-
1
-
-
0345600172
-
Classification and clinical manifestations of the hematopoietic stem cell disorders
-
Williams W, Beutler E, Erslev A, Lichtmann M (eds): New York, NY, McGraw-Hill
-
Lichtmann M: Classification and clinical manifestations of the hematopoietic stem cell disorders, in Williams W, Beutler E, Erslev A, Lichtmann M (eds): Hematology. New York, NY, McGraw-Hill, 1990, p 148
-
(1990)
Hematology
, pp. 148
-
-
Lichtmann, M.1
-
2
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DAG, Gralnick HR, Sultan C: Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 51:189, 1982
-
(1982)
Br J Haematol
, vol.51
, pp. 189
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.G.5
Gralnick, H.R.6
Sultan, C.7
-
3
-
-
0025355946
-
Childhood myelodysplasia: Suggested classification as myelodysplastic syndromes
-
Brandwein JM, Horsman D, Eaves A, Eaves CJ, Massing BG, Wadsworth LD, Rogers PCJ, Kalousek D: Childhood myelodysplasia: Suggested classification as myelodysplastic syndromes. Am J Pediatr Hematol Oncol 12:63, 1990
-
(1990)
Am J Pediatr Hematol Oncol
, vol.12
, pp. 63
-
-
Brandwein, J.M.1
Horsman, D.2
Eaves, A.3
Eaves, C.J.4
Massing, B.G.5
Wadsworth, L.D.6
Rogers, P.C.J.7
Kalousek, D.8
-
4
-
-
0026763828
-
Myelodysplastische erkrankungen im kindesalter
-
Niemeyer C, Stollmann-Gibbels B, Ebell W, Gaedicke G, Creutzig U: Myelodysplastische erkrankungen im Kindesalter. Kin Padiatr 204:190, 1992
-
(1992)
Kin Padiatr
, vol.204
, pp. 190
-
-
Niemeyer, C.1
Stollmann-Gibbels, B.2
Ebell, W.3
Gaedicke, G.4
Creutzig, U.5
-
5
-
-
0030977399
-
Chronic myelomonocytic leukemia in childhood: A retrospective analysis of 110 cases
-
Niemeyer C, Arico M, Basso G, Biondi A, Cantu Rajnoldi A, Creutzig U, Haas O, Harbott J, Hasle H, Kerndrup G, Locatelli F, Mann G, Stollmann-Gibbels B, van't Veer-Korhof E, van Wering E, Zimmermann M: Chronic myelomonocytic leukemia in childhood: A retrospective analysis of 110 cases. Blood 89:3534, 1997
-
(1997)
Blood
, vol.89
, pp. 3534
-
-
Niemeyer, C.1
Arico, M.2
Basso, G.3
Biondi, A.4
Cantu Rajnoldi, A.5
Creutzig, U.6
Haas, O.7
Harbott, J.8
Hasle, H.9
Kerndrup, G.10
Locatelli, F.11
Mann, G.12
Stollmann-Gibbels, B.13
Van't Veer-Korhof, E.14
Van Wering, E.15
Zimmermann, M.16
-
6
-
-
0026569705
-
Bone marrow dysfunctions preceding acute leukemia in children: A clinical study
-
Wegelius R: Bone marrow dysfunctions preceding acute leukemia in children: A clinical study. Leuk Res 16:71, 1992
-
(1992)
Leuk Res
, vol.16
, pp. 71
-
-
Wegelius, R.1
-
7
-
-
0028069002
-
The chronic myeloid leukaemias: Guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British cooperative Leukaemia group
-
Bennett J, Catovsky D, Daniel M, Flandrin G, Galton D, Gralnick H, Sultan C, Cox C: The chronic myeloid leukaemias: Guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia Group. Br J Haematol 87:746, 1994
-
(1994)
Br J Haematol
, vol.87
, pp. 746
-
-
Bennett, J.1
Catovsky, D.2
Daniel, M.3
Flandrin, G.4
Galton, D.5
Gralnick, H.6
Sultan, C.7
Cox, C.8
-
8
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P, Cox C, LeBeau M, Fenaux P, Morel M, Sanz G, Sanz M, Vallespi T, Hamblin T, Oscier D, Ohyashiki K, Toyama K, Aul C, Mufti G, Bennett J: International scoring system for evaluating prognosis in myelodysplastic syndromes. J Clin Oncol 89:2079, 1997
-
(1997)
J Clin Oncol
