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dc.contributor.authorBavunoglu, Işıl
dc.contributor.authorOzbakir, Fatma
dc.contributor.authorTabak, F
dc.contributor.authorMelikoglu, Melike
dc.contributor.authorSoysal, Teoman
dc.contributor.authorHekim, N
dc.contributor.authorYazici, Hasan
dc.contributor.authorYurdakul, Sebahattin
dc.contributor.authorHamuryudan, Vedat
dc.contributor.authorFresko, I
dc.date.accessioned2021-03-03T14:53:10Z
dc.date.available2021-03-03T14:53:10Z
dc.date.issued2005
dc.identifier.citationYurdakul S., Hekim N., Soysal T., Fresko I., Bavunoglu I., Ozbakir F., Tabak F., Melikoglu M., Hamuryudan V., Yazici H., "Fibrinolytic activity and d-dimer levels in Behcet's syndrome", CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.23, sa.4, 2005
dc.identifier.issn0392-856X
dc.identifier.othervv_1032021
dc.identifier.otherav_3bf8f37c-5aee-4433-9071-70959c7bd6d3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44260
dc.description.abstractObjective. Thrombophlebilis occurs in a third of patients with Behcets syndrome (BS). The thrombotic tendency in BS has been studied with inconclusive results perhaps due to the inadequate numbers of patients studied during the acute phase of the thrombosis as well as the lack of appropriate diseased controls. We have studied tissue-type plasminogen activator (t-PA) and its inhibitor (PAI-1), and d-dimer levels in BS patients with and without thrombosis both in the acute and chronic phases along with suitable diseased and healthy controls.
dc.language.isoeng
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleFibrinolytic activity and d-dimer levels in Behcet's syndrome
dc.typeMakale
dc.relation.journalCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.contributor.department, ,
dc.identifier.volume23
dc.identifier.issue4
dc.contributor.firstauthorID8454


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