-
1
-
-
0033780541
-
The management of neoplastic disorders of haematopoiesis in children with Down's syndrome
-
Lange B. The management of neoplastic disorders of haematopoiesis in children with Down's syndrome. Br J Haematol. 2000;110:512-524.
-
(2000)
Br J Haematol
, vol.110
, pp. 512-524
-
-
Lange, B.1
-
2
-
-
0036156450
-
Down syndrome and the transient myeloproliferative disorder: Why is it transient?
-
Taub JW, Ravindranath Y. Down syndrome and the transient myeloproliferative disorder: why is it transient? J Pediatr Hematol Oncol. 2002;24:6-8.
-
(2002)
J Pediatr Hematol Oncol
, vol.24
, pp. 6-8
-
-
Taub, J.W.1
Ravindranath, Y.2
-
3
-
-
0037355255
-
Transient leukaemia - A benign form of leukaemia in newborn infants with trisomy 21
-
Zipursky A. Transient leukaemia-a benign form of leukaemia in newborn infants with trisomy 21. Br J Haematol. 2003;120:930-938.
-
(2003)
Br J Haematol
, vol.120
, pp. 930-938
-
-
Zipursky, A.1
-
4
-
-
0036156276
-
Transient myeloproliferative disorder, a disorder with too few data and many unanswered questions: Does it contain an important piece of the puzzle to understanding hematopoiesis and acute myelogenous leukemia?
-
Gamis AS Hilden JM. Transient myeloproliferative disorder, a disorder with too few data and many unanswered questions: does it contain an important piece of the puzzle to understanding hematopoiesis and acute myelogenous leukemia? J Pediatr Hematol Oncol. 2002;24:2-5.
-
(2002)
J Pediatr Hematol Oncol
, vol.24
, pp. 2-5
-
-
Gamis, A.S.1
Hilden, J.M.2
-
6
-
-
0030986775
-
Leukemia and/or myeloproliferative syndrome in neonates with Down syndrome
-
Zipursky A, Brown E, Christensen H, Sutherland R, Doyle J. Leukemia and/or myeloproliferative syndrome in neonates with Down syndrome. Semin Perinatol. 1997;21:97-101.
-
(1997)
Semin Perinatol
, vol.21
, pp. 97-101
-
-
Zipursky, A.1
Brown, E.2
Christensen, H.3
Sutherland, R.4
Doyle, J.5
-
7
-
-
0034981492
-
Fetal hydrops and hepatosplenomegaly in the second half of pregnancy: A sign of myeloproliferative disorder in fetuses with trisomy 21
-
Smrcek JM, Baschat AA, Germer U, Gloeckner-Hofmann K, Gembruch U. Fetal hydrops and hepatosplenomegaly in the second half of pregnancy: a sign of myeloproliferative disorder in fetuses with trisomy 21. Ultrasound Obstet Gynecol. 2001;17:403-409.
-
(2001)
Ultrasound Obstet Gynecol
, vol.17
, pp. 403-409
-
-
Smrcek, J.M.1
Baschat, A.A.2
Germer, U.3
Gloeckner-Hofmann, K.4
Gembruch, U.5
-
8
-
-
0029838764
-
Myelodysplasia and acute myelogenous leukemia in Down's syndrome: A report of 40 children of the AML-BFM Study Group
-
Creutzig U, Ritter J, Vormoor J, et al J. Myelodysplasia and acute myelogenous leukemia in Down's syndrome: a report of 40 children of the AML-BFM Study Group. Leukemia. 1996;10:1677-1686.
-
(1996)
Leukemia
, vol.10
, pp. 1677-1686
-
-
Creutzig, U.1
Ritter, J.2
Vormoor, J.3
-
9
-
-
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, et al. 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. 1998;91:608-615.
-
(1998)
Blood
, vol.91
, pp. 608-615
-
-
Lange, B.1
Kobrinsky, N.2
Barnard, D.3
-
10
-
-
0342905433
-
Risks of leukaemia and solid tumours in individuals with Down's syndrome
-
Hasle H, Clemmensen IH, Mikkelsen M. Risks of leukaemia and solid tumours in individuals with Down's syndrome. Lancet. 2000;355:165-169.
