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dc.contributor.authorKoc, Basak
dc.contributor.authorZulfikar, Bulent
dc.date.accessioned2021-12-10T10:31:49Z
dc.date.available2021-12-10T10:31:49Z
dc.date.issued2021
dc.identifier.citationKoc B., Zulfikar B., "Inherited Rare Factor Deficiencies: Single-centre Experience", MEANDROS MEDICAL AND DENTAL JOURNAL, cilt.22, sa.1, ss.1-6, 2021
dc.identifier.othervv_1032021
dc.identifier.otherav_459e3840-f311-41d2-b794-cc8026dab4cb
dc.identifier.urihttp://hdl.handle.net/20.500.12627/170075
dc.identifier.urihttps://doi.org/10.4274/meandros.galenos.2020.55476
dc.description.abstractObjective: Bleeding is one of the most important problems in humans. Absence, deficiency or dysfunctions of protein factors in the coagulation system can cause prolonged bleeding, morbidity or mortality. Although factor VIII, factor IX and von Willebrand factor deficiencies are the most common, deficiencies in all other factors exist, called rare factor deficiencies. This study aimed to present the clinical presentations, laboratory findings, treatments, and surgical interventions in patients with rare factor deficiencies other than factor VII followed up in our clinic.
dc.language.isoeng
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectGeneral Medicine
dc.subjectHealth Sciences
dc.subjectTemel Tıp Bilimleri
dc.subjectFamily Practice
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleInherited Rare Factor Deficiencies: Single-centre Experience
dc.typeMakale
dc.relation.journalMEANDROS MEDICAL AND DENTAL JOURNAL
dc.contributor.departmentİstanbul Teknik Üniversitesi , ,
dc.identifier.volume22
dc.identifier.issue1
dc.identifier.startpage1
dc.identifier.endpage6
dc.contributor.firstauthorID2604775


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