-
1
-
-
0034054939
-
Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes, Grupo Cooperativo Espanol de Citogenetica Hematologica
-
Sole F., Espinet B., Sanz G.F., Cervera J., Calasanz M.J., Luno E.et al. Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes, Grupo Cooperativo Espanol de Citogenetica Hematologica. Br J. Haematol. 108:2000;346-356.
-
(2000)
Br J. Haematol.
, vol.108
, pp. 346-356
-
-
Sole, F.1
Espinet, B.2
Sanz, G.F.3
Cervera, J.4
Calasanz, M.J.5
Luno, E.6
-
2
-
-
0027511657
-
Karyotypic analysis in primary myelodysplastic syndromes
-
Noel P., Tefferi A., Pierre R.V., Jenkins R.B., Dewald G.W. Karyotypic analysis in primary myelodysplastic syndromes. Blood Rev. 7:1993;10-18.
-
(1993)
Blood Rev.
, vol.7
, pp. 10-18
-
-
Noel, P.1
Tefferi, A.2
Pierre, R.V.3
Jenkins, R.B.4
Dewald, G.W.5
-
4
-
-
0026536685
-
Chromosomal deletions in the myelodysplastic syndrome
-
Mufti G.J. Chromosomal deletions in the myelodysplastic syndrome. Leuk. Res. 16:1992;35-41.
-
(1992)
Leuk. Res.
, vol.16
, pp. 35-41
-
-
Mufti, G.J.1
-
5
-
-
0034988764
-
Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia
-
Tefferi A., Mesa R.A., Schroeder G., Hanson C.A., Li C.Y., Dewald G.W. Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia. Br. J. Haematol. 113:2001;763-771.
-
(2001)
Br. J. Haematol.
, vol.113
, pp. 763-771
-
-
Tefferi, A.1
Mesa, R.A.2
Schroeder, G.3
Hanson, C.A.4
Li, C.Y.5
Dewald, G.W.6
-
6
-
-
0029154197
-
Chromosome abnormalities in the myeloproliferative disorders
-
Dewald G.W., Wright P.I. Chromosome abnormalities in the myeloproliferative disorders. Semin. Oncol. 22:1995;341-354.
-
(1995)
Semin. Oncol.
, vol.22
, pp. 341-354
-
-
Dewald, G.W.1
Wright, P.I.2
-
9
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett J.M., Catovsky D., Daniel M.T., Flandrin G., Galton D.A., Gralnick H.R.et al. Proposals for the classification of the myelodysplastic syndromes. Br. J. Haematol. 51:1982;189-199.
-
(1982)
Br. J. Haematol.
, vol.51
, pp. 189-199
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.5
Gralnick, H.R.6
-
10
-
-
0032784783
-
World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997
-
Harris N.L., Jaffe E.S., Diebold J., Flandrin G., Muller-Hermelink H.K., Vardiman J.et al. World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997. J. Clin. Oncol. 17:1999;3835-3849.
-
(1999)
J. Clin. Oncol.
, vol.17
, pp. 3835-3849
-
-
Harris, N.L.1
Jaffe, E.S.2
Diebold, J.3
Flandrin, G.4
Muller-Hermelink, H.K.5
Vardiman, J.6
-
11
-
-
0031902192
-
Chromosomal abnormalities and molecular genetics of non-Hodgkin's lymphoma
-
Ong S.T., Le Beau M.M. Chromosomal abnormalities and molecular genetics of non-Hodgkin's lymphoma. Semin. Oncol. 25:1998;447-460.
-
(1998)
Semin. Oncol.
, vol.25
, pp. 447-460
-
-
Ong, S.T.1
Le Beau, M.M.2
-
13
-
-
0026669997
-
Loss of the Y chromosome from normal and neoplastic bone marrows
-
United Kingdom Cancer Cytogenetics Group (UKCCG)
-
Loss of the Y chromosome from normal and neoplastic bone marrows. United Kingdom Cancer Cytogenetics Group (UKCCG). Genes Chromosomes Cancer 1992;5:83-8.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 83-88
-
-
-
14
-
-
0033066538
-
Loss of the Y chromosome in bone marrow cells: Results on 1907 consecutive cases of leukaemia and preleukaemia
-
Herens C., Brasseur E., Jamar M., Vierset L., Schoenen I., Koulischer L. Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia. Clin. Lab. Haematol. 21:1999;17-20.
