Literature DB >> 10150888

Basic science and applications of in vivo microscopy.

W D Mathers1, W M Petroll, J V Jester, H D Cavanagh.   

Abstract

Confocal microscopy creates a scanned image from a point light source and point detection or a scanning slit to remove scattered light and improve optical resolution. This also results in optical sectioning of tissues. These capabilities can be employed to image structures in the human cornea, in vivo, both for research and for the diagnosis and treatment of human disease. Optical sections, when recombined, can lead to three-dimensional reconstructions from which very useful information is obtained. Investigators have found keratocyte density decreases from anterior to posterior in the stroma of the rabbit cornea. Surface epithelial desquamation can also be studied and the effects of contact lens use can be demonstrated. The instrument is also useful for diagnosing and guiding therapy for some human diseases such as Acanthamoeba keratitis. Colonies of bacteria may also be observed and treatment evaluated in patients with infectious crystalline keratopathy. Confocal microscopy can also image the retina.

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Year:  1995        PMID: 10150888     DOI: 10.1097/00055735-199508000-00015

Source DB:  PubMed          Journal:  Curr Opin Ophthalmol        ISSN: 1040-8738            Impact factor:   3.761


  2 in total

1.  Assessment of corneal thickness and keratocyte density in a rabbit model of laser in situ keratomileusis using scanning laser confocal microscopy.

Authors:  Michael D Twa; Michael J Giese
Journal:  Am J Ophthalmol       Date:  2011-08-25       Impact factor: 5.258

2.  Subclinical increased anterior stromal reflectivity with topical taprenepag isopropyl.

Authors:  Ronald A Schachar; Susan Raber; Kristina V Thomas; Beth Ann M Benetz; Loretta B Szczotka-Flynn; Min Zhang; Scott J Howell; Jonathan H Lass
Journal:  Cornea       Date:  2013-03       Impact factor: 2.651

  2 in total

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