Analysis of retinal sublayer thicknesses and rates of change in ABCA4-associated Stargardt disease
暂无分享,去创建一个
Adam P. DeLuca | Ian C. Han | E. Stone | C. Fortenbach | S. S. Whitmore | D. Critser | Jeremy M. Hoffmann | I. Han | A. DeLuca | Justine L. Cheng | Elizabeth L. Geary | Elizabeth L Geary | Elizabeth L. Geary
[1] Kazuhiro Kurokawa,et al. Cellular Scale Imaging of Transparent Retinal Structures and Processes Using Adaptive Optics Optical Coherence Tomography. , 2020, Annual review of vision science.
[2] Nathaniel T. Stevens,et al. Using multiple agreement methods for continuous repeated measures data: a tutorial for practitioners , 2020, BMC Medical Research Methodology.
[3] J. Sunness,et al. Abnormal Visual Function Outside the Area of Atrophy Defined by Short-Wavelength Fundus Autofluorescence in Stargardt Disease , 2020, Investigative ophthalmology & visual science.
[4] M. Michaelides,et al. Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease Symmetry , 2019, American journal of ophthalmology.
[5] M. Michaelides,et al. Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options , 2019, British Journal of Ophthalmology.
[6] Ian C. Han,et al. Scleral pits represent degeneration around the posterior ciliary arteries and are signs of disease severity in choroideremia , 2019, Eye.
[7] M. Vidal-Sanz,et al. Retinal Ganglion Cell Death as a Late Remodeling Effect of Photoreceptor Degeneration , 2019, International journal of molecular sciences.
[8] J. Sahel,et al. Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11. , 2019, JAMA ophthalmology.
[9] Simon S. Gao,et al. Correlation of Outer Retinal Degeneration and Choriocapillaris Loss in Stargardt Disease Using En Face Optical Coherence Tomography and Optical Coherence Tomography Angiography. , 2019, American journal of ophthalmology.
[10] Beatriz Munoz,et al. Reproducibility of Measurements of Retinal Structural Parameters Using Optical Coherence Tomography in Stargardt Disease , 2019, Translational vision science & technology.
[11] M. Michaelides,et al. Cross-Sectional and Longitudinal Assessment of the Ellipsoid Zone in Childhood-Onset Stargardt Disease , 2019, Translational vision science & technology.
[12] Glenn J. Jaffe,et al. A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies: Findings and Lessons Learned , 2019, Translational vision science & technology.
[13] S. Sadda,et al. Impact of segmentation density on spectral domain optical coherence tomography assessment in Stargardt disease , 2019, Graefe's Archive for Clinical and Experimental Ophthalmology.
[14] M. Michaelides,et al. Cross-Sectional and Longitudinal Assessment of Retinal Sensitivity in Patients With Childhood-Onset Stargardt Disease , 2018, Translational vision science & technology.
[15] J. Sallum,et al. Relative frequency of inherited retinal dystrophies in Brazil , 2018, Scientific Reports.
[16] B. Munoz,et al. Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12. , 2018, American journal of ophthalmology.
[17] A. Cideciyan,et al. Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10 , 2018, JAMA ophthalmology.
[18] M. Gillies,et al. Normative Data for Retinal-Layer Thickness Maps Generated by Spectral-Domain OCT in a White Population. , 2018, Ophthalmology. Retina.
[19] K. Tsunoda,et al. Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy , 2018, Ophthalmology.
[20] J. García-Feijóo,et al. Impacts of age and sex on retinal layer thicknesses measured by spectral domain optical coherence tomography with Spectralis , 2018, PloS one.
[21] Emily J Patterson,et al. Adaptive optics imaging of inherited retinal diseases , 2017, British Journal of Ophthalmology.
[22] J. Sahel,et al. Visual Acuity Change over 12 Months in the Prospective Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: ProgStar Report Number 6. , 2017, Ophthalmology.
[23] V. Greenstein,et al. A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt Disease , 2017, Investigative ophthalmology & visual science.
[24] Adam P. DeLuca,et al. Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease. , 2017, Ophthalmology.
[25] J. Handa,et al. Quantifying the Rate of Ellipsoid Zone Loss in Stargardt Disease. , 2017, American journal of ophthalmology.
[26] V. Greenstein,et al. Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease , 2017, Graefe's Archive for Clinical and Experimental Ophthalmology.
[27] B. J. Klevering,et al. Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt disease , 2017, PloS one.
[28] R. Adelman,et al. Novel therapeutics for Stargardt disease , 2017, Graefe's Archive for Clinical and Experimental Ophthalmology.
[29] M. Yaseri,et al. STARGARDT DISEASE: Beyond Flecks and Atrophy , 2017, Retina.
[30] W. MacNee,et al. Application of Mixed Effects Limits of Agreement in the Presence of Multiple Sources of Variability: Exemplar from the Comparison of Several Devices to Measure Respiratory Rate in COPD Patients , 2016, PLoS ONE.
[31] David J. Wilson,et al. Test–Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial , 2016, Translational vision science & technology.