-
(1999)
Clin. Lab. Haematol.
, vol.21
, pp. 17-20
-
-
Herens, C.1
Brasseur, E.2
Jamar, M.3
Vierset, L.4
Schoenen, I.5
Koulischer, L.6
-
15
-
-
0015416999
-
Age-associated aneuploidy: Loss of Y chromosome from human bone marrow cells with aging
-
Pierre R.V., Hoagland H.C. Age-associated aneuploidy: loss of Y chromosome from human bone marrow cells with aging. Cancer. 30:1972;889-894.
-
(1972)
Cancer
, vol.30
, pp. 889-894
-
-
Pierre, R.V.1
Hoagland, H.C.2
-
16
-
-
0023525879
-
Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia
-
Appelbaum F.R., Barrall J., Storb R., Ramberg R., Doney K., Sale G.E.et al. Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia. Exp. Hematol. 15:1987;1134-1139.
-
(1987)
Exp. Hematol.
, vol.15
, pp. 1134-1139
-
-
Appelbaum, F.R.1
Barrall, J.2
Storb, R.3
Ramberg, R.4
Doney, K.5
Sale, G.E.6
-
17
-
-
0023881064
-
Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques
-
Spurbeck J.L., Carlson R.O., Allen J.E., Dewald G.W. Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques. Cancer Genet. Cytogenet. 32:1988;59-66.
-
(1988)
Cancer Genet. Cytogenet.
, vol.32
, pp. 59-66
-
-
Spurbeck, J.L.1
Carlson, R.O.2
Allen, J.E.3
Dewald, G.W.4
-
19
-
-
0027725137
-
PG-M1: A new monoclonal antibody directed against a fixative-resistant epitope on the macrophage-restricted form of the CD68 molecule
-
Falini B., Flenghi L., Pileri S., Gambacorta M., Bigerna B., Durkop H.et al. PG-M1: a new monoclonal antibody directed against a fixative-resistant epitope on the macrophage-restricted form of the CD68 molecule. Am. J. Pathol. 142:1993;1359-1372.
-
(1993)
Am. J. Pathol.
, vol.142
, pp. 1359-1372
-
-
Falini, B.1
Flenghi, L.2
Pileri, S.3
Gambacorta, M.4
Bigerna, B.5
Durkop, H.6
-
20
-
-
0032854508
-
Bone marrow effects of anagrelide therapy in patients with myelofibrosis with myeloid metaplasia
-
Yoon S.Y., Li C.Y., Mesa R.A., Tefferi A. Bone marrow effects of anagrelide therapy in patients with myelofibrosis with myeloid metaplasia. Br. J. Haematol. 106:1999;682-688.
-
(1999)
Br. J. Haematol.
, vol.106
, pp. 682-688
-
-
Yoon, S.Y.1
Li, C.Y.2
Mesa, R.A.3
Tefferi, A.4
-
21
-
-
4243895778
-
Clonal T-cell and immunoglobulin gene rearrangements in myelodysplastic syndromes (MDS): A morphologic and immunoperoxidase study
-
Hanson C.A., Dayharsh G.A., Morice W.G., Hodnefield J.M., Steensma D.P. Clonal T-cell and immunoglobulin gene rearrangements in myelodysplastic syndromes (MDS): a morphologic and immunoperoxidase study. Leuk. Res. 25:2001;S12-S13.
-
(2001)
Leuk. Res.
, vol.25
, pp. 12-S13
-
-
Hanson, C.A.1
Dayharsh, G.A.2
Morice, W.G.3
Hodnefield, J.M.4
Steensma, D.P.5
-
22
-
-
0033592318
-
Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes
-
Dunn D.E., Tanawattanacharoen P., Boccuni P., Nagakura S., Green S.W., Kirby M.R.et al. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann. Intern. Med. 131:1999;401-408.
-
(1999)
Ann. Intern. Med.