-
(2000)
Lancet
, vol.355
, pp. 165-169
-
-
Hasle, H.1
Clemmensen, I.H.2
Mikkelsen, M.3
-
11
-
-
0029091379
-
Ultrastructural studies of the megakaryoblastic leukemias of Down syndrome
-
ZipurskyA, Christensen H, De Harven E. Ultrastructural studies of the megakaryoblastic leukemias of Down syndrome. Leuk Lymphoma. 1995;18:341-347.
-
(1995)
Leuk Lymphoma
, vol.18
, pp. 341-347
-
-
Zipursky, A.1
Christensen, H.2
De Harven, E.3
-
12
-
-
0034764037
-
Transient myeloproliferative disorder and acute myeloid leukemia in Down syndrome: An immunophenotypic analysis
-
Karandikar NJ, Aquino DB, McKenna RW, Kroft SH. Transient myeloproliferative disorder and acute myeloid leukemia in Down syndrome: an immunophenotypic analysis. Am J Clin Pathol. 2001;116:204-210.
-
(2001)
Am J Clin Pathol
, vol.116
, pp. 204-210
-
-
Karandikar, N.J.1
Aquino, D.B.2
McKenna, R.W.3
Kroft, S.H.4
-
13
-
-
0026639952
-
Mixed phenotype of blasts in acute megakaryocytic leukaemia and transient abnormal myelopoiesis in Down's syndrome
-
Yumura-Yagi K, Hara J, Kurahashi H, et al. Mixed phenotype of blasts in acute megakaryocytic leukaemia and transient abnormal myelopoiesis in Down's syndrome. Br J Haematol. 1992;81:520-525.
-
(1992)
Br J Haematol
, vol.81
, pp. 520-525
-
-
Yumura-Yagi, K.1
Hara, J.2
Kurahashi, H.3
-
14
-
-
0034655478
-
Immunophenotype of a transient myeloproliferative disorder in a newborn with trisomy 21
-
Girodon F, Favre B, Couillaud G, Carli PM, Parmeland C, Maynadie M. Immunophenotype of a transient myeloproliferative disorder in a newborn with trisomy 21. Cytometry. 2000;42:118-122.
-
(2000)
Cytometry
, vol.42
, pp. 118-122
-
-
Girodon, F.1
Favre, B.2
Couillaud, G.3
Carli, P.M.4
Parmeland, C.5
Maynadie, M.6
-
15
-
-
0037100420
-
Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): A study of the Groupe Francais de Cytogenetique Hematologique (GFCH)
-
Dastugue N, Lafage-Pochitaloff M, Pages MP, et al. Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Francais de Cytogenetique Hematologique (GFCH). Blood. 2002;100:618-626.
-
(2002)
Blood
, vol.100
, pp. 618-626
-
-
Dastugue, N.1
Lafage-Pochitaloff, M.2
Pages, M.P.3
-
16
-
-
0036727413
-
Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome
-
Wechsler J, Greene M, McDevitt MA, et al. Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome. Nat Genet. 2002;32:148-152.
-
(2002)
Nat Genet
, vol.32
, pp. 148-152
-
-
Wechsler, J.1
Greene, M.2
McDevitt, M.A.3
-
17
-
-
0038142390
-
Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis
-
Mundschau G, Gurbuxani S, Gamis AS, Greene ME, Arceci RJ, Crispino JD. Mutagenesis of GATA1 is an initiating event in Down syndrome leukemogenesis. Blood. 2003;101:4298-4300.
-
(2003)
Blood
, vol.101
, pp. 4298-4300
-
-
Mundschau, G.1
Gurbuxani, S.2
Gamis, A.S.3
Greene, M.E.4
Arceci, R.J.5
Crispino, J.D.6
-
18
-
-
0038142350
-
GATA1 A mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome
-
Hitzler JK, Cheung J, Li Y, Scherer SW, Zipursky A. GATA1 A. GATAL mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndrome. Blood. 2003;101:4301-4304.
