Allogeneic bone marrow transplantation in a child with severe aplastic anemia and hemophilia A

Author:

Ostronoff M,Ostronoff F,Campos G,Arruda S,Vaz C,Florencio R,Calixto R,Souto Maior A P,Sucupira A,Domingues M,Tagliari C

Publisher

Springer Science and Business Media LLC

Subject

Transplantation,Hematology

Reference13 articles.

1. Bolton-Maggs PH, Pasi KJ . Haemophilias A and B. Lancet 2003; 361: 1801–1809.

2. Morfini M, Longo G, Rossi Ferrini P, Azzi A, Zakrewska C, Ciappi S et al. Hypoplastic anemia in a hemophiliac first infused with a solvent/detergent treated factor VIII concentrate: the role of human B19 parvovirus. Am J Hematol 1992; 39: 149–150.

3. Matsui H, Sugimoto M, Tsuji S, Shima M, Giddings J, Yoshioka A . Transient hypoplastic anemia caused by primary human parvovirus B19 infection in a previously untreated patient with hemophilia transfused with a plasma-derived, monoclonal antibody-purified factor VIII concentrate. J Pediatr Hematol Oncol 1999; 21: 74–76.

4. Irfan M . Aplastic anemia in a patient with factor IX deficiency. J Pak Med Assoc 2000; 50: 397.

5. Wion KL, Kelly D, Summerfield JA, Tuddenham EG, Lawn RM . Distribution of factor VIII mRNA and antigen in human liver and other tissues. Nature 1985; 317: 726–729.

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