, vol.131
, pp. 401-408
-
-
Dunn, D.E.1
Tanawattanacharoen, P.2
Boccuni, P.3
Nagakura, S.4
Green, S.W.5
Kirby, M.R.6
-
24
-
-
0033995780
-
154 Chromosome anomalies in hematologic malignancies
-
Dewald G.W., Stupca P. 154 chromosome anomalies in hematologic malignancies. Leuk. Res. 24:2000;487-489.
-
(2000)
Leuk. Res.
, vol.24
, pp. 487-489
-
-
Dewald, G.W.1
Stupca, P.2
-
25
-
-
0022645855
-
Unbalanced 1;7 translocation and therapy-induced hematologic disorders: A possible relationship
-
Morrison-DeLap S.J., Kuffel D.G., Dewald G.W., Letendre L. Unbalanced 1;7 translocation and therapy-induced hematologic disorders: a possible relationship. Am. J. Hematol. 21:1986;39-47.
-
(1986)
Am. J. Hematol.
, vol.21
, pp. 39-47
-
-
Morrison-DeLap, S.J.1
Kuffel, D.G.2
Dewald, G.W.3
Letendre, L.4
-
26
-
-
0031730137
-
Myelodysplastic syndrome (MDS) with unbalanced t(1;7) after severe aplastic anemia (SAA) in childhood as a variant form of monosomy 7
-
Kikuchi A., Ohashi H., Hanada R., Yamamoto K. Myelodysplastic syndrome (MDS) with unbalanced t(1;7) after severe aplastic anemia (SAA) in childhood as a variant form of monosomy 7. Leukemia. 12:1998;2036-2038.
-
(1998)
Leukemia
, vol.12
, pp. 2036-2038
-
-
Kikuchi, A.1
Ohashi, H.2
Hanada, R.3
Yamamoto, K.4
-
27
-
-
0021254497
-
Hematologic manifestations associated with deletions of the long arm of chromosome 20
-
Davis M.P., Dewald G.W., Pierre R.V., Hoagland H.C. Hematologic manifestations associated with deletions of the long arm of chromosome 20. Cancer Genet. Cytogenet. 12:1984;63-71.
-
(1984)
Cancer Genet. Cytogenet.
, vol.12
, pp. 63-71
-
-
Davis, M.P.1
Dewald, G.W.2
Pierre, R.V.3
Hoagland, H.C.4
-
28
-
-
0027458441
-
The 5q-syndrome: A single-institution study of 43 consecutive patients
-
Mathew P., Tefferi A., Dewald G.W., Goldberg S.L., Su J., Hoagland H.C.et al. The 5q-syndrome: a single-institution study of 43 consecutive patients. Blood. 81:1993;1040-1045.
-
(1993)
Blood
, vol.81
, pp. 1040-1045
-
-
Mathew, P.1
Tefferi, A.2
Dewald, G.W.3
Goldberg, S.L.4
Su, J.5
Hoagland, H.C.6
-
29
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P., Cox C., LeBeau M.M., Fenaux P., Morel P., Sanz G.et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood. 89:1997;2079-2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
Fenaux, P.4
Morel, P.5
Sanz, G.6
-
30
-
-
0031975407
-
Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies
-
La Starza R., Wlodarska I., Aventin A., Falzetti D., Crescenzi B., Martelli M.F.et al. Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies. Blood. 91:1998;231-237.
-
(1998)
Blood
, vol.91
, pp. 231-237
-
-
La Starza, R.1
Wlodarska, I.2
Aventin, A.3
Falzetti, D.4
Crescenzi, B.5
Martelli, M.F.6
-
31
-
-
0036197441
-
Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: Report from an International Workshop
-
Olney H.J., Mitelman F., Johansson B., Mrozek K., Berger R., Rowley J.D. Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: report from an International Workshop. Genes Chromosomes Cancer. 33:2002;413-423.
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 413-423
-
-
Olney, H.J.1
Mitelman, F.2
Johansson, B.3
Mrozek, K.4
Berger, R.5
Rowley, J.D.6
-
32
-
-
0036194105
-
Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop
-
Block A.W., Carroll A.J., Hagemeijer A., Lm L.M., van Lom K., Olney H.J.et al. 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.W.1
Carroll, A.J.2
Hagemeijer, A.3
Lm, L.M.4
Van Lom, K.5
Olney, H.J.6
-
34
-
-
0027286442
-
Issues in the pathology and diagnosis of the chronic myeloproliferative disorders and the myelodysplastic syndromes
-
Dickstein J.I., Vardiman J.W. Issues in the pathology and diagnosis of the chronic myeloproliferative disorders and the myelodysplastic syndromes. Am. J. Clin. Pathol. 99:1993;513-525.
