Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1582
Full metadata record
DC FieldValueLanguage
dc.contributor.authorREGNO:BN0120001-
dc.date.accessioned2023-12-11T10:41:40Z-
dc.date.available2023-12-11T10:41:40Z-
dc.date.issued2023-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1582-
dc.description.abstractBackground: A well-known consequence of thalassemia patients who receive multiple blood transfusions throughout their lives is the development of alloimmunity, or allo-antibodies against donor red blood cells (RBCs). This leads to hemolysis of the donor's red blood cells, making the transfusion less effective and increasing the risk of secondary problems such as iron overload. This study was conducted to examine how common alloimmunization is in patients with thalassemia.en_US
dc.language.isoen_USen_US
dc.publisherKLE Academy of Higher Education and Research, Belagavien_US
dc.subjectKey Words: Alloimmunization, thalassemia major, thalassemia intermedia, blood transfusion, splenectomy, hemoglobin, allo-antibodies.en_US
dc.titleSTUDY OF ALLOIMMUNIZATION IN TRANSFUSION DEPENDENT THALASSEMIA PATIENTS AT A TERTIARY CARE HOSPTALen_US
dc.typeDissertationsen_US
Appears in Collections:Pathology

Files in This Item:
File Description SizeFormat 
BN0120001.pdf4.08 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.