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Items: 1 to 20 of 31


Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.

Jacobson SG, McGuigan DB 3rd, Sumaroka A, Roman AJ, Gruzensky ML, Sheplock R, Palma J, Schwartz SB, Aleman TS, Cideciyan AV.

Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):4847-4858. doi: 10.1167/iovs.16-19890.


Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa.

Smith TB, Parker M, Steinkamp PN, Weleber RG, Smith N, Wilson DJ; VPA Clinical Trial Study Group; EZ Working Group.

PLoS One. 2016 Feb 4;11(2):e0148022. doi: 10.1371/journal.pone.0148022. eCollection 2016.


Rates of decline in regions of the visual field defined by frequency-domain optical coherence tomography in patients with RPGR-mediated X-linked retinitis pigmentosa.

Birch DG, Locke KG, Felius J, Klein M, Wheaton DK, Hoffman DR, Hood DC.

Ophthalmology. 2015 Apr;122(4):833-9. doi: 10.1016/j.ophtha.2014.11.005. Epub 2014 Dec 31.


Antibody neutralization poses a barrier to intravitreal adeno-associated viral vector gene delivery to non-human primates.

Kotterman MA, Yin L, Strazzeri JM, Flannery JG, Merigan WH, Schaffer DV.

Gene Ther. 2015 Feb;22(2):116-26. doi: 10.1038/gt.2014.115. Epub 2014 Dec 11.


Targeted next generation sequencing for molecular diagnosis of Usher syndrome.

Aparisi MJ, Aller E, Fuster-García C, García-García G, Rodrigo R, Vázquez-Manrique RP, Blanco-Kelly F, Ayuso C, Roux AF, Jaijo T, Millán JM.

Orphanet J Rare Dis. 2014 Nov 18;9:168. doi: 10.1186/s13023-014-0168-7.


TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.

Jacobson SG, Cideciyan AV, Huang WC, Sumaroka A, Roman AJ, Schwartz SB, Luo X, Sheplock R, Dauber JM, Swider M, Stone EM.

Invest Ophthalmol Vis Sci. 2014 Jul 29;55(8):5354-64. doi: 10.1167/iovs.14-14570.


Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations.

Huang WC, Cideciyan AV, Roman AJ, Sumaroka A, Sheplock R, Schwartz SB, Stone EM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2014 Mar 20;55(3):1810-22. doi: 10.1167/iovs.13-13768.


A Comparison of Methods for Tracking Progression in X-Linked Retinitis Pigmentosa Using Frequency Domain OCT.

Ramachandran R, Zhou L, Locke KG, Birch DG, Hood DC.

Transl Vis Sci Technol. 2013 Nov;2(7):5. Epub 2013 Nov 11.


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 19;8(11):e79447. doi: 10.1371/journal.pone.0079447. eCollection 2013.


Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa.

Birch DG, Locke KG, Wen Y, Locke KI, Hoffman DR, Hood DC.

JAMA Ophthalmol. 2013 Sep;131(9):1143-50. doi: 10.1001/jamaophthalmol.2013.4160.


Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants.

Jacobson SG, Cideciyan AV, Peshenko IV, Sumaroka A, Olshevskaya EV, Cao L, Schwartz SB, Roman AJ, Olivares MB, Sadigh S, Yau KW, Heon E, Stone EM, Dizhoor AM.

Hum Mol Genet. 2013 Jan 1;22(1):168-83. doi: 10.1093/hmg/dds421. Epub 2012 Oct 3.


Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials.

Cideciyan AV, Swider M, Aleman TS, Feuer WJ, Schwartz SB, Russell RC, Steinberg JD, Stone EM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2012 Feb 21;53(2):841-52. doi: 10.1167/iovs.11-8415. Print 2012 Feb.


Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene.

Stone EM, Luo X, Héon E, Lam BL, Weleber RG, Halder JA, Affatigato LM, Goldberg JB, Sumaroka A, Schwartz SB, Cideciyan AV, Jacobson SG.

Invest Ophthalmol Vis Sci. 2011 Dec 28;52(13):9665-73. doi: 10.1167/iovs.11-8527.


Transition zones between healthy and diseased retina in choroideremia (CHM) and Stargardt disease (STGD) as compared to retinitis pigmentosa (RP).

Lazow MA, Hood DC, Ramachandran R, Burke TR, Wang YZ, Greenstein VC, Birch DG.

Invest Ophthalmol Vis Sci. 2011 Dec 20;52(13):9581-90. doi: 10.1167/iovs.11-8554.


Automated segmentation of outer retinal layers in macular OCT images of patients with retinitis pigmentosa.

Yang Q, Reisman CA, Chan K, Ramachandran R, Raza A, Hood DC.

Biomed Opt Express. 2011 Sep 1;2(9):2493-503. doi: 10.1364/BOE.2.002493. Epub 2011 Aug 1.


Structural and functional changes associated with normal and abnormal fundus autofluorescence in patients with retinitis pigmentosa.

Greenstein VC, Duncker T, Holopigian K, Carr RE, Greenberg JP, Tsang SH, Hood DC.

Retina. 2012 Feb;32(2):349-57. doi: 10.1097/IAE.0b013e31821dfc17.


Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS.

Invest Ophthalmol Vis Sci. 2011 Oct 7;52(11):7924-36. doi: 10.1167/iovs.11-8313.


Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.

Birch DG, Wen Y, Locke K, Hood DC.

Invest Ophthalmol Vis Sci. 2011 Sep 9;52(10):7141-7. doi: 10.1167/iovs.11-7509.


Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function.

Phillips JB, Blanco-Sanchez B, Lentz JJ, Tallafuss A, Khanobdee K, Sampath S, Jacobs ZG, Han PF, Mishra M, Titus TA, Williams DS, Keats BJ, Washbourne P, Westerfield M.

Dis Model Mech. 2011 Nov;4(6):786-800. doi: 10.1242/dmm.006429. Epub 2011 Jul 14.


Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.

Mustafi D, Kevany BM, Genoud C, Okano K, Cideciyan AV, Sumaroka A, Roman AJ, Jacobson SG, Engel A, Adams MD, Palczewski K.

FASEB J. 2011 Sep;25(9):3157-76. doi: 10.1096/fj.11-186767. Epub 2011 Jun 9.

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