American Journal of Hematology, 0361-8609

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  1. Bleeding phenotype and diagnostic characterization of patients with congenital platelet defects

    Blaauwgeers, M. W., Kruip, M. J. H. A., Beckers, E. A. M., Coppens, M., Eikenboom, J., van Galen, K. P. M., Tamminga, R. Y. J., Urbanus, R. T. & Schutgens, R. E. G., 14-Jul-2020, In : American Journal of Hematology. 6 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects

    Blaauwgeers, M. W., van Asten, I., Kruip, M. J. H. A., Beckers, E. A. M., Coppens, M., Eikenboom, J., van Galen, K. P. M., Huisman, A., Korporaal, S. J. A., Ploos van Amstel, H. K., Tamminga, R. Y. J., Urbanus, R. T. & Schutgens, R. E. G., 13-Nov-2019, In : American Journal of Hematology. 3 p.

    Research output: Contribution to journalLetterAcademicpeer-review

  3. BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand disease

    WiN Study Grp, Atiq, F., Fijnvandraat, K., van Galen, K. P. M., Laros-Van Gorkom, B. A. P., Meijer, K., de Meris, J., Coppens, M., Mauser-Bunschoten, E. P., Cnossen, M. H., van der Bom, J. G., Eikenboom, J. & Leebeek, F. W. G., Aug-2019, In : American Journal of Hematology. 94, 8, p. E201-E205 5 p.

    Research output: Contribution to journalLetterAcademicpeer-review

  4. X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations

    Campagna, D. R., de Bie, C. I., Schmitz-Abe, K., Sweeney, M., Sendamarai, A. K., Schmidt, P. J., Heeney, M. M., Yntema, H. G., Kannengiesser, C., Grandchamp, B., Niemeyer, C. M., Knoers, N. V. A. M., Swart, S., Marron, G., van Wijk, R., Raymakers, R. A., May, A., Markianos, K., Bottomley, S. S., Swinkels, D. W. & Fleming, M. D., 2014, In : American Journal of Hematology. 89, 3, p. 315-319 5 p.

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