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MEFV Mutations Modify the Clinical Presentation of Henoch-Schonlein Purpura

dc.contributor.authorUncu, Nermin
dc.contributor.authorKasapcopur, Oezguer
dc.contributor.authorKara, Nazli
dc.contributor.authorEkim, Mesiha
dc.contributor.authorArisoy, Nil
dc.contributor.authorOzcakar, Z. Birsin
dc.contributor.authorYalcinkaya, Fatos
dc.contributor.authorCakar, Nilguen
dc.contributor.authorAcar, Banu
dc.contributor.authorUguten, Deniz
dc.contributor.authorSoy, Derya
dc.date.accessioned2021-03-04T14:55:04Z
dc.date.available2021-03-04T14:55:04Z
dc.date.issued2008
dc.identifier.citationOzcakar Z. B. , Yalcinkaya F., Cakar N., Acar B., Kasapcopur O., Uguten D., Soy D., Kara N., Uncu N., Arisoy N., et al., "MEFV Mutations Modify the Clinical Presentation of Henoch-Schonlein Purpura", JOURNAL OF RHEUMATOLOGY, cilt.35, sa.12, ss.2427-2429, 2008
dc.identifier.issn0315-162X
dc.identifier.othervv_1032021
dc.identifier.otherav_84054bc8-66fb-400c-90a1-f68dad03a54d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/89826
dc.identifier.urihttps://doi.org/10.3899/jrheum.080405
dc.description.abstractObjective. To investigate the prevalence of MEFV gene mutations in Turkish patients with Henoch-Schonlein purpura (HSP) but with no symptoms of familial Mediterranean fever (FMF). In addition, we assessed the clinical and laboratory characteristics of HSP patients with and without MEFV mutations.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleMEFV Mutations Modify the Clinical Presentation of Henoch-Schonlein Purpura
dc.typeMakale
dc.relation.journalJOURNAL OF RHEUMATOLOGY
dc.contributor.departmentAnkara Üniversitesi , ,
dc.identifier.volume35
dc.identifier.issue12
dc.identifier.startpage2427
dc.identifier.endpage2429
dc.contributor.firstauthorID42319


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