-
1
-
-
55049097649
-
Myelodysplastic syndromes: Diagnosis and staging
-
Suppl
-
Malcovati L, Nimer SD. Myelodysplastic syndromes: diagnosis and staging. Cancer Control 15(Suppl), 4-13 (2008).
-
(2008)
Cancer Control
, vol.15
, pp. 4-13
-
-
Malcovati, L.1
Nimer, S.D.2
-
2
-
-
30144443817
-
The myelodysplastic syndromes: Diagnosis and treatment
-
Steensma DP, Bennett JM. The myelodysplastic syndromes: diagnosis and treatment. Mayo Clin. Proc. 81(1), 104-130 (2006). (Pubitemid 43054324)
-
(2006)
Mayo Clinic Proceedings
, vol.81
, Issue.1
, pp. 104-130
-
-
Steensma, D.P.1
Bennett, J.M.2
-
3
-
-
78951473511
-
Epidemiology, natural history, and practice patterns of patients with myelodysplastic syndromes in 2010
-
Sekeres MA. Epidemiology, natural history, and practice patterns of patients with myelodysplastic syndromes in 2010. J. Natl Compr. Canc. Netw. 9(1), 57-63 (2011).
-
(2011)
J. Natl Compr. Canc. Netw.
, vol.9
, Issue.1
, pp. 57-63
-
-
Sekeres, M.A.1
-
4
-
-
0030016365
-
Epidemiological characteristics of myelodysplastic syndrome in a well-defined French population
-
Maynadié M, Verret C, Moskovtchenko P et al. Epidemiological characteristics of myelodysplastic syndrome in a well-defined French population. Br. J. Cancer 74(2), 288-290 (1996). (Pubitemid 26254146)
-
(1996)
British Journal of Cancer
, vol.74
, Issue.2
, pp. 288-290
-
-
Maynadie, M.1
Verret, C.2
Moskovtchenko, P.3
Mugneret, F.4
Petrella, T.5
Caillot, D.6
Carli, P.M.7
-
5
-
-
33750020532
-
The incidence and outcome of myeloid malignancies in 2,112 adult patients in south East-England
-
Phekoo KJ, Richards MA, Møller H, Schey SA; South Thames Haematology Specialist Committee. The incidence and outcome of myeloid malignancies in 2,112 adult patients in southeast England. Haematologica 91(10), 1400-1404 (2006). (Pubitemid 44569817)
-
(2006)
Haematologica
, vol.91
, Issue.10
, pp. 1400-1404
-
-
Phekoo, K.J.1
Richards, M.A.2
Moller, H.3
Schey, S.A.4
-
6
-
-
0028955323
-
Incidence of myelodysplastic syndromes in a Swedish population
-
Rådlund A, Thiede T, Hansen S, Carlsson M, Engquist L. Incidence of myelodysplastic syndromes in a Swedish population. Eur. J. Haematol. 54(3), 153-156 (1995).
-
(1995)
Eur. J. Haematol.
, vol.54
, Issue.3
, pp. 153-156
-
-
Rådlund, A.1
Thiede, T.2
Hansen, S.3
Carlsson, M.4
Engquist, L.5
-
7
-
-
80055110031
-
Incidence and prevalence of myelodysplastic syndromes: Data from the Düsseldorf MDS-registry
-
Neukirchen J, Schoonen WM, Strupp C et al. Incidence and prevalence of myelodysplastic syndromes: data from the Düsseldorf MDS-registry. Leuk. Res. 35(12), 1591-1596 (2011).
-
(2011)
Leuk. Res.
, vol.35
, Issue.12
, pp. 1591-1596
-
-
Neukirchen, J.1
Schoonen, W.M.2
Strupp, C.3
-
8
-
-
47249150213
-
Epidemiology of myelodysplastic syndromes and chronic myeloproliferative disorders in the United States, 2001-2004, using data from the NAACCR and SEER programs
-
Rollison DE, Howlader N, Smith MT et al. Epidemiology of myelodysplastic syndromes and chronic myeloproliferative disorders in the United States, 2001-2004, using data from the NAACCR and SEER programs. Blood 112(1), 45-52 (2008).
-
(2008)
Blood
, vol.112
, Issue.1
, pp. 45-52
-
-
Rollison, D.E.1
Howlader, N.2
Smith, M.T.3
-
9
-
-
27644448871
-
Risk factors of myelodysplastic syndromes: A case-control study
-
DOI 10.1038/sj.leu.2403945, PII 2403945
-
Strom SS, Gu Y, Gruschkus SK, Pierce SA, Estey EH. Risk factors of myelodysplastic syndromes: A caseYcontrol study. Leukemia 19(11), 1912-1918 (2005). (Pubitemid 41553999)
-
(2005)
Leukemia
, vol.19
, Issue.11
, pp. 1912-1918
-
-
Strom, S.S.1
Gu, Y.2
Gruschkus, S.K.3
Pierce, S.A.4
Estey, E.H.5
-
10
-
-
73249121401
-
Smoking and alcohol intake as risk factors for myelodysplastic syndromes (MDS)
-
Du Y, Fryzek J, Sekeres MA, Taioli E. Smoking and alcohol intake as risk factors for myelodysplastic syndromes (MDS). Leuk. Res. 34(1), 1-5 (2010).
-
(2010)
Leuk. Res.
, vol.34
, Issue.1
, pp. 1-5
-
-
Du, Y.1
Fryzek, J.2
Sekeres, M.A.3
Taioli, E.4
-
11
-
-
78649916901
-
Are we nearer to curing patients with MDS?
-
Sekeres MA. Are we nearer to curing patients with MDS? Best Pract. Res. Clin. Haematol. 23(4), 481-487 (2010).
-
(2010)
Best Pract Res. Clin. Haematol.
