The effects of 2,3-diphosphoglycerate, adenosine triphosphate, and glycosylated hemoglobin on the hemoglobin-oxygen affinity of diabetic patients von Castilho, E M, Glass, M L, Manço, J C

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Multiple Pulmonary Thromboembolism Diagnosed by Two-Dimensional Echocardiography von Maciel, B.C., Neto, J.A Marin, Junior, L. Gallo, Maciel, L.M.Z., Iazigi, N., Evora, P.R., Manço, J.C.

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Survey of the anti–factor IX immunoglobulin profiles in patients with hemophilia B using a fluorescence‐based immunoassay von Boylan, B., Rice, A. S., Neff, A. T., Manco‐Johnson, M. J., Kempton, C. L., Miller, C. H., Abshire, T. C., Dunn, A., Bockenstedt, P. L., Brettler, D. B., Di Paola, J. A., Radhi, M., Lentz, S. R., Massey, G., Barrett, J. C., Shapiro, A. D., Tarantino, M., Wicklund, B. M., Knoll, C., Escobar, M. A., Eyster, M. E., Gill, J. C., Leissinger, C., Yaish, H.

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Characterization of the anti‐factor VIII immunoglobulin profile in patients with hemophilia A by use of a fluorescence‐based immunoassay von Boylan, B., Rice, A. S., Dunn, A. L., Tarantino, M. D., Brettler, D. B., Barrett, J. C., Miller, C. H., Abshire, T. C., Kempton, C. L., Bockenstedt, P. L., Di Paola, J. A., Radhi, M., Lentz, S. R., Massey, G., Neff, A. T., Shapiro, A. D., Wicklund, B. M., Manco‐Johnson, M. J., Knoll, C., Escobar, M. A., Elaine Eyster, M., Gill, J. C., Leissinger, C., Yaish, H.

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Limit of detection and threshold for positivity of the Centers for Disease Control and Prevention assay for factor VIII inhibitors von Miller, C. H., Boylan, B., Shapiro, A. D., Lentz, S. R., Wicklund, B. M., Abshire, T. C., Dunn, A. L., Kempton, C. L., Soucie, J. M., Bethea, F., Payne, A., Bockenstedt, P. L., Brettler, D. B., Di Paola, J. A., Radhi, M., Neff, A. T., Tarantino, M. D., Manco‐Johnson, M. J., Knoll, C., Escobar, M. A., Eyster, M. E., Gill, J. C., Leissinger, C., Yaish, H.

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Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations von Boylan, B., Rice, A. S., De Staercke, C., Eyster, M. E., Yaish, H. M., Knoll, C. M., Bean, C. J., Miller, C. H., Abshire, T. C., Dunn, A., Kempton, C. L., Bockenstedt, P. L., Brettler, D. B., Di Paola, J. A., Radhi, M., Lentz, S. R., Massey, G., Barrett, J. C., Neff, A. T., Shapiro, A. D., Tarantino, M., Wicklund, B. M., Manco‐Johnson, M. J., Escobar, M. A., Gill, J. C., Leissinger, C.

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Experimental Chronic Wasting Disease (CWD) in the Ferret von Sigurdson, C.J., Mathiason, C.K., Perrott, M.R., Eliason, G.A., Spraker, T.R., Glatzel, M., Manco, G., Bartz, J.C., Miller, M.W., Hoover, E.A.

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Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study von Young, G., Manco‐Johnson, M., Gill, J. C., Dimichele, D. M., Tarantino, M. D., Abshire, T., Nugent, D. J.

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Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States von Flood, V.H, Christopherson, P.A, Gill, J.C, Friedman, K.D, Haberichter, S.L, Bellissimo, D.B, Udani, R.A, Dasgupta, M, Hoffmann, R.G, Ragni, M.V, Shapiro, A.D, Lusher, J.M, Lentz, S.R, Abshire, T.C, Leissinger, C, Hoots, W.K, Manco-Johnson, M.J, Gruppo, R.A, Boggio, L.N, Montgomery, K.T, Goodeve, A.C, James, P.D, Lillicrap, D, Peake, I.R, Montgomery, R.R

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