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Page 1
Factor XII: form determines function.
de Maat S, Maas C. de Maat S, et al. Among authors: maas c. J Thromb Haemost. 2016 Aug;14(8):1498-506. doi: 10.1111/jth.13383. Epub 2016 Aug 2. J Thromb Haemost. 2016. PMID: 27282310 Free article. Review.
Contact system activation on endothelial cells.
de Maat S, de Groot PG, Maas C. de Maat S, et al. Among authors: maas c. Semin Thromb Hemost. 2014 Nov;40(8):887-94. doi: 10.1055/s-0034-1395159. Epub 2014 Nov 11. Semin Thromb Hemost. 2014. PMID: 25389102 Review.
Response to letter regarding article, "plasmin cleavage of von willebrand factor as an emergency bypass for ADAMTS13 deficiency in thrombotic microangiopathy".
Tersteeg C, de Maat S, De Meyer SF, Smeets MW, Barendrecht AD, Roest M, Pasterkamp G, Fijnheer R, Vanhoorelbeke K, de Groot PG, Maas C. Tersteeg C, et al. Among authors: maas c. Circulation. 2015 Jan 13;131(2):e19-20. doi: 10.1161/CIRCULATIONAHA.114.012802. Circulation. 2015. PMID: 25583061 No abstract available.
Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III.
Björkqvist J, de Maat S, Lewandrowski U, Di Gennaro A, Oschatz C, Schönig K, Nöthen MM, Drouet C, Braley H, Nolte MW, Sickmann A, Panousis C, Maas C, Renné T. Björkqvist J, et al. Among authors: maas c. J Clin Invest. 2015 Aug 3;125(8):3132-46. doi: 10.1172/JCI77139. Epub 2015 Jul 20. J Clin Invest. 2015. PMID: 26193639 Free PMC article.
379 results