American Journal of Hematology, 0361-8609

Journal

  1. 2020
  2. 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. (2020). Bleeding phenotype and diagnostic characterization of patients with congenital platelet defects. American Journal of Hematology, 95(10), 1142-1147. https://doi.org/10.1002/ajh.25910
  3. 2019
  4. 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. (2019). The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects. American Journal of Hematology. https://doi.org/10.1002/ajh.25667
  5. 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. (2019). BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand disease. American Journal of Hematology, 94(8), E201-E205. https://doi.org/10.1002/ajh.25499
  6. 2017
  7. Pasricha, S-R., Lim, P. J., Duarte, T., Casu, C., Mleczko-Sanecka, K., Suciu, M., Areas, J., Da Silva, A. R., Frost, J., McHugh, K., Porto, G., Draper, S., Gooding, S., Olinga, P., Muckenthaler, M., Rivella, S., Hughes, J., Milne, T., Armitage, A., & Drakesmith, H. (2017). Hepcidin is an HDAC3 regulated gene and its expression is determined by promoter-associated histone acetylation. American Journal of Hematology, 92(8), E351-E351.
  8. 2016
  9. 2015
  10. Sanders, Y. V., Fijnvandraat, K., Boender, J., Mauser-Bunschoten, E. P., van der Bom, J. G., de Meris, J., Smiers, F. J., Granzen, B., Brons, P., Tamminga, R. Y. J., Cnossen, M. H., Leebeek, F. W. G., & WiN Study Grp (2015). Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleeding. American Journal of Hematology, 90(12), 1142-1148. https://doi.org/10.1002/ajh.24195
  11. Poire, X., Labopin, M., Cornelissen, J. J., Volin, L., Richard Espiga, C., Veelken, J. H., Milpied, N., Cahn, J-Y., Yacoub-Agha, I., van Imhoff, G. W., Michallet, M., Michaux, L., Nagler, A., & Mohty, M. (2015). Outcome of conditioning intensity in acute myeloid leukemia with monosomal karyotype in patients over 45 year-old: A study from the acute leukemia working party (ALWP) of the European group of blood and marrow transplantation (EBMT). American Journal of Hematology, 90(8), 719-724. https://doi.org/10.1002/ajh.24069
  12. 2014
  13. Gambacorti-Passerini, C., BrĂ¼mmendorf, T. H., Kim, D-W., Turkina, A. G., Masszi, T., Assouline, S., Durrant, S., Kantarjian, H. M., Khoury, H. J., Zaritskey, A., Shen, Z-X., Jin, J., Vellenga, E., Pasquini, R., Mathews, V., Cervantes, F., Besson, N., Turnbull, K., Leip, E., ... Cortes, J. E. (2014). Bosutinib efficacy and safety in chronic phase chronic myeloid leukemia after imatinib resistance or intolerance: Minimum 24-month follow-up. American Journal of Hematology, 89(7), 732-742. https://doi.org/10.1002/ajh.23728
  14. Spronk, H. M. H., de Jong, A-M., de Boer, H., Maass, A., Verheule, S., Lau, D., Rienstra, M., Kamphuisen, P. W., ten Cate, H., Crijns, H., van Gelder, I., van Zonneveld, A. J., & Schotten, U. (2014). HYPERCOAGULABILITY PROMOTES ATRIAL FIBROSIS AND FIBRILLATION. American Journal of Hematology, 89(6), E58-E58.
  15. 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., ... Fleming, M. D. (2014). X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations. American Journal of Hematology, 89(3), 315-319. https://doi.org/10.1002/ajh.23616
  16. 2011
  17. 2010
  18. Nur, E., Mairuhu, W., Biemond, B. J., van Zanten, A. P., Schnog, J-J. B., Brandjes, D. P., Otten, H-M., & CURAMA study grp (2010). Urinary markers of bone resorption, pyridinoline and deoxypyridinoline, are increased in sickle cell patients with further increments during painful crisis. American Journal of Hematology, 85(11), 902-904. https://doi.org/10.1002/ajh.21856
  19. 2009
  20. Nichols, W. L., Rick, M. E., Ortel, T. L., Montgomery, R. R., Sadler, J. E., Yawn, B. P., James, A. H., Hultin, M. B., Manco-Johnson, M. J., & Weinstein, M. (2009). Clinical and laboratory diagnosis of von Willebrand disease: A synopsis of the 2008 NHLBI/NIH guidelines. American Journal of Hematology, 84(6), 366-370. https://doi.org/10.1002/ajh.21405
  21. 2008
  22. van Beers, E. J., Nur, E., Schaefer-Prokop, C. M., Mac Gillavry, M. R., van Esser, J. W. J., Brandjes, D. P. M., Kappers-Klunne, M. C., Duits, A. J., Muskiet, F. A. J., Schnog, J-J. B., Biemond, B. J., & CURAMA study grp (2008). Cardiopulmonary imaging, functional and laboratory studies in sickle cell disease associated pulmonary hypertension. American Journal of Hematology, 83(11), 850-854. https://doi.org/10.1002/ajh.21272
  23. 2005
  24. Gertz, MA., Comenzo, R., Falk, RH., Fermand, JP., Hazenberg, BP., Hawkins, PN., Merlini, G., Moreau, P., Ronco, P., Sanchorawala, N. V., Sezer, O., Solomon, A., & Grateau, G. (2005). Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis. American Journal of Hematology, 79(4), 319-328. https://doi.org/10.1002/ajh.20381
  25. 2002
  26. van der Dijs, F. P. L., Fokkema, M. R., Dijck-Brouwer, D. A. J., Niessink, B., van der Wal, T. I. C., Schnog, J-J. B., Duits, A. J., Muskiet, F. D., & Muskiet, F. A. J. (2002). Optimization of folic acid, vitamin B-12, and vitamin B-6 supplements in pediatric patients with sickle cell disease. American Journal of Hematology, 69(4), 239-246. https://doi.org/10.1002/ajh.10083
  27. 1998
  28. van der Dijs, FPL., Schnog, JJB., Brouwer, DAJ., Velvis, HJR., van den Berg, GA., Bakker, AJ., Duits, AJ., & Muskiet, FD. (1998). Elevated homocysteine levels indicate suboptimal folate status in pediatric sickle cell patients. American Journal of Hematology, 59(3), 192-198.
  29. Schnog, JJB., Lard, LR., Rojer, RA., Van der Dijs, FPL., Muskiet, FAJ., & Duits, AJ. (1998). New concepts in assessing sickle cell disease severity. American Journal of Hematology, 58(1), 61-66.

ID: 2185555