-
1
-
-
68149178285
-
Refractory cytopenia with multilineage dysplasia
-
IARC Press, Lyon, S. Swerdlow, E. Campo, N. Lee Harris, E. Jaffe, S. Pileri, H. Stein, J. Thiele, J. Vardiman (Eds.)
-
Brunning R., Bennett J., Matutes E., Orazi A., Vardiman J., Thiele J. Refractory cytopenia with multilineage dysplasia. WHO classification of tumours of haematopoietic and lymphoid tissues 2008, 98-99. IARC Press, Lyon. 4th ed. S. Swerdlow, E. Campo, N. Lee Harris, E. Jaffe, S. Pileri, H. Stein, J. Thiele, J. Vardiman (Eds.).
-
(2008)
WHO classification of tumours of haematopoietic and lymphoid tissues
, pp. 98-99
-
-
Brunning, R.1
Bennett, J.2
Matutes, E.3
Orazi, A.4
Vardiman, J.5
Thiele, J.6
-
2
-
-
68149124150
-
Refractory anaemia with ring sideroblasts
-
IARC Press, Lyon, S. Swerdlow, E. Campo, N. Lee Harris, E. Jaffe, S. Pileri, H. Stein, J. Thiele, J. Vardiman (Eds.)
-
Hasserjian R., Gattermann N., Bennett J., Brunning R., Thiele J. Refractory anaemia with ring sideroblasts. WHO classification of tumours of haematopoietic and lymphoid tissues 2008, 96-97. IARC Press, Lyon. 4th ed. S. Swerdlow, E. Campo, N. Lee Harris, E. Jaffe, S. Pileri, H. Stein, J. Thiele, J. Vardiman (Eds.).
-
(2008)
WHO classification of tumours of haematopoietic and lymphoid tissues
, pp. 96-97
-
-
Hasserjian, R.1
Gattermann, N.2
Bennett, J.3
Brunning, R.4
Thiele, J.5
-
3
-
-
0033757263
-
Valdiation of the WHO proposals for a new classification of primary myelodysplastic syndromes: a retrospective analysis of 1600 patients
-
Germing U., Gattermann N., Strupp C., Aivado M., Aul C. Valdiation of the WHO proposals for a new classification of primary myelodysplastic syndromes: a retrospective analysis of 1600 patients. Leuk Res 2000, 24:983-992.
-
(2000)
Leuk Res
, vol.24
, pp. 983-992
-
-
Germing, U.1
Gattermann, N.2
Strupp, C.3
Aivado, M.4
Aul, C.5
-
4
-
-
44849143798
-
The role of iron transporter ABCB7 in refractory anemia with ring sideroblasts
-
Boultwood J., Pellagati A., Nikpour M., Pushkaran B., Fidler C., Cattan H., et al. The role of iron transporter ABCB7 in refractory anemia with ring sideroblasts. PLoS One 2008, 3:e1970.
-
(2008)
PLoS One
, vol.3
-
-
Boultwood, J.1
Pellagati, A.2
Nikpour, M.3
Pushkaran, B.4
Fidler, C.5
Cattan, H.6
-
5
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K., Sanada M., Shiraishi Y., Nowak D., Nagata Y., Yamamoto R., et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 2011, 478:64-69.
-
(2011)
Nature
, vol.478
, pp. 64-69
-
-
Yoshida, K.1
Sanada, M.2
Shiraishi, Y.3
Nowak, D.4
Nagata, Y.5
Yamamoto, R.6
-
6
-
-
80054010617
-
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts
-
Papaemmanuil E., Cazzola M., Boultwood J., Malcovati L., Vyas P., Bowen D., et al. Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. N Engl J Med 2011, 365:1384-1395.
-
(2011)
N Engl J Med
, vol.365
, pp. 1384-1395
-
-
Papaemmanuil, E.1
Cazzola, M.2
Boultwood, J.3
Malcovati, L.4
Vyas, P.5
Bowen, D.6
-
7
-
-
0043169105
-
Refractory cytopenia with multilineage dysplasia
-
IARC Press, Lyon, E. Jaffe, N. Harris, H. Stein, J. Vardiman (Eds.)
-
Brunning R., Bennett J., Flandrin G., Matutes E., Head D., Vardiman J., et al. Refractory cytopenia with multilineage dysplasia. World Health Organization classification of tumours. Tumours of haematopoietic and lymphoid tissues 2001, 70. IARC Press, Lyon. 3rd ed. E. Jaffe, N. Harris, H. Stein, J. Vardiman (Eds.).
