Bianchi, P., Fermo, E., Lezon-Geyda, K., Gallagher, P. G., Morton, D. H., Barcellini, W., … Grace, R. F. (2015). Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants. In BLOOD (Vol. 126). Orlando, FL: AMER SOC HEMATOLOGY.

Bianchi, Paola, Elisa Fermo, Kimberly Lezon-Geyda, Patrick G. Gallagher, D Holmes Morton, Wilma Barcellini, Bertil Glader, et al. “Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants.” In BLOOD, Vol. 126. AMER SOC HEMATOLOGY, 2015.

Bianchi P, Fermo E, Lezon-Geyda K, Gallagher PG, Morton DH, Barcellini W, et al. Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants. In: BLOOD. AMER SOC HEMATOLOGY; 2015.

Bianchi, Paola, et al. “Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants.” BLOOD, vol. 126, no. 23, AMER SOC HEMATOLOGY, 2015.

Bianchi P, Fermo E, Lezon-Geyda K, Gallagher PG, Morton DH, Barcellini W, Glader B, Eber SW, Despotovic JM, Knoll CM, Yaish HM, Newburger PF, Rothman J, Thompson AA, Ravindranath Y, Nottage KA, Wang H, van Beers EJ, Kunz J, Wlodarski MW, Sharma M, Rose MJ, Pastore YD, Giardina PJ, Rhodes M, Kuo K, Guo D, London WB, Grace RF. Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants. BLOOD. AMER SOC HEMATOLOGY; 2015.