Basit öğe kaydını göster

dc.contributor.authorYozgat, A.K.
dc.contributor.authorLeblebisatan, G.
dc.contributor.authorAkbayram, S.
dc.contributor.authorÖzel, S.Ç.
dc.contributor.authorKarakaş, Z.
dc.contributor.authorErduran, E.
dc.contributor.authorYılmaz, Ş.
dc.contributor.authorKoçak, Ü.
dc.contributor.authorÜnal, Ş.
dc.contributor.authorÖzdemir, G.N.
dc.contributor.authorAlbayrak, M.
dc.date.accessioned2021-12-21T08:40:49Z
dc.date.available2021-12-21T08:40:49Z
dc.date.issued2020
dc.identifier.issn13007777
dc.identifier.urihttps://doi.org/10.4274/tjh.galenos.2020.2019.0380
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/1211
dc.description.abstractObjective: Immune thrombocytopenia (ITP) is a rare autoimmune disease and hematologic disorder characterized by reduced platelet counts that can result in significant symptoms, such as bleeding, bruising, epistaxis, or petechiae. The thrombopoietin recept
dc.language.isoEnglish
dc.publisherTurkish Society of Hematology
dc.rightsAll Open Access, Bronze, Green
dc.titleOutcomes of eltrombopag treatment and development of iron deficiency in children with immune thrombocytopenia in Turkey [İmmün trombositopenili çocuk hastalarda eltrombopag tedavisi ve tedaviye bağlı demir eksikliği]
dc.typeArticle
dc.relation.journalTurkish Journal of Hematology
dc.identifier.issue3
dc.identifier.startpage139
dc.identifier.endpage144
dc.identifier.volume37
dc.identifier.doi10.4274/tjh.galenos.2020.2019.0380
dc.relation.issue3
dc.relation.volume37


Bu öğenin dosyaları:

Thumbnail

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster