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Li, Bojun; Billur, Ramya; Maurer, Muriel C; Kohler, Hans-Peter; Raddatz Müller, Pascale; Alberio, Lorenzo; Schroeder, Verena (2018). Proline 36 of the Factor XIII Activation Peptide Plays a Crucial Role in Substrate Recognition and Zymogen Activation. Thrombosis and haemostasis, 118(12), pp. 2037-2045. Thieme 10.1055/s-0038-1675600
Li, Bojun; Borhany, Munira; Abid, Madiha; Kohler, Hans-Peter; Schroeder, Verena (2018). Identification of a novel nonsense mutation leading to congenital factor XIII deficiency. Thrombosis research, 165, pp. 83-85. Elsevier 10.1016/j.thromres.2018.03.019
Schroeder, Verena; Handrková, Helena; Dodt, Johannes; Kohler, Hans-Peter (2015). Free factor XIII activation peptide affects factor XIII function. British journal of haematology, 168(5), pp. 757-759. Wiley-Blackwell 10.1111/bjh.13144
Borhany, M.; Handrkova, Helena; Cairo, A.; Schroeder, Verena; Fatima, N.; Naz, A.; Amanat, S.; Shamsi, T.; Peyvandi, F.; Kohler, Hans-Peter (2014). Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations. Haemophilia, 20(4), pp. 568-574. Blackwell Science 10.1111/hae.12340
Isenegger, Jörg; Meier, Niklaus; Lämmle, Bernhard; Alberio, Lorenzo; Fischer, Urs; Nedeltchev, Krassen; Gralla, Jan; Kohler, Hans-Peter; Mattle, Heinrich; Arnold, Marcel (2010). D-Dimers Predict Stroke Subtype when Assessed Early. Cerebrovascular diseases, 29(1), pp. 82-86. Basel: Karger 10.1159/000256652
Castaman, G; Giacomelli, S H; Ivaskevicius, V; Schroeder, Verena; Kohler, Hans-Peter; Dragani, A; Biasioli, C; Oldenburg, J; Madeo, D; Rodeghiero, F (2008). Molecular characterization of five Italian families with inherited severe factor XIII deficiency. Haemophilia, 14(1), pp. 96-102. Wiley 10.1111/j.1365-2516.2007.01603.x
