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dc.contributor.authorGokler, G
dc.contributor.authorKotogyan, A
dc.contributor.authorDemirkesen, C
dc.contributor.authorMat, MC
dc.date.accessioned2021-03-02T20:39:42Z
dc.date.available2021-03-02T20:39:42Z
dc.date.issued1997
dc.identifier.citationMat M., Gokler G., Demirkesen C., Kotogyan A., "Intraepidermal IgA pustulosis", JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, cilt.9, sa.2, ss.161-165, 1997
dc.identifier.issn0926-9959
dc.identifier.othervv_1032021
dc.identifier.otherav_03170ecf-d2cc-4072-92d7-d685a6c44529
dc.identifier.urihttp://hdl.handle.net/20.500.12627/8022
dc.identifier.urihttps://doi.org/10.1016/s0926-9959(97)00040-8
dc.description.abstractBackground Intraepidermal IgA pustulosis is a rare vesiculopustular condition characterized by intercellular IgA deposits, neutrophilic infiltration and mild acantholysis. This condition is usually reported in middle-aged or elderly people. We present the clinical, histological and immunofluorescence data of a child with this condition.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectDERMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectDermatoloji
dc.titleIntraepidermal IgA pustulosis
dc.typeMakale
dc.relation.journalJOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
dc.contributor.department, ,
dc.identifier.volume9
dc.identifier.issue2
dc.identifier.startpage161
dc.identifier.endpage165
dc.contributor.firstauthorID119374


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