-
1
-
-
0022869420
-
Chromosome abnormalities in the myelodysplastic syndromes
-
S. Heim, and F. Mitelman Chromosome abnormalities in the myelodysplastic syndromes Clin Haematol 15 1986 1003 1021
-
(1986)
Clin Haematol
, vol.15
, pp. 1003-1021
-
-
Heim, S.1
Mitelman, F.2
-
2
-
-
57649119892
-
Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: A report from the US with a focus on some undefined single chromosomal abnormalities
-
O. Pozdnyakova, P.M. Miron, and G. Tang Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities Cancer 113 2008 3331 3340
-
(2008)
Cancer
, vol.113
, pp. 3331-3340
-
-
Pozdnyakova, O.1
Miron, P.M.2
Tang, G.3
-
3
-
-
23744513172
-
Incidence and prognostic significance of karyotype abnormalities in de novo primary myelodysplastic syndromes: A study on 331 patients from a single institution
-
P. Bernasconi, C. Klersy, and M. Boni Incidence and prognostic significance of karyotype abnormalities in de novo primary myelodysplastic syndromes: a study on 331 patients from a single institution Leukemia 19 2005 1424 1431
-
(2005)
Leukemia
, vol.19
, pp. 1424-1431
-
-
Bernasconi, P.1
Klersy, C.2
Boni, M.3
-
4
-
-
25444484409
-
Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes
-
F. Sole, E. Luno, and C. Sanzo Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes Haematologica 90 2005 1168 1178
-
(2005)
Haematologica
, vol.90
, pp. 1168-1178
-
-
Sole, F.1
Luno, E.2
Sanzo, C.3
-
5
-
-
39649094569
-
New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: Evidence from a core dataset of 2124 patients
-
D. Haase, U. Germing, and J. Schanz New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients Blood 110 2007 4385 4395
-
(2007)
Blood
, vol.110
, pp. 4385-4395
-
-
Haase, D.1
Germing, U.2
Schanz, J.3
-
6
-
-
68149162241
-
Myelodysplastic syndrome with isolated del(5q)
-
S. Swerdlow, E. Campo, N.L. Harris, IARC Lyon
-
R. Hasserjian, M.M. Le Beau, and A.F. List Myelodysplastic syndrome with isolated del(5q) S. Swerdlow, E. Campo, N.L. Harris, WHO classification of tumours of haematopietic and lymphoid tissues 2008 IARC Lyon 102 103
-
(2008)
WHO Classification of Tumours of Haematopietic and Lymphoid Tissues
, pp. 102-103
-
-
Hasserjian, R.1
Le Beau, M.M.2
List, A.F.3
-
7
-
-
0016348695
-
Distinct haematological disorder with deletion of long arm of no. 5 chromosome
-
H. Van den Berghe, J.J. Cassiman, G. David, J.P. Fryns, J.L. Michaux, and G. Sokal Distinct haematological disorder with deletion of long arm of no. 5 chromosome Nature 251 1974 437 438
-
(1974)
Nature
, vol.251
, pp. 437-438
-
-
Van Den Berghe, H.1
Cassiman, J.J.2
David, G.3
Fryns, J.P.4
Michaux, J.L.5
Sokal, G.6
-
9
-
-
10744229499
-
Clinical, morphological, cytogenetic, and prognostic features of patients with myelodysplastic syndromes and del(5q) including band q31
-
A.A. Giagounidis, U. Germing, and S. Haase Clinical, morphological, cytogenetic, and prognostic features of patients with myelodysplastic syndromes and del(5q) including band q31 Leukemia 18 2004 113 119
-
(2004)
Leukemia
, vol.18
, pp. 113-119
-
-
Giagounidis, A.A.1
Germing, U.2
Haase, S.3
-
10
-
-
0029065975
-
Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion
-
S. Lewis, D. Oscier, and J. Boultwood Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion Am J Hematol 49 1995 194 200
-
(1995)
Am J Hematol
, vol.49
, pp. 194-200
-
-
Lewis, S.1
Oscier, D.2
Boultwood, J.3
-
11
-
-
51449104487
-
Myelodysplastic syndromes associated with interstitial deletion of chromosome 5q: Clinicopathologic correlations and new insights from the pre-lenalidomide era
-
S.G. Holtan, R. Santana-Davila, and G.W. Dewald Myelodysplastic syndromes associated with interstitial deletion of chromosome 5q: clinicopathologic correlations and new insights from the pre-lenalidomide era Am J Hematol 83 2008 708 713
-
(2008)
Am J Hematol
, vol.83
, pp. 708-713
-
-
Holtan, S.G.1
Santana-Davila, R.2
Dewald, G.W.3
-
12
-
-
77954658029
-
