Research

  1. 2003
  2. 2002
  3. Bodmer, D., Janssen, N. V., Jonkers, Y., van den Berg, E., Dijkhuizen, T., Debiec-Rychter, M., Schoenmakers, E., & van Kessel, AG. (2002). Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13 similar to q22 breakpoints. Cancer Genetics and Cytogenetics, 136(2), 95-100. [PII S0165-4608(02)00517-4].
  4. Fisher, C., van den Berg , E., & Molenaar, W. (2002). Adult fibrosarcoma. In CDM. Fletcher, KK. Unni, & F. Mertens (Eds.), World Health Organization Classification of Tumours : Pathology and Genetics of Tumours of Soft Tissue and Bone (pp. 100-101). IARC Press.
  5. Folpe, A., van den Berg, E., & Molenaar, W. (2002). Low grade fibromyxoid sarcoma. In World Health Organization Classification of Tumours : Pathology and Genetics of Tumours of Soft Tissue and Bone (pp. 104-105). IARC Press.
  6. Molenaar, W., & van den Berg, E. (2002). Myxofibrosarcoma. In CDM. Fletcher, KK. Unni, & F. Mertens (Eds.), World Health Organization Classification of Tumours : Pathology and Genetics of Tumours of Soft Tissue and Bone (pp. 102-103). IARC Press.
  7. Fletcher, CDM., van den Berg, E., & Molenaar, W. (2002). Pleomorphic malignant fibrous histiocytoma/undifferentiated high grade sarcoma. In CDM. Fletcher, KK. Unni, & F. Mertens (Eds.), World Health Organization Classification of Tumours (pp. 120-122). IARC Press.
  8. Meis-Kindblom, JM., van den Berg, E., & Molenaar, W. (2002). Sclerosong epithelioid fibrosarcoma. In CDM. Fletcher, KK. Unni, & F. Mertens (Eds.), World Health Organization Clssification of Tumours: Pathology and Genetics of Tumours of Soft Tissue and Bone. (pp. 106-107). IARC Press.
  9. 2001
  10. Slater, RM., Drunen, EV., Kroes, WG., Weghuis, DO., van den Berg, E., Smit, EM., van der Does-van den Berg, A., van Wering, E., Hahlen, K., Carroll, AJ., Raimondi, SC., & Beverloo, HB. (2001). t(7;12)(q36;p13) and t(7;12)(q32;p13) - translocations involving ETV6 in children 18 months of age or younger with myeloid disorders. Leukemia, 15(6), 915-920.
  11. 2000
  12. Janssen, JJWM., van der Holt, B., Schuurhuis, GJ., Vellenga, E., Verhoef, GEG., Ossenkoppele, GJ., van den Berg, E., Hagemeijer, A., Slater, R., Nieuwint, AWM., & Cornelissen, JJ. (2000). Mobilisation of haemopoietic progenitors in CML: a second course of intensive chemotherapy does not improve Ph-negativity in stem cell harvests. Bone marrow transplantation, 25(11), 1147-1155.
  13. Simons, A., Schepens, M., Jeuken, J., Sprenger, S., van de Zande, G., Bjerkehagen, B., Forus, A., Weibolt, V., Molenaar, I., van den Berg-de Ruiter, E., Myklebost, O., Bridge, J., Geurts van Kessel, A., & Suijkerbuijk, R. (2000). Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma. Cancer Genetics and Cytogenetics, 118(2), 89-98.
  14. 1999
  15. Kamps, WA., Bokkerink, JPM., Hahlen, K., Hermans, J., Riehm, H., Gadner, H., Schrappe, M., Slater, R., van den Berg-de Ruiter, E., Smets, LA., de Vaan, GAM., Weening, RS., van Weerden, JF., van Wering, ER., & van der Does-van den Berg, A. (1999). Intensive treatment of children with acute lymphoblastic leukemia according to ALL-BFM-86 without cranial radiotherapy: Results of Dutch Childhood Leukemia Study Group protocol ALL-7 (1988-1991). Blood, 94(4), 1226-1236.
  16. 1998
  17. Bodmer, D., Eleveld, MJ., Ligtenberg, MJL., Weterman, MAJ., Janssen, BAP., Smeets, DFCM., de Wit, PEJ., van den Berg, A., van den Berg, E., Koolen, MI., & van Kessel, AG. (1998). An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation. American Journal of Human Genetics, 62(6), 1475-1483.
  18. Speleman, F., van den Berg, E., Dhooge, C., Oosterhuis, W., Redeker, B., De Potter, CR., Tamminga, RYJ., Van Roy, N., & Mannens, M. (1998). Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma. GENES CHROMOSOMES & CANCER, 21(3), 265-269.
  19. 1996
  20. Mastik, M. F., Plaat, B. E. C., Molenaar, W. M., Hoekstra, H. J., de Graaf, S. S. N., & van den Berg, E. (1996). t(11;22)(q24;q12) in an extrarenal malignant rhabdoid tumor. Cancer Genetics and Cytogenetics, 91, 164.
  21. 1995
  22. Dijkhuizen, T., Van den Berg, E., Wilbrink, M., Weterman, M., Geurts van Kessel, A., Störkel, S., Folkers, R. P., Braam, A., & De Jong, B. (1995). Distinct Xp11.2 breakpoints in two renal cell carcinomas exhibiting X;autosome translocations. GENES CHROMOSOMES & CANCER, 14(1), 43-50. https://doi.org/10.1002/gcc.2870140108
  23. Echten, J. V., van den Berg-de Ruiter, E., Baarlen, J. V., Noort, G. V., Vermey, A., Dam, A., & Molenaar, W. M. (1995). An important role for chromosome 17, band q25, in the histogenesis of alveolar soft part sarcoma. Cancer Genetics and Cytogenetics, 82(1), 57-61.
  24. 1994
  25. van den Berg, E., Molenaar, W. M., Echten, J. V., Dam, A., Mensink, H. J., & Jong, B. D. (1994). Cytogenetic analysis of a leiomyosarcoma of the kidney. Cancer Genetics and Cytogenetics, 72(2), 126-129. https://doi.org/10.1016/0165-4608(94)90127-9
  26. Weghuis, D. O., Stoepker, M. E., Leeuw, B. D., van den Berg, E., Suijkerbuijk, R. F., Molenaar, W. M., Jong, B. D., & Kessel, A. G. V. (1994). A synovial sarcoma with a complex t(X;18;5;4) and a break in the ornithine aminotransferase (OAT)L1 cluster on Xp11.2. GENES CHROMOSOMES & CANCER, 9, 288-291.
  27. Leeuw, B. D., Suijkerbuijk, R. F., Weghuis, D. O., Meloni, A. M., Stenman, G., Kindblom, L. G., Balemans, M., van den Berg, E., Molenaar, W. M., & Sandberg, A. A. (1994). Distinct Xp11.2 breakpoint regions in synovial sarcoma revealed by metaphase and interphase FISH: relationship to histologic subtypes. Cancer Genetics and Cytogenetics, 73(2), 89-94.
  28. 1993
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