-
1
-
-
0018178963
-
Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia
-
Mitelman F., Brandt L., and Nilsson P.G. Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia. Blood 52 (1978) 1229-1237
-
(1978)
Blood
, vol.52
, pp. 1229-1237
-
-
Mitelman, F.1
Brandt, L.2
Nilsson, P.G.3
-
2
-
-
0017715976
-
Non-industrial exposure to benzene as leukaemogenic risk factor
-
Brandt L., Nilsson P.G., and Mitelman F. Non-industrial exposure to benzene as leukaemogenic risk factor. Lancet 2 (1977) 1074
-
(1977)
Lancet
, vol.2
, pp. 1074
-
-
Brandt, L.1
Nilsson, P.G.2
Mitelman, F.3
-
3
-
-
0014955268
-
Multiple myeloma and acute myelomonocytic leukemia: report of four cases possibly related to melphalan
-
Kyle R.A., Pierre R.V., and Bayrd E.D. Multiple myeloma and acute myelomonocytic leukemia: report of four cases possibly related to melphalan. N Engl J Med 283 (1970) 1121-1125
-
(1970)
N Engl J Med
, vol.283
, pp. 1121-1125
-
-
Kyle, R.A.1
Pierre, R.V.2
Bayrd, E.D.3
-
4
-
-
0017661030
-
Acute nonlymphocytic leukemia: a delayed complication of Hodgkin's disease therapy: analysis of 109 cases
-
Cadman E.C., Capizzi R.L., and Bertino J.R. Acute nonlymphocytic leukemia: a delayed complication of Hodgkin's disease therapy: analysis of 109 cases. Cancer 40 (1977) 1280-1296
-
(1977)
Cancer
, vol.40
, pp. 1280-1296
-
-
Cadman, E.C.1
Capizzi, R.L.2
Bertino, J.R.3
-
5
-
-
0017766069
-
Acute leukaemia after treatment of lymphoma
-
Rowley J.D., Golomb H.M., and Vardiman J. Acute leukaemia after treatment of lymphoma. N Engl Med 297 (1977) 1013
-
(1977)
N Engl Med
, vol.297
, pp. 1013
-
-
Rowley, J.D.1
Golomb, H.M.2
Vardiman, J.3
-
6
-
-
0018889957
-
Dysmyelopoietic syndrome: sequential clinical and cytogenetic studies
-
Streuli R.A., Testa J.R., Vardiman J.W., Mintz U., Golomb H.M., and Rowley J.D. Dysmyelopoietic syndrome: sequential clinical and cytogenetic studies. Blood 55 (1980) 636-644
-
(1980)
Blood
, vol.55
, pp. 636-644
-
-
Streuli, R.A.1
Testa, J.R.2
Vardiman, J.W.3
Mintz, U.4
Golomb, H.M.5
Rowley, J.D.6
-
7
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multi-fluor FISH
-
Speicher M.R., Gwyn Ballard S., and Ward D.C. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 12 (1996) 368-375
-
(1996)
Nat Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Gwyn Ballard, S.2
Ward, D.C.3
-
8
-
-
0022135739
-
Proposed revised criteria for the classification of acute myeloid leukemia. A report of the French-American-British Cooperative Group
-
Bennett J.M., Catovsky D., Daniel M.T., Flandrin G., Galton D.A., Gralnick H.R., and Sultan C. Proposed revised criteria for the classification of acute myeloid leukemia. A report of the French-American-British Cooperative Group. Ann Intern Med 103 (1985) 620-625
-
(1985)
Ann Intern Med
, vol.103
, pp. 620-625
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.5
Gralnick, H.R.6
Sultan, C.7
-
9
-
-
0003477486
-
-
Jaffe E.S., Harris N.L., Stein H., and Vardiman J.W. (Eds), IARC Press, Lyon
-
In: Jaffe E.S., Harris N.L., Stein H., and Vardiman J.W. (Eds). World Health Organisation classification of tumours. Pathology and genetics of tumours of haematopoietic and lymphoid tissues (2001), IARC Press, Lyon
-
(2001)
World Health Organisation classification of tumours. Pathology and genetics of tumours of haematopoietic and lymphoid tissues
-
-
-
10
-
-
0020629324
-
Fluorodeoxyuridine synchronization of bone marrow cultures
-
Weber L.M., and Garson O.M. Fluorodeoxyuridine synchronization of bone marrow cultures. Cancer Genet Cytogenet 8 (1983) 123-132
-
(1983)
Cancer Genet Cytogenet
, vol.8
, pp. 123-132
-
-
Weber, L.M.1
Garson, O.M.2
-
12
-
-
0035074295
-
