- URN to cite this document:
- urn:nbn:de:bvb:355-epub-748694
- DOI to cite this document:
- 10.5283/epub.74869
Abstract
Acquired aplastic anemia is a bone marrow failure syndrome characterized by hypocellular bone marrow and peripheral blood pancytopenia. Frequent clinical responses to calcineurin inhibition and antithymocyte globulin strongly suggest critical roles for hematopoietic stem/progenitor cell–reactive T-cell clones in disease pathophysiology; however, their exact contribution and antigen specificities ...

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