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Ivaskevicius, V; Biswas, A; Loreth, R; Schroeder, V; Ohlenforst, S; Rott, H; Krause, M; Kohler, H-P; Scharrer, I; Oldenburg, J (2010). 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. Haemophilia, 16(4), pp. 675-682. Oxford: Blackwell Science 10.1111/j.1365-2516.2010.02207.x
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
Ivaskevicius, V; Windyga, J; Baran, B; Schroeder, V; Junen, J; Bykowska, K; Seifried, E; Kohler, H P; Oldenburg, J (2007). Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations. Haemophilia, 13(5), pp. 649-657. Oxford: Blackwell Science 10.1111/j.1365-2516.2007.01517.x
Ivaskevicius, V; Seitz, R; Kohler, HP; Schroeder, V; Muszbek, L; Ariens, RA; Seifried, E; Oldenburg, J; Study, Group (2007). International registry on factor XIII deficiency: a basis formed mostly on European data. Thrombosis and haemostasis, 97(6), pp. 914-921. Stuttgart: Schattauer 10.1160/TH07-01-0034
