Fibrinogen kaiserslautern (γ 380 Lys to Asn) : a new glycosylated fibrinogen variant with delayed polymerization von RIDGWAY, H. J, BRENNAN, S. O, LORETH, R. M, GEORGE, P. M

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Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene von HERRMANN, F. H., WULFF, K., AUERSWALD, G., SCHULMAN, S., ASTERMARK, J., BATOROVA, A., KREUZ, W., POLLMANN, H., RUIZ-SAEZ, A., DE BOSCH, N., SALAZAR-SANCHEZ, L.

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Pregnancy-associated risk for venous thromboembolism and pregnancy outcome in women homozygous for factor V Leiden von Pabinger, I, Nemes, L, Rintelen, C, Koder, S, Lechler, E, Loreth, R M, Kyrle, P A, Scharrer, I, Sas, G, Lechner, K, Mannhalter, C, Ehrenforth, S

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65. Fibrinogen Kaiserslautern (γ 380 Lys to Asn): morphological and physical properties as a clue for the thrombotic tendency in the propositi? von Loreth, R M, Collet, J -P, Brennan, S O

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61. Fibrinogen Kaiserslautern III: a new variant of congenital dysfibrinogenemia (Aα 16 Arg → Cys) von Loreth, R M, Meyer, M, Berger, H H, Albert, F W

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Fibrinogen Kaiserslautern III: A New Case of Congenital Dysfibrinogenemia with Aα 16 Arg → Cys Substitution von Loreth, R.M., Meyer, M., Albert, F.W.

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Haemophilia A in a female caused by coincidence of a Swyer syndrome and a missense mutation in factor VIII gene von Loreth, Ralph M., El-Maarri, Osman, Schröder, Jörg, Budde, Ulrich, Herrmann, Falko H., Oldenburg, Johannes

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Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V von Herrmann, Falko H, Wulff, Karin, Strey, Rüdiger, Siegemund, Annelie, Astermark, Jan, Schulman, Sam

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Was bringt die Volumentherapie mit HES 200/0,5 im Vergleich zur Gelatine-Lösung bei Patienten mit einem akuten ischämischen Hirninfarkt: eine randomisierte Doppelblindstudie von Treib, J, Wössner, R, Hoock, SB, Herber, M, Loreth, RM, Albert, FW

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Fibrinogen kaiserslautern III: a new case of congenital dysfibrinogenemia with aalpha 16 arg-->cys substitution von Loreth, R M, Meyer, M, Albert, F W

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Phylogenetic analysis of SARS-CoV-2 in Boston highlights the impact of superspreading events von Lemieux, Jacob E, Siddle, Katherine J, Shaw, Bennett M, Loreth, Christine, Schaffner, Stephen F, Gladden-Young, Adrianne, Adams, Gordon, Fink, Timelia, Tomkins-Tinch, Christopher H, Krasilnikova, Lydia A, DeRuff, Katherine C, Rudy, Melissa, Bauer, Matthew R, Lagerborg, Kim A, Normandin, Erica, Chapman, Sinéad B, Reilly, Steven K, Anahtar, Melis N, Lin, Aaron E, Carter, Amber, Myhrvold, Cameron, Kemball, Molly E, Chaluvadi, Sushma, Cusick, Caroline, Flowers, Katelyn, Neumann, Anna, Cerrato, Felecia, Farhat, Maha, Slater, Damien, Harris, Jason B, Branda, John A, Hooper, David, Gaeta, Jessie M, Baggett, Travis P, O'Connell, James, Gnirke, Andreas, Lieberman, Tami D, Philippakis, Anthony, Burns, Meagan, Brown, Catherine M, Luban, Jeremy, Ryan, Edward T, Turbett, Sarah E, LaRocque, Regina C, Hanage, William P, Gallagher, Glen R, Madoff, Lawrence C, Smole, Sandra, Pierce, Virginia M, Rosenberg, Eric, Sabeti, Pardis C, Park, Daniel J, MacInnis, Bronwyn L

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Amyloid-β Peptide Induces Mitochondrial Dysfunction by Inhibition of Preprotein Maturation von Mossmann, Dirk, Vögtle, F.-Nora, Taskin, Asli Aras, Teixeira, Pedro Filipe, Ring, Julia, Burkhart, Julia M., Burger, Nils, Pinho, Catarina Moreira, Tadic, Jelena, Loreth, Desiree, Graff, Caroline, Metzger, Friedrich, Sickmann, Albert, Kretz, Oliver, Wiedemann, Nils, Zahedi, René P., Madeo, Frank, Glaser, Elzbieta, Meisinger, Chris

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Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2) von KNOEBL, P., MARCO, P., BAUDO, F., COLLINS, P., HUTH‐KÜHNE, A., NEMES, L., PELLEGRINI, F., TENGBORN, L., LÉVESQUE, H.

