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dc.contributor.authorOzkaya, O
dc.contributor.authorCanturk, F
dc.contributor.authorAlayli, G
dc.contributor.authorAkpolat, I
dc.contributor.authorBelet, U
dc.contributor.authorDiren, B
dc.date.accessioned2020-06-21T15:43:18Z
dc.date.available2020-06-21T15:43:18Z
dc.date.issued2004
dc.identifier.issn0300-9742
dc.identifier.urihttps://doi.org/10.1080/03009740310004117
dc.identifier.urihttps://hdl.handle.net/20.500.12712/21572
dc.descriptionozkaya, ozan/0000-0002-0198-1221; DIREN, HALDUN BARIS/0000-0001-8958-2040en_US
dc.descriptionWOS: 000220516400010en_US
dc.descriptionPubMed: 15163115en_US
dc.description.abstractFamilial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limiting attacks of joint, chest and abdominal associated with fever. We present an unusual case of FMF with prolonged arthritis and amyloidosis. Familial Mediterranean fever should be considered in the differential diagnosis of prolonged hip pain, even in the absence of symptoms or signs of FMF.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Asen_US
dc.relation.isversionof10.1080/03009740310004117en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleAn unusual presentation of familial Mediterranean fever with prolonged hip pain and amyloidosisen_US
dc.typeeditorialen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume33en_US
dc.identifier.issue2en_US
dc.identifier.startpage123en_US
dc.identifier.endpage125en_US
dc.relation.journalScandinavian Journal of Rheumatologyen_US
dc.relation.publicationcategoryDiğeren_US


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