摘要:

AbstractAn adolescent male patient developed functional asplenia in the course of graft versus host disease (GVHD) after successful allogeneic bone marrow transplantation (BMT) for aplastic anemia. Coincident with the onset of the asplenia, amelioration of the ongoing GVHD was observed. Unexpectedly, after 34 months of functional asplenia, the organ regained its function without evidence of graft rejection or reactivation of GVHD.

ISSN:0361-8609    

DOI:10.1002/ajh.2830120112

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1982

数据来源: WILEY

摘要:

AbstractRecent advances in defining the molecular basis for the thalassemia syndromes are discussed. We now realize that the causes of the thalassemia phenotype are diverse and include gene deletions, nuclear RNA processing defects, nonsense mutations, fusion genes, termination codon mutants, and unstable globin chains.

ISSN:0361-8609    

DOI:10.1002/ajh.2830120113

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1982

数据来源: WILEY

ISSN:0361-8609    

DOI:10.1002/ajh.2830120114

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1982

数据来源: WILEY

ISSN:0361-8609    

DOI:10.1002/ajh.2830120101

出版商:Wiley Subscription Services, Inc., A Wiley Company    

年代:1982

数据来源: WILEY