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dc.contributor.authorAltiparmak, MR
dc.contributor.authorSerdengecti, K
dc.contributor.authorKilicarslan, I
dc.contributor.authorBilir, M
dc.contributor.authorOygar, D
dc.date.accessioned2021-03-06T08:05:18Z
dc.date.available2021-03-06T08:05:18Z
dc.date.issued2002
dc.identifier.citationAltiparmak M., Oygar D., Bilir M., Kilicarslan I., Serdengecti K., "A rare cause of focal segmental glomerulosclerosis: Sarcoidosis", NEPHRON, cilt.90, ss.211-212, 2002
dc.identifier.issn0028-2766
dc.identifier.otherav_df4d0cb6-a265-44f0-a119-3715ecf80f45
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/147103
dc.identifier.urihttps://doi.org/10.1159/000049044
dc.description.abstractA 58-year-old female patient diagnosed as having sarcoidosis 23 years ago developed nephrotic syndrome. No pathology was found which could explain this, so it was attributed to her sarcoidosis. Renal biopsy showed global and segmental sclerosis. The occurrence of focal segmentary glomerulosclerosis in a case of sarcoidosis is rare. In systemic sarcoidosis it is thought that T-cell dysfunction may play a role in the pathogenesis of glomerulonephritis. When treatment is considered, corticosteroid therapy may be used according to the clinical status at diagnosis as well as on follow-up of the patient. Copyright (C) 2002 S. KargerAG, Basel.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectNefroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleA rare cause of focal segmental glomerulosclerosis: Sarcoidosis
dc.typeMakale
dc.relation.journalNEPHRON
dc.contributor.department, ,
dc.identifier.volume90
dc.identifier.issue2
dc.identifier.startpage211
dc.identifier.endpage212
dc.contributor.firstauthorID164556


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