| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0161-6420(80)35106-3 |
| P698 | PubMed publication ID | 6165950 |
| P2093 | author name string | M Yanoff | |
| R C Eagle | |||
| V B Bernardino | |||
| A C Lucier | |||
| P2860 | cites work | Participation of the retinal pigment epithelium in the rod outer segment renewal process | Q28609982 |
| Fundus fluorescein angiography in fundus flavimaculatus and Stargardts disease | Q41659243 | ||
| Stargardt's Disease and Fundus Flavimaculatus | Q41667241 | ||
| Über familiäre, progressive Degeneration in der Maculagegend des Auges | Q55921174 | ||
| Patterned dystrophies of the retinal pigment epithelium | Q57462512 | ||
| Pigment epithelial dystrophy in the dog | Q67833290 | ||
| Fundus flavimaculatus. A clinical classification | Q67876698 | ||
| P433 | issue | 12 | |
| P304 | page(s) | 1189-1200 | |
| P577 | publication date | 1980-12-01 | |
| P1433 | published in | Ophthalmology | Q7098109 |
| P1476 | title | Retinal pigment epithelial abnormalities in fundus flavimaculatus: a light and electron microscopic study | |
| P478 | volume | 87 |
| Q39865129 | A clinical review of Stargardt's disease and/or fundus flavimaculatus with follow-up |
| Q55670938 | A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1 |
| Q89000215 | A non-retinoid antagonist of retinol-binding protein 4 rescues phenotype in a model of Stargardt disease without inhibiting the visual cycle |
| Q28141384 | A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease |
| Q24324625 | A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy |
| Q28609934 | A2E, a byproduct of the visual cycle |
| Q33777110 | Accelerated accumulation of lipofuscin pigments in the RPE of a mouse model for ABCA4-mediated retinal dystrophies following Vitamin A supplementation |
| Q40093241 | Acute exudative polymorphous vitelliform maculopathy |
| Q42467879 | Age-related changes in the basement membrane of the retinal pigment epithelium of Rpe65 -/- and wild-type mice |
| Q64077492 | An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease |
| Q33245800 | Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography |
| Q49107499 | Asymmetric fundus flavimaculatus/Stargardt's disease, associated with unilateral myopia |
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| Q46453340 | Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation |
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| Q57797592 | Bisretinoids mediate light sensitivity resulting in photoreceptor cell degeneration in mice lacking the receptor tyrosine kinase Mer |
| Q37158866 | Centrifugal expansion of fundus autofluorescence patterns in Stargardt disease over time |
| Q69626644 | Chorioretinal juncture. Multiple extramacular drusen |
| Q72849843 | Clinical biochemical and pathologic correlations in Bietti's crystalline dystrophy |
| Q50788774 | Color vision in Stargardt's disease |
| Q30500872 | Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease |
| Q34699966 | Correlations among near-infrared and short-wavelength autofluorescence and spectral-domain optical coherence tomography in recessive Stargardt disease |
| Q37307033 | Dark adaptation in patients with Best vitelliform macular dystrophy |
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| Q35000428 | Distinct characteristics of inferonasal fundus autofluorescence patterns in stargardt disease and retinitis pigmentosa |
| Q93613862 | Electrophysiological analysis of Stargardt's disease fundus flavimaculatus group |
| Q33634255 | Electrophysiological findings in Stargardt's-fundus flavimaculatus disease |
| Q39829821 | Electrophysiology and inherited retinal disorders |
| Q38651022 | Epithelium-capillary interactions in the eye: the retinal pigment epithelium and the choriocapillaris. |
| Q34165112 | Evaluation of phenotypic similarities between Stargardt flavimaculatus and retinal pigment epithelial pattern dystrophies. |
| Q70047278 | Fleck retina in Kjellin's syndrome |
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| Q37440969 | Functional Analysis of Retinal Flecks in Stargardt Disease |
| Q92267392 | Functional Relevance and Structural Correlates of Near Infrared and Short Wavelength Fundus Autofluorescence Imaging in ABCA4-Related Retinopathy |
| Q34166719 | Fundus autofluorescence and photoreceptor cell rosettes in mouse models |
| Q33809041 | Fundus autofluorescence and the bisretinoids of retina |
| Q36014786 | Fundus autofluorescence in exudative age-related macular degeneration |
| Q68040431 | Fundus flavimaculatus and subretinal neovascularization |
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| Q34213037 | Funduscopically controlled scotometry. |
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| Q67935526 | Histopathology of Incipient Fundus Flavimaculatus |
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| Q42155444 | Hyperautofluorescence in outer retinal layers thinning |
| Q71969631 | Indocyanine Green Angiography in Stargardt's Flavimaculatus |
| Q35581414 | Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects |
| Q38932332 | Inhibition of autophagy induces retinal pigment epithelial cell damage by the lipofuscin fluorophore A2E. |
| Q34199909 | Inhibition of the visual cycle by A2E through direct interaction with RPE65 and implications in Stargardt disease. |