, vol.89
, pp. 2079
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.3
Fenaux, P.4
Morel, M.5
Sanz, G.6
Sanz, M.7
Vallespi, T.8
Hamblin, T.9
Oscier, D.10
Ohyashiki, K.11
Toyama, K.12
Aul, C.13
Mufti, G.14
Bennett, J.15
-
9
-
-
0026063878
-
Selective hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors
-
Emanuel PD, Bates LJ, Castleberry RP, Gualtieri RJ, Zuckerman KS: Selective hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors. Blood 77:925, 1991
-
(1991)
Blood
, vol.77
, pp. 925
-
-
Emanuel, P.D.1
Bates, L.J.2
Castleberry, R.P.3
Gualtieri, R.J.4
Zuckerman, K.S.5
-
10
-
-
0026756459
-
Myelodysplastic syndromes in childhood: A population based study of nine cases
-
Hasle H, Jacobsen BB, Pedersen NT: Myelodysplastic syndromes in childhood: A population based study of nine cases. Br J Haematol 81:495, 1992
-
(1992)
Br J Haematol
, vol.81
, pp. 495
-
-
Hasle, H.1
Jacobsen, B.B.2
Pedersen, N.T.3
-
11
-
-
0030712155
-
Occurrence of myeloproliferative disorder in patients with Noonan syndrome
-
Bader-Meunier B, Tchernia G, Mielot F, Fontaine J, Thomas C, Lyonnet S, Lavergne JM, Dommergues JP: Occurrence of myeloproliferative disorder in patients with Noonan syndrome. J Pediatr 130:885, 1997
-
(1997)
J Pediatr
, vol.130
, pp. 885
-
-
Bader-Meunier, B.1
Tchernia, G.2
Mielot, F.3
Fontaine, J.4
Thomas, C.5
Lyonnet, S.6
Lavergne, J.M.7
Dommergues, J.P.8
-
12
-
-
0021233189
-
Subacute and chronic myelomonocytic leukemia in children (juvenile CML)
-
Castro-Malaspina H, Schaison G, Passe S, Pasquier A, Berger R, Bayle-Weisgerber C, Miller D, Seligmann M, Bernard J: Subacute and chronic myelomonocytic leukemia in children (juvenile CML). Cancer 54:675, 1984
-
(1984)
Cancer
, vol.54
, pp. 675
-
-
Castro-Malaspina, H.1
Schaison, G.2
Passe, S.3
Pasquier, A.4
Berger, R.5
Bayle-Weisgerber, C.6
Miller, D.7
Seligmann, M.8
Bernard, J.9
-
13
-
-
0028910402
-
Childhood monosomy 7: Epidemiology, biology and mechanistic implications
-
Luna-Fineman S, Shannon K, Lange B: Childhood monosomy 7: Epidemiology, biology and mechanistic implications. Blood 85:1985, 1995
-
(1995)
Blood
, vol.85
, pp. 1985
-
-
Luna-Fineman, S.1
Shannon, K.2
Lange, B.3
-
14
-
-
0028967873
-
Pediatric myelodysplasia: A study of 68 children and a new prognostic scoring system
-
Passmore S, Hann C, Stiller P, Ramani G, Swansbury B, Gibbons B, Reeves B, Chessells J: Pediatric myelodysplasia: A study of 68 children and a new prognostic scoring system. Blood 85:1742, 1995
-
(1995)
Blood
, vol.85
, pp. 1742
-
-
Passmore, S.1
Hann, C.2
Stiller, P.3
Ramani, G.4
Swansbury, B.5
Gibbons, B.6
Reeves, B.7
Chessells, J.8
-
15
-
-
0030280090
-
Juvenile myelomonocytic leukemia: Molecular understanding and prospects of therapy
-
Emanuel P, Shannon K, Castelberry R: Juvenile myelomonocytic leukemia: molecular understanding and prospects of therapy. Mol Med Today 2:468, 1996
-
(1996)
Mol Med Today
, vol.2
, pp. 468
-
-
Emanuel, P.1
Shannon, K.2
Castelberry, R.3
-
16
-
-
0030843626
-
Juvenile myelomonocytic leukemia
-
Arico M, Biondi A, Pui C: Juvenile myelomonocytic leukemia. Blood 90:479, 1997
-
(1997)
Blood
, vol.90
, pp. 479
-
-
Arico, M.1
Biondi, A.2
Pui, C.3
-
17
-
-
0142099097
-
Response: Differentiating juvenile myelomonocytic leukemia from infectious disease
-