, vol.23
, Issue.4
, pp. 481-487
-
-
Sekeres, M.A.1
-
12
-
-
18144454198
-
Genetic testing in the myelodysplastic syndromes: Molecular insights into hematologic diversity
-
Steensma DP, List AF. Genetic testing in the myelodysplastic syndromes: molecular insights into hematologic diversity. Mayo Clin. Proc. 80(5), 681-698 (2005). (Pubitemid 40628827)
-
(2005)
Mayo Clinic Proceedings
, vol.80
, Issue.5
, pp. 681-698
-
-
Steensma, D.P.1
List, A.F.2
-
13
-
-
55749114037
-
Characteristics of US patients with myelodysplastic syndromes: Results of six cross-sectional physician surveys
-
Sekeres MA, Schoonen WM, Kantarjian H et al. Characteristics of US patients with myelodysplastic syndromes: results of six cross-sectional physician surveys. J. Natl Cancer Inst. 100(21), 1542-1551 (2008).
-
(2008)
J. Natl Cancer Inst.
, vol.100
, Issue.21
, pp. 1542-1551
-
-
Sekeres, M.A.1
Schoonen, W.M.2
Kantarjian, H.3
-
14
-
-
33947499579
-
Efficacy of growth factors compared to other therapies for low-risk myelodysplastic syndromes
-
DOI 10.1111/j.1365-2141.2007.06546.x
-
Golshayan AR, Jin T, Maciejewski J et al. Efficacy of growth factors compared to other therapies for low-risk myelodysplastic syndromes. Br. J. Haematol. 137(2), 125-132 (2007). (Pubitemid 46474717)
-
(2007)
British Journal of Haematology
, vol.137
, Issue.2
, pp. 125-132
-
-
Golshayan, A.-R.1
Jin, T.2
Maciejewski, J.3
Fu, A.Z.4
Bershadsky, B.5
Kattan, M.W.6
Kalaycio, M.E.7
Sekeres, M.A.8
-
15
-
-
49049116574
-
Erythropoietin and granulocyte-colony stimulating factor treatment associated with improved survival in myelodysplastic syndrome
-
Jädersten M, Malcovati L, Dybedal I et al. Erythropoietin and granulocyte-colony stimulating factor treatment associated with improved survival in myelodysplastic syndrome. J. Clin. Oncol. 26(21), 3607-3613 (2008).
-
(2008)
J. Clin. Oncol.
, vol.26
, Issue.21
, pp. 3607-3613
-
-
Jädersten, M.1
Malcovati, L.2
Dybedal, I.3
-
16
-
-
33749438404
-
Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion
-
DOI 10.1056/NEJMoa061292
-
List A, Dewald G, Bennett J et al.; Myelodysplastic Syndrome-003 Study Investigators. Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion. N. Engl. J. Med. 355(14), 1456-1465 (2006). (Pubitemid 44511560)
-
(2006)
New England Journal of Medicine
, vol.355
, Issue.14
, pp. 1456-1465
-
-
List, A.1
Dewald, G.2
Bennett, J.3
Giagounidis, A.4
Raza, A.5
Feldman, E.6
Powell, B.7
Greenberg, P.8
Thomas, D.9
Stone, R.10
Reeder, C.11
Wride, K.12
Patin, J.13
Schmidt, M.14
Zeldis, J.15
Knight, R.16
-
17
-
-
79957455541
-
Management of lower-risk myelodysplastic syndromes: The art and evidence
-
Komrokji RS, Sekeres MA, List AF. Management of lower-risk myelodysplastic syndromes: The art and evidence. Curr. Hematol. Malig. Rep. 6(2), 145-153 (2011).
-
(2011)
Curr. Hematol. Malig. Rep.
, vol.6
, Issue.2
, pp. 145-153
-
-
Komrokji, R.S.1
Sekeres, M.A.2
List, A.F.3
-
18
-
-
84862538596
-
Immunosuppressive therapy for myelodysplastic syndromes
-
Dobbelstein C, Ganser A. Immunosuppressive therapy for myelodysplastic syndromes. Curr. Pharm. Des. 18(22), 3184-3189 (2012).
-
(2012)
Curr. Pharm. Des.
, vol.18
, Issue.22
, pp. 3184-3189
-
-
Dobbelstein, C.1
Ganser, A.2
-
19
-
-
62849104641
-
Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: A randomised, open-label, Phase III study
-
International Vidaza High-Risk MDS Survival Study Group
-
Fenaux P, Mufti GJ, Hellstrom-Lindberg E et al.; International Vidaza High-Risk MDS Survival Study Group. Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: A randomised, open-label, Phase III study. Lancet Oncol. 10(3), 223-232 (2009).
-
(2009)
Lancet Oncol.
, vol.10
, Issue.3
, pp. 223-232
-
-
Fenaux, P.1
Mufti, G.J.2
Hellstrom-Lindberg, E.3
-
20
-
-
79956294708
-
Low-dose decitabine versus best supportive care in elderly patients with intermediate- or high-risk myelodysplastic syndrome (MDS) ineligible for intensive chemotherapy: final results of the randomized Phase III study of the European Organisation for Research and Treatment of Cancer Leukemia Group and the German MDS Study Group
-
Lübbert M, Suciu S, Baila L et al. Low-dose decitabine versus best supportive care in elderly patients with intermediate- or high-risk myelodysplastic syndrome (MDS) ineligible for intensive chemotherapy: final results of the randomized Phase III study of the European Organisation for Research and Treatment of Cancer Leukemia Group and the German MDS Study Group. J. Clin. Oncol. 29(15), 1987-1996 (2011).
-
(2011)
J. Clin. Oncol.
, vol.29
, Issue.15
, pp. 1987-1996
-
-
Lübbert, M.1
Suciu, S.2
Baila, L.3
-
21
-
-
33646071894
-
Decitabine improves patient outcomes in myelodysplastic syndromes: Results of a Phase III randomized study
-
Kantarjian H, Issa JP, Rosenfeld CS et al. Decitabine improves patient outcomes in myelodysplastic syndromes: results of a Phase III randomized study. Cancer 106(8), 1794-1803 (2006).