-
(2003)
Blood
, vol.101
, pp. 4301-4304
-
-
Hitzler, J.K.1
Cheung, J.2
Li, Y.3
Scherer, S.W.4
Zipursky, A.5
-
19
-
-
0042243593
-
Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
-
Rainis L, Bercovich D, Strehl S, et al. Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood. 2003;102:981-986.
-
(2003)
Blood
, vol.102
, pp. 981-986
-
-
Rainis, L.1
Bercovich, D.2
Strehl, S.3
-
20
-
-
0037906527
-
Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder
-
Groet J, McElwaine S, Spinelli M, et al. Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder. Lancet. 2003;361:1617-1620.
-
(2003)
Lancet
, vol.361
, pp. 1617-1620
-
-
Groet, J.1
McElwaine, S.2
Spinelli, M.3
-
21
-
-
0036720398
-
The roles of FLT3 in hematopoiesis and leukemia
-
Gilliland DG, Griffin JD. The roles of FLT3 in hematopoiesis and leukemia. Blood. 2002;100:1532-1542.
-
(2002)
Blood
, vol.100
, pp. 1532-1542
-
-
Gilliland, D.G.1
Griffin, J.D.2
-
22
-
-
0036725138
-
A leukemogenic twist for GATA1
-
Look AT. A leukemogenic twist for GATA1. Nat Genet. 2002;32:83-84.
-
(2002)
Nat Genet
, vol.32
, pp. 83-84
-
-
Look, A.T.1
-
23
-
-
0029876726
-
The transcriptional control of hematopoiesis
-
Shivdasani RA, Orkin SH. The transcriptional control of hematopoiesis. Blood. 1996;87:4025-4039.
-
(1996)
Blood
, vol.87
, pp. 4025-4039
-
-
Shivdasani, R.A.1
Orkin, S.H.2
-
24
-
-
0034303586
-
Diversification of haematopoieic stem cells to specific lineages
-
Orkin SH. Diversification of haematopoieic stem cells to specific lineages. Nature Reviews Genetics. 2000;1:57-64.
-
(2000)
Nature Reviews Genetics
, vol.1
, pp. 57-64
-
-
Orkin, S.H.1
-
25
-
-
0035480007
-
Hematopoietic development: A balancing act
-
Cantor AB Orkin SH. Hematopoietic development: a balancing act. Curr Opin Genet Dev. 2001;11:513-519.
-
(2001)
Curr Opin Genet Dev
, vol.11
, pp. 513-519
-
-
Cantor, A.B.1
Orkin, S.H.2
-
26
-
-
0030926006
-
A lineage-selective knockout establishes the critical role of transcription factor GATA-1 in megakaryocyte growth and platelet development
-
Shivdasani RA, Fujiwara Y, McDevitt MA, Orkin SH. A lineage-selective knockout establishes the critical role of transcription factor GATA-1 in megakaryocyte growth and platelet development. EMBO J. 1997;16:3965-3973.
-
(1997)
EMBO J
, vol.16
, pp. 3965-3973
-
-
Shivdasani, R.A.1
Fujiwara, Y.2
McDevitt, M.A.3
Orkin, S.H.4
-
27
-
-
0033134831
-
Consequences of GATA-1 deficiency in megakaryocytes and platelets
-
Vyas P, Ault K, Jackson CW, Orkin SH, Shivdasani RA. Consequences of GATA-1 deficiency in megakaryocytes and platelets. Blood. 1999;93:2867-2875.
-
(1999)
Blood
, vol.93
, pp. 2867-2875
-
-
Vyas, P.1
Ault, K.2
Jackson, C.W.3
Orkin, S.H.4
Shivdasani, R.A.5
-
28
-
-
0034052854
-
Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1
-
Nichols KE, Crispino JD Poncz M, et al. Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1, Nat Genet. 2000;24:266-270.