Niemeyer C, Fenu S, Hasle H, Mann G, Stary J, van Wering E: Response: Differentiating juvenile myelomonocytic leukemia from infectious disease. Blood 91:365, 1998
-
(1998)
Blood
, vol.91
, pp. 365
-
-
Niemeyer, C.1
Fenu, S.2
Hasle, H.3
Mann, G.4
Stary, J.5
Van Wering, E.6
-
18
-
-
0021162175
-
Bone marrow histology in myelodysplastic syndromes. II prognostic value of abnormal localization of immature precursors in MDS
-
Tricot G, De Wolf-Peeters C, Vlietinck P, Werwilghen R: Bone marrow histology in myelodysplastic syndromes. II Prognostic value of abnormal localization of immature precursors in MDS. Br J Haematol 58:217, 1984
-
(1984)
Br J Haematol
, vol.58
, pp. 217
-
-
Tricot, G.1
De Wolf-Peeters, C.2
Vlietinck, P.3
Werwilghen, R.4
-
19
-
-
33845382806
-
Nonparametric estimation from incomplete observations
-
Kaplan E, Meier P: Nonparametric estimation from incomplete observations. J Am Stat Assoc 53:457, 1958
-
(1958)
J Am Stat Assoc
, vol.53
, pp. 457
-
-
Kaplan, E.1
Meier, P.2
-
20
-
-
0017365573
-
Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. Analysis and examples
-
Peto R, Pike M, Armitage P, Breslow N, Cox D, Howard S, Mantel N, McPherson K, Peto J, Smith P: Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. Analysis and examples. Br J Cancer 35:1, 1977
-
(1977)
Br J Cancer
, vol.35
, pp. 1
-
-
Peto, R.1
Pike, M.2
Armitage, P.3
Breslow, N.4
Cox, D.5
Howard, S.6
Mantel, N.7
McPherson, K.8
Peto, J.9
Smith, P.10
-
21
-
-
0031406504
-
Equal participation of minority patients in U.S. National pediatric cancer clinical trials
-
Bleyer W, Tejeda H, Murphy S, Brawley O, Smith M, Ungerleider R: Equal participation of minority patients in U.S. national pediatric cancer clinical trials. J Pediatr Hematol Oncol 19:423, 1997
-
(1997)
J Pediatr Hematol Oncol
, vol.19
, pp. 423
-
-
Bleyer, W.1
Tejeda, H.2
Murphy, S.3
Brawley, O.4
Smith, M.5
Ungerleider, R.6
-
22
-
-
9044229714
-
Morphologic, immunologic, and cytogenetic classification of acute myeloid leukemia and myelodysplastic syndrome in childhood: A report from the children's cancer group
-
Barnard D, Kalousek DK, Wiersma SR, Lange BJ, Benjamin DR, Arthur DC, Burckley JD, Kobrinsky N, Neudorf S, Sanders J, Miller LP, DeSwarte J, Shina DC, Hammond GD, Woods WG: Morphologic, immunologic, and cytogenetic classification of acute myeloid leukemia and myelodysplastic syndrome in childhood: A report from the Children's Cancer Group. Leukemia 10:5, 1996
-
(1996)
Leukemia
, vol.10
, pp. 5
-
-
Barnard, D.1
Kalousek, D.K.2
Wiersma, S.R.3
Lange, B.J.4
Benjamin, D.R.5
Arthur, D.C.6
Burckley, J.D.7
Kobrinsky, N.8
Neudorf, S.9
Sanders, J.10
Miller, L.P.11
DeSwarte, J.12
Shina, D.C.13
Hammond, G.D.14
Woods, W.G.15
-
23
-
-
0027478524
-
T(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia
-
Wessels J, Febbe W, van der Keur D, Landegent J, van der Plas D, den Ottolander G, Roozendaal K, Beverstock G: t(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia. Cancer Genet Cytogenet 65:7, 1993
-
(1993)
Cancer Genet Cytogenet
, vol.65
, pp. 7
-
-
Wessels, J.1
Febbe, W.2
Van Der Keur, D.3
Landegent, J.4
Van Der Plas, D.5
Den Ottolander, G.6
Roozendaal, K.7
Beverstock, G.8
-
24
-
-
0027979146
-
Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders
-
Shannon KM, O'Connell P, Martin GA, Paderanga D, Olson K, Dinndorf P, McCormick F: Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med 330:597, 1994