-
(2006)
Cancer
, vol.106
, Issue.8
, pp. 1794-1803
-
-
Kantarjian, H.1
Issa, J.P.2
Rosenfeld, C.S.3
-
22
-
-
84857633196
-
Combination strategies in myelodysplastic syndromes
-
Ornstein MC, Sekeres MA. Combination strategies in myelodysplastic syndromes. Int. J. Hematol. 95(1), 26-33 (2012).
-
(2012)
Int. J. Hematol.
, vol.95
, Issue.1
, pp. 26-33
-
-
Ornstein, M.C.1
Sekeres, M.A.2
-
23
-
-
79958696276
-
Cytogenetic abnormalities in myelodysplastic syndrome: An overview
-
Kawankar N, Vundinti BR. Cytogenetic abnormalities in myelodysplastic syndrome: An overview. Hematology 16(3), 131-138 (2011).
-
(2011)
Hematology
, vol.16
, Issue.3
, pp. 131-138
-
-
Kawankar, N.1
Vundinti, B.R.2
-
24
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P, Cox C, LeBeau MM et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 89(6), 2079-2088 (1997). (Pubitemid 27132124)
-
(1997)
Blood
, vol.89
, Issue.6
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
Fenaux, P.4
Morel, P.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
-
25
-
-
53149113768
-
Proposal for a new risk model in myelodysplastic syndrome that accounts for events not considered in the original International Prognostic Scoring System
-
Kantarjian H, O'Brien S, Ravandi F et al. Proposal for a new risk model in myelodysplastic syndrome that accounts for events not considered in the original International Prognostic Scoring System. Cancer 113(6), 1351-1361 (2008).
-
(2008)
Cancer
, vol.113
, Issue.6
, pp. 1351-1361
-
-
Kantarjian, H.1
O'Brien, S.2
Ravandi, F.3
-
26
-
-
84866621729
-
Revised international prognostic scoring system for myelodysplastic syndromes
-
Greenberg PL, Tuechler H, Schanz J et al. Revised international prognostic scoring system for myelodysplastic syndromes. Blood 120(12), 2454-2465 (2012).
-
(2012)
Blood
, vol.120
, Issue.12
, pp. 2454-2465
-
-
Greenberg, P.L.1
Tuechler, H.2
Schanz, J.3
-
27
-
-
43149119716
-
International Working Group on MDS cytogenetics: October 2007 meeting report
-
Slovak ML, Dewald GW. International Working Group on MDS cytogenetics: October 2007 meeting report. Leuk Res 32(9), 1329-1332 (2008).
-
(2008)
Leuk Res
, vol.32
, Issue.9
, pp. 1329-1332
-
-
Slovak, M.L.1
Dewald, G.W.2
-
28
-
-
22144453267
-
Adequate cytogenetic examination in myelodysplastic syndromes: Analysis of 529 patients
-
DOI 10.1016/j.leukres.2005.01.019, PII S0145212605000664
-
Steidl C, Steffens R, Gassmann W et al. Adequate cytogenetic examination in myelodysplastic syndromes: Analysis of 529 patients. Leuk. Res. 29(9), 987-993 (2005). (Pubitemid 40982592)
-
(2005)
Leukemia Research
, vol.29
, Issue.9
, pp. 987-993
-
-
Steidl, C.1
Steffens, R.2
Gassmann, W.3
Hildebrandt, B.4
Hilgers, R.5
Germing, U.6
Trumper, L.7
Haase, D.8
-
30
-
-
39649094569
-
New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: Evidence from a core dataset of 2124 patients
-
DOI 10.1182/blood-2007-03-082404
-
Haase D, Germing U, Schanz J et al. 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(13), 4385-4395 (2007). (Pubitemid 351377805)
-
(2007)
Blood
, vol.110
, Issue.13
, pp. 4385-4395
-
-
Haase, D.1
Germing, U.2
Schanz, J.3
Pfeilstocker, M.4
Nosslinger, T.5
Hildebrandt, B.6
Kundgen, A.7
Lubbert, M.8
Kunzmann, R.9
Giagounidis, A.A.N.10
Aul, C.11
Trumper, L.12
Krieger, O.13
Stauder, R.14
Muller, T.H.15
Wimazal, F.16
Valent, P.17
Fonatsch, C.18
Steidl, C.19
-
31
-
-
25444484409
-
Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes
-
Solé F, Luño E, Sanzo C et al. Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes. Haematologica 90(9), 1168-1178 (2005). (Pubitemid 41375276)
-
(2005)
Haematologica
, vol.90
, Issue.9
, pp. 1168-1178
-
-
Sole, F.1
Luno, E.2
Sanzo, C.3
Espinet, B.4
Sanz, G.F.5
Cervera, J.6
Calasanz, M.J.7
Cigudosa, J.C.8
Milla, F.9
Ribera, J.M.10
Bureo, E.11
Martin, M.L.12
Arranz, E.13
Florensa, L.14
-
32
-
-
79956318358
-
Coalesced multicentric analysis of 2351 patients with myelodysplastic syndromes indicates an underestimation of poor-risk cytogenetics of myelodysplastic syndromes in the international prognostic scoring system
-
Schanz J, Steidl C, Fonatsch C et al. Coalesced multicentric analysis of 2351 patients with myelodysplastic syndromes indicates an underestimation of poor-risk cytogenetics of myelodysplastic syndromes in the international prognostic scoring system. J. Clin. Oncol. 29(15), 1963-1970 (2011).
-
(2011)
J. Clin. Oncol.
, vol.29
, Issue.15
, pp. 1963-1970
-
-
Schanz, J.1
Steidl, C.2
Fonatsch, C.3
-
33
-
-
84858830672
-
New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge
-
Schanz J, Tüchler H, Solé F et al. New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge. J. Clin. Oncol. 30(8), 820-829 (2012).
-
(2012)
J. Clin. Oncol.
, vol.30
, Issue.8
, pp. 820-829
-
-
Schanz, J.1
Tüchler, H.2
Solé, F.3
-
34
-
-
84864051730
-
Cytogenetic risk stratification in myelodysplastic syndromes: Are we there yet?
-
author reply 2704
-
Pardanani A, Tefferi A. Cytogenetic risk stratification in myelodysplastic syndromes: Are we there yet? J. Clin. Oncol. 30(21), 2703-2704; author reply 2704 (2012).