-
(1993)
Am. J. Clin. Pathol.
, vol.99
, pp. 513-525
-
-
Dickstein, J.I.1
Vardiman, J.W.2
-
36
-
-
0034305979
-
Problematic WHO reclassification of myelodysplastic syndromes: Members of the International MDS Study Group
-
Greenberg P., Anderson J., de Witte T., Estey E., Fenaux P., Gupta P.et al. Problematic WHO reclassification of myelodysplastic syndromes: members of the International MDS Study Group. J. Clin. Oncol. 18:2000;3447-3452.
-
(2000)
J. Clin. Oncol.
, vol.18
, pp. 3447-3452
-
-
Greenberg, P.1
Anderson, J.2
De Witte, T.3
Estey, E.4
Fenaux, P.5
Gupta, P.6
-
37
-
-
0026580044
-
Minimal diagnostic criteria for the myelodysplastic syndrome in clinical practice
-
Tricot G.J. Minimal diagnostic criteria for the myelodysplastic syndrome in clinical practice. Leuk. Res. 16:1992;5-6.
-
(1992)
Leuk. Res.
, vol.16
, pp. 5-6
-
-
Tricot, G.J.1
-
38
-
-
0034472615
-
Myelodysplasia or myeloneoplasia: Thoughts on the nosology of clonal myeloid diseases
-
Lichtman M.A. Myelodysplasia or myeloneoplasia: thoughts on the nosology of clonal myeloid diseases. Blood Cells Mol. Dis. 26:2000;572-581.
-
(2000)
Blood Cells Mol. Dis.
, vol.26
, pp. 572-581
-
-
Lichtman, M.A.1
-
39
-
-
0026077438
-
Normal cytogenetic values for bone marrow based on studies of bone marrow transplant donors
-
Kuffel D.G., Schultz C.G., Ash R.C., Dewald G.W. Normal cytogenetic values for bone marrow based on studies of bone marrow transplant donors. Cancer Genet. Cytogenet. 55:1991;39-48.
-
(1991)
Cancer Genet. Cytogenet.
, vol.55
, pp. 39-48
-
-
Kuffel, D.G.1
Schultz, C.G.2
Ash, R.C.3
Dewald, G.W.4
-
40
-
-
0028091121
-
Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells
-
Raynaud S.D., Brunet B., Chischportich M., Bayle J., Gratecos N., Pesce A.et al. Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells. Leukemia. 8:1994;245-249.
-
(1994)
Leukemia
, vol.8
, pp. 245-249
-
-
Raynaud, S.D.1
Brunet, B.2
Chischportich, M.3
Bayle, J.4
Gratecos, N.5
Pesce, A.6
-
41
-
-
13044312738
-
Detection of abnormal pretransplant clones in progenitor cells of patients who developed myelodysplasia after autologous transplantation
-
Abruzzese E., Radford J.E., Miller J.S., Vredenburgh J.J., Rao P.N., Pettenati M.J.et al. Detection of abnormal pretransplant clones in progenitor cells of patients who developed myelodysplasia after autologous transplantation. Blood. 94:1999;1814-1819.
-
(1999)
Blood
, vol.94
, pp. 1814-1819
-
-
Abruzzese, E.1
Radford, J.E.2
Miller, J.S.3
Vredenburgh, J.J.4
Rao, P.N.5
Pettenati, M.J.6
-
42
-
-
0021365147
-
Recurrent chromosomal defects are found in most patients with acute non-lymphocytic leukemia
-
Yunis J.J. Recurrent chromosomal defects are found in most patients with acute non-lymphocytic leukemia. Cancer Genet. Cytogenet. 11:1984;125-137.
-
(1984)
Cancer Genet. Cytogenet.
