Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/23088
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dc.contributor.authorSiamopoulou-Mavridou, A.en
dc.contributor.authorMavridis, A. K.en
dc.contributor.authorDimou, G.en
dc.contributor.authorDrosos, A. A.en
dc.date.accessioned2015-11-24T19:30:24Z-
dc.date.available2015-11-24T19:30:24Z-
dc.identifier.issn0770-3198-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/23088-
dc.rightsDefault Licence-
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAntibodies, Antinuclear/analysisen
dc.subjectCentral Nervous System/pathologyen
dc.subjectFemaleen
dc.subjectFollow-Up Studiesen
dc.subjectGreece/epidemiologyen
dc.subjectHumansen
dc.subjectJoints/pathologyen
dc.subjectKidney/pathologyen
dc.subjectLupus Erythematosus, Systemic/epidemiology/*immunology/*pathologyen
dc.subjectMaleen
dc.subjectSkin/pathologyen
dc.titleClinical and serological spectrum of systemic lupus erythematosus in Greek childrenen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/1790634-
heal.identifier.secondaryhttp://www.springerlink.com/content/34g7n26t3250qm73/fulltext.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1991-
heal.abstractIn the present study 19 Greek Caucasian children with systemic lupus erythematosus (SLE), onset before the age of 16, were followed up for 1-12 years (mean 5.6 yrs.). Diagnosis was determined early in 14 patients and delayed by 2 to 6 years in 5. The clinical manifestations and laboratory findings did not differ significantly from those reported in adults with lupus. The major organ system involvement at onset and early course were skin and joints (80%) followed by kidneys (42%). During the course of the disease 26% of the children developed central nervous system (CNS) involvement. All the patients were treated with steroids and/or cytotoxic drugs in severe uncontrolled progressive disease. At the mean 5.6 years follow-up most patients were in remission on small doses of steroids; one patient still presents signs of active lupus nephritis and one patient died from sepsis. All the patients with CNS involvement recovered without permanent CNS residue.en
heal.journalNameClin Rheumatolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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