Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients by Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén

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Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients by Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén

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Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. by Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén

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PB2064: THE COMPLETE STUDY: A SINGLE ARM, MULTICENTER OBSERVATIONAL STUDY TO EVALUATE EFFECTIVENESS OF PEGCETACOPLAN UNDER REAL WORLD CONDITIONS IN PATIENTS WITH PAROXYSMAL NOCTURN... by Régis Peffault de Latour, Jeff Szer, Austin Kulasekararaj, Anna Gaya, Simona Sica, Matthias Nölte, Regina Horneff, Lethagen Stefan

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Efficacy of rFVIIIFc versus Emicizumab for the Treatment of Patients with Hemophilia A without Inhibitors: Matching-Adjusted Indirect Comparison of A-LONG and HAVEN Trials by Klamroth R, Wojciechowski P, Aballéa S, Diamand F, Hakimi Z, Nazir J, Abad-Franch L, Lethagen S, Santagostino E, Tarantino MD

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Managing surgery in hemophilia with recombinant factor VIII Fc and factor IX Fc: Data on safety and effectiveness from phase 3 pivotal studies by Pratima Chowdary, Margareta Holmström, Johnny N. Mahlangu, Margaret C. Ozelo, Ingrid Pabinger, K. John Pasi, Margaret V. Ragni, Amy Shapiro, Chris Barnowski, Stefan Lethagen

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