-
(1994)
N Engl J Med
, vol.330
, pp. 597
-
-
Shannon, K.M.1
O'Connell, P.2
Martin, G.A.3
Paderanga, D.4
Olson, K.5
Dinndorf, P.6
McCormick, F.7
-
25
-
-
0028224348
-
Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland DG: Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77:307, 1994
-
(1994)
Cell
, vol.77
, pp. 307
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
26
-
-
0029888193
-
Myelodysplastic syndrome with t(5;12)(q31;p12-p13) and eosinophilia: A pediatric case with review of the literature
-
Pellier I, LeMoine P, Rialland X, Francois S, Baranger L, Blanchet O, Larget-Piet L, Ifrah N: Myelodysplastic syndrome with t(5;12)(q31;p12-p13) and eosinophilia: A pediatric case with review of the literature. J Pediatric Hematol Oncol 18:285, 1996
-
(1996)
J Pediatric Hematol Oncol
, vol.18
, pp. 285
-
-
Pellier, I.1
LeMoine, P.2
Rialland, X.3
Francois, S.4
Baranger, L.5
Blanchet, O.6
Larget-Piet, L.7
Ifrah, N.8
-
27
-
-
9044251606
-
Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells
-
Bollag G, Clapp D, Shih S, Adler F, Zhang Y, Thompson P, Lange B, Freedman M, McCormick F, Jacks T: Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells. Nat Genet 12:144, 1996
-
(1996)
Nat Genet
, vol.12
, pp. 144
-
-
Bollag, G.1
Clapp, D.2
Shih, S.3
Adler, F.4
Zhang, Y.5
Thompson, P.6
Lange, B.7
Freedman, M.8
McCormick, F.9
Jacks, T.10
-
29
-
-
0028344097
-
Mutations of the N-ras gene in juvenile chronic myelogenous leukemia
-
Miyauchi J, Asada M, Sasaki M, Tsunematsu Y, Kojima S, Mizutani S: Mutations of the N-ras gene in juvenile chronic myelogenous leukemia. Blood 83:2248, 1994
-
(1994)
Blood
, vol.83
, pp. 2248
-
-
Miyauchi, J.1
Asada, M.2
Sasaki, M.3
Tsunematsu, Y.4
Kojima, S.5
Mizutani, S.6
-
30
-
-
0030947237
-
Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders
-
Side L, Taylor B, Cayouett M, Conner E, Thompson P, Luce M, Shannon K: Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders. N Engl J Med 336:1713, 1997
-
(1997)
N Engl J Med
, vol.336
, pp. 1713
-
-
Side, L.1
Taylor, B.2
Cayouett, M.3
Conner, E.4
Thompson, P.5
Luce, M.6
Shannon, K.7
-
31
-
-
9044248952
-
Myelodysplastic syndromes in childhood: Report of 49 patients from a French multicenter study. French society of paediatric haematology and immunology
-
Bader-Meunier B, Mielot F, Tchernia G, Buisine J, Delsol G, Duchayne E, Lemerle S, Leverger G, de Lumley L, Manel AM: Myelodysplastic syndromes in childhood: Report of 49 patients from a French multicenter study. French Society of Paediatric Haematology and Immunology. Br J Haematol 92:344, 1996
-
(1996)
Br J Haematol
, vol.92
, pp. 344
-
-
Bader-Meunier, B.1
Mielot, F.2
Tchernia, G.3
Buisine, J.4
Delsol, G.5
Duchayne, E.6
Lemerle, S.7
Leverger, G.8
De Lumley, L.9
Manel, A.M.10
-
32
-
-
0032125716
-
Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without clinical evidence of neurofibromatosis, type 1
-
Side L, Emanuel P, Taylor B, Franklin J, Thompson P, Castleberry R, Shannon K: Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without clinical evidence of neurofibromatosis, type 1. Blood 92:267, 1998
-
(1998)
Blood
, vol.92
, pp. 267
-
-
Side, L.1
Emanuel, P.2
Taylor, B.3
Franklin, J.4
Thompson, P.5
Castleberry, R.6
Shannon, K.7
-
33
-
-
16744366910
-
Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome: Children's cancer group studies 2861 and 2891
