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Glanzmann thrombasthenia: Cerrahpasa Medical Faculty experience

dc.contributor.authorApak, Hilmi
dc.contributor.authorOzdemir, Gul Nihal
dc.contributor.authorKutlubay, Busra
dc.contributor.authorTuysuz, Gulen
dc.contributor.authorCelkan, Tülin Tıraje
dc.date.accessioned2021-03-05T19:19:22Z
dc.date.available2021-03-05T19:19:22Z
dc.date.issued2012
dc.identifier.citationKutlubay B., Ozdemir G. N. , Tuysuz G., Apak H., Celkan T. T. , "Glanzmann thrombasthenia: Cerrahpasa Medical Faculty experience", TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.47, ss.104-106, 2012
dc.identifier.issn1306-0015
dc.identifier.othervv_1032021
dc.identifier.otherav_ceb47bcb-ba1c-479b-8a9d-96187b241785
dc.identifier.urihttp://hdl.handle.net/20.500.12627/136728
dc.identifier.urihttps://doi.org/10.4274/tpa.823
dc.description.abstractAim: Glazmann thrombasthenia is a rare autosomal recessive disease characterized by a defect in platelet aggregation. Here we report the management of children with Glazmann thrombasthenia followed up at Cerrahpasa Medical Faculty Pediatric Hematology Department.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectPEDİATRİ
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.titleGlanzmann thrombasthenia: Cerrahpasa Medical Faculty experience
dc.typeMakale
dc.relation.journalTURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume47
dc.identifier.issue2
dc.identifier.startpage104
dc.identifier.endpage106
dc.contributor.firstauthorID32780


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