1. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations. (1st October 2013) Authors: Katona, É.; Muszbek, L.; Devreese, K.; Kovács, K. B.; Bereczky, Z.; Jonkers, M.; Shemirani, A. H.; Mondelaers, V.; Ermens, A. A. M. Journal: Haemophilia Issue: Volume 20:Number 1(2014:Jan.) Page Start: 114 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia. Issue 4 (17th March 2017) Authors: Casini, A.; Vilar, R.; Beauverd, Y.; Aslan, D.; Devreese, K.; Mondelaers, V.; Alberio, L.; Gubert, C.; de Moerloose, P.; Neerman‐Arbez, M. Journal: Haemophilia Issue: Volume 23:Issue 4(2017) Page Start: 583 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