, vol.11
, pp. 125-137
-
-
Yunis, J.J.1
-
43
-
-
0035110260
-
Bone marrow cytogenetic abnormalities of aplastic anemia
-
Keung Y.K., Pettenati M.J., Cruz J.M., Powell B.L., Woodruff R.D., Buss D.H. Bone marrow cytogenetic abnormalities of aplastic anemia. Am. J. Hematol. 66:2001;167-171.
-
(2001)
Am. J. Hematol.
, vol.66
, pp. 167-171
-
-
Keung, Y.K.1
Pettenati, M.J.2
Cruz, J.M.3
Powell, B.L.4
Woodruff, R.D.5
Buss, D.H.6
-
44
-
-
0035124250
-
Three cases of typical aplastic anemia associated with a Philadelphia chromosome
-
Suzan F., Terre C., Garcia I., Bastie J., Baumelou E., Gluckman E.et al. Three cases of typical aplastic anemia associated with a Philadelphia chromosome. Br. J. Haematol. 112:2001;385-387.
-
(2001)
Br. J. Haematol.
, vol.112
, pp. 385-387
-
-
Suzan, F.1
Terre, C.2
Garcia, I.3
Bastie, J.4
Baumelou, E.5
Gluckman, E.6
-
45
-
-
0030777064
-
Aplastic anemia or aplastic preleukemic syndrome?
-
Jameel T., Anwar M., Abdi S.I., Saleem M., Ahmad P.A., Khattak M.F. Aplastic anemia or aplastic preleukemic syndrome? Ann. Hematol. 75:1997;189-193.
-
(1997)
Ann. Hematol.
, vol.75
, pp. 189-193
-
-
Jameel, T.1
Anwar, M.2
Abdi, S.I.3
Saleem, M.4
Ahmad, P.A.5
Khattak, M.F.6
-
47
-
-
0028234052
-
Myelodysplasia in a patient with preexisting paroxysmal nocturnal haemoglobinuria: A clonal disease originating from within a clonal disease
-
Longo L., Bessler M., Beris P., Swirsky D., Luzzatto L. Myelodysplasia in a patient with preexisting paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease. Br. J. Haematol. 87:1994;401-403.
-
(1994)
Br. J. Haematol.
, vol.87
, pp. 401-403
-
-
Longo, L.1
Bessler, M.2
Beris, P.3
Swirsky, D.4
Luzzatto, L.5
-
48
-
-
0028229227
-
Myelodysplasia following paroxysmal nocturnal haemoglobinuria: Evidence for the emergence of a separate clone
-
van Kamp H., Smit J.W., van den Berg E., Ruud Halie M., Vellenga E. Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone. Br. J. Haematol. 87:1994;399-400.
-
(1994)
Br. J. Haematol.
, vol.87
, pp. 399-400
-
-
Van Kamp, H.1
Smit, J.W.2
Van den Berg, E.3
Ruud Halie, M.4
Vellenga, E.5
-
49
-
-
0029790993
-
Myelodysplasia following aplastic anemia-paroxysmal nocturnal haemoglobinuria syndrome after treatment with immunosuppression and G-CSF: Evidence for the emergence of a separate clone
-
Jin J.Y., Tooze J.A., Marsh J.C., Matthey F., Gordon-Smith E.C. Myelodysplasia following aplastic anemia-paroxysmal nocturnal haemoglobinuria syndrome after treatment with immunosuppression and G-CSF: evidence for the emergence of a separate clone. Br. J. Haematol. 94:1996;510-512.
-
(1996)
Br. J. Haematol.
, vol.94
, pp. 510-512
-
-
Jin, J.Y.1
Tooze, J.A.2
Marsh, J.C.3
Matthey, F.4
Gordon-Smith, E.C.5
-
50
-
-
0034048199
-
Myelodysplastic syndrome and aplastic anemia-diagnostic and conceptual uncertainties
-
Barrett J. Myelodysplastic syndrome and aplastic anemia-diagnostic and conceptual uncertainties. Leuk. Res. 24:2000;595-596.
-
(2000)
Leuk. Res.
, vol.24
, pp. 595-596
-
-
Barrett, J.1
-
51
-
-
0029846342
-
Hematologic disorders associated with deletions of chromosome 20q: A clinicopathologic study of 107 patients
-
Kurtin P.J., Dewald G.W., Shields D.J., Hanson C.A. Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients. Am. J. Clin. Pathol. 106:1996;680-688.