WHO-defined 'myelodysplastic syndrome with isolated del(5q)' in 88 consecutive patients: Survival data, leukemic transformation rates and prevalence of JAK2, MPL and IDH mutations
-
M.M. Patnaik, T.L. Lasho, and C.M. Finke WHO-defined 'myelodysplastic syndrome with isolated del(5q)' in 88 consecutive patients: survival data, leukemic transformation rates and prevalence of JAK2, MPL and IDH mutations Leukemia 24 2010 1283 1289
-
(2010)
Leukemia
, vol.24
, pp. 1283-1289
-
-
Patnaik, M.M.1
Lasho, T.L.2
Finke, C.M.3
-
13
-
-
0027458441
-
The 5q - Syndrome: A single-institution study of 43 consecutive patients
-
P. Mathew, A. Tefferi, and G.W. Dewald 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
-
14
-
-
78651307662
-
Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q
-
M. Mallo, J. Cervera, and J. Schanz Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q Leukemia 25 2011 110 120
-
(2011)
Leukemia
, vol.25
, pp. 110-120
-
-
Mallo, M.1
Cervera, J.2
Schanz, J.3
-
15
-
-
33749438404
-
Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion
-
A. List, G. Dewald, and J. Bennett Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion N Engl J Med 355 2006 1456 1465
-
(2006)
N Engl J Med
, vol.355
, pp. 1456-1465
-
-
List, A.1
Dewald, G.2
Bennett, J.3
-
16
-
-
13444256401
-
Efficacy of lenalidomide in myelodysplastic syndromes
-
A. List, S. Kurtin, and D.J. Roe Efficacy of lenalidomide in myelodysplastic syndromes N Engl J Med 352 2005 549 557
-
(2005)
N Engl J Med
, vol.352
, pp. 549-557
-
-
List, A.1
Kurtin, S.2
Roe, D.J.3
-
17
-
-
38349088899
-
Identification of RPS14 as a 5q - Syndrome gene by RNA interference screen
-
B.L. Ebert, J. Pretz, and J. Bosco Identification of RPS14 as a 5q - syndrome gene by RNA interference screen Nature 451 2008 335 339
-
(2008)
Nature
, vol.451
, pp. 335-339
-
-
Ebert, B.L.1
Pretz, J.2
Bosco, J.3
-
18
-
-
73849128091
-
A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q - Syndrome
-
J.L. Barlow, L.F. Drynan, and D.R. Hewett A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q - syndrome Nat Med 16 2010 59 66
-
(2010)
Nat Med
, vol.16
, pp. 59-66
-
-
Barlow, J.L.1
Drynan, L.F.2
Hewett, D.R.3
-
19
-
-
33745213401
-
The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrow
-
W. Ingram, N.C. Lea, and J. Cervera The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrow Leukemia 20 2006 1319 1321
-
(2006)
Leukemia
, vol.20
, pp. 1319-1321
-
-
Ingram, W.1
Lea, N.C.2
Cervera, J.3
-
22
-
-
0015090542
-
Quantitation of bone marrow reticulin - A normal range
-
D.E. Bauermeister Quantitation of bone marrow reticulin - a normal range Am J Clin Pathol 56 1971 24 31
-
(1971)
Am J Clin Pathol
, vol.56
, pp. 24-31
-
-
Bauermeister, D.E.1
-
23
-
-
0018675904
-
The reticulin content of bone marrow in acute leukaemia in adults
-
A. Manoharan, R. Horsley, and W.R. Pitney The reticulin content of bone marrow in acute leukaemia in adults Br J Haematol 43 1979 185 190
-
(1979)
Br J Haematol
, vol.43
, pp. 185-190
-
-
Manoharan, A.1
Horsley, R.2
Pitney, W.R.3
-
25
-
-
34247899182
-
Amplification refractory mutation system, a highly sensitive and simple polymerase chain reaction assay, for the detection of JAK2 V617F mutation in chronic myeloproliferative disorders
-
Q. Chen, P. Lu, A.V. Jones, N.C. Cross, R.T. Silver, and Y.L. Wang Amplification refractory mutation system, a highly sensitive and simple polymerase chain reaction assay, for the detection of JAK2 V617F mutation in chronic myeloproliferative disorders J Mol Diagn 9 2007 272 276
-
(2007)
J Mol Diagn
, vol.9
, pp. 272-276
-
-
Chen, Q.1
Lu, P.2
Jones, A.V.3
Cross, N.C.4
Silver, R.T.5
Wang, Y.L.6
-
26
-
-
45149113001
-
JAK2 Mutations are present in all cases of polycythemia vera
-
Y.L. Wang, K. Vandris, and A. Jones JAK2 Mutations are present in all cases of polycythemia vera Leukemia 22 2008 1289
-
(2008)
Leukemia
, vol.22
, pp. 1289
-
-
Wang, Y.L.1
Vandris, K.2
Jones, A.3
-
28
-
-
0003575142
-
-
Common toxicity criteria 1999: http://www.eortc.be/services/doc/ctc/ ctcv20-4-30-992.pdf.
