aplastic anemia | Page 40 | Aplastic Anemia & MDS International Foundation

aplastic anemia

Improved outcome of patients older than 30 years receiving HLA-identical sibling hematopoietic stem cell transplantation for severe acquired aplastic anemia using fludarabine-based conditioning: a comparison with conventional conditioning regimen.

Author(s): 
Maury S, Bacigalupo A, Anderlini P, Aljurf M, Marsh J, Socié G, Oneto R, Passweg JR; Severe Aplastic Anemia Working Party, European Group for Blood and Marrow Transplantation (EBMT-SAAWP).
Primary Author: 
Maury S
Journal Title: 
Haematologica
Original Publication Date: 
Sep 2009

Older age is a limitation for HLA-identical sibling hematopoietic stem cell transplantation (HSCT) as

Bone Marrow Diseases: 

Survival of patients with documented autologous recovery after SCT for severe aplastic anemia: a study by the WPSAA of the EBMT.

Author(s): 
Piccin A, McCann S, Socié G, Oneto R, Bacigalupo A, Locasciulli A, Marsh J, Schrezenmeier H, Tichelli A, Hand E, Lawler M, Passweg J; Aplastic Anaemia Working Party of the European Group for Blood and Marrow Transplantation.
Primary Author: 
Piccin A
Journal Title: 
Biol Blood Marrow Transplant
Original Publication Date: 
Nov 2009

Graft rejection, with persistent pancytopenia, is well documented after allogeneic BMT (hematopoietic SCT

Bone Marrow Diseases: 

Fludarabine, cyclophosphamide, antithymocyte globulin, with or without low dose total body irradiation, for alternative donor transplants, in acquired severe aplastic anemia: a retrospective study from the EBMT-SAA working party.

Author(s): 
Bacigalupo A, Socie' G, Lanino E, Prete A, Locatelli F, Locasciulli A, Cesaro S, Shimoni A, Marsh J, Brune M, Van Lint MT, Oneto R, Passweg J; Severe Aplastic Anemia Working Party of the European Group for Blood and Marrow Transplantation.
Primary Author: 
Bacigalupo A
Journal Title: 
Haematologica
Original Publication Date: 
May 2010

BACKGROUND:

We analyzed

Bone Marrow Diseases: 

Paroxysmal nocturnal hemoglobinuria clones in severe aplastic anemia patients treated with horse anti-thymocyte globulin plus cyclosporine.

Author(s): 
Scheinberg P, Marte M, Nunez O, Young NS.
Primary Author: 
Scheinberg P
Journal Title: 
Haematologica
Original Publication Date: 
Jul 2010

BACKGROUND:

Clones of glycosylphosphatidylinositol-anchor protein-deficient cells are