Retinal diseases and disorders such as Retinal Vein Occlusion, Diabetic Retinopathy, Age-Related Macular Degeneration, and Retinal Tear or Detachments are among the top causes of blindness in the world. Though there are sophisticated technologies available today to diagnose these diseases on a macroscopic level, no existing technology enables us to view the microstructures of the retina and understand their physiological changes prior to the onset of, during the development of, and during the treatment of these diseases. A novel technology called two-photon microscopy, which is based on the principle of Confocal Laser Scanning Microscopy and Two-Photon Excitation is being explored for its application in imaging the microstructures of the re...
Two-photon fluorescence microscopy allows three-dimensional imaging of biological specimens in vivo....
Noninvasive imaging of visual system components in vivo is critical for understanding the causal mec...
zekowsky-Schroeder R, et al. Two-photon microscopy and fluorescence lifetime imaging of retinal pigm...
Retinal diseases and disorders such as Retinal Vein Occlusion, Diabetic Retinopathy, Age-Related Mac...
The human eye consists of many complex layers and microstructures that interact with one another t...
High-resolution imaging techniques capable of detecting identifiable endogenous fluorophores in the ...
Minimal-invasive imaging of ocular surface pathologies aims at securing clinical diagnosis without t...
Since its inception more than 15 years ago, two-photon laser scanning microscopy (2PLSM) has found w...
Although confocal microscopy provides an efficient means of fluorescence imaging, many obstacles inc...
PURPOSE: To record the distribution and spectrum of human retinal pigment epithelial cell lipofuscin...
Fluorescence optical microscopy is one of the most important tools to investigate biological samples...
Fluorescence optical microscopy is one of the most important tools to investigate biological samples...
Two-photon microscopy is a fluorescence imaging technique which provides distinct advantages in thre...
Two-photon microscopy is a fluorescence imaging technique which provides distinct advantages in thre...
Thesis (Ph. D.)--University of Rochester. Institute of Optics, 2007. Missing pages 8-9.The ability t...
Two-photon fluorescence microscopy allows three-dimensional imaging of biological specimens in vivo....
Noninvasive imaging of visual system components in vivo is critical for understanding the causal mec...
zekowsky-Schroeder R, et al. Two-photon microscopy and fluorescence lifetime imaging of retinal pigm...
Retinal diseases and disorders such as Retinal Vein Occlusion, Diabetic Retinopathy, Age-Related Mac...
The human eye consists of many complex layers and microstructures that interact with one another t...
High-resolution imaging techniques capable of detecting identifiable endogenous fluorophores in the ...
Minimal-invasive imaging of ocular surface pathologies aims at securing clinical diagnosis without t...
Since its inception more than 15 years ago, two-photon laser scanning microscopy (2PLSM) has found w...
Although confocal microscopy provides an efficient means of fluorescence imaging, many obstacles inc...
PURPOSE: To record the distribution and spectrum of human retinal pigment epithelial cell lipofuscin...
Fluorescence optical microscopy is one of the most important tools to investigate biological samples...
Fluorescence optical microscopy is one of the most important tools to investigate biological samples...
Two-photon microscopy is a fluorescence imaging technique which provides distinct advantages in thre...
Two-photon microscopy is a fluorescence imaging technique which provides distinct advantages in thre...
Thesis (Ph. D.)--University of Rochester. Institute of Optics, 2007. Missing pages 8-9.The ability t...
Two-photon fluorescence microscopy allows three-dimensional imaging of biological specimens in vivo....
Noninvasive imaging of visual system components in vivo is critical for understanding the causal mec...
zekowsky-Schroeder R, et al. Two-photon microscopy and fluorescence lifetime imaging of retinal pigm...