-
(1999)
Common Toxicity Criteria
-
-
-
29
-
-
80053956542
-
Treatment by Lenalidomide in lower risk myelodysplastic syndrome with 5q deletion - The GFM experience
-
F. Le Bras, M. Sebert, and C. Kelaidi Treatment by Lenalidomide in lower risk myelodysplastic syndrome with 5q deletion - the GFM experience Leuk Res 35 2011 1444 1448
-
(2011)
Leuk Res
, vol.35
, pp. 1444-1448
-
-
Le Bras, F.1
Sebert, M.2
Kelaidi, C.3
-
30
-
-
70449378917
-
The heterogeneous prognosis of patients with myelodysplastic syndrome and chromosome 5 abnormalities: How does it relate to the original lenalidomide experience in MDS?
-
H. Kantarjian, S. O'Brien, and F. Ravandi The heterogeneous prognosis of patients with myelodysplastic syndrome and chromosome 5 abnormalities: how does it relate to the original lenalidomide experience in MDS? Cancer 115 2009 5202 5209
-
(2009)
Cancer
, vol.115
, pp. 5202-5209
-
-
Kantarjian, H.1
O'Brien, S.2
Ravandi, F.3
-
31
-
-
0036235310
-
Myeloid disorders with deletion of 5q as the sole karyotypic abnormality: The clinical and pathologic spectrum
-
L.T. Washington, D. Doherty, A. Glassman, J. Martins, S. Ibrahim, and R. Lai Myeloid disorders with deletion of 5q as the sole karyotypic abnormality: the clinical and pathologic spectrum Leuk Lymphoma 43 2002 761 765
-
(2002)
Leuk Lymphoma
, vol.43
, pp. 761-765
-
-
Washington, L.T.1
Doherty, D.2
Glassman, A.3
Martins, J.4
Ibrahim, S.5
Lai, R.6
-
32
-
-
39749117093
-
Chromosome 5q deletion: Specific diagnoses and cytogenetic details among 358 consecutive cases from a single institution
-
R. Santana-Davila, S.G. Holtan, and G.W. Dewald Chromosome 5q deletion: specific diagnoses and cytogenetic details among 358 consecutive cases from a single institution Leuk Res 32 2008 407 411
-
(2008)
Leuk Res
, vol.32
, pp. 407-411
-
-
Santana-Davila, R.1
Holtan, S.G.2
Dewald, G.W.3
-
33
-
-
65449150965
-
Efficacy and safety of lenalidomide in intermediate-2 or high-risk myelodysplastic syndromes with 5q deletion: Results of a phase 2 study
-
L. Ades, S. Boehrer, and T. Prebet Efficacy and safety of lenalidomide in intermediate-2 or high-risk myelodysplastic syndromes with 5q deletion: results of a phase 2 study Blood 113 2009 3947 3952
-
(2009)
Blood
, vol.113
, pp. 3947-3952
-
-
Ades, L.1
Boehrer, S.2
Prebet, T.3
-
34
-
-
77649303359
-
Patients with del(5q) MDS who fail to achieve sustained erythroid or cytogenetic remission after treatment with lenalidomide have an increased risk for clonal evolution and AML progression
-
G. Gohring, A. Giagounidis, and G. Busche Patients with del(5q) MDS who fail to achieve sustained erythroid or cytogenetic remission after treatment with lenalidomide have an increased risk for clonal evolution and AML progression Ann Hematol 89 2010 365 374
-
(2010)
Ann Hematol
, vol.89
, pp. 365-374
-
-
Gohring, G.1
Giagounidis, A.2
Busche, G.3
-
35
-
-
40849131212
-
Unusual clonal evolution involving 5q in a case of myelodysplastic syndrome with deletion 5q 31 treated with lenalidomide
-
V. Eclache, A. Da Rocha, G. Le Roux, and P. Fenaux Unusual clonal evolution involving 5q in a case of myelodysplastic syndrome with deletion 5q 31 treated with lenalidomide Haematologica 93 2008 315 316
