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Pasquier, E; De Saint Martin, L; Kohler, H P; Schroeder, V (2012). Factor XIII plasma levels in women with unexplained recurrent pregnancy loss. Journal of thrombosis and haemostasis, 10(4), pp. 723-725. Oxford: Wiley-Blackwell 10.1111/j.1538-7836.2012.04657.x
Hess, K; Alzahrani, S H; Mathai, M; Schroeder, V; Carter, A M; Howell, G; Koko, T; Strachan, M W J; Price, J F; Smith, K A; Grant, P J; Ajjan, R A (2012). A novel mechanism for hypofibrinolysis in diabetes: the role of complement C3. Diabetologia, 55(4), pp. 1103-1113. Heidelberg: Springer 10.1007/s00125-011-2301-7
Castaman, G; Giacomelli, S H; Schroeder, V; Sanna, S; Valdrè, L; Morfini, M; Banov, L; Kohler, H P; Rodeghiero, F (2012). Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiency. Haemophilia, 18(1), e6-e8. Oxford: Blackwell Science 10.1111/j.1365-2516.2011.02622.x
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
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
