File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Imaging of the lamina cribrosa in glaucoma: Perspectives of pathogenesis and clinical applications

TitleImaging of the lamina cribrosa in glaucoma: Perspectives of pathogenesis and clinical applications
Authors
KeywordsOptical coherence tomography
Glaucoma
Lamina cribrosa
Intraocular pressure
Issue Date2013
Citation
Current Eye Research, 2013, v. 38, n. 9, p. 903-909 How to Cite?
AbstractThe lamina cribrosa (LC) is a sieve-like structure in the sclera where retinal ganglion cell axons exit from the eye. The LC has been known to play a critical role in the pathogenesis of glaucoma. With the advent of imaging technologies, such as enhanced depth imaging, spectral-domain optical coherence tomography (OCT) enables us to unveil the LC in vivo features. The application of adaptive optics technology and a compensatory image-processing algorithm has further improved the visualization of the beams and pores and neural pathways of the LC and the scleral insertion sites. Monitoring the changes of these structures in relation to acute and chronic elevation of intraocular pressure would be germane to decipher the relationship between the stress and strain response of the LC and optic nerve damage and improve our understanding of glaucoma pathophysiology. While the impact of investigating the integrity of LC is substantive, considerable challenges remain for imaging the LC. Nevertheless, with the rapid development of the OCT technology, it is expected that some of these limitations can be overcome and the potentials of LC imaging will be unraveled. © Informa Healthcare USA, Inc.
Persistent Identifierhttp://hdl.handle.net/10722/298044
ISSN
2023 Impact Factor: 1.7
2023 SCImago Journal Rankings: 0.741
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKim, Tae Woo-
dc.contributor.authorKagemann, Larry-
dc.contributor.authorGirard, Michaël J.A.-
dc.contributor.authorStrouthidis, Nicholas G.-
dc.contributor.authorSung, Kyung Rim-
dc.contributor.authorLeung, Christopher K.-
dc.contributor.authorSchuman, Joel S.-
dc.contributor.authorWollstein, Gadi-
dc.date.accessioned2021-04-08T03:07:32Z-
dc.date.available2021-04-08T03:07:32Z-
dc.date.issued2013-
dc.identifier.citationCurrent Eye Research, 2013, v. 38, n. 9, p. 903-909-
dc.identifier.issn0271-3683-
dc.identifier.urihttp://hdl.handle.net/10722/298044-
dc.description.abstractThe lamina cribrosa (LC) is a sieve-like structure in the sclera where retinal ganglion cell axons exit from the eye. The LC has been known to play a critical role in the pathogenesis of glaucoma. With the advent of imaging technologies, such as enhanced depth imaging, spectral-domain optical coherence tomography (OCT) enables us to unveil the LC in vivo features. The application of adaptive optics technology and a compensatory image-processing algorithm has further improved the visualization of the beams and pores and neural pathways of the LC and the scleral insertion sites. Monitoring the changes of these structures in relation to acute and chronic elevation of intraocular pressure would be germane to decipher the relationship between the stress and strain response of the LC and optic nerve damage and improve our understanding of glaucoma pathophysiology. While the impact of investigating the integrity of LC is substantive, considerable challenges remain for imaging the LC. Nevertheless, with the rapid development of the OCT technology, it is expected that some of these limitations can be overcome and the potentials of LC imaging will be unraveled. © Informa Healthcare USA, Inc.-
dc.languageeng-
dc.relation.ispartofCurrent Eye Research-
dc.subjectOptical coherence tomography-
dc.subjectGlaucoma-
dc.subjectLamina cribrosa-
dc.subjectIntraocular pressure-
dc.titleImaging of the lamina cribrosa in glaucoma: Perspectives of pathogenesis and clinical applications-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.3109/02713683.2013.800888-
dc.identifier.pmid23768229-
dc.identifier.pmcidPMC5536835-
dc.identifier.scopuseid_2-s2.0-84880872076-
dc.identifier.volume38-
dc.identifier.issue9-
dc.identifier.spage903-
dc.identifier.epage909-
dc.identifier.eissn1460-2202-
dc.identifier.isiWOS:000322319800001-
dc.identifier.issnl0271-3683-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats