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A case with Henoch-Schonlein purpura concomitant with MTHFR C677T polymorphism

dc.contributor.authorHatipoglu, Nevin
dc.contributor.authorKasapcopur, Ozgur
dc.contributor.authorAydogan, Gonul
dc.contributor.authorBicer, Suat
dc.contributor.authorImseytoglu, Gokhan
dc.contributor.authorOzdemir, Pinar G.
dc.date.accessioned2021-03-05T08:48:41Z
dc.date.available2021-03-05T08:48:41Z
dc.identifier.citationOzdemir P. G. , Aydogan G., Hatipoglu N., Bicer S., Imseytoglu G., Kasapcopur O., "A case with Henoch-Schonlein purpura concomitant with MTHFR C677T polymorphism", ACTA PAEDIATRICA, cilt.97, ss.252, 2008
dc.identifier.issn0803-5253
dc.identifier.othervv_1032021
dc.identifier.otherav_9ad24ab4-97d4-46ac-9cd9-70500a06722c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/104064
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleA case with Henoch-Schonlein purpura concomitant with MTHFR C677T polymorphism
dc.typeMakale
dc.relation.journalACTA PAEDIATRICA
dc.contributor.departmentBakirkoy Children''s & Maternity Hospital , ,
dc.identifier.volume97
dc.identifier.startpage252
dc.identifier.endpage252
dc.contributor.firstauthorID188285


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