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Efficacy and safety of simultaneous immunomagnetic CD34+ cell selection and breast cancer cell purging in peripheral blood progenitor cell samples used for hematopoietic rescue after high-dose therapy.
Mohr M, Hilgenfeld E, Fietz T, Hoppe B, Koenigsmann M, Hoffmann M, Knauf WU, Cassens U, Sibrowski W, Kienast J, Thiel E, Berdel WE. Mohr M, et al. Among authors: hilgenfeld e. Clin Cancer Res. 1999 May;5(5):1035-40. Clin Cancer Res. 1999. PMID: 10353736 Clinical Trial.
Is there a place for 2-CDA in the treatment of B-CLL?
Mitterbauer M, Hilgenfeld E, Wilfing A, Jäger U, Knauf WU. Mitterbauer M, et al. Among authors: hilgenfeld e. Leukemia. 1997 Apr;11 Suppl 2:S35-7. Leukemia. 1997. PMID: 9178836 Review.
Multicolor karyotyping in acute myeloid leukemia.
Tchinda J, Volpert S, McNeil N, Neumann T, Kennerknecht I, Ried T, Büchner T, Serve H, Berdel WE, Horst J, Hilgenfeld E. Tchinda J, et al. Among authors: hilgenfeld e. Leuk Lymphoma. 2003 Nov;44(11):1843-53. doi: 10.1080/10428190310001603605. Leuk Lymphoma. 2003. PMID: 14738135 Review.
Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
Hilgenfeld E, Padilla-Nash H, McNeil N, Knutsen T, Montagna C, Tchinda J, Horst J, Ludwig WD, Serve H, Büchner T, Berdel WE, Schröck E, Ried T. Hilgenfeld E, et al. Br J Haematol. 2001 May;113(2):305-17. doi: 10.1046/j.1365-2141.2001.02723.x. Br J Haematol. 2001. PMID: 11380393 Free article.
Analysis of B-cell neoplasias by spectral karyotyping (SKY).
Hilgenfeld E, Padilla-Nash H, Schröck E, Ried T. Hilgenfeld E, et al. Curr Top Microbiol Immunol. 1999;246:169-74. doi: 10.1007/978-3-642-60162-0_21. Curr Top Microbiol Immunol. 1999. PMID: 10396053 Review.
Spectral karyotyping in cancer cytogenetics.
Hilgenfeld E, Montagna C, Padilla-Nash H, Stapleton L, Heselmeyer-Haddad K, Ried T. Hilgenfeld E, et al. Methods Mol Med. 2002;68:29-44. doi: 10.1385/1-59259-135-3:029. Methods Mol Med. 2002. PMID: 11901510 No abstract available.
MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site.
Slater DJ, Hilgenfeld E, Rappaport EF, Shah N, Meek RG, Williams WR, Lovett BD, Osheroff N, Autar RS, Ried T, Felix CA. Slater DJ, et al. Among authors: hilgenfeld e. Oncogene. 2002 Jul 11;21(30):4706-14. doi: 10.1038/sj.onc.1205572. Oncogene. 2002. PMID: 12096348
37 results