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Asdas responses in patients with axial Spondyloarthritis starting bdmards: results from a multicentre prospective cohort

dc.contributor.authorSantos, M. E.
dc.contributor.authorRamiro, S.
dc.contributor.authorvan der Heijde, D.
dc.contributor.authorLandewe, R.
dc.date.accessioned2024-10-31T11:40:47Z
dc.date.available2024-10-31T11:40:47Z
dc.date.issued2024
dc.description.abstractASAS and EULAR recommend the use of an improvement ≥1.1 in ASDAS at 12 weeks to determine the continuation of a bDMARD. However, it is debated whether improvements can occur and whether patients’ characteristics influence (time to) response.eng
dc.identifier.eissn1593-098X
dc.identifier.issn0392-856X
dc.identifier.urihttp://hdl.handle.net/10400.1/26188
dc.language.isoeng
dc.peerreviewedyes
dc.publisherClinical and Experimental Rheumatology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleAsdas responses in patients with axial Spondyloarthritis starting bdmards: results from a multicentre prospective cohorteng
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferenceDate2024
oaire.citation.conferencePlaceGhent, Belgium
oaire.citation.endPage84
oaire.citation.issue9
oaire.citation.startPage84
oaire.citation.titleClinical and Experimental Rheumatology / Fourteenth International Congress on Spondyloarthritides
oaire.citation.volume42
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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