ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease von James, Paula D., Connell, Nathan T., Ameer, Barbara, Di Paola, Jorge, Eikenboom, Jeroen, Giraud, Nicolas, Haberichter, Sandra, Jacobs-Pratt, Vicki, Konkle, Barbara, McLintock, Claire, McRae, Simon, R. Montgomery, Robert, O'Donnell, James S., Scappe, Nikole, Sidonio, Robert, Flood, Veronica H., Husainat, Nedaa, Kalot, Mohamad A., Mustafa, Reem A.

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A conditional knockout mouse model reveals endothelial cells as the principal and possibly exclusive source of plasma factor VIII von Fahs, Scot A., Hille, Matthew T., Shi, Qizhen, Weiler, Hartmut, Montgomery, Robert R.

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The endothelial cell receptor stabilin-2 regulates VWF-FVIII complex half-life and immunogenicity von Swystun, Laura L, Lai, Jesse D, Notley, Colleen, Georgescu, Ilinca, Paine, A Simonne, Mewburn, Jeff, Nesbitt, Kate, Schledzewski, Kai, Géraud, Cyrill, Kzhyshkowska, Julia, Goerdt, Sergij, Hopman, Wilma, Montgomery, Robert R, James, Paula D, Lillicrap, David

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The impact of aberrant von Willebrand factor-GPIbα interaction on megakaryopoiesis and platelets in humanized type 2B von Willebrand disease model mouse von Kanaji, Sachiko, Morodomi, Yosuke, Weiler, Hartmut, Zarpellon, Alessandro, Montgomery, Robert R, Ruggeri, Zaverio M, Kanaji, Taisuke

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The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels von Rydz, Natalia, Swystun, Laura L., Notley, Colleen, Paterson, Andrew D., Riches, J. Jacob, Sponagle, Kate, Boonyawat, Boonchai, Montgomery, Robert R., James, Paula D., Lillicrap, David

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Platelet hyperreactivity explains the bleeding abnormality and macrothrombocytopenia in a murine model of sitosterolemia von Kanaji, Taisuke, Kanaji, Sachiko, Montgomery, Robert R., Patel, Shailendra B., Newman, Peter J.

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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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Leukocyte proteases cleave von Willebrand factor at or near the ADAMTS13 cleavage site von Raife, Thomas J., Cao, Wenjing, Atkinson, Bonnie S., Bedell, Bruce, Montgomery, Robert R., Lentz, Steven R., Johnson, George F., Zheng, X. Long

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Life in the shadow of a dominant partner: the FVIII-VWF association and its clinical implications for hemophilia A von Pipe, Steven W., Montgomery, Robert R., Pratt, Kathleen P., Lenting, Peter J., Lillicrap, David

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Low VWF levels in children and lack of association with bleeding in children undergoing tonsillectomy von Gill, Joan Cox, Conley, Stephen F., Johnson, Victoria P., Christopherson, Pamela A., Haberichter, Sandra L., Diaz, Christina D., Strong, Tatyana C., Zhang, Jian, Simpson, Pippa, Abshire, Thomas C., Montgomery, Robert R., Flood, Veronica H.

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von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene von Sadler, Brooke, Christopherson, Pamela A., Haller, Gabe, Montgomery, Robert R., Di Paola, Jorge

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Correction of Murine Bernard–Soulier Syndrome by Lentivirus-mediated Gene Therapy von Kanaji, Sachiko, Kuether, Erin L, Fahs, Scot A, Schroeder, Jocelyn A, Ware, Jerry, Montgomery, Robert R, Shi, Qizhen

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The severe spontaneous bleeding phenotype in a novel hemophilia A rat model is rescued by platelet FVIII expression von Shi, Qizhen, Mattson, Jeremy G., Fahs, Scot A., Geurts, Aron M., Weiler, Hartmut, Montgomery, Robert R.

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Ristocetin dependent cofactor activity in von Willebrand disease diagnosis: Limitations of relying on a single measure von Christopherson, Pamela A., Haberichter, Sandra L., Flood, Veronica H., Sicking, Ursula O., Abshire, Thomas C., Montgomery, Robert R., Weiler, H., Lillicrap, D., James, P., O’Donnell, J., Ng, C., Di Paola, J., Sadler, B., 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.

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Evaluation of von Willebrand Factor and von Willebrand Factor Propeptide in Models of Vascular Endothelial Cell Activation, Perturbation, and/or Injury von Brott, David A., Katein, Anne, Thomas, Heath, Lawton, Michael, Montgomery, Robert R., Richardson, Rudy J., Louden, Calvert S.

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The heads and the tails of malaria and VWF von Montgomery, Robert R.

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von Willebrand factor binding to myosin assists in coagulation von Flood, Veronica H., Slobodianuk, Tricia L., Keesler, Daniel, Lohmeier, Hannah K., Fahs, Scot, Zhang, Liyun, Simpson, Pippa, Montgomery, Robert R.

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Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States von Flood, Veronica H., Christopherson, Pamela A., Gill, Joan Cox, Friedman, Kenneth D., Haberichter, Sandra L., Bellissimo, Daniel B., Udani, Rupa A., Dasgupta, Mahua, Hoffmann, Raymond G., Ragni, Margaret V., Shapiro, Amy D., Lusher, Jeanne M., Lentz, Steven R., Abshire, Thomas C., Leissinger, Cindy, Hoots, W. Keith, Manco-Johnson, Marilyn J., Gruppo, Ralph A., Boggio, Lisa N., Montgomery, Kate T., Goodeve, Anne C., James, Paula D., Lillicrap, David, Peake, Ian R., Montgomery, Robert R.

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Variability in International Society on Thrombosis and Haemostasis-Scientific and Standardization Committee endorsed Bleeding Assessment Tool (ISTH-BAT) score with normal aging in... von Doherty, Dearbhla, Grabell, Julie, Christopherson, Pamela A., Montgomery, Robert R., Coller, Barry S., Lavin, Michelle, O’Donnell, James S., James, Paula D.

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The impact of GPIbα on platelet‐targeted FVIII gene therapy in hemophilia A mice with pre‐existing anti‐FVIII immunity von Chen, Juan, Schroeder, Jocelyn A., Luo, Xiaofeng, Montgomery, Robert R., Shi, Qizhen

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