A Comparison of Fundus Autofluorescence and Retinal Structure in Patients with Stargardt Disease
Gomes et al.
IOVS 2009;50:3953-3959.
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Phenotypic Variability Due to a Novel Glu292Lys Variation in Exon 8 of the BEST1 Gene Causing Best Macular Dystrophy
Sohn et al.
Arch Ophthalmol 2009;127:913-920.
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Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence
Rath et al.
Br J Ophthalmol 2008;92:623-629.
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Macular Dystrophy Associated With the A3243G Mitochondrial DNA Mutation: Distinct Retinal and Associated Features, Disease Variability, and Characterization of Asymptomatic Family Members
Michaelides et al.
Arch Ophthalmol 2008;126:320-328.
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Autofluorescence Characteristics of Early, Atrophic, and High-Risk Fellow Eyes in Age-Related Macular Degeneration
Smith et al.
IOVS 2006;47:5495-5504.
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Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography
Querques et al.
Br J Ophthalmol 2006;90:1157-1162.
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Fundus autofluorescence in age-related macular degeneration: an epiphenomenon?
Hopkins et al.
IOVS 2006;47:2269-2271.
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ABCA4-Associated Retinal Degenerations Spare Structure and Function of the Human Parapapillary Retina
Cideciyan et al.
IOVS 2005;46:4739-4746.
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Autofluorescence Characteristics of Normal Foveas and Reconstruction of Foveal Autofluorescence from Limited Data Subsets
Smith et al.
IOVS 2005;46:2940-2946.
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Isolation and characterization of a retinal pigment epithelial cell fluorophore: An all-trans-retinal dimer conjugate
Fishkin et al.
Proc. Natl. Acad. Sci. USA 2005;102:7091-7096.
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Assessment of Central Visual Function in Stargardt's Disease/Fundus Flavimaculatus with Ultrahigh-Resolution Optical Coherence Tomography
Ergun et al.
IOVS 2005;46:310-316.
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Loss of Synchronized Retinal Phagocytosis and Age-related Blindness in Mice Lacking {alpha}v{beta}5 Integrin
Nandrot et al.
JEM 2004;200:1539-1545.
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Fundus Autofluorescence and Vitelliform Macular Dystrophy
Chung and Spaide
Arch Ophthalmol 2004;122:1078-1079.
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Photopic and Scotopic Fine Matrix Mapping of Retinal Areas of Increased Fundus Autofluorescence in Patients with Age-Related Maculopathy
Scholl et al.
IOVS 2004;45:574-583.
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Fundus autofluorescence imaging compared with different confocal scanning laser ophthalmoscopes
Bellmann et al.
Br J Ophthalmol 2003;87:1381-1386.
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The genetics of inherited macular dystrophies
Michaelides et al.
J. Med. Genet. 2003;40:641-650.
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An Early-Onset Autosomal Dominant Macular Dystrophy (MCDR3) Resembling North Carolina Macular Dystrophy Maps to Chromosome 5
Michaelides et al.
IOVS 2003;44:2178-2183.
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An Autosomal Dominant Bull's-Eye Macular Dystrophy (MCDR2) that Maps to the Short Arm of Chromosome 4
Michaelides et al.
IOVS 2003;44:1657-1662.
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Spectral Profiling of Autofluorescence Associated with Lipofuscin, Bruch's Membrane, and Sub-RPE Deposits in Normal and AMD Eyes
Marmorstein et al.
IOVS 2002;43:2435-2441.
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Clinical Variations in Assessment of Bull's-eye Maculopathy
Kurz-Levin et al.
Arch Ophthalmol 2002;120:567-575.
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Age-Related Accumulation and Spatial Distribution of Lipofuscin in RPE of Normal Subjects
Delori et al.
IOVS 2001;42:1855-1866.
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Phenotypic Subtypes of Stargardt Macular Dystrophy-Fundus Flavimaculatus
Lois et al.
Arch Ophthalmol 2001;119:359-369.
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Ultrastructural Changes Associated with Accumulation of Inclusion Bodies in Rat Retinal Pigment Epithelium
Okubo et al.
IOVS 2000;41:4305-4312.
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Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease
Lois et al.
Br J Ophthalmol 2000;84:741-745.
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Laser imaging of the retina
SHARP et al.
Br J Ophthalmol 1999;83:1241-1245.
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Intrafamilial Variation of Phenotype in Stargardt Macular Dystrophy-Fundus Flavimaculatus
Lois et al.
IOVS 1999;40:2668-2675.
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Clinical Features of Codon 172 RDS Macular Dystrophy: Similar Phenotype in 12 Families
Downes et al.
Arch Ophthalmol 1999;117:1373-1383.
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Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope
Lois et al.
Br J Ophthalmol 1999;83:276-279.
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Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6q
Reichel et al.
Br J Ophthalmol 1998;82:1162-1168.
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What Is the Future of Research in Age-Related Macular Disease?
Bird
Arch Ophthalmol 1997;115:1311-1313.
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