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dc.contributor.authorDiz-Küçükkaya, Reyhan
dc.contributor.authorLopez, Jose A.
dc.date.accessioned2014-12-15T13:59:32Z
dc.date.available2014-12-15T13:59:32Z
dc.date.issued2013
dc.identifier.citationDiz-Kücükkaya R, López JA. Inherited disorders of platelets: membrane glycoprotein disorders. Hematology/Oncology Clinics of North America. 2013; 27(3): 613-627. doi: 10.1016/j.hoc.2013.03.005.en_US
dc.identifier.issn0889-8588
dc.identifier.urihttps://www.clinicalkey.com/#!/content/playContent/1-s2.0-S0889858813000324en_US
dc.identifier.urihttps://hdl.handle.net/11446/601en_US
dc.descriptionİstanbul Bilim Üniversitesi, Tıp Fakültesi.en_US
dc.description.abstractPlatelet membrane glycoproteins play a key role in hemostasis and thrombosis. Although disorders of platelet membrane glycoproteins are rare, their effects on the lives of those affected are very important. Severe deficiencies manifest themselves early during childhood with mucocutaneous bleeding. Mild deficiencies may not be diagnosed until adulthood or until the hemostatic system is stressed by surgery or trauma. The diagnosis of these disorders requires detailed laboratory investigation. Management of bleeding in patients with inherited platelet disorders requires both preventive measures and the treatment of individual bleeding episodes according to severity. The study of platelet membrane disorders also has yielded important insights into the functions of affected proteins, information that has produced some of the most successful antithrombotic drugs currently in use.en_US
dc.language.isoengen_US
dc.publisherWB Saundersen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectplatelet glycoproteinsen_US
dc.subjectbernard-soulier syndromeen_US
dc.subjectglanzmann thrombastheniaen_US
dc.subjectinherited bleeding tendencyen_US
dc.subjectplatelet disordersen_US
dc.titleInherited disorders of platelets membrane glycoprotein disordersen_US
dc.typearticleen_US
dc.relation.journalHematology/Oncology Clinics of North Americaen_US
dc.departmentDBÜ, Tıp Fakültesien_US
dc.identifier.issue3
dc.identifier.volume27
dc.identifier.startpage613
dc.identifier.endpage627
dc.contributor.authorIDTR116136en_US
dc.relation.publicationcategoryBelirsizen_US


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