Limitations of chromosome classification by multicolor karyotyping
-
Lee C., Gisselsson D., Jin C., Nordgren A., Ferguson D.O., Blennow E., Fletcher J.A., and Morton C. Limitations of chromosome classification by multicolor karyotyping. Am J Hum Genet 68 (2001) 1043-1047
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1043-1047
-
-
Lee, C.1
Gisselsson, D.2
Jin, C.3
Nordgren, A.4
Ferguson, D.O.5
Blennow, E.6
Fletcher, J.A.7
Morton, C.8
-
13
-
-
0031788987
-
Cytogenetically unrelated clones in therapy-related myelodysplasia and acute myeloid leukemia: experience from the Copenhagen series updated to 180 consecutive cases
-
Pedersen-Bjergaard J., Timshel S., Andersen M.K., Thöger Andersen A.S., and Philip P. Cytogenetically unrelated clones in therapy-related myelodysplasia and acute myeloid leukemia: experience from the Copenhagen series updated to 180 consecutive cases. Genes Chromosomes Cancer 23 (1998) 337-349
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 337-349
-
-
Pedersen-Bjergaard, J.1
Timshel, S.2
Andersen, M.K.3
Thöger Andersen, A.S.4
Philip, P.5
-
14
-
-
0032052825
-
FISH investigation of 5q and 7q deletions in MDS/AML reveals hidden translocations, insertions and fragmentations of the same chromosomes
-
Lessard M., Herry A., Berthou C., Leglise M.C., Abgrall J.F., Morice P., and Flandrin G. FISH investigation of 5q and 7q deletions in MDS/AML reveals hidden translocations, insertions and fragmentations of the same chromosomes. Leukemia Res 22 (1998) 303-312
-
(1998)
Leukemia Res
, vol.22
, pp. 303-312
-
-
Lessard, M.1
Herry, A.2
Berthou, C.3
Leglise, M.C.4
Abgrall, J.F.5
Morice, P.6
Flandrin, G.7
-
15
-
-
85084722183
-
Balanced translocations involving chromosome bands 11q23 and 21q22 are highly characteristic of myelodysplasia and leukaemia following therapy with cytostatic agents targeting at DNA-topoisomerase
-
Pedersen-Bjergaard J., and Philip P. Balanced translocations involving chromosome bands 11q23 and 21q22 are highly characteristic of myelodysplasia and leukaemia following therapy with cytostatic agents targeting at DNA-topoisomerase. Blood 17 (1991) 1147-1148
-
(1991)
Blood
, vol.17
, pp. 1147-1148
-
-
Pedersen-Bjergaard, J.1
Philip, P.2
-
16
-
-
0036197783
-
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop
-
Bloomfield C.D., Archer K.J., Mrozek K., Lillington D.M., Kaneko Y., Head D.R., Dal Cin P., and Raimondi S.C. 11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop. Genes Chromosomes Cancer 33 (2002) 362-378
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 362-378
-
-
Bloomfield, C.D.1
Archer, K.J.2
Mrozek, K.3
Lillington, D.M.4
Kaneko, Y.5
Head, D.R.6
Dal Cin, P.7
Raimondi, S.C.8
-
17
-
-
0030792867
-
All patients with the t(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders
-
Rowley J.D., Reshmi S., Sobulo O., Musvee T., Anastasi J., Raimondi S., Schneider N.R., Barredo J.C., Cantu E.S., Schlegelberger B., Behm F., Doggett N.A., Borrow J., and Zeleznik-Le N. All patients with the t(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders. Blood 90 (1997) 535-541
-
(1997)
Blood
, vol.90
, pp. 535-541
-
-
Rowley, J.D.1
Reshmi, S.2
Sobulo, O.3
Musvee, T.4
Anastasi, J.5
Raimondi, S.6
Schneider, N.R.7
Barredo, J.C.8
Cantu, E.S.9
Schlegelberger, B.10
Behm, F.11
Doggett, N.A.12
Borrow, J.13
Zeleznik-Le, N.14
-
18
-
-
0036194105
-
Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: report from an international workshop
-
Block A.M.W., Caroll A.J., Hajemeijer A., Michaux L., van Lom K., Olney H.J., and Baer M.R. Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: report from an international workshop. Genes Chromosomes Cancer 33 (2002) 401-412
