1. Camitta BM. Pathogenesis and treatment of aplastic anemia. Rinsho Ketsueki. 1984. 25:459–469.
2. Pitcher LA, Hann IM, Evans JP, Veys P, Chessells JM, Webb DK. Improved prognosis for acquired aplastic anaemia. Arch Dis Child. 1999. 80:158–162.
Article
3. Camitta BM, Thomas ED, Nathan DG, et al. A prospective study of androgens and bone marrow transplantation for treatment of severe aplastic anemia. Blood. 1979. 53:504–514.
Article
4. Bacigalupo A, Passweg J. Diagnosis and treatment of acquired aplastic anemia. Hematol Oncol Clin North Am. 2009. 23:159–170.
Article
5. Camitta BM, Storb R, Thomas ED. Aplastic anemia (first of two parts): pathogenesis, diagnosis, treatment, and prognosis. N Engl J Med. 1982. 306:645–652.
6. Camitta BM, Storb R, Thomas ED. Aplastic anemia (second of two parts): pathogenesis, diagnosis, treatment, and prognosis. N Engl J Med. 1982. 306:712–718.
7. Dunn DE, Tanawattanacharoen P, Boccuni P, et al. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann Intern Med. 1999. 131:401–408.
Article
8. Rosenfeld SJ, Kimball J, Vining D, Young NS. Intensive immunosuppression with antithymocyte globulin and cyclosporine as treatment for severe acquired aplastic anemia. Blood. 1995. 85:3058–3065.
Article
9. Rosenfeld S, Follmann D, Nunez O, Young NS. Antithymocyte globulin and cyclosporine for severe aplastic anemia: association between hematologic response and long-term outcome. JAMA. 2003. 289:1130–1135.
Article
10. Young NS, Calado RT, Scheinberg P. Current concepts in the pathophysiology and treatment of aplastic anemia. Blood. 2006. 108:2509–2519.
Article
11. Sebastiani G, Pantopoulos K. Disorders associated with systemic or local iron overload: from pathophysiology to clinical practice. Metallomics. 2011. 3:971–986.
Article
12. Quarta A, Melpignano A, Quarta G. Oral iron chelator deferasirox in the treatment of secondary hemochromatosis following bone marrow transplantation in a patient with severe aplastic anemia. Acta Haematol. 2011. 125:219–221.
Article
13. Wali R, Fadoo Z, Adil S, Naqvi MA. Aplastic anemia: clinicohaematological features, treatment and outcome analysis. J Coll Physicians Surg Pak. 2011. 21:219–222.
14. Najean Y, Pecking A. Prognostic factors in acquired aplastic anemia. A study of 352 cases. Am J Med. 1979. 67:564–571.
15. Williams DM, Lynch RE, Cartwright GE. Prognostic factors in aplastic anaemia. Clin Haematol. 1978. 7:467–474.
Article
16. Rozman C, Marin P, Grañena A, et al. Prognosis in acquired aplastic anaemia. A multivariate statistical analysis of 80 cases. Scand J Haematol. 1981. 26:321–329.
Article
17. Camitta BM, Thomas ED, Nathan DG, et al. Severe aplastic anemia: a prospective study of the effect of early marrow transplantation on acute mortality. Blood. 1976. 48:63–70.
Article
18. Hormann A, Berchthold W, Rhyner K, Wiedemann-Sigg C, Gmür J. Prognosis in acquired aplastic anemia. Acta Haematol. 1984. 71:81–89.
Article
19. Scheinberg P, Wu CO, Nunez O, Young NS. Predicting response to immunosuppressive therapy and survival in severe aplastic anaemia. Br J Haematol. 2009. 144:206–216.
Article
20. Bacigalupo A, Hows J, Gluckman E, et al. Bone marrow transplantation (BMT) versus immunosuppression for the treatment of severe aplastic anaemia (SAA): a report of the EBMT SAA working party. Br J Haematol. 1988. 70:177–182.
Article
21. Sleijfer DT, Mulder NH, Nieweg HO. The value of prognostic indices in aplastic anaemia. Blut. 1981. 42:69–78.
Article