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Journal of Thrombosis and Haemostasis : JTH|January 3, 2013
New developments in the area of factor XIIIV Schroeder, H P KohlerJournal of Thrombosis and Haemostasis : JTH|June 18, 2015
The activation peptide of coagulation factor XIII is vital for its expression and stabilityH Handrkova, V Schroeder, H P KohlerThrombosis Research|January 5, 2002
Influence of blood coagulation factor XIII and FXIII Val34Leu on plasma clot formation measured by thrombelastographyV Schroeder, T Chatterjee, H P KohlerSwiss Medical Weekly|June 28, 2007
Congenital factor XIII deficiency in Switzerland: from the worldwide first case in 1960 to its molecular characterisation in 2005V Schroeder, D Durrer, E Meili, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutationsV Ivaskevicius, J Windyga, B Baran, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 17, 2013
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutationsM Borhany, H Handrkova, A Cairo, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 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 deficiencyV Ivaskevicius, A Biswas, R Loreth, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.Hamostaseologie|August 24, 2002
[Role of coagulation factor XIII in cardio- and cerebrovascular diseases]H P Kohler, V SchröderPageof 25