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dc.contributor.authorYozgat, Ayca Koca
dc.contributor.authorLeblebisatan, Goksel
dc.contributor.authorAkbayram, Sinan
dc.contributor.authorOzel, Simge Cinar
dc.contributor.authorKarakas, Zeynep
dc.contributor.authorErduran, Erol
dc.contributor.authorYilmaz, Sebnem
dc.contributor.authorKocak, Ulker
dc.contributor.authorUnal, Sule
dc.contributor.authorOzdemir, Gul Nihal
dc.contributor.authorAlbayrak, Meryem
dc.date.accessioned2021-12-21T08:47:57Z
dc.date.available2021-12-21T08:47:57Z
dc.date.issued2020
dc.identifier.issn1300-7777
dc.identifier.issn1308-5263
dc.identifier.urihttps://doi.org/10.4274/tjh.galenos.2020.2019.0380
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/2328
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.publisherGalenos Yayıncılık
dc.rightsgold, Green Published
dc.titleOutcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey
dc.typeArticle
dc.relation.journalTurkısh 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


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