-
(2012)
J. Clin. Oncol.
, vol.30
, Issue.21
, pp. 2703-2704
-
-
Pardanani, A.1
Tefferi, A.2
-
35
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar R, Stevenson K, Abdel-Wahab O et al. Clinical effect of point mutations in myelodysplastic syndromes. N. Engl. J. Med. 364(26), 2496-2506 (2011).
-
(2011)
N. Engl. J. Med.
, vol.364
, Issue.26
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
Abdel-Wahab, O.3
-
36
-
-
79955945973
-
Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and relat-ed myeloid malignancies
-
Tiu RV, Gondek LP, O'Keefe CL et al. Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and relat-ed myeloid malignancies. Blood 117(17), 4552-4560 (2011).
-
(2011)
Blood
, vol.117
, Issue.17
, pp. 4552-4560
-
-
Tiu, R.V.1
Gondek, L.P.2
O'Keefe, C.L.3
-
37
-
-
38949123096
-
Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML
-
DOI 10.1182/blood-2007-05-092304
-
Gondek LP, Tiu R, O'Keefe CL, Sekeres MA, Theil KS, Maciejewski JP. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. Blood 111(3), 1534-1542 (2008). (Pubitemid 351213443)
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1534-1542
-
-
Gondek, L.P.1
Tiu, R.2
O'Keefe, C.L.3
Sekeres, M.A.4
Theil, K.S.5
Maciejewski, J.P.6
-
38
-
-
79952164235
-
Unraveling the molecular pathophysiology of myelodysplastic syndromes
-
Bejar R, Levine R, Ebert BL. Unraveling the molecular pathophysiology of myelodysplastic syndromes. J. Clin. Oncol. 29(5), 504-515 (2011).
-
(2011)
J. Clin. Oncol.
, vol.29
, Issue.5
, pp. 504-515
-
-
Bejar, R.1
Levine, R.2
Ebert, B.L.3
-
39
-
-
36148993604
-
Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
-
DOI 10.1182/blood-2007-03-079673
-
Mohamedali A, Gäken J, Twine NA et al. Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes. Blood 110(9), 3365-3373 (2007). (Pubitemid 350106331)
-
(2007)
Blood
, vol.110
, Issue.9
, pp. 3365-3373
-
-
Mohamedali, A.1
Gaken, J.2
Twine, N.A.3
Ingram, W.4
Westwood, N.5
Lea, N.C.6
Hayden, J.7
Donaldson, N.8
Aul, C.9
Gattermann, N.10
Giagounidis, A.11
Germing, U.12
List, A.F.13
Mufti, G.J.14
-
40
-
-
17044453376
-
Primary myelodysplastic syndrome with normal cytogenetics: utility of 'FISH panel testing' and M-FISH
-
Ketterling RP, Wyatt WA, VanWier SA et al. Primary myelodysplastic syndrome with normal cytogenetics: utility of 'FISH panel testing' and M-FISH. Leuk. Res. 26(3), 235-240 (2002).
-
(2002)
Leuk. Res.
, vol.26
, Issue.3
, pp. 235-240
-
-
Ketterling, R.P.1
Wyatt, W.A.2
VanWier, S.A.3
-
41
-
-
33847772851
-
Clinical relevance of cytogenetics in myelodysplastic syndromes
-
DOI 10.1196/annals.1386.034, Estrogens and Human Diseases
-
Bernasconi P, Boni M, Cavigliano PM et al. Clinical relevance of cytogenetics in myelodysplastic syndromes. Ann. NY Acad. Sci. 1089, 395-410 (2006). (Pubitemid 47092089)
-
(2006)
Annals of the New York Academy of Sciences
, vol.1089
, pp. 395-410
-
-
Bernasconi, P.1
Boni, M.2
Cavigliano, P.M.3
Calatroni, S.4
Giardini, I.5
Rocca, B.6
Zappatore, R.7
Dambruoso, I.8
Caresana, M.9
-
42
-
-
67650462718
-
Usefulness of classic cytogenetic testing compared to fluorescence in situ hybridization in genetic diagnosis of 58 patients with myelodysplastic syndromes
-
Skonieczka K, Duszenko E, Wyrowinska E, Haus O. Usefulness of classic cytogenetic testing compared to fluorescence in situ hybridization in genetic diagnosis of 58 patients with myelodysplastic syndromes. Pol. Arch. Med. Wewn. 119(6), 366-372 (2009).
-
(2009)
Pol. Arch. Med. Wewn.
, vol.119
, Issue.6
, pp. 366-372
-
-
Skonieczka, K.1
Duszenko, E.2
Wyrowinska, E.3
Haus, O.4
-
43
-
-
39049162350
-
Conventional and molecular cytogenetic features of myelodysplastic syndrome in China
-
Chen L, Li J, Zhu Y et al. Conventional and molecular cytogenetic features of myelodysplastic syndrome in China. Exp. Oncol. 29(4), 299-303 (2007). (Pubitemid 351236320)
-
(2007)
Experimental Oncology
, vol.29
, Issue.4
, pp. 299-303
-
-
Chen, L.-J.1
Li, J.-Y.2
Zhu, Y.3
Qiu, H.-R.4
Pan, J.-L.5
Wang, R.6
Qian, S.-X.7
Xu, W.8
Xue, Y.-Q.9
-
44
-
-
76749133549
-
FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q)
-
Makishima H, Rataul M, Gondek LP et al. FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q). Leuk. Res. 34(4), 447-453 (2010).
-
(2010)
Leuk. Res.
, vol.34
, Issue.4
, pp. 447-453
-
-
Makishima, H.1
Rataul, M.2
Gondek, L.P.3
-
45
-
-
68949213291
-
Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies
-
Maciejewski JP, Tiu RV, O'Keefe C. Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies. Br. J. Haematol. 146(5), 479-488 (2009).
-
(2009)
Br. J. Haematol.
