Results 131 to 140 of about 1,571,779 (177)
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Oncology, 2009
Kinetic studies of leukemic blast cells (LBC) and erythroblasts were carried out in 20 cases of acute myeloblasts leukemia (AML), and the results were compared with those observed in dividing granulocytic precursors (DGP) and erythroblasts in a control group of 16 normal subjects.
J. Sánchez-Fayos +3 more
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Kinetic studies of leukemic blast cells (LBC) and erythroblasts were carried out in 20 cases of acute myeloblasts leukemia (AML), and the results were compared with those observed in dividing granulocytic precursors (DGP) and erythroblasts in a control group of 16 normal subjects.
J. Sánchez-Fayos +3 more
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International Journal of Hematology, 2022
This study examined the prognostic impact of erythroblast predominance (EP) in 61 patients with myelodysplastic syndromes (MDS) (n = 51) or acute myeloid leukemia (n = 10) treated with azacitidine. Median age was 78 years. EP, defined as > 40% erythroblasts and M/E
Akihito Matsuoka +3 more
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This study examined the prognostic impact of erythroblast predominance (EP) in 61 patients with myelodysplastic syndromes (MDS) (n = 51) or acute myeloid leukemia (n = 10) treated with azacitidine. Median age was 78 years. EP, defined as > 40% erythroblasts and M/E
Akihito Matsuoka +3 more
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International Journal of Hematology, 2001
We assessed the in vitro chemosensitivity of acute erythroblastic and megakaryoblastic leukemia cells from children with Down syndrome (DS) compared to non-DS children. We conducted in vitro tests using the MTT assay of bone marrow samples from 12 children with DS and 16 children without DS.
S, Yamada +8 more
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We assessed the in vitro chemosensitivity of acute erythroblastic and megakaryoblastic leukemia cells from children with Down syndrome (DS) compared to non-DS children. We conducted in vitro tests using the MTT assay of bone marrow samples from 12 children with DS and 16 children without DS.
S, Yamada +8 more
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Derivative (1;7)(q10;p10) in a Patient with de novo Acute Erythroblastic Leukemia (AML-M6)
Cancer Genetics and Cytogenetics, 1999A rare association of der(1;7)(q10;p10) with de novo acute erythroblastic leukemia (AML-M6) in a 63-year-old male is reported. While this unbalanced 1;7 translocation, der(1;7), has been reported often in therapy-related myelodysplastic syndrome (t-MDS) or therapy-related acute myeloid leukemia (t-AML), its associations with de novo AML-FAB-M6 have ...
N, Obara +4 more
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Acta Haematologica, 1999
The frequencies of erythroblasts with micronuclei (EBM) and erythroblasts with aberrant nuclear shapes (EBAN) in bone marrow were evaluated in 60 patients with untreated myelodysplastic syndrome (MDS), and also in 21 patients with acute leukemia before and after treatment, and the results were compared regarding cytogenetic patterns.
H, Yashige +4 more
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The frequencies of erythroblasts with micronuclei (EBM) and erythroblasts with aberrant nuclear shapes (EBAN) in bone marrow were evaluated in 60 patients with untreated myelodysplastic syndrome (MDS), and also in 21 patients with acute leukemia before and after treatment, and the results were compared regarding cytogenetic patterns.
H, Yashige +4 more
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Hématologie, 2017
Le syndrome 8p11 est un syndrome rare dont le pronostic defavorable est du a une progression rapide vers une leucemie aigue myeloide (LAM) ou vers un lymphome lymphoblastique. Il resulte d’une mutation acquise impliquant le gene FGFR1 situe en p11 sur le chromosome 8 (translocation ou insertion chromosomiques).
Cécile Torregrosa +9 more
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Le syndrome 8p11 est un syndrome rare dont le pronostic defavorable est du a une progression rapide vers une leucemie aigue myeloide (LAM) ou vers un lymphome lymphoblastique. Il resulte d’une mutation acquise impliquant le gene FGFR1 situe en p11 sur le chromosome 8 (translocation ou insertion chromosomiques).
Cécile Torregrosa +9 more
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Leukemia Research, 2017
We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%,
Tomoyuki, Uchida +3 more
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We reviewed the cases of 68 consecutive patients who were diagnosed with myelodysplastic syndrome (MDS, n=61) or acute erythroleukemia (AEL, n=7) according to the World Health Organization (WHO) 2008 criteria and had previously been treated with azacitidine, a hypomethylating agent. Fifteen MDS patients had bone marrow erythroblast frequencies of ≥50%,
Tomoyuki, Uchida +3 more
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[Acute basophilic leukemia with an intense erythroblastic reaction].
Sangre, 1994A patient is presented who had acute basophilic leukaemia with intense erythroblastic reaction. The patient, a 66 year-old man, complained of general malaise, increased abdominal perimeter and melena. Leucocytosis, as well as severe anaemia and thrombocytopenia, were found in his peripheral blood.
M, Batlle +5 more
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Acta Haematologica, 2011
Patients with near-tetraploid acute myeloid leukemia (NT-AML) typically have poor survival. We present the case of a 67-year-old Caucasian male with NT-AML M0 who had an unusually long first complete remission of 51 months and an overall survival of 80 months.
Petr, Lemež +11 more
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Patients with near-tetraploid acute myeloid leukemia (NT-AML) typically have poor survival. We present the case of a 67-year-old Caucasian male with NT-AML M0 who had an unusually long first complete remission of 51 months and an overall survival of 80 months.
Petr, Lemež +11 more
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Leukemia Research, 2000
Erythroblastic and/or megakaryocytic dysplasia (EMD) was evaluated in diagnostic bone marrow smears of 43 consecutively treated patients under 65 years with de novo acute myeloid leukemia (AML) M0-M5 according to FAB criteria. The evaluation was possible in 39 (91%) patients, i.e.
P, Lemez, J, Gáliková, T, Haas
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Erythroblastic and/or megakaryocytic dysplasia (EMD) was evaluated in diagnostic bone marrow smears of 43 consecutively treated patients under 65 years with de novo acute myeloid leukemia (AML) M0-M5 according to FAB criteria. The evaluation was possible in 39 (91%) patients, i.e.
P, Lemez, J, Gáliková, T, Haas
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