Structural evaluation in inherited retinal diseases

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dc.authoridCabral de Guimaraes, Thales Antonio/0000-0002-7936-6851
dc.authoridDaich Varela, Malena/0000-0003-4960-4510
dc.authorwosidESENER, BURAK/ABF-7689-2021
dc.authorwosidCabral de Guimarães, Thales Antônio/AAD-9236-2022
dc.contributor.authorVarela, Malena Daich
dc.contributor.authorEsener, Burak
dc.contributor.authorHashem, Shaima A.
dc.contributor.authorde Guimaraes, Thales Antonio Cabral
dc.contributor.authorGeorgiou, Michalis
dc.contributor.authorMichaelides, Michel
dc.date.accessioned2024-08-04T20:50:14Z
dc.date.available2024-08-04T20:50:14Z
dc.date.issued2021
dc.departmentİnönü Üniversitesien_US
dc.description.abstractOphthalmic genetics is a field that has been rapidly evolving over the last decade, mainly due to the flourishing of translational medicine for inherited retinal diseases (IRD). In this review, we will address the different methods by which retinal structure can be objectively and accurately assessed in IRD. We review standard-of-care imaging for these patients: colour fundus photography, fundus autofluorescence imaging and optical coherence tomography (OCT), as well as higher-resolution and/or newer technologies including OCT angiography, adaptive optics imaging, fundus imaging using a range of wavelengths, magnetic resonance imaging, laser speckle flowgraphy and retinal oximetry, illustrating their utility using paradigm genotypes with on-going therapeutic efforts/trials.en_US
dc.description.sponsorshipWellcome Trust [099173/Z/12/Z]; National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust; UCL Institute of Ophthalmology; Moorfields Eye Charity; Retina UK; Foundation Fighting Blindness; Wellcome Trust [099173/Z/12/Z] Funding Source: Wellcome Trusten_US
dc.description.sponsorshipThis work has been supported by grants from The Wellcome Trust (099173/Z/12/Z), the National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, Moorfields Eye Charity, Retina UK and the Foundation Fighting Blindness (no specific grant/award number for the latter).en_US
dc.identifier.doi10.1136/bjophthalmol-2021-319228
dc.identifier.endpage1631en_US
dc.identifier.issn0007-1161
dc.identifier.issn1468-2079
dc.identifier.issue12en_US
dc.identifier.pmid33980508en_US
dc.identifier.scopus2-s2.0-85106045031en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage1623en_US
dc.identifier.urihttps://doi.org/10.1136/bjophthalmol-2021-319228
dc.identifier.urihttps://hdl.handle.net/11616/99935
dc.identifier.volume105en_US
dc.identifier.wosWOS:000726907900004en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherBmj Publishing Groupen_US
dc.relation.ispartofBritish Journal of Ophthalmologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectimagingen_US
dc.subjectgeneticsen_US
dc.subjectclinical trialen_US
dc.subjectretinaen_US
dc.subjectdystrophyen_US
dc.titleStructural evaluation in inherited retinal diseasesen_US
dc.typeReview Articleen_US

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