, vol.146
, Issue.5
, pp. 479-488
-
-
Maciejewski, J.P.1
Tiu, R.V.2
O'Keefe, C.3
-
46
-
-
1642473037
-
Genomic microarrays in the spotlight
-
DOI 10.1016/j.tig.2003.12.008
-
Mantripragada KK, Buckley PG, Diaz de Ståhl T, Dumanski JP. Genomic microarrays in the spotlight. Trends Genet. 20(2), 87-94 (2004). (Pubitemid 38121360)
-
(2004)
Trends in Genetics
, vol.20
, Issue.2
, pp. 87-94
-
-
Mantripragada, K.K.1
Buckley, P.G.2
Diaz De Stahl, T.3
Dumanski, J.P.4
-
47
-
-
33846389406
-
High-Resolution Genomic Arrays Facilitate Detection of Novel Cryptic Chromosomal Lesions in Myelodysplastic Syndromes
-
DOI 10.1016/j.exphem.2006.09.016, PII S0301472X06006370
-
O'Keefe CL, Tiu R, Gondek LP et al. High-resolution genomic arrays facilitate detection of novel cryptic chromosomal lesions in myelodysplastic syndromes. Exp. Hematol. 35(2), 240-251 (2007). (Pubitemid 46135810)
-
(2007)
Experimental Hematology
, vol.35
, Issue.2
, pp. 240-251
-
-
O'Keefe, C.L.1
Tiu, R.2
Gondek, L.P.3
Powers, J.4
Theil, K.S.5
Kalaycio, M.6
Lichtin, A.7
Sekeres, M.A.8
Maciejewski, J.P.9
-
48
-
-
79952452217
-
Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance
-
Thiel A, Beier M, Ingenhag D et al. Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance. Leukemia 25(3), 387-399 (2011).
-
(2011)
Leukemia
, vol.25
, Issue.3
, pp. 387-399
-
-
Thiel, A.1
Beier, M.2
Ingenhag, D.3
-
49
-
-
84857099656
-
Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromes
-
Kolquist KA, Schultz RA, Furrow A et al. Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromes. Cancer Genet. 204(11), 603-628 (2011).
-
(2011)
Cancer Genet.
, vol.204
, Issue.11
, pp. 603-628
-
-
Kolquist, K.A.1
Schultz, R.A.2
Furrow, A.3
-
50
-
-
78149424920
-
Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes
-
Slovak ML, Smith DD, Bedell V et al. Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/ myeloproliferative syndromes. Mol. Cytogenet. 3, 23 (2010).
-
(2010)
Mol. Cytogenet.
, vol.3
, Issue.23
-
-
Slovak, M.L.1
Smith, D.D.2
Bedell, V.3
-
51
-
-
54049105351
-
High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival
-
Starczynowski DT, Vercauteren S, Telenius A et al. High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival. Blood 112(8), 3412-3424 (2008).
-
(2008)
Blood
, vol.112
, Issue.8
, pp. 3412-3424
-
-
Starczynowski, D.T.1
Vercauteren, S.2
Telenius, A.3
-
52
-
-
34447552512
-
Getting it right: Designing microarray (and not 'microawry') comparative genomic hybridization studies for cancer research
-
DOI 10.1038/labinvest.3700593, PII 3700593
-
Tan DS, Lambros MB, Natrajan R, Reis-Filho JS. Getting it right: designing microarray (and not 'microawry') comparative genomic hybridization studies for cancer research. Lab. Invest. 87(8), 737-754 (2007). (Pubitemid 47077258)
-
(2007)
Laboratory Investigation
, vol.87
, Issue.8
, pp. 737-754
-
-
Tan, D.S.P.1
Lambros, M.B.K.2
Natrajan, R.3
Reis-Filho, J.S.4
-
53
-
-
84859383178
-
Detection of copy number alterations in acute myeloid leukemia and myelodysplastic syndromes
-
Jacoby MA, Walter MJ. Detection of copy number alterations in acute myeloid leukemia and myelodysplastic syndromes. Expert Rev. Mol. Diagn. 12(3), 253-264 (2012).
-
(2012)
Expert Rev. Mol. Diagn.
, vol.12
, Issue.3
, pp. 253-264
-
-
Jacoby, M.A.1
Walter, M.J.2
-
54
-
-
35448931911
-
Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes
-
DOI 10.1016/j.exphem.2007.08.009, PII S0301472X07004973
-
Gondek LP, Haddad AS, O'Keefe CL et al. Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes. Exp. Hematol. 35(11), 1728-1738 (2007). (Pubitemid 47633771)
-
(2007)
Experimental Hematology
, vol.35
, Issue.11
, pp. 1728-1738
-
-
Gondek, L.P.1
Haddad, A.S.2
O'Keefe, C.L.3
Tiu, R.4
Wlodarski, M.W.5
Sekeres, M.A.6
Theil, K.S.7
Maciejewski, J.P.8
-
55
-
-
70350438115
-
Groupe Francophone des Myélodysplasies. TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs)
-
Kosmider O, Gelsi-Boyer V, Cheok M et al.; Groupe Francophone des Myélodysplasies. TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs). Blood 114(15), 3285-3291 (2009).
-
(2009)
Blood
, vol.114
, Issue.15
, pp. 3285-3291
-
-
Kosmider, O.1
Gelsi-Boyer, V.2
Cheok, M.3
-
56
-
-
67649876132
-
Acquired mutations in TET2 are common in myelodysplastic syndromes
-
Langemeijer SM, Kuiper RP, Berends M et al. Acquired mutations in TET2 are common in myelodysplastic syndromes. Nat. Genet. 41(7), 838-842 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.7
, pp. 838-842
-
-
Langemeijer, S.M.1
Kuiper, R.P.2
Berends, M.3
-
57
-
-
79960229916
-
Impact of TET2 mutations on response rate to azacitidine in myelodysplastic syndromes and low blast count acute myeloid leukemias
-
Groupe Francophone des Myelodysplasies (GFM).
-
Itzykson R, Kosmider O, Cluzeau T et al.; Groupe Francophone des Myelodysplasies (GFM). Impact of TET2 mutations on response rate to azacitidine in myelodysplastic syndromes and low blast count acute myeloid leukemias. Leukemia 25(7), 1147-1152 (2011).