-
(1996)
Am. J. Clin. Pathol.
, vol.106
, pp. 680-688
-
-
Kurtin, P.J.1
Dewald, G.W.2
Shields, D.J.3
Hanson, C.A.4
-
52
-
-
0028871987
-
Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia
-
Pedersen-Bjergaard J., Pedersen M., Roulston D., Philip P. Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia. Blood. 86:1995;3542-3552.
-
(1995)
Blood
, vol.86
, pp. 3542-3552
-
-
Pedersen-Bjergaard, J.1
Pedersen, M.2
Roulston, D.3
Philip, P.4
-
53
-
-
0020056752
-
Thrombocytopenia as presenting symptom of preleukaemia in three patients
-
Tricot G., Criel A., Verwilghen R.L. Thrombocytopenia as presenting symptom of preleukaemia in three patients. Scand. J. Haematol. 28:1982;243-250.
-
(1982)
Scand. J. Haematol.
, vol.28
, pp. 243-250
-
-
Tricot, G.1
Criel, A.2
Verwilghen, R.L.3
-
54
-
-
0026475228
-
Refractory thrombocytopenia: A myelodysplastic syndrome that may mimic immune thrombocytopenic purpura
-
Menke D.M., Colon-Otero G., Cockerill K.J., Jenkins R.B., Noel P., Pierre R.V. Refractory thrombocytopenia: a myelodysplastic syndrome that may mimic immune thrombocytopenic purpura. Am. J. Clin. Pathol. 98:1992;502-510.
-
(1992)
Am. J. Clin. Pathol.
, vol.98
, pp. 502-510
-
-
Menke, D.M.1
Colon-Otero, G.2
Cockerill, K.J.3
Jenkins, R.B.4
Noel, P.5
Pierre, R.V.6
-
55
-
-
8944225498
-
Idiopathic thrombocytopenic purpura: A practice guideline developed by explicit methods for the American Society of Hematology
-
George J.N., Woolf S.H., Raskob G.E., Wasser J.S., Aledort L.M., Ballem P.J.et al. Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology. Blood. 88:1996;3-40.
-
(1996)
Blood
, vol.88
, pp. 3-40
-
-
George, J.N.1
Woolf, S.H.2
Raskob, G.E.3
Wasser, J.S.4
Aledort, L.M.5
Ballem, P.J.6
-
56
-
-
0024423204
-
Refractory anemia with excess of blasts in transformation hematologic and clinical study of 52 patients
-
Michels S.D., Saumur J., Arthur D.C., Robison L.L., Brunning R.D. Refractory anemia with excess of blasts in transformation hematologic and clinical study of 52 patients. Cancer. 64:1989;2340-2346.
-
(1989)
Cancer
, vol.64
, pp. 2340-2346
-
-
Michels, S.D.1
Saumur, J.2
Arthur, D.C.3
Robison, L.L.4
Brunning, R.D.5
-
57
-
-
0028365777
-
Trisomy 6 as the sole chromosome abnormality in myeloid disorders
-
Jonveaux P., Fenaux P., Berger R. Trisomy 6 as the sole chromosome abnormality in myeloid disorders. Cancer Genet. Cytogenet. 74:1994;150-152.
-
(1994)
Cancer Genet. Cytogenet.
, vol.74
, pp. 150-152
-
-
Jonveaux, P.1
Fenaux, P.2
Berger, R.3
-
58
-
-
0035863018
-
Trisomy 14 in myeloid malignancies: Report of two cases and review of the literature
-
Horton Y.M., Johnson P.R. Trisomy 14 in myeloid malignancies: report of two cases and review of the literature. Cancer Genet. Cytogenet. 124:2001;172-174.
-
(2001)
Cancer Genet. Cytogenet.
