dc.contributor.author | Selcuk, Hakan | |
dc.contributor.author | Hasiloglu, Zehra Isik | |
dc.contributor.author | Tasmali, Koray | |
dc.contributor.author | Albayram, Sait | |
dc.contributor.author | Islak, Civan | |
dc.contributor.author | Erer, Burak | |
dc.date.accessioned | 2021-03-03T12:12:38Z | |
dc.date.available | 2021-03-03T12:12:38Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | Hasiloglu Z. I. , Albayram S., Tasmali K., Erer B., Selcuk H., Islak C., "A case of primary Sjogren's syndrome presenting primarily with central nervous system vasculitic involvement", RHEUMATOLOGY INTERNATIONAL, cilt.32, sa.3, ss.805-807, 2012 | |
dc.identifier.issn | 0172-8172 | |
dc.identifier.other | av_2c90ce2f-8d08-465a-9beb-a073b5fac9de | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/34652 | |
dc.identifier.uri | https://doi.org/10.1007/s00296-011-1824-z | |
dc.description.abstract | Sjogren's syndrome is primarily a chronic systemic autoimmune disease that affects exocrine organs. Neurologic symptoms frequently present as peripheral neuropathy due to small vessel vasculitis. Type and prevalence of central nervous system involvement are still controversial. In this report, we present a 35-year-old woman with primary Sjogren's syndrome with central nervous system vasculitic involvement. | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | İmmünoloji ve Romatoloji | |
dc.subject | İç Hastalıkları | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | ROMATOLOJİ | |
dc.title | A case of primary Sjogren's syndrome presenting primarily with central nervous system vasculitic involvement | |
dc.type | Makale | |
dc.relation.journal | RHEUMATOLOGY INTERNATIONAL | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 32 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 805 | |
dc.identifier.endpage | 807 | |
dc.contributor.firstauthorID | 203648 | |