-
Lange B, Kobrinsky N, Barnard D, Arthur D, Buckley J, Howells W, Gold S, Sanders J, Neudorf S, Smith F, Woods W: Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome: Children's Cancer Group Studies 2861 and 2891. Blood 91:608, 1998
-
(1998)
Blood
, vol.91
, pp. 608
-
-
Lange, B.1
Kobrinsky, N.2
Barnard, D.3
Arthur, D.4
Buckley, J.5
Howells, W.6
Gold, S.7
Sanders, J.8
Neudorf, S.9
Smith, F.10
Woods, W.11
-
34
-
-
0025959243
-
Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the international fanconi anemia registry
-
Auerbach A, Allen R: Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry. Cancer Genet Cytogenet 51:1, 1991
-
(1991)
Cancer Genet Cytogenet
, vol.51
, pp. 1
-
-
Auerbach, A.1
Allen, R.2
-
35
-
-
0028328265
-
Identification of a nonsense mutation in the granulocyte-colony stimulating factor receptor in severe congenital neutropenia
-
Dong F, Hoefsloot L, Schelen A, Broeders C, Meijer Y, Veerman A, Touw I, Lowenberg B: Identification of a nonsense mutation in the granulocyte-colony stimulating factor receptor in severe congenital neutropenia. Proc Natl Acad Sci USA 91:4480, 1994
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 4480
-
-
Dong, F.1
Hoefsloot, L.2
Schelen, A.3
Broeders, C.4
Meijer, Y.5
Veerman, A.6
Touw, I.7
Lowenberg, B.8
-
36
-
-
0028206608
-
Granulocyte colony-stimulating factor (G-CSF) production and G-CSF receptor structure in patients with congenital neutropenia
-
Guba S, Sartor C, Hutchinson R, Boxer L, Emerson S: Granulocyte colony-stimulating factor (G-CSF) production and G-CSF receptor structure in patients with congenital neutropenia. Blood 83:1486, 1994
-
(1994)
Blood
, vol.83
, pp. 1486
-
-
Guba, S.1
Sartor, C.2
Hutchinson, R.3
Boxer, L.4
Emerson, S.5
-
37
-
-
0028807618
-
Monosomy 7 and activating RAS mutations accompany malignant transformation in patients with congenital neutropenia
-
Kalra R, Dale D, Freedman M, Bonilla M, Weinblatt M, Ganser A, Bowman P, Abish S, Priest J, Oseas R, Shannon K: Monosomy 7 and activating RAS mutations accompany malignant transformation in patients with congenital neutropenia. Blood 86:4579, 1995
-
(1995)
Blood
, vol.86
, pp. 4579
-
-
Kalra, R.1
Dale, D.2
Freedman, M.3
Bonilla, M.4
Weinblatt, M.5
Ganser, A.6
Bowman, P.7
Abish, S.8
Priest, J.9
Oseas, R.10
Shannon, K.11
-
38
-
-
0027372507
-
Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: A report on 408 cases
-
Morel P, Hebbar M, Lai JL, Duhamel A, Preudomme C, Wattel E, Bauters F, Fenaux P: Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: A report on 408 cases. Leukemia 7:1315, 1993
-
(1993)
Leukemia
, vol.7
, pp. 1315
-
-
Morel, P.1
Hebbar, M.2
Lai, J.L.3
Duhamel, A.4
Preudomme, C.5
Wattel, E.6
Bauters, F.7
Fenaux, P.8
-
39
-
-
0026502986
-
Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: Epidemiology and molecular analysis
-
Shannon KM, Watterson J, Johnson P, O'Connell P, Lange B, Shah N, Steinherz P, Kan YW, Priest JR: Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: Epidemiology and molecular analysis. Blood 79:1311, 1992
-
(1992)
Blood
, vol.79
, pp. 1311
-
-
Shannon, K.M.1
Watterson, J.2
Johnson, P.3
O'Connell, P.4
Lange, B.5
Shah, N.6
Steinherz, P.7
Kan, Y.W.8
Priest, J.R.9
-
40
-
-
0022368551
-
Childhood bone marrow monosomy 7 syndrome: A familial disorder?