-
(2008)
Haematologica
, vol.93
, pp. 315-316
-
-
Eclache, V.1
Da Rocha, A.2
Le Roux, G.3
Fenaux, P.4
-
36
-
-
73149108856
-
Clonal heterogeneity in the 5q - Syndrome: P53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression
-
M. Jadersten, L. Saft, and A. Pellagatti Clonal heterogeneity in the 5q - syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression Haematologica 94 2009 1762 1766
-
(2009)
Haematologica
, vol.94
, pp. 1762-1766
-
-
Jadersten, M.1
Saft, L.2
Pellagatti, A.3
-
37
-
-
77956516658
-
Persistent malignant stem cells in del(5q) myelodysplasia in remission
-
R. Tehranchi, P.S. Woll, and K. Anderson Persistent malignant stem cells in del(5q) myelodysplasia in remission N Engl J Med 363 2010 1025 1037
-
(2010)
N Engl J Med
, vol.363
, pp. 1025-1037
-
-
Tehranchi, R.1
Woll, P.S.2
Anderson, K.3
-
38
-
-
21344440357
-
The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
-
D.P. Steensma, G.W. Dewald, and T.L. Lasho The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes Blood 106 2005 1207 1209
-
(2005)
Blood
, vol.106
, pp. 1207-1209
-
-
Steensma, D.P.1
Dewald, G.W.2
Lasho, T.L.3
-
39
-
-
33748177825
-
The JAK2-V617F mutation and essential thrombocythemia features in a subset of patients with refractory anemia with ring sideroblasts (RARS)
-
M. Boissinot, R. Garand, M. Hamidou, and S. Hermouet The JAK2-V617F mutation and essential thrombocythemia features in a subset of patients with refractory anemia with ring sideroblasts (RARS) Blood 108 2006 1781 1782
-
(2006)
Blood
, vol.108
, pp. 1781-1782
-
-
Boissinot, M.1
Garand, R.2
Hamidou, M.3
Hermouet, S.4
-
40
-
-
33750299561
-
The JAK2 V617F mutation is rare in RARS but common in RARS-T
-
M.M. Ceesay, N.C. Lea, and W. Ingram The JAK2 V617F mutation is rare in RARS but common in RARS-T Leukemia 20 2006 2060 2061
-
(2006)
Leukemia
, vol.20
, pp. 2060-2061
-
-
Ceesay, M.M.1
Lea, N.C.2
Ingram, W.3
-
41
-
-
33846891352
-
9/L) and ringed sideroblasts more than 15% considered as MDS/MPD, unclassifiable
-
9/L) and ringed sideroblasts more than 15% considered as MDS/MPD, unclassifiable Blood 109 2007 1334 1335
-
(2007)
Blood
, vol.109
, pp. 1334-1335
-
-
Gattermann, N.1
Billiet, J.2
Kronenwett, R.3
-
42
-
-
77952097487
-
JAK2(V617F) mutation in myelodysplastic syndrome (MDS) with del(5q) arises in genetically discordant clones
-
L. Sokol, G. Caceres, K. Rocha, K.J. Stockero, D.W. Dewald, and A.F. List JAK2(V617F) mutation in myelodysplastic syndrome (MDS) with del(5q) arises in genetically discordant clones Leuk Res 34 2010 821 823
-
(2010)
Leuk Res
, vol.34
, pp. 821-823
-
-
Sokol, L.1
Caceres, G.2
Rocha, K.3
Stockero, K.J.4
Dewald, D.W.5
List, A.F.6
-
43
-
-
77649282030
-
JAK2 V617F mutation is associated with 5q - Syndrome in Chinese
-
K.F. Wong, W.S. Wong, L.L. Siu, T.C. Lau, and N.P. Chan JAK2 V617F mutation is associated with 5q - syndrome in Chinese Leuk Lymphoma 50 2009 1333 1335
-
(2009)
Leuk Lymphoma
, vol.50
, pp. 1333-1335
-
-
Wong, K.F.1
Wong, W.S.2
Siu, L.L.3
Lau, T.C.4
Chan, N.P.5
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