-
(2000)
Nat Genet
, vol.24
, pp. 266-270
-
-
Nichols, K.E.1
Crispino, J.D.2
Poncz, M.3
-
29
-
-
0035412362
-
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation
-
Freson K, Devriendt K, Matthijs G, et al. Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation. Blood. 2001;98:85-92.
-
(2001)
Blood
, vol.98
, pp. 85-92
-
-
Freson, K.1
Devriendt, K.2
Matthijs, G.3
-
30
-
-
0037081819
-
Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation
-
Freson K, Matthijs G, Thys C, et al. Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation. Hum Mol Genet. 2002;11:147-152.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 147-152
-
-
Freson, K.1
Matthijs, G.2
Thys, C.3
-
31
-
-
0037105495
-
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction
-
Yu C, Niakan KK, Matsushita M, Stamatoyannopoulos G, Orkin SH, Raskind WH. X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction. Blood. 2002;100:2040-2045.
-
(2002)
Blood
, vol.100
, pp. 2040-2045
-
-
Yu, C.1
Niakan, K.K.2
Matsushita, M.3
Stamatoyannopoulos, G.4
Orkin, S.H.5
Raskind, W.H.6
-
32
-
-
0035525746
-
X-linked thrombocytopenia caused by a novel mutation of GATA-1
-
Mehaffey MG, Newton AL, Gandhi MJ, Crossley M, Drachman JG. X-linked thrombocytopenia caused by a novel mutation of GATA-1. Blood. 2001;98:2681-2688.
-
(2001)
Blood
, vol.98
, pp. 2681-2688
-
-
Mehaffey, M.G.1
Newton, A.L.2
Gandhi, M.J.3
Crossley, M.4
Drachman, J.G.5
-
33
-
-
0031471132
-
Backtracking leukemia to birth: Identification of clonotypic gene fusion sequences in neonatal blood spots
-
Gale K, Ford A, Repp R, et al. Backtracking leukemia to birth: identification of clonotypic gene fusion sequences in neonatal blood spots. Proc Natl Acad Sci USA. 1997;94:13950-13954.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13950-13954
-
-
Gale, K.1
Ford, A.2
Repp, R.3
-
34
-
-
0033619452
-
Prenatal origin of acute lymphoblastic leukaemia in children
-
Wiemels JL, Cazzaniga G, Daniotti M, et al. Prenatal origin of acute lymphoblastic leukaemia in children. Lancet. 1999;354:1499-1503.
-
(1999)
Lancet
, vol.354
, pp. 1499-1503
-
-
Wiemels, J.L.1
Cazzaniga, G.2
Daniotti, M.3
-
35
-
-
0037092955
-
In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia
-
Wiemels J, Xiao Z, Buffler P, et al. In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia. Blood. 2002;99:3801-3805.
-
(2002)
Blood
, vol.99
, pp. 3801-3805
-
-
Wiemels, J.1
Xiao, Z.2
Buffler, P.3
-
36
-
-
0037062496
-
Chromosome translocations and covert leukemic clones are generated during normal fetal development
-
Mori H, Colman S, Xiao Z, et al. Chromosome translocations and covert leukemic clones are generated during normal fetal development. Proc Natl Acad Sci U S A. 2002;99:8242-8247.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 8242-8247
-
-
Mori, H.1
Colman, S.2
Xiao, Z.3
-
37
-
-
0014707398
-
Malformations and leukemia in children with Down's syndrome
-
Fabia J, Drolette M. Malformations and leukemia in children with Down's syndrome. Pediatrics. 1970;45:60-70.
-
(1970)
Pediatrics
, vol.45
, pp. 60-70
-
-
Fabia, J.1
Drolette, M.2
-
38
-
-
0031750106
-
A tumor profile in Down syndrome
-
Satge D, Sommelet D, GeneixA, Nishi M, Malet P, Vekemans M. A tumor profile in Down syndrome. Am J Med Genet. 1998;78:207-216.
-
(1998)
Am J Med Genet
, vol.78
, pp. 207-216
-
-
Satge, D.1
Sommelet, D.2
Geneix, A.3
Nishi, M.4
Malet, P.5
Vekemans, M.6
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