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POS0815- Differences in giant cell arteritis manifestations according to the ultrasound pattern of disease involvement

dc.contributor.authorMartinho, J.
dc.contributor.authorSousa Bandeira, M. J.
dc.contributor.authorBarreira, S. C.
dc.contributor.authorDourado, E.
dc.contributor.authorCruz-Machado, A. R.
dc.contributor.authorTeixeira, V.
dc.contributor.authorMacieira, C.
dc.contributor.authorKhmelinskii, N.
dc.contributor.authorFonseca, J. E.
dc.contributor.authorPonte, C.
dc.date.accessioned2023-01-23T15:57:13Z
dc.date.available2023-01-23T15:57:13Z
dc.date.issued2022-06
dc.description.abstractGiant cell arteritis (GCA) is the most common form of primary systemic vasculitis in patients aged >50 years. It predominantly affects the cranial arteries; however, extra-cranial disease involving the aorta and its major branches, known as large-vessel GCA (LV-GCA), can be present in 20-80% of cases, depending on the imaging modality used for screening the disease.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1136/annrheumdis-2022-eular.3866pt_PT
dc.identifier.eissn1468-2060
dc.identifier.urihttp://hdl.handle.net/10400.1/18898
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Publishing Grouppt_PT
dc.titlePOS0815- Differences in giant cell arteritis manifestations according to the ultrasound pattern of disease involvementpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage697pt_PT
oaire.citation.issueSuppl 1pt_PT
oaire.citation.startPage697.1pt_PT
oaire.citation.titleAnnals of the Rheumatic Diseasespt_PT
oaire.citation.volume81pt_PT
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT

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