[32] Justis P. Ehlers,et al. ELLIPSOID ZONE MAPPING AND OUTER RETINAL ASSESSMENT IN STARGARDT DISEASE , 2016, Retina.
[33] J. Sunness,et al. MAPPING THE DENSE SCOTOMA AND ITS ENLARGEMENT IN STARGARDT DISEASE , 2016, Retina.
[34] Michel Michaelides,et al. Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options , 2016, British Journal of Ophthalmology.
[35] Fang Wang,et al. Optical Coherence Tomographic Analysis of Retina in Retinitis Pigmentosa Patients , 2016, Ophthalmic Research.
[36] S. Sadda,et al. COMPARISON OF MANUAL AND SEMIAUTOMATED FUNDUS AUTOFLUORESCENCE ANALYSIS OF MACULAR ATROPHY IN STARGARDT DISEASE PHENOTYPE , 2016, Retina.
[37] Donald C Hood,et al. Near-infrared autofluorescence: its relationship to short-wavelength autofluorescence and optical coherence tomography in recessive stargardt disease. , 2015, Investigative ophthalmology & visual science.
[38] P. Rosenfeld,et al. Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies , 2015, The Lancet.
[39] V. Greenstein,et al. Correlations among near-infrared and short-wavelength autofluorescence and spectral-domain optical coherence tomography in recessive Stargardt disease. , 2014, Investigative ophthalmology & visual science.
[40] G. Rebolleda,et al. Measurement of retinal nerve fiber layer and macular ganglion cell–inner plexiform layer with spectral-domain optical coherence tomography in patients with optic nerve head drusen , 2014, Graefe's Archive for Clinical and Experimental Ophthalmology.
[41] A. J. Roman,et al. Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations. , 2014, Investigative ophthalmology & visual science.
[42] R. Glynn,et al. Regression Methods when the Eye is the Unit of Analysis , 2012, Ophthalmic epidemiology.
[43] R. Molday,et al. ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer , 2012, Nature Communications.
[44] V. Greenstein,et al. Transition zones between healthy and diseased retina in choroideremia (CHM) and Stargardt disease (STGD) as compared to retinitis pigmentosa (RP). , 2011, Investigative ophthalmology & visual science.
[45] G. Fishman,et al. Spectral-domain OCT peripapillary retinal nerve fibre layer thickness measurements in patients with stargardt disease , 2010, British Journal of Ophthalmology.
[46] Vikram S Brar,et al. Normative data for macular thickness by high-definition spectral-domain optical coherence tomography (spectralis). , 2009, American journal of ophthalmology.
[47] Xiaodong Wu,et al. Automated 3-D Intraretinal Layer Segmentation of Macular Spectral-Domain Optical Coherence Tomography Images , 2009, IEEE Transactions on Medical Imaging.
[48] A. Bird,et al. Fundus autofluorescence in Stargardt macular dystrophy-fundus flavimaculatus. , 2004, American journal of ophthalmology.
[49] Jean Bennett,et al. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence. , 2004, Human molecular genetics.
[50] B. Jones,et al. Neural remodeling in retinal degeneration , 2003, Progress in Retinal and Eye Research.
[51] B. Lorenz,et al. Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype–phenotype correlation , 2002, Graefe's Archive for Clinical and Experimental Ophthalmology.
[52] D. K. Roberts,et al. Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia , 2002, The British journal of ophthalmology.
[53] A. Bird,et al. Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. , 2001, Archives of ophthalmology.
[54] A. Bird,et al. Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus. , 1999, Investigative ophthalmology & visual science.
[55] D. Birch,et al. Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice , 1999, Cell.
[56] J. Lupski,et al. Corrigendum: A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy , 1997, Nature Genetics.
[57] J. Lupski,et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy , 1997, Nature Genetics.
[58] G. Fishman,et al. Frequency of optic disc or parapapillary nerve fiber layer drusen in retinitis pigmentosa. , 1997, Ophthalmology.
[59] J. Weiter,et al. In vivo measurement of lipofuscin in Stargardt's disease--Fundus flavimaculatus. , 1995, Investigative ophthalmology & visual science.
[60] J. L. Stone,et al. Morphometric analysis of macular photoreceptors and ganglion cells in retinas with retinitis pigmentosa. , 1992, Archives of ophthalmology.
[61] D. Altman,et al. STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT , 1986, The Lancet.
[62] G. Fishman,et al. Drusen of the optic nerve associated with retinitis pigmentosa. , 1985, Archives of ophthalmology.
[63] A. Beckett,et al. AKUFO AND IBARAPA. , 1965, Lancet.
[64] Angela Jain,et al. Findings and Lessons Learnt , 2021 .
[65] A. Cideciyan,et al. Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3. , 2017, Ophthalmology. Retina.
[66] M. Sonka,et al. Retinal Imaging and Image Analysis , 2010, IEEE Reviews in Biomedical Engineering.
[67] W. Spencer. Drusen of the optic disk and aberrant axoplasmic transport. The XXXIV Edward Jackson memorial lecture. , 1978, American journal of ophthalmology.