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 401-412
-
-
Block, A.M.W.1
Caroll, A.J.2
Hajemeijer, A.3
Michaux, L.4
van Lom, K.5
Olney, H.J.6
Baer, M.R.7
-
19
-
-
11844252560
-
A new translocation t(9;11)(q34;p15) fuses NUP98 to a novel homeobox partner gene, PRRX2, in a therapy-related acute myeloid leukemia
-
Gervais C., Mauvieux L., Perrusson N., Helias C., Struski S., Leymarie V., Lioure B., and Lessard M. A new translocation t(9;11)(q34;p15) fuses NUP98 to a novel homeobox partner gene, PRRX2, in a therapy-related acute myeloid leukemia. Leukemia 19 (2005) 145-148
-
(2005)
Leukemia
, vol.19
, pp. 145-148
-
-
Gervais, C.1
Mauvieux, L.2
Perrusson, N.3
Helias, C.4
Struski, S.5
Leymarie, V.6
Lioure, B.7
Lessard, M.8
-
20
-
-
0036262776
-
Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overexpression of 21q, 11q, and 22q
-
Mrozek K., Heinonen K., Theil K., and Bloomfield C. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overexpression of 21q, 11q, and 22q. Genes Chromosomes Cancer 34 (2002) 137-153
-
(2002)
Genes Chromosomes Cancer
, vol.34
, pp. 137-153
-
-
Mrozek, K.1
Heinonen, K.2
Theil, K.3
Bloomfield, C.4
-
21
-
-
0023253682
-
Trisomy 9 in hematologic disorders: possible association with primary thrombocytosis
-
Cournoyer D., Noel P., Schmidt M.A., and Dewald G.W. Trisomy 9 in hematologic disorders: possible association with primary thrombocytosis. Cancer Genet Cytogenet 27 (1987) 73-78
-
(1987)
Cancer Genet Cytogenet
, vol.27
, pp. 73-78
-
-
Cournoyer, D.1
Noel, P.2
Schmidt, M.A.3
Dewald, G.W.4
-
22
-
-
0023689044
-
Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients
-
Groupe Français de Cytogenetique Hematologique. Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients. Cancer Genet Cytogenet 32 (1988) 157-168
-
(1988)
Cancer Genet Cytogenet
, vol.32
, pp. 157-168
-
-
Groupe Français de Cytogenetique Hematologique1
-
23
-
-
0023713372
-
A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course
-
Swolin B., Weinfeld A., and Westin J. A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course. Blood 72 (1988) 386-395
-
(1988)
Blood
, vol.72
, pp. 386-395
-
-
Swolin, B.1
Weinfeld, A.2
Westin, J.3
-
24
-
-
21344472778
-
Gain of 9p due to an unbalanced rearrangement der(9;18): a recurrent clonal abnormality in chronic myeloproliferative disorders
-
Bacher U., Haferlach T., and Schoch C. Gain of 9p due to an unbalanced rearrangement der(9;18): a recurrent clonal abnormality in chronic myeloproliferative disorders. Cancer Genet Cytogenet 160 (2005) 179-183
-
(2005)
Cancer Genet Cytogenet
, vol.160
, pp. 179-183
-
-
Bacher, U.1
Haferlach, T.2
Schoch, C.3
-
25
-
-
0033984674
-
Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere
-
Andersen M.K., and Pedersen-Bjergaard J. Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere. Leukemia 14 (2000) 105-111
-
(2000)
Leukemia
, vol.14
, pp. 105-111
-
-
Andersen, M.K.1
Pedersen-Bjergaard, J.2
-
26
-
-
0031982894
-
Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with 17p deletion
-
Sterkers Y., Preudhomme C., Lai J.L., Demory J.L., Caulier M.T., Wattel E., Bordessoule D., Bauters F., and Fenaux P. Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with 17p deletion. Blood 91 (1998) 616-622
-
(1998)
Blood
, vol.91
, pp. 616-622
-
-
Sterkers, Y.1
Preudhomme, C.2
Lai, J.L.3
Demory, J.L.4
Caulier, M.T.5
Wattel, E.6
Bordessoule, D.7
Bauters, F.8
Fenaux, P.9
-
27
-
-
0028928283
-
Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoiesis and a high incidence of P53 mutations
-
Lai J.L., Preudhomme C., Zandecki M., Flactif M., Vanrumbeke M., Lepelley P., Wattel E., and Fenaux P. Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoiesis and a high incidence of P53 mutations. Leukemia 9 (1995) 370-381