-
(2011)
Leukemia
, vol.25
, Issue.7
, pp. 1147-1152
-
-
Itzykson, R.1
Kosmider, O.2
Cluzeau, T.3
-
58
-
-
78149454504
-
Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value
-
Smith AE, Mohamedali AM, Kulasekararaj A et al. Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value. Blood 116(19), 3923-3932 (2010).
-
(2010)
Blood
, vol.116
, Issue.19
, pp. 3923-3932
-
-
Smith, A.E.1
Mohamedali, A.M.2
Kulasekararaj, A.3
-
59
-
-
65549139174
-
Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations
-
Harada Y, Harada H. Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations. J. Cell. Physiol. 220(1), 16-20 (2009).
-
(2009)
J. Cell. Physiol.
, vol.220
, Issue.1
, pp. 16-20
-
-
Harada, Y.1
Harada, H.2
-
60
-
-
79251640863
-
Molecular mechanisms that produce secondary MDS/AML by RUNX1/AML1 point mutations
-
Harada Y, Harada H. Molecular mechanisms that produce secondary MDS/AML by RUNX1/AML1 point mutations. J. Cell. Biochem. 112(2), 425-432 (2011).
-
(2011)
J. Cell. Biochem.
, vol.112
, Issue.2
, pp. 425-432
-
-
Harada, Y.1
Harada, H.2
-
61
-
-
4444302228
-
Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation
-
DOI 10.1182/blood-2004-02-0754
-
Christiansen DH, Andersen MK, Pedersen-Bjergaard J. Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation. Blood 104(5), 1474-1481 (2004). (Pubitemid 39166527)
-
(2004)
Blood
, vol.104
, Issue.5
, pp. 1474-1481
-
-
Christiansen, D.H.1
Andersen, M.K.2
Pedersen-Bjergaard, J.3
-
62
-
-
1542373639
-
High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
-
DOI 10.1182/blood-2003-09-3074
-
Harada H, Harada Y, Niimi H, Kyo T, Kimura A, Inaba T. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood 103(6), 2316-2324 (2004). (Pubitemid 38326252)
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2316-2324
-
-
Harada, H.1
Harada, Y.2
Niimi, H.3
Kyo, T.4
Kimura, A.5
Inaba, T.6
-
63
-
-
12444314088
-
Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
-
DOI 10.1111/j.1600-0609.2004.00363.x
-
Steensma DP, Gibbons RJ, Mesa RA, Tefferi A, Higgs DR. Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia. Eur. J. Haematol. 74(1), 47-53 (2005). (Pubitemid 40143686)
-
(2005)
European Journal of Haematology
, vol.74
, Issue.1
, pp. 47-53
-
-
Steensma, D.P.1
Gibbons, R.J.2
Mesa, R.A.3
Tefferi, A.4
Higgs, D.R.5
-
64
-
-
33644659923
-
Characterization of Asxl1, a murine homolog of Additional sex combs, and analysis of the Asx-like gene family
-
DOI 10.1016/j.gene.2005.10.033, PII S0378111905006591
-
Fisher CL, Randazzo F, Humphries RK, Brock HW. Characterization of Asxl1, a murine homolog of additional sex combs, and analysis of the Asx-like gene family. Gene 369, 109-118 (2006). (Pubitemid 43327337)
-
(2006)
Gene
, vol.369
, Issue.1-2
, pp. 109-118
-
-
Fisher, C.L.1
Randazzo, F.2
Humphries, R.K.3
Brock, H.W.4
-
65
-
-
77952421834
-
Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia
-
Boultwood J, Perry J, Pellagatti A et al. Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia. Leukemia 24(5), 1062-1065 (2010).
-
(2010)
Leukemia
, vol.24
, Issue.5
, pp. 1062-1065
-
-
Boultwood, J.1
Perry, J.2
Pellagatti, A.3
-
66
-
-
79959317767
-
Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes
-
Thol F, Friesen I, Damm F et al. Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes. J. Clin. Oncol. 29(18), 2499-2506 (2011).
-
(2011)
J. Clin. Oncol.
, vol.29
, Issue.18
, pp. 2499-2506
-
-
Thol, F.1
Friesen, I.2
Damm, F.3
-
67
-
-
77952426827
-
Mutations of IDH1 and IDH2 genes in early and accelerated phases of myelodysplastic syndromes and MDS/myeloproliferative neoplasms
-
Kosmider O, Gelsi-Boyer V, Slama L et al. Mutations of IDH1 and IDH2 genes in early and accelerated phases of myelodysplastic syndromes and MDS/myeloproliferative neoplasms. Leukemia 24(5), 1094-1096 (2010).
-
(2010)
Leukemia
, vol.24
, Issue.5
, pp. 1094-1096
-
-
Kosmider, O.1
Gelsi-Boyer, V.2
Slama, L.3
-
68
-
-
77955087290
-
Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes
-
Nikoloski G, Langemeijer SM, Kuiper RP et al. Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes. Nat. Genet. 42(8), 665-667 (2010).
-
(2010)
Nat. Genet.
, vol.42
, Issue.8
, pp. 665-667
-
-
Nikoloski, G.1
Langemeijer, S.M.2
Kuiper, R.P.3
-
69
-
-
77957987676
-
Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies
-
Makishima H, Jankowska AM, Tiu RV et al. Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies. Leukemia 24(10), 1799-1804 (2010).
-
(2010)
Leukemia
, vol.24
, Issue.10
, pp. 1799-1804
-
-
Makishima, H.1
Jankowska, A.M.2
Tiu, R.V.3
-
70
-
-
79956145260
-
Overexpression of the EZH2 RING1 and BMI1 genes is common in myelodysplastic syndromes: Relation to adverse epigenetic alteration and poor prognostic scoring
-
Xu F, Li X, Wu L et al. Overexpression of the EZH2, RING1 and BMI1 genes is common in myelodysplastic syndromes: relation to adverse epigenetic alteration and poor prognostic scoring. Ann. Hematol. 90(6), 643-653 (2011).