-
Carroll WL, Morgan R, Glader BE: Childhood bone marrow monosomy 7 syndrome: A familial disorder? J Pediatr 107:578, 1985
-
(1985)
J Pediatr
, vol.107
, pp. 578
-
-
Carroll, W.L.1
Morgan, R.2
Glader, B.E.3
-
41
-
-
0026655447
-
Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7
-
Shannon KM, Turhan AG, Rogers PC, Kan YW: Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7. Genomics 14:121, 1992
-
(1992)
Genomics
, vol.14
, pp. 121
-
-
Shannon, K.M.1
Turhan, A.G.2
Rogers, P.C.3
Kan, Y.W.4
-
42
-
-
0026591778
-
Recombinant human granulocyte-colony stimulating factor in the treatment of patients with chronic benign granulocytopenia and congenital agranulocytosis (Kostmann's syndrome)
-
Imashuku S, Tsuchida M, Sasaki M, Shimokawa T, Nakamura H, Matsuyama T, Taniguchi N, Oda M, Higuchi S, Ishimoto K: Recombinant human granulocyte-colony stimulating factor in the treatment of patients with chronic benign granulocytopenia and congenital agranulocytosis (Kostmann's syndrome). Acta Paediatr 81:133, 1992
-
(1992)
Acta Paediatr
, vol.81
, pp. 133
-
-
Imashuku, S.1
Tsuchida, M.2
Sasaki, M.3
Shimokawa, T.4
Nakamura, H.5
Matsuyama, T.6
Taniguchi, N.7
Oda, M.8
Higuchi, S.9
Ishimoto, K.10
-
43
-
-
1842295700
-
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias
-
Fischer K, Fröhling S, Scherer S, McAllisterBrown J, Scholl C, Stilgenbauer S, Tsui L, Lichter P, Döhner H: Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias. Blood 89:2036, 1997
-
(1997)
Blood
, vol.89
, pp. 2036
-
-
Fischer, K.1
Fröhling, S.2
Scherer, S.3
McAllisterBrown, J.4
Scholl, C.5
Stilgenbauer, S.6
Tsui, L.7
Lichter, P.8
Döhner, H.9
-
44
-
-
0023551999
-
Molecular characterization of chromosome 7 long arm deletions in myeloid disorders
-
Kere J, Ruutu T, Lahtinen R, de la Chapelle A: Molecular characterization of chromosome 7 long arm deletions in myeloid disorders. Blood 70:1349, 1987
-
(1987)
Blood
, vol.70
, pp. 1349
-
-
Kere, J.1
Ruutu, T.2
Lahtinen, R.3
De La Chapelle, A.4
-
45
-
-
0024495676
-
Chromosome 7 long arm deletion in myeloid disorders: A narrow breakpoint region in 7q22 defined by molecular mapping
-
Kere J, Ruutu T, Davies KA, Roninson IB, Watkins PC, Winqvist R, de la Chapelle A: Chromosome 7 long arm deletion in myeloid disorders: A narrow breakpoint region in 7q22 defined by molecular mapping. Blood 73:230, 1989
-
(1989)
Blood
, vol.73
, pp. 230
-
-
Kere, J.1
Ruutu, T.2
Davies, K.A.3
Roninson, I.B.4
Watkins, P.C.5
Winqvist, R.6
De La Chapelle, A.7
-
46
-
-
0029821113
-
Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases
-
LeBeau M, Espinosa R, Davis E, Eisenbart J, Larson R, Green E: Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases. Blood 88:1930, 1996
-
(1996)
Blood
, vol.88
, pp. 1930
-
-
LeBeau, M.1
Espinosa, R.2
Davis, E.3
Eisenbart, J.4
Larson, R.5
Green, E.6
-
47
-
-
0029743347
-
Intensive chemotherapy in childhood myelodysplastic syndrome. A comparison with results in acute myeloid leukemia
-
Hasle H, Kerndrup G, Yssing M, Clausen N, Ostergaard E, Jacobsen N, Brock Jacobsen B: Intensive chemotherapy in childhood myelodysplastic syndrome. A comparison with results in acute myeloid leukemia. Leukemia 10:1269, 1996
