Contemporary management of primary immune thrombocytopenia in adults von LAKSHMANAN, S., CUKER, A.

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The HIT Expert Probability (HEP) Score: a novel pre‐test probability model for heparin‐induced thrombocytopenia based on broad expert opinion von CUKER, A., AREPALLY, G., CROWTHER, M. A., RICE, L., DATKO, F., HOOK, K., PROPERT, K. J., KUTER, D. J., ORTEL, T. L., KONKLE, B. A., CINES, D. B.

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Recombinant porcine sequence factor VIII (rpFVIII) for acquired haemophilia A: practical clinical experience of its use in seven patients von Tarantino, M. D., Cuker, A., Hardesty, B., Roberts, J. C., Sholzberg, M.

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Laboratory measurement of the direct oral anticoagulants: Indications and impact on management in clinical practice von Wright, C., Brown, R., Cuker, A.

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Inappropriate documentation of heparin allergy in the medical record because of misdiagnosis of heparin‐induced thrombocytopenia: frequency and consequences von McMahon, C. M., Tanhehco, Y. C., Cuker, A.

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Diagnostic accuracy of IgG‐specific versus polyspecific enzyme‐linked immunoassays in heparin‐induced thrombocytopenia: a systematic review and meta‐analysis von Husseinzadeh, H. D., Gimotty, P. A., Pishko, A. M., Buckley, M., Warkentin, T. E., Cuker, A.

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Evaluation of the utility of the ISTH-BAT in haemophilia carriers: a multinational study von James, P. D., Mahlangu, J., Bidlingmaier, C., Mingot-Castellano, M. E., Chitlur, M., Fogarty, P. F., Cuker, A., Mancuso, M. E., Holme, P. A., Grabell, J., Satkunam, N., Hopman, W. M., Mathew, P.

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Molecular pathogenesis and heterogeneity in type 3 VWD families in U.S. Zimmerman program von Christopherson, Pamela A., Haberichter, Sandra L., Flood, Veronica H., Perry, Crystal L., Sadler, Brooke E., Bellissimo, Daniel B., Di Paola, Jorge, Montgomery, Robert R., Abshire, T, Weiler, H, Lillicrap, D, James, P, O’Donnell, J, Ng, C, Bennett, C, Sidonio, R, Manco‐Johnson, M, Journeycake, J, Zia, A, Lusher, J, Rajpurkar, M, Shapiro, A, Lentz, S, Gill, J, Leissinger, C, Ragni, M, Tarantino, M, Roberts, J, Hord, J, Strouse, J, Ma, A, Valentino, L, Boggio, L, Sharathkumar, A, Gruppo, R, Kerlin, B, Kulkarni, R, Green, D, Hoots, K, Brown, D, Mahoney, D, Mathias, L, Bedros, A, Diamond, C, Neff, A, DiMichele, D, Giardina, P, Cohen, A, Paidas, M, Werner, E, Matsunaga, A, Shafer, F, Konkle, B, Cuker, A, Kouides, P, Stein, D

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Prevalence of and risk factors for cerebral microbleeds among adult patients with haemophilia A or B von Husseinzadeh, H., Chiasakul, T., Gimotty, P. A., Pukenas, B., Wolf, R., Kelty, M., Chiang, E., Fogarty, P. F., Cuker, A.

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Prevalence and impact of obesity in people with haemophilia: Review of literature and expert discussion around implementing weight management guidelines von Kahan, S., Cuker, A., Kushner, R. F., Maahs, J., Recht, M., Wadden, T., Willis, T., Majumdar, S., Ungar, D., Cooper, D.

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Heparin-induced thrombocytopenia (HIT) in 2011: An epidemic of overdiagnosis von Cuker, Adam

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Recombinant factor VIIa addition to haemophilic blood perfused over collagen/tissue factor can sufficiently bypass the factor IXa/VIIIa defect to rescue fibrin generation von Li, R., Panckeri, K. A., Fogarty, P. F., Cuker, A., Diamond, S. L.

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Interlaboratory agreement in the monitoring of unfractionated heparin using the anti‐factor Xa‐correlated activated partial thromboplastin time von CUKER, A., PTASHKIN, B., KONKLE, B. A., PIPE, S. W., WHINNA, H. C., ZHENG, X. L., CINES, D. B., POLLAK, E. S.

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Distinguishing opinion from evidence in guidelines von Schünemann, Holger J, Zhang, Yuqing, Oxman, Andrew D

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Similarity in joint function limitation in Type 3 von Willebrand's disease and moderate haemophilia A von Sood, S. L., Cuker, A., Wang, C., Metjian, A. D., Chiang, E. Y., Soucie, J. M., Konkle, B. A.

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How I treat heparin-induced thrombocytopenia von Cuker, Adam, Cines, Douglas B.

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Crucial role for the VWF A1 domain in binding to type IV collagen von Flood, Veronica H., Schlauderaff, Abraham C., Haberichter, Sandra L., Slobodianuk, Tricia L., Jacobi, Paula M., Bellissimo, Daniel B., Christopherson, Pamela A., Friedman, Kenneth D., Gill, Joan Cox, Hoffmann, Raymond G., Montgomery, Robert R.

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Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant von George, Lindsey A, Sullivan, Spencer K, Giermasz, Adam, Rasko, John E.J, Samelson-Jones, Benjamin J, Ducore, Jonathan, Cuker, Adam, Sullivan, Lisa M, Majumdar, Suvankar, Teitel, Jerome, McGuinn, Catherine E, Ragni, Margaret V, Luk, Alvin Y, Hui, Daniel, Wright, J. Fraser, Chen, Yifeng, Liu, Yun, Wachtel, Katie, Winters, Angela, Tiefenbacher, Stefan, Arruda, Valder R, van der Loo, Johannes C.M, Zelenaia, Olga, Takefman, Daniel, Carr, Marcus E, Couto, Linda B, Anguela, Xavier M, High, Katherine A

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Laboratory variability in the diagnosis of type 2 VWD variants von DiGiandomenico, Stefanie, Christopherson, Pamela A., Haberichter, Sandra L., Abshire, Thomas C., Montgomery, Robert R., Flood, Veronica H., Valentino, L., Abshire, T., Dunn, A., Bennett, C., Lusher, J., Rajpurkar, M., Hoots, W. K., Brown, D., Shapiro, A., Paola, J. Di, Lentz, S., Gill, J., Leissinger, C., Ragni, M., Hord, J., Manco‐Johnson, M., Ma, A., Boggio, L., Sharathkumar, A., Gruppo, R., Kerlin, B., Journeycake, J., Kulkarni, R., Mahoney, D, Mathias, L., Bedros, A., Diamond, C., Neff, A., Paroskie, A., DiMichele, D., Giardina, P., Cohen, A., Paidas, M., Werner, E., Matsunaga, A., Singer, T., Tarantino, M., Roberts, J., Shafer, F., Konkle, B., Cuker, A., Kouides, P., Stein, D., Manco‐Johnson, M., Dunn, A., Bennett, C., Journeycake, J., Lusher, J., Rajpurkar, M., Shapiro, A., Lentz, S., Lillicrap, D., James, P., Leissinger, C., Roberts, J., Ragni, M.

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SUPPLEMENT • Building Diversity, Equity, and Inclusion in the Ocean Sciences Autobiographical Sketches von Kappel, Ellen

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