| Q48156633 | Insights into autofluorescence patterns in Stargardt macular dystrophy using ultra-wide-field imaging. |
| Q28140171 | Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice |
| Q34135516 | Interpretations of fundus autofluorescence from studies of the bisretinoids of the retina |
| Q44844820 | Intraocular PAS-positive macrophages simulating Whipple's disease |
| Q35862230 | Keypathophysiologic pathways in age-related macular disease |
| Q36481342 | Light and inherited retinal degeneration |
| Q37645850 | Light exposure stimulates formation of A2E oxiranes in a mouse model of Stargardt's macular degeneration |
| Q36290158 | Lipofuscin-associated photo-oxidative stress during fundus autofluorescence imaging |
| Q44953248 | Lipofuscinosis of the cornea. A clinicopathologic study of three cases |
| Q41719920 | Long-term follow-up of Stargardt's disease and fundus flavimaculatus |
| Q40110908 | Mechanisms of Maculopathy |
| Q34502476 | Mechanistic studies of ABCR, the ABC transporter in photoreceptor outer segments responsible for autosomal recessive Stargardt disease |
| Q37415582 | Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence Study |
| Q35303893 | Multifocal electroretinography in patients with Stargardt's macular dystrophy |
| Q38736594 | Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease. |
| Q36172144 | Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus |
| Q28345269 | North Carolina macular dystrophy: clinicopathologic correlation |
| Q42464369 | Ocular clinicopathologic correlation of Hallervorden-Spatz syndrome with acanthocytosis and pigmentary retinopathy |
| Q42009911 | Ophthaproblem. Juvenile macular dystrophy (fundus flavimaculatus or Stargardt's disease). |
| Q91644266 | Optical Coherence Tomography Angiography Imaging in Inherited Retinal Diseases |
| Q58397659 | Pattern Dystrophy of the Retinal Pigment Epithelium |
| Q52559503 | Photoreceptor cells as a source of fundus autofluorescence in recessive Stargardt disease. |
| Q36067981 | Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front |
| Q90283905 | Progression of Anterograde Trans-Synaptic Degeneration in the Human Retina Is Modulated by Axonal Convergence and Divergence |
| Q45291946 | Proliferative Vitreoretinopathy in Fundus Flavimaculatus |
| Q72187617 | Prolonged rod dark adaptation in patients with cone-rod dystrophy |
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| Q30883183 | Quantitative evaluation of fundus autofluorescence imaged "in vivo" in eyes with retinal disease |
| Q27304733 | Quantitative fundus autofluorescence distinguishes ABCA4-associated and non-ABCA4-associated bull's-eye maculopathy |
| Q30543909 | Quantitative fundus autofluorescence in healthy eyes. |
| Q30577468 | Quantitative fundus autofluorescence in recessive Stargardt disease |
| Q34053070 | Quantitative measurements of autofluorescence with the scanning laser ophthalmoscope |
| Q34888843 | Relationship between foveal cone structure and clinical measures of visual function in patients with inherited retinal degenerations |
| Q30712714 | Reproducibility of fundus autofluorescence measurements obtained using a confocal scanning laser ophthalmoscope |
| Q34330950 | Retinal pigment epithelial acid lipase activity and lipoprotein receptors: effects of dietary omega-3 fatty acids. |
| Q70645637 | Retinitis pigmentosa: a quantitative study of the apical membrane of normal and dystrophic human retinal pigment epithelial cells in tissue culture in relation to phagocytosis |
| Q36969143 | Spectral-domain OCT peripapillary retinal nerve fibre layer thickness measurements in patients with stargardt disease |
| Q34165042 | Stargardt's disease and fundus flavimaculatus: evaluation of morphologic progression and intrafamilial co-existence. |
| Q68100556 | Stargardt's disease. Family studies |
| Q72566834 | Stargardt's disease/fundus flavimaculatus: psychophysical and electrophysiologic results |
| Q73939439 | Stargardt's macular dystrophy |
| Q37172298 | Structures and biogenetic analysis of lipofuscin bis-retinoids |
| Q37477052 | Symptomatic abnormalities of dark adaptation in patients with age-related Bruch's membrane change |
| Q34212290 | The Kearns-Sayre syndrome: a light and electron microscopic study. |
| Q28645952 | The Project MACULA Retinal Pigment Epithelium Grading System for Histology and Optical Coherence Tomography in Age-Related Macular Degeneration |
| Q70568872 | The atypical pigmentary retinopathy of Kearns-Sayre syndrome. A light and electron microscopic study |
| Q69454559 | The dark choroid in posterior retinal dystrophies |
| Q33641154 | The dark choroid in posterior retinal dystrophies |
| Q35213761 | The genetics of inherited macular dystrophies |
| Q28114964 | The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR) |
| Q40969774 | The variable expressivity of a family with central areolar pigment epithelial dystrophy |
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| Q42212373 | Three-dimensional spectral domain optical coherence tomography in Stargardt disease and fundus flavimaculatus |
| Q69393647 | Transplantation of retinal pigment epithelium using a pars plana approach |
| Q34960196 | Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration |
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