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dc.contributor.authorYazganoglu, K. Didem
dc.contributor.authorBÜYÜKBABANİ, Nesimi
dc.contributor.authorBAYKAL, Can
dc.date.accessioned2022-02-18T10:01:03Z
dc.date.available2022-02-18T10:01:03Z
dc.identifier.citationBAYKAL C., BÜYÜKBABANİ N., Yazganoglu K. D. , "Primary cutaneous CD30(+)lymphoproliferative disorders", TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, cilt.40, 2006
dc.identifier.othervv_1032021
dc.identifier.otherav_74319599-cd79-4cda-bc7c-3dc02ee13455
dc.identifier.urihttp://hdl.handle.net/20.500.12627/178428
dc.description.abstractBackground: Primary cutaneous CD30(+) lymphoproliferative disorders (LPDs) includes primary cutaneous anaplastic large cell lymphoma (C-ALCL) and lymphomatoid papulosis (LyP). Though both diseases have some common clinical features the therapy and prognosis of the diseases are different. We evaluated the common and different clinical features of both diseases in our patients.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectHealth Sciences
dc.subjectDermatology
dc.subjectDERMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDermatoloji
dc.subjectDahili Tıp Bilimleri
dc.titlePrimary cutaneous CD30(+)lymphoproliferative disorders
dc.typeMakale
dc.relation.journalTURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY
dc.contributor.departmentİstanbul Teknik Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume40
dc.contributor.firstauthorID3373708


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