Karin Fijnvandraat

Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A

Eckhardt, C. L., van Velzen, A. S., Peters, M., Astermark, J., Brons, P. P., Castaman, G., Cnossen, M. H., Dors, N., Escuriola-Ettingshausen, C., Hamulyak, K., Hart, D. P., Hay, C. R. M., Haya, S., van Heerde, W. L., Hermans, C., Holmström, M., Jimenez-Yuste, V., Keenan, R. D., Klamroth, R., Laros-van Gorkom, B. A. P., & 25 othersLeebeek, F. W. G., Liesner, R., Mäkipernaa, A., Male, C., Mauser-Bunschoten, E., Mazzucconi, M. G., McRae, S., Meijer, K., Mitchell, M., Morfini, M., Nijziel, M., Oldenburg, J., Peerlinck, K., Petrini, P., Platokouki, H., Reitter-Pfoertner, S. E., Santagostino, E., Schinco, P., Smiers, F. J., Siegmund, B., Tagliaferri, A., Yee, T. T., Kamphuisen, P. W., van der Bom, J. G. & Fijnvandraat, K., 2013, In: Blood. 122, 11, p. 1954-1962

Research output: Contribution to journal › Article › Academic › peer-review

Molecular and clinical predictors of inhibitor risk and its prevention and treatment in mild hemophilia A

Castaman, G. & Fijnvandraat, K., 2014, In: Blood. 124, 15, p. 2333-2336

Research output: Contribution to journal › Article › Academic › peer-review

Diagnosis and management of haemophilia

Fijnvandraat, K., Cnossen, M. H., Leebeek, F. W. G. & Peters, M., 2012, In: BMJ (Clinical research ed.). 344, p. e2707

Research output: Contribution to journal › Review article › Academic › peer-review

Long-term follow-up of children with sickle cell disease diagnosed by newborn screening in the Netherlands: Overview of morbidity and mortality

Vuong, C., Eckhardt, C. L., Heijboer, H., Suijker, M. H., de Ligt, L. A., Voigt, A. L. A., Leeflang, M. M. G., Bartels, M., Brons, P., Hooimeijer, L., Rettenbacher, E., Smiers, F. J., Stein-Wit, M. A., van der Veer, A., Verbaan, A., Cnossen, M. H. & Fijnvandraat, K., Aug 2024, In: American journal of hematology. 99, 8, p. 1606-1609 4 p.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

Efanesoctocog Alfa Prophylaxis for Children with Severe Hemophilia A

Malec, L., Peyvandi, F., Chan, A. K. C., Königs, C., Zulfikar, B., Yuan, H., Simpson, M., Román, M. T. Á., Carcao, M., Staber, J. M., Dunn, A. L., Chou, S-C., d’Oiron, R., Albisetti, M., Demissie, M., Santagostino, E., Yarramaneni, A., Wong, N., Abad-Franch, L., Gunawardena, S., & 1 othersXTEND-Kids Trial Group, 18 Jul 2024, In: New England journal of medicine. 391, 3, p. 235-246 12 p.

Research output: Contribution to journal › Article › Academic › peer-review

Transcriptional and functional profiling identifies inflammation and endothelial-to-mesenchymal transition as potential drivers for phenotypic heterogeneity within a cohort of endothelial colony forming cells

Laan, S. N. J., de Boer, S., Dirven, R. J. & SYMPHONY consortium, Jul 2024, In: Journal of thrombosis and haemostasis. 22, 7, p. 2027-2038 12 p.

Research output: Contribution to journal › Article › Academic › peer-review