ECMO produces very rapid changes in primary hemostasis detected by PFA-200 during lung transplantation: An observational study von Garaj, Michal, Francesconi, Alessandro, Durila, Miroslav, Vajter, Jaromir, Holubová, Gabriela, Hrachovinová, Ingrid

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Extracorporeal membrane oxygenation seems to induce impairment of primary hemostasis pathology as measured by a Multiplate analyzer: An observational retrospective study von Garaj, Michal, Durila, Miroslav, Vajter, Jaromir, Solcova, Michaela, Marecek, Frantisek, Hrachovinová, Ingrid

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Evaluation of von willebrand factor with a fully magnetically levitated centrifugal continuous flow left ventricular assist device in advanced heart failure von Netuka, Ivan, Kvasnička, Tomáš, Kvasnička, Jan, Hrachovinová, Ingrid, Ivák, Peter, Mareček, František, Bílková, Jana, Malíková, Ivana, Jančová, Michaela, Malý, Jiří, Sood, Poornima, Sundareswaran, Kartik S, Connors, Jean M, Mehra, Mandeep R

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Molecular basis and outcomes of atypical haemolytic uraemic syndrome in Czech children von Štolbová, Šárka, Bezdíčka, Martin, Seeman, Tomas, Prohászka, Zoltán, Csuka, Dorottya, Hrachovinová, Ingrid, Burkert, Jan, Šimánková, Naděžda, Průhová, Štěpánka, Zieg, Jakub

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A novel Kunitz protein with proposed dual function from Eudiplozoon nipponicum (Monogenea) impairs haemostasis and action of complement in vitro von Jedličková, Lucie, Dvořák, Jan, Hrachovinová, Ingrid, Ulrychová, Lenka, Kašný, Martin, Mikeš, Libor

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Correction to: Molecular basis and outcomes of a typical haemolytic uraemic syndrome in Czech children von Štolbová, Šárka, Bezdíčka, Martin, Seeman, Tomas, Prohászka, Zoltán, Csuka, Dorottya, Hrachovinová, Ingrid, Burkert, Jan, Šimánková, Naděžda, Průhová, Štěpánka, Zieg, Jakub

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Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population von Provaznikova, Dana, Matyskova, Miloslava, Capova, Irena, Grancarova, Dagmar, Drbohlavova, Eva, Slechtova, Marie, Hrachovinova, Ingrid

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Pro-Coagulant State Resulting from High Levels of Soluble P-Selectin in Blood von Andre, Patrick, Hartwell, Daqing, Hrachovinova, Ingrid, Safaripour, Simin, Wagner, Denisa D

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Identifying risk factors and optimizing standard of care for patients with acquired haemophilia A: Results from a Czech patient cohort von Salaj, Peter, Geierová, Vera, Ivanová, Eva, Loužil, Jan, Pohlreichová, Viera, Hrachovinová, Ingrid, Dulíček, Petr

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Interaction of P-selectin and PSGL-1 generates microparticles that correct hemostasis in a mouse model of hemophilia A von Wagner, Denisa D, Hrachovinová, Ingrid, Cambien, Beatrice, Hafezi-Moghadam, Ali, Kappelmayer, János, Camphausen, Raymond T, Widom, Angela, Xia, Lijun, Kazazian, Haig H, Schaub, Robert G, McEver, Rodger P

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Diagnostic strategies in disorders of hemostasis von Hrachovinová, Ingrid

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A common origin of the 4143insA ADAMTS13 mutation von Schneppenheim, Reinhard, Hovinga, Johanna A. Kremer, Becker, Tim, Budde, Ulrich, Karpman, Diana, Brockhaus, Wolfgang, Hrachovinová, Ingrid, Korczowski, Bartosz, Oyen, Florian, Rittich, Šimon, von Rosen, Johannes, Tjønnfjord, Geir E., Pimanda, John E., Wienker, Thomas F., Lämmle, Bernhard

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Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura von Tarasco, Erika, Bütikofer, Lukas, Friedman, Kenneth D., George, James N., Hrachovinova, Ingrid, Knöbl, Paul N., Matsumoto, Masanori, von Krogh, Anne Sophie, Aebi-Huber, Isabella, Cermakova, Zuzana, Górska-Kosicka, Magdalena, Jalowiec, Katarzyna A., Largiadèr, Carlo R., Prohászka, Zoltán, Sinkovits, György, Windyga, Jerzy, Lämmle, Bernhard, Kremer Hovinga, Johanna A.

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Fibrinogen Šumperk II: Dysfibrinogenemia in an individual with two coding mutations von Kotlín, Roman, Suttnar, Jiří, Čápová, Irena, Hrachovinová, Ingrid, Urbánková, Marie, Dyr, Jan Evangelista

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First Experiences with the Measurement of Thrombin Generation (TGA) on the Ceveron® Alpha in the Routine Lab von Wagner, Lieselotte, Luddington, Roger, Wiens, Lilli, Grigorov, Alexandre, Hrachovinová, Ingrid, Binder, Bernd

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Novel homozygous fibrinogen Aα chain truncation causes severe afibrinogenemia with life threatening complications in a two-year-old boy von Štikarová, Jana, Blatný, Jan, Kotlín, Roman, Suttnar, Jiří, Zapletal, Ondřej, Pimková, Kristýna, Májek, Pavel, Hrachovinová, Ingrid, Dyr, Jan E

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Congenital dysfibrinogenemia Aα Gly13Glu associated with bleeding during pregnancy von Kotlín, Roman, Zichová, Kateřina, Suttnar, Jiří, Reicheltová, Zuzana, Salaj, Peter, Hrachovinová, Ingrid, Dyr, Jan E

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The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: key findings at enrollment until 2017 von van Dorland, Hendrika A, Taleghani, Magnus Mansouri, Sakai, Kazuya, Friedman, Kenneth D, George, James N, Hrachovinova, Ingrid, Knöbl, Paul N, von Krogh, Anne Sophie, Schneppenheim, Reinhard, Aebi-Huber, Isabella, Bütikofer, Lukas, Largiadèr, Carlo R, Cermakova, Zuzana, Kokame, Koichi, Miyata, Toshiyuki, Yagi, Hideo, Terrell, Deirdra R, Vesely, Sara K, Matsumoto, Masanori, Lämmle, Bernhard, Fujimura, Yoshihiro, Kremer Hovinga, Johanna A

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Two novel fibrinogen variants in the C-terminus of the Bβ-chain: fibrinogen Rokycany and fibrinogen Znojmo von Kotlín, Roman, Reicheltová, Zuzana, Suttnar, Jiří, Salaj, Peter, Hrachovinová, Ingrid, Riedel, Tomáš, Malý, Martin, Oravec, Milan, Kvasnička, Jan, Dyr, Jan Evangelista

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Diagnosing Czech Patients with Inherited Platelet Disorders von Louzil, Jan, Stikarova, Jana, Provaznikova, Dana, Hrachovinova, Ingrid, Fenclova, Tereza, Musil, Jan, Radek, Martin, Kaufmanova, Jirina, Geierova, Vera, Ceznerova, Eliska, Salaj, Peter, Kotlin, Roman

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