophthalmol Vis Sci. 2014 Oct 16;55(11):7467-78. doi: 10.1167/iovs.13-13825.

PMID:
25324290
13.

Retinal morphology of patients with achromatopsia during early childhood: implications for gene therapy.

Yang P, Michaels KV, Courtney RJ, Wen Y, Greninger DA, Reznick L, Karr DJ, Wilson LB, Weleber RG, Pennesi ME.

JAMA Ophthalmol. 2014 Jul;132(7):823-31. doi: 10.1001/jamaophthalmol.2014.685.

PMID:
24676353
14.

Characterization of stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging.

Ritter M, Zotter S, Schmidt WM, Bittner RE, Deak GG, Pircher M, Sacu S, Hitzenberger CK, Schmidt-Erfurth UM; Macula Study Group Vienna.

Invest Ophthalmol Vis Sci. 2013 Sep 27;54(9):6416-25. doi: 10.1167/iovs.12-11550.

PMID:
23882696
15.

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;96(2):213-7. doi: 10.1136/bjo.2011.203638. Epub 2011 May 10.

PMID:
21558291
16.

Acute Zonal Cone Photoreceptor Outer Segment Loss.

Aleman TS, Sandhu HS, Serrano LW, Traband A, Lau MK, Adamus G, Avery RA.

JAMA Ophthalmol. 2017 May 1;135(5):487-490. doi: 10.1001/jamaophthalmol.2017.0451.

PMID:
28384671
17.

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;120(4):809-20. doi: 10.1016/j.ophtha.2012.09.057. Epub 2013 Jan 3.

PMID:
23290749
18.

Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

Wissinger B, Dangel S, J├Ągle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.

Invest Ophthalmol Vis Sci. 2008 Feb;49(2):751-7. doi: 10.1167/iovs.07-0471.

PMID:
18235024
19.

Cone abnormalities in fundus albipunctatus associated with RDH5 mutations assessed using adaptive optics scanning laser ophthalmoscopy.

Makiyama Y, Ooto S, Hangai M, Ogino K, Gotoh N, Oishi A, Yoshimura N.

Am J Ophthalmol. 2014 Mar;157(3):558-70.e1-4. doi: 10.1016/j.ajo.2013.10.021. Epub 2013 Nov 16.

PMID:
24246574
20.

Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.

Thiadens AA, Somervuo V, van den Born LI, Roosing S, van Schooneveld MJ, Kuijpers RW, van Moll-Ramirez N, Cremers FP, Hoyng CB, Klaver CC.

Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5952-7. doi: 10.1167/iovs.10-5680. Epub 2010 Jun 23.

PMID:
20574029

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