-
(2011)
Ann. Hematol.
, vol.90
, Issue.6
, pp. 643-653
-
-
Xu, F.1
Li, X.2
Wu, L.3
-
71
-
-
84866749552
-
Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes
-
Bejar R, Stevenson KE, Caughey BA et al. Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. J. Clin. Oncol. 30(27), 3376-3382 (2012).
-
(2012)
J. Clin. Oncol.
, vol.30
, Issue.27
, pp. 3376-3382
-
-
Bejar, R.1
Stevenson, K.E.2
Caughey, B.A.3
-
72
-
-
79960255863
-
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes
-
Walter MJ, Ding L, Shen D et al. Recurrent DNMT3A mutations in patients with myelodysplastic syndromes. Leukemia 25(7), 1153-1158 (2011).
-
(2011)
Leukemia
, vol.25
, Issue.7
, pp. 1153-1158
-
-
Walter, M.J.1
Ding, L.2
Shen, D.3
-
73
-
-
82855177869
-
Rare occurrence of DNMT3A mutations in myelodysplastic syndromes
-
Thol F, Winschel C, Lüdeking A et al. Rare occurrence of DNMT3A mutations in myelodysplastic syndromes. Haematologica 96(12), 1870-1873 (2011).
-
(2011)
Haematologica
, vol.96
, Issue.12
, pp. 1870-1873
-
-
Thol, F.1
Winschel, C.2
Lüdeking, A.3
-
74
-
-
0038581265
-
Comparative genomic organization of the cbl genes
-
DOI 10.1016/S0378-1119(03)00471-2
-
Nau MM, Lipkowitz S. Comparative genomic organization of the cbl genes. Gene 308, 103-113 (2003). (Pubitemid 36597828)
-
(2003)
Gene
, vol.308
, Issue.1-2
, pp. 103-113
-
-
Nau, M.M.1
Lipkowitz, S.2
-
75
-
-
74949108515
-
Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies
-
Makishima H, Cazzolli H, Szpurka H et al. Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies. J. Clin. Oncol. 27(36), 6109-6116 (2009).
-
(2009)
J. Clin. Oncol.
, vol.27
, Issue.36
, pp. 6109-6116
-
-
Makishima, H.1
Cazzolli, H.2
Szpurka, H.3
-
76
-
-
81355154527
-
A high occurrence of acquisition and/or expansion of C-CBL mutant clones in the progression of high-risk myelodysplastic syndrome to acute myeloid leukemia
-
Kao HW, Sanada M, Liang DC et al. A high occurrence of acquisition and/or expansion of C-CBL mutant clones in the progression of high-risk myelodysplastic syndrome to acute myeloid leukemia. Neoplasia 13(11), 1035-1042 (2011).
-
(2011)
Neoplasia
, vol.13
, Issue.11
, pp. 1035-1042
-
-
Kao, H.W.1
Sanada, M.2
Liang, D.C.3
-
77
-
-
77955081371
-
Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias
-
Rocquain J, Carbuccia N, Trouplin V et al. Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias. BMC Cancer 10, 401 (2010).
-
(2010)
BMC Cancer
, vol.10
, pp. 401
-
-
Rocquain, J.1
Carbuccia, N.2
Trouplin, V.3
-
78
-
-
77957806536
-
IDH1 mutations in patients with myelodysplastic syndromes are associated with an unfavorable prognosis
-
Thol F, Weissinger EM, Krauter J et al. IDH1 mutations in patients with myelodysplastic syndromes are associated with an unfavorable prognosis. Haematologica 95(10), 1668-1674 (2010).
-
(2010)
Haematologica
, vol.95
, Issue.10
, pp. 1668-1674
-
-
Thol, F.1
Weissinger, E.M.2
Krauter, J.3
-
79
-
-
77954660316
-
Recurrent IDH mutations in high-risk myelodysplastic syndrome or acute myeloid leukemia with isolated del(5q)
-
Pardanani A, Patnaik MM, Lasho TL et al. Recurrent IDH mutations in high-risk myelodysplastic syndrome or acute myeloid leukemia with isolated del(5q). Leukemia 24(7), 1370-1372 (2010).
-
(2010)
Leukemia
, vol.24
, Issue.7
, pp. 1370-1372
-
-
Pardanani, A.1
Patnaik, M.M.2
Lasho, T.L.3
-
80
-
-
84856725273
-
Differential prognostic effect of IDH1 versus IDH2 mutations in myelodysplastic syndromes: A Mayo Clinic study of 277 patients
-
Patnaik MM, Hanson CA, Hodnefield JM et al. Differential prognostic effect of IDH1 versus IDH2 mutations in myelodysplastic syndromes: A Mayo Clinic study of 277 patients. Leukemia 26(1), 101-105 (2012).
-
(2012)
Leukemia
, vol.26
, Issue.1
, pp. 101-105
-
-
Patnaik, M.M.1
Hanson, C.A.2
Hodnefield, J.M.3
-
81
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K, Sanada M, Shiraishi Y et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 478(7367), 64-69 (2011).
-
(2011)
Nature
, vol.478
, Issue.7367
, pp. 64-69
-
-
Yoshida, K.1
Sanada, M.2
Shiraishi, Y.3
-
82
-
-
84871236747
-
Emerging roles of the spliceosomal machinery in myelodysplastic syndromes and other hematological disorders
-
Visconte V, Makishima H, Maciejewski JP, Tiu RV. Emerging roles of the spliceosomal machinery in myelodysplastic syndromes and other hematological disorders. Leukemia 26(12):2447-2454 (2012).
-
(2012)
Leukemia
, vol.26
, Issue.12
, pp. 2447-2454
-
-
Visconte, V.1
Makishima, H.2
Maciejewski, J.P.3
Tiu, R.V.4
-
83
-
-
84859597590
-
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
-
Makishima H, Visconte V, Sakaguchi H et al. Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis. Blood 119(14), 3203-3210 (2012).
