Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 273


High-resolution images of retinal structure in patients with choroideremia.

Syed R, Sundquist SM, Ratnam K, Zayit-Soudry S, Zhang Y, Crawford JB, MacDonald IM, Godara P, Rha J, Carroll J, Roorda A, Stepien KE, Duncan JL.

Invest Ophthalmol Vis Sci. 2013 Feb 1;54(2):950-61. doi: 10.1167/iovs.12-10707.


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 4;55(10):6381-97. doi: 10.1167/iovs.13-13454.


Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data.

Preising MN, Wegscheider E, Friedburg C, Poloschek CM, Wabbels BK, Lorenz B.

Ophthalmology. 2009 Jun;116(6):1201-9.e1-2. doi: 10.1016/j.ophtha.2009.01.016.


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. doi: 10.1167/iovs.11-8600.


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.


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 1;52(3):1557-66. doi: 10.1167/iovs.10-6549.


Cone structure imaged with adaptive optics scanning laser ophthalmoscopy in eyes with nonneovascular age-related macular degeneration.

Zayit-Soudry S, Duncan JL, Syed R, Menghini M, Roorda AJ.

Invest Ophthalmol Vis Sci. 2013 Nov 15;54(12):7498-509. doi: 10.1167/iovs.13-12433.


Clinical and genetic studies in a family with a new splice-site mutation in the choroideremia gene.

Contestabile MT, Piane M, Cascone NC, Pasquale N, Ciarnella A, Recupero SM, Chessa L.

Mol Vis. 2014 Mar 15;20:325-33.


Clinical characteristics of a large choroideremia pedigree carrying a novel CHM mutation.

Huang AS, Kim LA, Fawzi AA.

Arch Ophthalmol. 2012 Sep;130(9):1184-9. doi: 10.1001/archophthalmol.2012.1117.


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.


Adaptive optics microperimetry and OCT images show preserved function and recovery of cone visibility in macular telangiectasia type 2 retinal lesions.

Wang Q, Tuten WS, Lujan BJ, Holland J, Bernstein PS, Schwartz SD, Duncan JL, Roorda A.

Invest Ophthalmol Vis Sci. 2015 Jan 13;56(2):778-86. doi: 10.1167/iovs.14-15576.


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;131(1):67-74. doi: 10.1001/2013.jamaophthalmol.2.


Progression of retinal pigment epithelial alterations during long-term follow-up in female carriers of choroideremia and report of a novel CHM mutation.

Renner AB, Fiebig BS, Cropp E, Weber BH, Kellner U.

Arch Ophthalmol. 2009 Jul;127(7):907-12. doi: 10.1001/archophthalmol.2009.123.


Multimodal assessment of choroideremia patients defines pre-treatment characteristics.

Seitz IP, Zhour A, Kohl S, Llavona P, Peter T, Wilhelm B, Zrenner E, Ueffing M, Bartz-Schmidt KU, Fischer MD.

Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2143-50. doi: 10.1007/s00417-015-2976-4.


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.


Molecular analysis of the choroideremia gene related clinical findings in two families with choroideremia.

Lin Y, Liu X, Luo L, Qu B, Jiang S, Yang H, Liang X, Ye S, Liu Y.

Mol Vis. 2011;17:2564-9.


Clinical and functional findings in choroideremia due to complete deletion of the CHM gene.

Mura M, Sereda C, Jablonski MM, MacDonald IM, Iannaccone A.

Arch Ophthalmol. 2007 Aug;125(8):1107-13.


Large gene deletion and changes in corneal endothelial cells in a family with choroideremia.

Lee SY, Yu WK, Lin PK.

Invest Ophthalmol Vis Sci. 2015 Feb 26;56(3):1887-93. doi: 10.1167/iovs.14-16302.


Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutation.

Yoon MK, Roorda A, Zhang Y, Nakanishi C, Wong LJ, Zhang Q, Gillum L, Green A, Duncan JL.

Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1838-47. doi: 10.1167/iovs.08-2029.


Multimodal Approach to Monitoring and Investigating Cone Structure and Function in an Inherited Macular Dystrophy.

Ziccardi L, Giannini D, Lombardo G, Serrao S, Dell'Omo R, Nicoletti A, Bertelli M, Lombardo M.

Am J Ophthalmol. 2015 Aug;160(2):301-312.e6. doi: 10.1016/j.ajo.2015.04.024.

Items per page

Supplemental Content

Support Center