Zobrazeno 1 - 10
of 156
pro vyhledávání: '"DC Arthur"'
Autor:
NA Heerema, DC Arthur, H Sather, V Albo, J Feusner, BJ Lange, PG Steinherz, P Zeltzer, D Hammond, GH Reaman
Publikováno v:
Blood. 83:2274-2284
Cytogenetic analyses of pretreatment bone marrows were performed at local institutions as part of Childrens Cancer Group (CCG) protocol CCG- 107 for infants less than 1 year of age with previously untreated acute lymphoblastic leukemia (ALL). Cytogen
Autor:
Edward D. Ball, SL Allen, FR Davey, Robert J. Mayer, James D. Griffin, R B Davis, W Noll, Doris H. Wurster-Hill, MT Elghetany, DC Arthur
Publikováno v:
Blood. 77:2242-2250
We studied the expression of cell surface antigens associated with myeloid and lymphoid leukemias on bone marrow-derived blast cells from 339 patients with newly diagnosed de novo acute myeloid leukemia (AML) enrolled on Cancer and Leukemia Group B (
Autor:
Fatih M. Uckun, Hn, Sather, Ps, Gaynon, Dc, Arthur, Me, Trigg, Dg, Tubergen, Nachman J, Pg, Steinherz, Mg, Sensel, Gh, Reaman
Publikováno v:
Europe PubMed Central
Leukemic cells from a significant number of children with acute lymphoblastic leukemia (ALL) express protein antigens characteristic of both lymphoid and myeloid cells, yet the clinical significance of this immunophenotype has remained controversial.
Autor:
K Mrozek, Cp Karakousis, Cd Bloomfield, Fr Davey, C Perezmesa, E Mrozek, Mj Pettenati, Sr Frankel, R. Tantravahi, Dc Arthur, Unm Rao, Mm Lebeau, Prk Koduru
Publikováno v:
International Journal of Oncology.
An unbalanced translocation between chromosomes 1 and 16, der(16)t(1;16), resulting in trisomy 1q and loss of genetic material from 16q, has been thus far suggested to constitute a nonrandom secondary abnormality in two types of closely related solid
Autor:
H Dohner, DC Arthur, ED Ball, RE Sobol, FR Davey, D Lawrence, L Gordon, SR Patil, RB Surana, JR Testa
Publikováno v:
Blood. 76(8)
A new recurring chromosome abnormality was identified in 8 of 621 consecutive successfully karyotyped adults with de novo acute leukemia. These eight patients had trisomy 13 as the sole cytogenetic abnormality. On central morphologic review, five cas
Autor:
Rs, Shapiro, Kenneth McClain, Frizzera G, Kj, Gajl-Peczalska, Jh, Kersey, Br, Blazar, Dc, Arthur, Df, Patton, Js, Greenberg, Burke B
Publikováno v:
Europe PubMed Central
B cell lymphoproliferative disorders (BLPD) developed in eight patients following bone marrow transplantation (BMT) for leukemia (five patients) or immunodeficiency (three patients). Recipients of T depleted marrow from a mismatched donor were at par
Autor:
EG Levine, DC Arthur, J Machnicki, G Frizzera, D Hurd, B Peterson, KJ Gajl- Peczalska, CD Bloomfield
Publikováno v:
Blood. 74:1796-1800
The identification of recurring chromosomal translocations has provided clues to the gene regions important in lymphoma development. Among 157 patients with non-Hodgkin lymphoma studied by cytogenetic analysis, four new recurring translocations have
Publikováno v:
Blood. 66(6)
Although many recurring chromosome abnormalities have been found in malignant lymphoma (ML) in recent years, their relationship to histology remains largely undefined. We have correlated, in the same tumor mass, chromosome findings with histology, de
Autor:
DC Arthur, CD Bloomfield
Publikováno v:
Blood. 61(5)
Recently, several specific chromosomal abnormalities have been associated with distinctive clinical and/or morphological subtypes of acute nonlymphocytic leukemia (ANLL). To further investigate the clinical utility of karyotype analysis in ANLL, we h
Publikováno v:
Blood. 66(2)
The clinical, morphological, immunologic, and cytogenetic features of seven cases of chronic granulated T cell lymphocytosis with neutropenia were studied. The disorder was characterized by moderate blood and bone marrow lymphocytosis, neutropenia, p