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dc.contributor.authorKilic, Betul
dc.contributor.authorAydin, Kursad
dc.contributor.authorAyaz, Akif
dc.contributor.authorTelhan, Leyla
dc.contributor.authorAnak, Sema
dc.contributor.authorNepesov, Serdar
dc.contributor.authorYaman, Yontem
dc.contributor.authorElli, Murat
dc.contributor.authorBayram, Nihan
dc.contributor.authorOzdilli, Kursat
dc.contributor.authorKiykim, Ayca
dc.contributor.authorCakir, Deniz
dc.date.accessioned2023-02-21T08:20:23Z
dc.date.available2023-02-21T08:20:23Z
dc.date.issued2022
dc.identifier.citationNepesov S., Yaman Y., Elli M., Bayram N., Ozdilli K., Kiykim A., Cakir D., Kilic B., Aydin K., Ayaz A., et al., "Clinical, Genetic, and Outcome Characteristics of Pediatric Patients with Primary Hemophagocytic Lymphohistiocytosis", TURKISH ARCHIVES OF PEDIATRICS, cilt.57, sa.4, ss.398-405, 2022
dc.identifier.issn2757-6256
dc.identifier.otherav_18d83e10-1b46-495d-b135-f8f32857d525
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/186572
dc.identifier.urihttps://doi.org/10.5152/turkarchpediatr.2022.21314
dc.description.abstractObjectIive: In this study, we sought to describe the clinical, laboratory, and genetic characteristics of patients diagnosed with primary hemophagocytic lymphohistiocytosis. Thus, we aimed to evaluate the early diagnosis and appropriate treatment options for pediatric hemophagocytic lymphohistiocytosis patients.
dc.language.isoeng
dc.subjectPediatri, Perinatoloji ve Çocuk Sağlığı
dc.subjectSağlık Bilimleri
dc.subjectPediatri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.titleClinical, Genetic, and Outcome Characteristics of Pediatric Patients with Primary Hemophagocytic Lymphohistiocytosis
dc.typeMakale
dc.relation.journalTURKISH ARCHIVES OF PEDIATRICS
dc.contributor.departmentİstanbul Medipol Üniversitesi , ,
dc.identifier.volume57
dc.identifier.issue4
dc.identifier.startpage398
dc.identifier.endpage405
dc.contributor.firstauthorID4067673


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