Mortality in systemic sclerosis

dc.contributor.authorKarassa, F. B.en
dc.contributor.authorIoannidis, J. P.en
dc.date.accessioned2015-11-24T19:03:38Z
dc.date.available2015-11-24T19:03:38Z
dc.identifier.issn0392-856X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19918
dc.rightsDefault Licence-
dc.subjectAge Factorsen
dc.subjectBiological Markers/blooden
dc.subjectCause of Deathen
dc.subjectEpidemiologic Research Designen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectOdds Ratioen
dc.subjectScleroderma, Diffuse/*mortalityen
dc.subjectScleroderma, Limited/*mortalityen
dc.subjectSex Factorsen
dc.titleMortality in systemic sclerosisen
heal.abstractSystemic sclerosis is a rare and potentially devastating connective tissue disease. It is highly heterogeneous in terms of clinical presentation, extent and severity of organ involvement, immunologic abnormalities, and clinical course. Although clinical outcomes appear to have improved in recent years, the disease continues to cause substantial excess mortality. In this review, we have systematically collected the published studies addressing the mortality burden in patients with scleroderma in comparison with the general population, as well as studies exploring the most important potential predictors of mortality. Results of these studies are presented and discussed, with emphasis on methodological limitations. Suggestions are made for the design, conduct, and reporting of further research on these themes.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/19026149-
heal.journalNameClin Exp Rheumatolen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2008-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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