Zobrazeno 1 - 10
of 131
pro vyhledávání: '"C D Bloomfield"'
Autor:
Richard M. Stone, E. Panina, Julia Krzykalla, Joseph Brandwein, Thomas W. Prior, A. Benner, Hartmut Döhner, I. Gathmann, E. Tiecke, A. Ganser, Lars Bullinger, Agnes Gambietz, C. D. Bloomfield, Frederick R. Appelbaum, S. Amadori, K Döhner, Bruno C. Medeiros, Michael Heuser, J. Herzig, F. Lo-Coco, Martin S. Tallman, A. Dolnik, Tamara J. Blätte, Nikolaus Jahn, R. A. Larson, Celine Pallaud, G. Ehninger, C. Thiede
Publikováno v:
HemaSphere. 3:436
Autor:
M R, Baer, S L, George, B L, Sanford, K, Mrózek, J E, Kolitz, J O, Moore, R M, Stone, B L, Powell, M A, Caligiuri, C D, Bloomfield, R A, Larson, John, Lister
Publikováno v:
Leukemia. 25:800-807
Untreated de novo (n=421) and secondary (n=189) acute myeloid leukemia (AML) patients≥60 years received intensified chemotherapy, including daunorubicin 60mg/m2 and etoposide 100mg/m2 during days 1, 2, 3 with cytarabine 100mg/m2 during days 1–7,
Autor:
C A, Westbrook, A L, Hooberman, C, Spino, R K, Dodge, R A, Larson, F, Davey, D H, Wurster-Hill, R E, Sobol, C, Schiffer, C D, Bloomfield
Publikováno v:
Blood. 80:2983-2990
The Philadelphia (Ph1) chromosome, or its molecular counterpart, the BCR-ABL fusion gene, is a rare but important prognostic indicator in childhood acute lymphoblastic leukemia (ALL), but its impact on adult ALL has not been well ascertained. A prosp
Autor:
C D, Bloomfield, A S, Ruppert, K, Mrózek, J E, Kolitz, J O, Moore, R J, Mayer, C G, Edwards, L J, Sterling, J W, Vardiman, A J, Carroll, M J, Pettenati, J, Stamberg, J C, Byrd, G, Marcucci, R A, Larson
Publikováno v:
Annals of hematology. 83
Publikováno v:
Genes, chromosomescancer. 31(2)
The presence of an extra ring chromosome containing material from 17q and 22q, or, less frequently, a t(17;22)(q22;q13), is a cytogenetic hallmark of dermatofibrosarcoma protuberans (DFSP). However, occasionally tumors with other, atypical karyotypes
Publikováno v:
International journal of hematology. 72(3)
The majority of adults diagnosed with acute myeloid leukemia (AML) display acquired cytogenetic aberrations at presentation. Numerous recurring chromosomal abnormalities have been and continue to be identified in AML. In many instances, genes altered
Autor:
S P, Whitman, M P, Strout, G, Marcucci, A G, Freud, L L, Culley, N J, Zeleznik-Le, K, Mrózek, K S, Theil, U R, Kees, C D, Bloomfield, M A, Caligiuri
Publikováno v:
Cancer research. 61(1)
A partial nontandem duplication (PNTD) of mixed lineage leukemia (MLL) gene is described in B-cell acute lymphoid leukemia without structural cytogenetic abnormalities at 11q23 and 9p22. A duplicated portion of MLL is interrupted by the insertion of
Autor:
N L, Harris, E S, Jaffe, J, Diebold, G, Flandrin, H K, Muller-Hermelink, J, Vardiman, T A, Lister, C D, Bloomfield
Publikováno v:
Annals of oncology : official journal of the European Society for Medical Oncology. 10(12)
Since 1995, the European Association of Pathologists (EAHP) and the Society for Hematopathology (SH) have been developing a new World Health Organization (WHO) Classification of hematologic malignancies. The classification includes lymphoid, myeloid,
Publikováno v:
Hematological oncology. 17(1)
Autor:
M, Wetzler, R K, Dodge, K, Mrózek, A J, Carroll, R, Tantravahi, A W, Block, M J, Pettenati, M M, Le Beau, S R, Frankel, C C, Stewart, T P, Szatrowski, C A, Schiffer, R A, Larson, C D, Bloomfield
Publikováno v:
Blood. 93(11)
The Cancer and Leukemia Group B (CALGB) has been conducting a prospective cytogenetic companion study (CALGB 8461) to all CALGB treatment protocols for newly diagnosed adults with acute lymphoblastic leukemia (ALL). These protocols underwent a signif