Structural and functional changes associated with normal and abnormal fundus autofluorescence in patients with retinitis pigmentosa.
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Clinical applications of fundus autofluorescence in retinal diseaseQuantitative fundus autofluorescence in healthy eyes.Quantifying Fundus Autofluorescence in Patients With Retinitis PigmentosaFunctional principal component analysis reveals discriminating categories of retinal pigment epithelial morphology in mice.Early structural anomalies observed by high-resolution imaging in two related cases of autosomal-dominant retinitis pigmentosaComparison of near-infrared and short-wavelength autofluorescence in retinitis pigmentosa.Multimodal Imaging of Central Retinal Disease Progression in a 2-Year Mean Follow-up of Retinitis PigmentosaBilateral Concordance of the Fundus Hyperautofluorescent Ring in Typical Retinitis Pigmentosa Patients.Therapeutic margins in a novel preclinical model of retinitis pigmentosa.In vivo dark-field imaging of the retinal pigment epithelium cell mosaic.Correction of Monogenic and Common Retinal Disorders with Gene Therapy.Fundus-driven perimetry (microperimetry) compared to conventional static automated perimetry: similarities, differences, and clinical applications.Fundus autofluorescence applications in retinal imaging.A challenge to the striking genotypic heterogeneity of retinitis pigmentosa: a better understanding of the pathophysiology using the newest genetic strategies.Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal Imaging.MULTIMODAL IMAGING OF DISEASE-ASSOCIATED PIGMENTARY CHANGES IN RETINITIS PIGMENTOSA.In Vivo Imaging of Cx3cr1gfp/gfp Reporter Mice with Spectral-domain Optical Coherence Tomography and Scanning Laser Ophthalmoscopy.QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY.Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features.Characterization of Retinitis Pigmentosa Using Fluorescence Lifetime Imaging Ophthalmoscopy (FLIO).
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P2860
Structural and functional changes associated with normal and abnormal fundus autofluorescence in patients with retinitis pigmentosa.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 2012
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Structural and functional chan ...... nts with retinitis pigmentosa.
@en
Structural and functional chan ...... nts with retinitis pigmentosa.
@nl
type
label
Structural and functional chan ...... nts with retinitis pigmentosa.
@en
Structural and functional chan ...... nts with retinitis pigmentosa.
@nl
prefLabel
Structural and functional chan ...... nts with retinitis pigmentosa.
@en
Structural and functional chan ...... nts with retinitis pigmentosa.
@nl
P2093
P2860
P1433
P1476
Structural and functional chan ...... nts with retinitis pigmentosa.
@en
P2093
Donald C Hood
Jonathan P Greenberg
Karen Holopigian
Ronald E Carr
Stephen H Tsang
Tobias Duncker
Vivienne C Greenstein
P2860
P304
P356
10.1097/IAE.0B013E31821DFC17
P577
2012-02-01T00:00:00Z