, vol.124
, pp. 172-174
-
-
Horton, Y.M.1
Johnson, P.R.2
-
59
-
-
0033787922
-
Trisomy 15 is frequently observed as a minor clone in patients with anemia/MDS/NHL and as a major clone in patients with AML
-
Batanian J.R., Slovak M.L., Mohamed A., Dobin S., Luthardt F.W., Keitges E.A. Trisomy 15 is frequently observed as a minor clone in patients with anemia/MDS/NHL and as a major clone in patients with AML. Cancer Genet. Cytogenet. 121:2000;186-189.
-
(2000)
Cancer Genet. Cytogenet.
, vol.121
, pp. 186-189
-
-
Batanian, J.R.1
Slovak, M.L.2
Mohamed, A.3
Dobin, S.4
Luthardt, F.W.5
Keitges, E.A.6
-
60
-
-
0025166263
-
Clonal karyotype abnormalities and clinical progress in the myelodysplastic syndrome
-
Geddes A.A., Bowen D.T., Jacobs A. Clonal karyotype abnormalities and clinical progress in the myelodysplastic syndrome. Br. J. Haematol. 76:1990;194-202.
-
(1990)
Br. J. Haematol.
, vol.76
, pp. 194-202
-
-
Geddes, A.A.1
Bowen, D.T.2
Jacobs, A.3
-
61
-
-
0021879865
-
Major karyotypic abnormalities in a near-tetraploid erythroleukemia
-
Kocova M.J., Sandberg A.A. Major karyotypic abnormalities in a near-tetraploid erythroleukemia. Cancer Genet. Cytogenet. 17:1985;143-150.
-
(1985)
Cancer Genet. Cytogenet.
, vol.17
, pp. 143-150
-
-
Kocova, M.J.1
Sandberg, A.A.2
-
62
-
-
0032188805
-
The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1612 patients entered into the MRC AML 10 trial, The Medical Research Council Adult and Children's Leukaemia Working Parties
-
Grimwade D., Walker H., Oliver F., Wheatley K., Harrison C., Harrison G.et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1612 patients entered into the MRC AML 10 trial, The Medical Research Council Adult and Children's Leukaemia Working Parties. Blood. 92:1998;2322-2333.
-
(1998)
Blood
, vol.92
, pp. 2322-2333
-
-
Grimwade, D.1
Walker, H.2
Oliver, F.3
Wheatley, K.4
Harrison, C.5
Harrison, G.6
-
63
-
-
0028609646
-
Interstitial 9q-deletion in a case of acute myeloid leukemia-M2 arising from a granulocytic sarcoma
-
Lunde J.H., Allen E.F. Interstitial 9q-deletion in a case of acute myeloid leukemia-M2 arising from a granulocytic sarcoma. Cancer Genet. Cytogenet. 78:1994;239-241.
-
(1994)
Cancer Genet. Cytogenet.
, vol.78
, pp. 239-241
-
-
Lunde, J.H.1
Allen, E.F.2
-
64
-
-
0021205863
-
A new translocation, t(1;3)(p36;q21), in myelodysplastic disorders
-
Moir D.J., Jones P.A., Pearson J., Duncan J.R., Cook P., Buckle V.J. A new translocation, t(1;3)(p36;q21), in myelodysplastic disorders. Blood. 64:1984;553-555.
-
(1984)
Blood
, vol.64
, pp. 553-555
-
-
Moir, D.J.1
Jones, P.A.2
Pearson, J.3
Duncan, J.R.4
Cook, P.5
Buckle, V.J.6
-
65
-
-
0031002366
-
Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1q
-
Mogul M.J., Brady K., Brothman A.R., Adams R., Peterson F.B., Beatty P.G. Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1q. Cancer Genet. Cytogenet. 95:1997;210-212.
-
(1997)
Cancer Genet. Cytogenet.
, vol.95
, pp. 210-212
-
-
Mogul, M.J.1
Brady, K.2
Brothman, A.R.3
Adams, R.4
Peterson, F.B.5
Beatty, P.G.6
-
66
-
-
0032934759
-
Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridization
-
Aventin A., La Starza R., Martinez C., Wlodarska I., Boogaerts M., Van den Berghe H. Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridization. Cancer Genet. Cytogenet. 108:1999;48-52.
-
(1999)
Cancer Genet. Cytogenet.
