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dc.contributor.authorUgurlu, Serdal
dc.contributor.authorHamuryudan, Vedat
dc.contributor.authorHacioglu, Aysa
dc.contributor.authorAdibnia, Yasaman
dc.contributor.authorOzdogan, Huri
dc.date.accessioned2021-03-06T07:47:23Z
dc.date.available2021-03-06T07:47:23Z
dc.identifier.citationUgurlu S., Hacioglu A., Adibnia Y., Hamuryudan V., Ozdogan H., "Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever", ORPHANET JOURNAL OF RARE DISEASES, cilt.12, 2017
dc.identifier.issn1750-1172
dc.identifier.othervv_1032021
dc.identifier.otherav_dde292c2-0f83-4d1d-a5de-2e87cd33ca6c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/146181
dc.identifier.urihttps://doi.org/10.1186/s13023-017-0642-0
dc.description.abstractBackground: There is no established treatment of AA amyloidosis, a long-term complication of various chronic inflammatory diseases associated with increased mortality, such as familial Mediterranian fever (FMF). Recently there are few reports pointing out that tocilizumab(TCZ), an anti IL-6 agent may be effective in AA amyloidosis resistant to conventional treatments. We report our data on the effect of TCZ in patients with FMF complicated with AA amyloidosis.
dc.language.isoeng
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.titleTocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
dc.typeMakale
dc.relation.journalORPHANET JOURNAL OF RARE DISEASES
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume12
dc.contributor.firstauthorID242469


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