-
(1995)
Leukemia
, vol.9
, pp. 370-381
-
-
Lai, J.L.1
Preudhomme, C.2
Zandecki, M.3
Flactif, M.4
Vanrumbeke, M.5
Lepelley, P.6
Wattel, E.7
Fenaux, P.8
-
28
-
-
0025368831
-
Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemias
-
Laï J.L., Zandecki M., Fenaux P., Le Baron F., Bauters F., Cosson A., and Deminatti M. Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemias. Cancer Genet Cytogenet 46 (1990) 173-183
-
(1990)
Cancer Genet Cytogenet
, vol.46
, pp. 173-183
-
-
Laï, J.L.1
Zandecki, M.2
Fenaux, P.3
Le Baron, F.4
Bauters, F.5
Cosson, A.6
Deminatti, M.7
-
29
-
-
0035057424
-
Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents
-
Andersen M.K., Christiansen D.H., Kirchhoff M., and Pedersen-Bjergaard J. Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents. Genes Chromosomes Cancer 31 (2001) 33-41
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 33-41
-
-
Andersen, M.K.1
Christiansen, D.H.2
Kirchhoff, M.3
Pedersen-Bjergaard, J.4
-
30
-
-
0036132094
-
Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH
-
Van Limbergen H., Poppe B., Michaux L., Herens C., Brown J., Noens L., Berneman Z., De Bock R., De Paepe A., and Speleman F. Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH. Genes Chromosomes Cancer 33 (2002) 60-72
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 60-72
-
-
Van Limbergen, H.1
Poppe, B.2
Michaux, L.3
Herens, C.4
Brown, J.5
Noens, L.6
Berneman, Z.7
De Bock, R.8
De Paepe, A.9
Speleman, F.10
-
31
-
-
0028276190
-
Acute leukaemia after hydroxyurea therapy in polycythemia vera and allied disorders: prospective study of efficacy and leukaemogenicity with therapeutic implications
-
Weinfeld A., Swolin B., and Westin J. Acute leukaemia after hydroxyurea therapy in polycythemia vera and allied disorders: prospective study of efficacy and leukaemogenicity with therapeutic implications. Eur J Haematol 52 (1994) 134-139
-
(1994)
Eur J Haematol
, vol.52
, pp. 134-139
-
-
Weinfeld, A.1
Swolin, B.2
Westin, J.3
-
32
-
-
2442677684
-
The leukemia controversy in myeloproliferative disorders: is it a natural progression of disease, a secondary sequela of therapy, or a combination of both?
-
Barbui T. The leukemia controversy in myeloproliferative disorders: is it a natural progression of disease, a secondary sequela of therapy, or a combination of both?. Semin Hematol 41 (2004) 15-17
-
(2004)
Semin Hematol
, vol.41
, pp. 15-17
-
-
Barbui, T.1
-
33
-
-
0021255719
-
Chromosome analysis of 63 cases of secondary nonlymphoid blood disorders: a cooperative study
-
Groupe Français de Cytogénétique Hématologique. Chromosome analysis of 63 cases of secondary nonlymphoid blood disorders: a cooperative study. Cancer Genetics Cytogenetics 12 (1984) 95-104
-
(1984)
Cancer Genetics Cytogenetics
, vol.12
, pp. 95-104
-
-
Groupe Français de Cytogénétique Hématologique1
-
34
-
-
13844276894
-
Role of multiplex FISH in identifying chromosome involvement in myelodysplastic syndromes and acute myeloid leukemias with complex karyotypes: a report on 28 cases
-
Barouk-Simonet E., Soenen-Cornu V., Roumier C., Cosson A., Laï J.-L., Fenaux P., and Preudhomme C. Role of multiplex FISH in identifying chromosome involvement in myelodysplastic syndromes and acute myeloid leukemias with complex karyotypes: a report on 28 cases. Cancer Genet Cytogenet 157 (2005) 118-126
-
(2005)
Cancer Genet Cytogenet
, vol.157
, pp. 118-126
-
-
Barouk-Simonet, E.1
Soenen-Cornu, V.2
Roumier, C.3
Cosson, A.4
Laï, J.-L.5
Fenaux, P.6
Preudhomme, C.7
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