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Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry von Baudo, Francesco, Collins, Peter, Huth-Kühne, Angela, Lévesque, Hervé, Marco, Pascual, Nemes, László, Pellegrini, Fabio, Tengborn, Lilian, Knoebl, Paul

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Pathogenicity of Human Anti-PLA2R1 Antibodies in Minipigs: A Pilot Study von Reinhard, Linda, Wiech, Thorsten, Reitmeier, Aline, Lassé, Moritz, Machalitza, Maya, Heumann, Asmus, Ferru, Nicoletta, Loreth, Desiree, Schröder, Marie-Luise, Hutzfeldt, Arvid, Stahl, Felix R., Peine, Sven, Gröne, Hermann-Josef, Meyer-Schwesinger, Catherine, Rinschen, Markus M., Stahl, Rolf A.K., Hoxha, Elion

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Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA von Earnest, Rebecca, Uddin, Rockib, Matluk, Nicholas, Renzette, Nicholas, Turbett, Sarah E., Siddle, Katherine J., Loreth, Christine, Adams, Gordon, Tomkins-Tinch, Christopher H., Petrone, Mary E., Rothman, Jessica E., Breban, Mallery I., Koch, Robert Tobias, Billig, Kendall, Fauver, Joseph R., Vogels, Chantal B.F., Bilguvar, Kaya, De Kumar, Bony, Landry, Marie L., Peaper, David R., Omerza, Greg, Grieser, Heather, Meak, Sim, Martha, John, Dewey, Hannah B., King, Ewa, Huard, Richard C., Novitsky, Vlad, Darpolor, Josephine, Manne, Akarsh, Kantor, Rami, Smole, Sandra C., Brown, Catherine M., Fink, Timelia, Lang, Andrew S., Gallagher, Glen R., Pitzer, Virginia E., Sabeti, Pardis C., Gabriel, Stacey, MacInnis, Bronwyn L., Altajar, Ahmad, DeJesus, Alexandra, Brito, Anderson, Watkins, Anne E., Muyombwe, Anthony, Blumenstiel, Brendan S., Neal, Caleb, Kalinich, Chaney C., Liu, Chen, Castaldi, Christopher, Pearson, Claire, Bernard, Clare, Nolet, Corey M., Buzby, Erika, Laszlo, Eva, Reagan, Faye L., Vicente, Gina, Rooke, Heather M., Munger, Heidi, Johnson, Hillary, Tikhonova, Irina R., Ott, Isabel M., Razeq, Jafar, Meldrim, James C., Brown, Jessica, Wang, Jianhui, Vostok, Johanna, Beauchamp, John P., Grimsby, Jonna L., Messer, Katelyn S., Vernest, Kyle, Green, Lisa M., Webber, Lori, Gagne, Luc, Ray, Marianne C., Fisher, Marissa E., Barter, Mary, Lee, Matthew D., DeFelice, Matthew T., Cipicchio, Michelle C., Smith, Natasha L., Fitzgerald, Nicholas A., Kerantzas, Nicholas, Hui, Pei, Harrington, Rachel, Haye, Rashida, Lynch, Ryan, Cofsky, Seana, Clancy, Selina, Mane, Shrikant, Ash, Stephanie, Baez, Stephanie, Fleming, Steve, Murphy, Steven, Alpert, Tara, Mandese, Zoe M., Adams, Mark D., Park, Daniel J., Lemieux, Jacob E., Grubaugh, Nathan D.

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Multimodal surveillance of SARS-CoV-2 at a university enables development of a robust outbreak response framework von Petros, Brittany A., Paull, Jillian S., Tomkins-Tinch, Christopher H., Loftness, Bryn C., DeRuff, Katherine C., Nair, Parvathy, Gionet, Gabrielle L., Benz, Aaron, Brock-Fisher, Taylor, Hughes, Michael, Yurkovetskiy, Leonid, Mulaudzi, Shandukani, Leenerman, Emma, Nyalile, Thomas, Moreno, Gage K., Specht, Ivan, Sani, Kian, Adams, Gordon, Babet, Simone V., Baron, Emily, Blank, Jesse T., Boehm, Chloe, Botti-Lodovico, Yolanda, Brown, Jeremy, Buisker, Adam R., Burcham, Timothy, Chylek, Lily, Cronan, Paul, Dauphin, Ann, Desreumaux, Valentine, Doss, Megan, Flynn, Belinda, Gladden-Young, Adrianne, Glennon, Olivia, Harmon, Hunter D., Hook, Thomas V., Kary, Anton, King, Clay, Loreth, Christine, Marrs, Libby, McQuade, Kyle J., Milton, Thorsen T., Mulford, Jada M., Oba, Kyle, Pearlman, Leah, Schifferli, Mark, Schmidt, Madelyn J., Tandus, Grace M., Tyler, Andy, Vodzak, Megan E., Krohn Bevill, Kelly, Colubri, Andres, MacInnis, Bronwyn L., Ozsoy, A. Zeynep, Parrie, Eric, Sholtes, Kari, Siddle, Katherine J., Fry, Ben, Luban, Jeremy, Park, Daniel J., Marshall, John, Bronson, Amy, Schaffner, Stephen F., Sabeti, Pardis C.

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Accelerating bioinformatics implementation in public health von Libuit, Kevin G, Doughty, Emma L, Otieno, James R, Ambrosio, Frank, Kapsak, Curtis J, Smith, Emily A, Wright, Sage M, Scribner, Michelle R, Petit Iii, Robert A, Mendes, Catarina Inês, Huergo, Marcela, Legacki, Gregory, Loreth, Christine, Park, Daniel J, Sevinsky, Joel R

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Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate®) in the management of perioperative haemostasis in von Willebrand disease patients un... von Windyga, J, von Depka-Prondzinski, M

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Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency von IVASKEVICIUS, V., BISWAS, A., LORETH, R., SCHROEDER, V., OHLENFORST, S., ROTT, H., KRAUSE, M., KOHLER, H.-P., SCHARRER, I., OLDENBURG, J.

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