Selected Publications

Teachey D.T., Manno C.S., Axsom K.M., Andrews C.S., Choi J.K., Greenbraum B.H., McMann J.M., Sullivan K.E., Travis S.F., Grupp S.A.: Unmasking Evans syndrome: T-cell phenotype and apoptotic response reveal autoimmune lymphoproliferative syndrome (ALPS). Blood 105(6): 2443-2448, 2005.

Axsom K.M., Manno C.S.: Treatment of hemophilia with genetic engineering. Transfusion Alternatives in Transfusion Medicine 6(2): 46-54, 2004.

Rheingold S.A., Burnham J.M., Rutstein R., Manno C.S.: HIV infection presenting as severe autoimmune hemolytic anemia with disseminated intravascular coagulation in an infant. J Ped Hematol/Onco. 26(1): 9-12, 2004.

Manno C.S, Chew A.J., Hutchinson S., Larson P.J., Herzog R.W., Arruda V.R., Tai S.J., Ragni M.V., Thompson A., Ozelo M., Couto L.B., Leonard D.G.B., Johnson F.A., McClelland A., Sallan C., Skarsgard E., Flake A.W., Kay M.A., High K.A., Glader B.: AAV mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B. Blood 101: 2963-2972, 2003.

Manno C.S.: The promise of thrid generation recombinant therapy and gene therapy. Semin Hematol 40(suppl 3): 23-28, 2003.

Manno C.S.: Gene therapy for hemophilia. Curr Opin in Hematol 9(6): 511-515, 2002.

Roseff S.D., Luban N.L.C., Manno C.S.: Guidelines for assessing appropriateness of pediatric transfusion. Transfusion 42: 1398-1413, 2002.

Kay M.A., Manno C.S., Ragni M.V., Larson P.J., Couto L.B., McClelland A., Glader B., Chew A.J., Tai S., Herzog R.W., Arruda V., Johnson F., Scallan C., Skarsgard E., Flake A.W., High K.A.: Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector. Nat Genet 24(3): 257-261, 2001.

Manno C.S.: Gene therapy for hemophilia. Biotech Medical. 19: 3, 2001.

Eder A., Manno C.S.: Does red cell T-activation matter? Br J Hematol 114: 25-30, 2001.