-
(2012)
Blood
, vol.119
, Issue.14
, pp. 3203-3210
-
-
Makishima, H.1
Visconte, V.2
Sakaguchi, H.3
-
84
-
-
80054010617
-
Chronic myeloid disorders working group of the international cancer genome consortium. Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts
-
Papaemmanuil E, Cazzola M, Boultwood J et al.; Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium. Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. N. Engl. J. Med. 365(15), 1384-1395 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, Issue.15
, pp. 1384-1395
-
-
Papaemmanuil, E.1
Cazzola, M.2
Boultwood, J.3
-
85
-
-
84855841586
-
SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value
-
Patnaik MM, Lasho TL, Hodnefield JM et al. SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value. Blood 119(2), 569-572 (2012).
-
(2012)
Blood
, vol.119
, Issue.2
, pp. 569-572
-
-
Patnaik, M.M.1
Lasho, T.L.2
Hodnefield, J.M.3
-
86
-
-
23444460414
-
A comparative review of classification systems in myelodysplastic syndromes (MDS)
-
DOI 10.1053/j.seminoncol.2005.06.021, PII S0093775405002630, Evolving Trends in the Treatment of MDS: Immunomodulation and Beyond
-
Bennett JM. A comparative review of classification systems in myelodysplastic syndromes (MDS). Semin. Oncol. 32(4 Suppl. 5), S3-S10 (2005). (Pubitemid 41111984)
-
(2005)
Seminars in Oncology
, vol.32
, Issue.SUPPL. 5
-
-
Bennett, J.M.1
-
87
-
-
0037272767
-
Guidelines for the diagnosis and therapy of adult myelodysplastic syndromes
-
DOI 10.1046/j.1365-2141.2003.03907.x
-
Bowen D, Culligan D, Jowitt S et al.; UK MDS Guidelines Group. Guidelines for the diagnosis and therapy of adult myelodysplastic syndromes. Br. J. Haematol. 120(2), 187-200 (2003). (Pubitemid 36194166)
-
(2003)
British Journal of Haematology
, vol.120
, Issue.2
, pp. 187-200
-
-
Bowen, D.1
Culligan, D.2
Jowitt, S.3
Kelsey, S.4
Mufti, G.5
Oscier, D.6
Parker, J.7
-
88
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett JM, Catovsky D, Daniel MT et al. Proposals for the classification of the myelodysplastic syndromes. Br. J. Haematol. 51(2), 189-199 (1982). (Pubitemid 12073508)
-
(1982)
British Journal of Haematology
, vol.51
, Issue.2
, pp. 189-199
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
-
89
-
-
70349256226
-
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: Rationale and important changes
-
The 2008 Revision Of The World Health Organization
-
Vardiman JW, Thiele J, Arber DA et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 114(5), 937-951 (2009).
-
(2009)
Blood
, vol.114
, Issue.5
, pp. 937-951
-
-
Vardiman, J.W.1
Thiele, J.2
Arber, D.A.3
-
90
-
-
34548219420
-
Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes
-
DOI 10.1200/JCO.2006.08.5696
-
Malcovati L, Germing U, Kuendgen A et al. Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes. J. Clin. Oncol. 25(23), 3503-3510 (2007). (Pubitemid 47315575)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.23
, pp. 3503-3510
-
-
Malcovati, L.1
Germing, U.2
Kuendgen, A.3
Della Porta, M.G.4
Pascutto, C.5
Invernizzi, R.6
Giagounidis, A.7
Hildebrandt, B.8
Bernasconi, P.9
Knipp, S.10
Strupp, C.11
Lazzarino, M.12
Aul, C.13
Cazzola, M.14
-
91
-
-
80053186861
-
Impact of the degree of anemia on the outcome of patients with myelodysplastic syndrome and its integration into the WHO classification-based prognostic scoring system (wpss)
-
Malcovati L, Della Porta MG, Strupp C et al. Impact of the degree of anemia on the outcome of patients with myelodysplastic syndrome and its integration into the WHO classification-based Prognostic Scoring System (WPSS). Haematologica 96(10), 1433-1440 (2011).
-
(2011)
Haematologica
, vol.96
, Issue.10
, pp. 1433-1440
-
-
Malcovati, L.1
Della Porta, M.G.2
Strupp, C.3
-
92
-
-
40749135870
-
A prognostic score for patients with lower risk myelodysplastic syndrome
-
DOI 10.1038/sj.leu.2405070, PII 2405070
-
Garcia-Manero G, Shan J, Faderl S et al. A prognostic score for patients with lower risk myelodysplastic syndrome. Leukemia 22(3), 538-543 (2008). (Pubitemid 351386723)
-
(2008)
Leukemia
, vol.22
, Issue.3
, pp. 538-543
-
-
Garcia-Manero, G.1
Shan, J.2
Faderl, S.3
Cortes, J.4
Ravandi, F.5
Borthakur, G.6
Wierda, W.G.7
Pierce, S.8
Estey, E.9
Liu, J.10
Huang, X.11
Kantarjian, H.12
-
93
-
-
84873388359
-
Validating the Lower-Risk MD Anderson Prognostic Scoring System (LR-PSS) and the Revised International Prognostic Scoring System (IPSS-R) for Patients with Myelodysplastic Syndrome
-
San Diego, CA, USA, 10-13 December 2011.
-
Sekeres MA, Elsen P, Tiu RV et al. Validating the Lower-Risk MD Anderson Prognostic Scoring System (LR-PSS) and the Revised International Prognostic Scoring System (IPSS-R) for Patients with Myelodysplastic Syndrome. Presented at: 53rd ASH General Meeting. San Diego, CA, USA, 10-13 December 2011.
-
Presented at: 53rd ASH General Meeting
-
-
Sekeres, M.A.1
Elsen, P.2
Tiu, R.V.3
-
94
-
-
77958591628
-
ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia
-
Gelsi-Boyer V, Trouplin V, Roquain J et al. ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia. Br. J. Haematol. 151(4), 365-375 (2010).
-
(2010)
Br. J. Haematol.
, vol.151
, Issue.4
, pp. 365-375
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Roquain, J.3
|