-
(1996)
Leukemia
, vol.10
, pp. 1269
-
-
Hasle, H.1
Kerndrup, G.2
Yssing, M.3
Clausen, N.4
Ostergaard, E.5
Jacobsen, N.6
Brock Jacobsen, B.7
-
48
-
-
0030765385
-
Effect of diagnosis (refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, or acute myeloid leukemia [AML]) on outcome of AML-type chemotherapy
-
Estey E, Thall P, Beran M, Kantarjian H, Pierce S, Keating M: Effect of diagnosis (refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, or acute myeloid leukemia [AML]) on outcome of AML-type chemotherapy. Blood 90:2969, 1997
-
(1997)
Blood
, vol.90
, pp. 2969
-
-
Estey, E.1
Thall, P.2
Beran, M.3
Kantarjian, H.4
Pierce, S.5
Keating, M.6
-
49
-
-
0021967211
-
Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with acute nonlymphocytic leukemia
-
Woods WG, Nesbit ME, Buckley J, Lampkin BC, McCreadie S, Kim TH, Piomelli S, Kersey JH, Feig S, Bernstein I, Hammond D: Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with acute nonlymphocytic leukemia. J Clin Oncol 3:3, 1985
-
(1985)
J Clin Oncol
, vol.3
, pp. 3
-
-
Woods, W.G.1
Nesbit, M.E.2
Buckley, J.3
Lampkin, B.C.4
McCreadie, S.5
Kim, T.H.6
Piomelli, S.7
Kersey, J.H.8
Feig, S.9
Bernstein, I.10
Hammond, D.11
-
50
-
-
10544241963
-
Role of allogeneic bone marrow transplantation for the treatment of myelodysplastic syndromes in childhood
-
Locatelli F, Zecca M, Niemeyer C, Angelucci E, Arcese G, Bender-Gotze C, Bonetti F, Burdach S, Dini G, Ebell W, Friedrich W, Hasle H, Hermann J, Jacobsen N, Klingebiel T: Role of allogeneic bone marrow transplantation for the treatment of myelodysplastic syndromes in childhood. Bone Marrow Transplant 18:63, 1996
-
(1996)
Bone Marrow Transplant
, vol.18
, pp. 63
-
-
Locatelli, F.1
Zecca, M.2
Niemeyer, C.3
Angelucci, E.4
Arcese, G.5
Bender-Gotze, C.6
Bonetti, F.7
Burdach, S.8
Dini, G.9
Ebell, W.10
Friedrich, W.11
Hasle, H.12
Hermann, J.13
Jacobsen, N.14
Klingebiel, T.15
-
51
-
-
18844465770
-
Allogeneic bone marrow transplantation for chronic myelomonocytic leukemia in childhood: A report from the European working group on Myelodysplastic syndrome in childhood
-
Locatelli F, Niemeyer C, Angelucci E, Bender-Gotze C, Burdach S, Ebell W, Friedrich W, Hasle H, Herman J, Jacobsen N: Allogeneic bone marrow transplantation for chronic myelomonocytic leukemia in childhood: A report from the European Working Group on Myelodysplastic Syndrome in Childhood. J Clin Oncol 15:566, 1997
-
(1997)
J Clin Oncol
, vol.15
, pp. 566
-
-
Locatelli, F.1
Niemeyer, C.2
Angelucci, E.3
Bender-Gotze, C.4
Burdach, S.5
Ebell, W.6
Friedrich, W.7
Hasle, H.8
Herman, J.9
Jacobsen, N.10
-
52
-
-
0023924301
-
Allogeneic marrow transplantation for children with juvenile chronic myelogenous leukemia
-
Sanders JE, Buckner CD, Thomas ED, Fleischer R, Sullivan KM, Appelbaum FA, Storb R: Allogeneic marrow transplantation for children with juvenile chronic myelogenous leukemia. Blood 71:1144, 1988
-
(1988)
Blood
, vol.71
, pp. 1144
-
-
Sanders, J.E.1
Buckner, C.D.2
Thomas, E.D.3
Fleischer, R.4
Sullivan, K.M.5
Appelbaum, F.A.6
Storb, R.7
|