, vol.108
, pp. 48-52
-
-
Aventin, A.1
La Starza, R.2
Martinez, C.3
Wlodarska, I.4
Boogaerts, M.5
Van den Berghe, H.6
-
67
-
-
0026703970
-
Chromosome analyses in patients with myelodysplastic syndromes: Correlation with bone marrow histopathology and prognostic significance
-
Werner M., Maschek H., Kaloutsi V., Choritz H., Georgii A. Chromosome analyses in patients with myelodysplastic syndromes: correlation with bone marrow histopathology and prognostic significance. Virchows Arch. A Pathol. Anat. Histopathol. 421:1992;47-52.
-
(1992)
Virchows Arch. A Pathol. Anat. Histopathol.
, vol.421
, pp. 47-52
-
-
Werner, M.1
Maschek, H.2
Kaloutsi, V.3
Choritz, H.4
Georgii, A.5
-
68
-
-
0023801666
-
Childhood myelodysplastic syndromes with 11p15 translocation
-
Inaba T., Hayashi Y., Hanada R., Nakashima M., Yamamoto K., Nishida T. Childhood myelodysplastic syndromes with 11p15 translocation. Cancer Genet. Cytogenet. 34:1988;41-46.
-
(1988)
Cancer Genet. Cytogenet.
, vol.34
, pp. 41-46
-
-
Inaba, T.1
Hayashi, Y.2
Hanada, R.3
Nakashima, M.4
Yamamoto, K.5
Nishida, T.6
-
69
-
-
0032809702
-
A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignancies
-
Chen Z., Richkind K., Roherty S., Velasco J., Lytle C., Brothman A.R.et al. A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignancies. Cancer Genet. Cytogenet. 113:1999;162-165.
-
(1999)
Cancer Genet. Cytogenet.
, vol.113
, pp. 162-165
-
-
Chen, Z.1
Richkind, K.2
Roherty, S.3
Velasco, J.4
Lytle, C.5
Brothman, A.R.6
-
70
-
-
0031945625
-
Secondary acute leukemia and myelodysplastic syndrome with 11q23 abnormalities: EU concerted action 11q23 workshop
-
Secker-Walker L.M., Moorman A.V., Bain B.J., Mehta A.B. Secondary acute leukemia and myelodysplastic syndrome with 11q23 abnormalities: EU concerted action 11q23 workshop. Leukemia. 12:1998;840-844.
-
(1998)
Leukemia
, vol.12
, pp. 840-844
-
-
Secker-Walker, L.M.1
Moorman, A.V.2
Bain, B.J.3
Mehta, A.B.4
-
71
-
-
0029827390
-
3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia
-
Shi G., Weh H.J., Martensen S., Seeger D., Hossfeld D.K. 3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia. Cytogenet. Cell Genet. 74:1996;295-299.
-
(1996)
Cytogenet. Cell Genet.
, vol.74
, pp. 295-299
-
-
Shi, G.1
Weh, H.J.2
Martensen, S.3
Seeger, D.4
Hossfeld, D.K.5
-
72
-
-
0022877297
-
Cytogenetic studies in 18 patients with secondary blood disorders
-
Benitez J., Carbonell F., Ferro T., Prieto F., Sanchez Fayos J. Cytogenetic studies in 18 patients with secondary blood disorders. Cancer Genet. Cytogenet. 22:1986;309-317.
-
(1986)
Cancer Genet. Cytogenet.
, vol.22
, pp. 309-317
-
-
Benitez, J.1
Carbonell, F.2
Ferro, T.3
Prieto, F.4
Sanchez Fayos, J.5
-
73
-
-
0024423029
-
Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts
-
Dewald G.W., Brecher M., Travis L.B., Stupca P.J. Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts. Cancer Genet. Cytogenet. 42:1989;173-185.
-
(1989)
Cancer Genet. Cytogenet.
, vol.42
, pp. 173-185
-
-
Dewald, G.W.1
Brecher, M.2
Travis, L.B.3
Stupca, P.J.4
-
74
-
-
0020053658
-
Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia
-
Dewald G.W., Pierre R.V., Phyliky R.L. Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia. Blood. 59:1982;100-105.
-
(1982)
Blood
, vol.59
, pp. 100-105
-
-
Dewald, G.W.1
Pierre, R.V.2
Phyliky, R.L.3
|