-
(2001)
World Health Organization classification of tumours. Tumours of haematopoietic and lymphoid tissues
, pp. 70
-
-
Brunning, R.1
Bennett, J.2
Flandrin, G.3
Matutes, E.4
Head, D.5
Vardiman, J.6
-
9
-
-
55549136382
-
Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts
-
Mufti G., Bennett J., Goasguen J., Bain B., Baumann I., Brunning R., et al. Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts. Haematologica 2011, 93:1712-1717.
-
(2011)
Haematologica
, vol.93
, pp. 1712-1717
-
-
Mufti, G.1
Bennett, J.2
Goasguen, J.3
Bain, B.4
Baumann, I.5
Brunning, R.6
-
10
-
-
85009854501
-
Comparison of chromosome banding analysis, interphase- and hypermetaphase-FISH, qualitative and quantitative PCR for diagnosis and for follow-up in chronic myeloid leukemia: a study on 350 cases
-
Schoch C., Schnittger S., Bursch S., Gerstner D., Hochhaus A., Berger U., et al. Comparison of chromosome banding analysis, interphase- and hypermetaphase-FISH, qualitative and quantitative PCR for diagnosis and for follow-up in chronic myeloid leukemia: a study on 350 cases. Leukemia 2002, 16:53-59.
-
(2002)
Leukemia
, vol.16
, pp. 53-59
-
-
Schoch, C.1
Schnittger, S.2
Bursch, S.3
Gerstner, D.4
Hochhaus, A.5
Berger, U.6
-
11
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P., Cox C., LeBeau M.M., Fenaux P., Morel P., Sanz G., et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997, 89:2079-2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
Fenaux, P.4
Morel, P.5
Sanz, G.6
-
12
-
-
34548044732
-
Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia
-
Dicker F., Haferlach C., Kern W., Haferlach T., Schnittger S. Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia. Blood 2007, 110:1308-1316.
-
(2007)
Blood
, vol.110
, pp. 1308-1316
-
-
Dicker, F.1
Haferlach, C.2
Kern, W.3
Haferlach, T.4
Schnittger, S.5
-
13
-
-
33646575624
-
Implications of NRAS mutations in AML: a study of 2502 patients
-
Bacher U., Haferlach T., Schoch C., Kern W., Schnittger S. Implications of NRAS mutations in AML: a study of 2502 patients. Blood 2006, 107:3847-3853.
-
(2006)
Blood
, vol.107
, pp. 3847-3853
-
-
Bacher, U.1
Haferlach, T.2
Schoch, C.3
Kern, W.4
Schnittger, S.5
-
14
-
-
0034097609
-
Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML
-
Schnittger S., Kinkelin U., Schoch C., Heinecke A., Haase D., Haferlach T., et al. Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML. Leukemia 2000, 14:796-804.
-
(2000)
Leukemia
, vol.14
, pp. 796-804
-
-
Schnittger, S.1
Kinkelin, U.2
Schoch, C.3
Heinecke, A.4
Haase, D.5
Haferlach, T.6
-
15
-
-
0036659931
-
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
-
Schnittger S., Schoch C., Dugas M., Kern W., Staib P., Wuchter C., et al. Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood 2002, 100:59-66.
-
(2002)
Blood
, vol.100
, pp. 59-66
-
-
Schnittger, S.1
Schoch, C.2
Dugas, M.3
Kern, W.4
Staib, P.5
Wuchter, C.6
-
16
-
-
39649094569
-
New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients
-
Haase D., Germing U., Schanz J., Pfeilstöcker M., Nösslinger T., Hildebrandt B., 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 2007, 110:4385-4395.
-
(2007)
Blood
, vol.110
, pp. 4385-4395
-
-
Haase, D.1
Germing, U.2
Schanz, J.3
Pfeilstöcker, M.4
Nösslinger, T.5
Hildebrandt, B.6
-
17
-
-
33845935489
-
Prospective validation of the WHO proposals for the classification of myelodysplastic syndromes
-
Germing U., Strupp C., Kuendgen A., Isa S., Knipp S., Hildebrandt B., et al. Prospective validation of the WHO proposals for the classification of myelodysplastic syndromes. Haematologica 2006, 91:1596-1604.
-
(2006)
Haematologica
, vol.91
, pp. 1596-1604
-
-
Germing, U.1
Strupp, C.2
Kuendgen, A.3
Isa, S.4
Knipp, S.5
Hildebrandt, B.6
-
18
-
-
33646813836
-
Classification and scoring systems in myelodysplastic syndromes: a retrospective analysis of 311 patients
-
Navarro I., Ruiz M., Cabello A., Collado R., Ferrer R., Hueso J., et al. Classification and scoring systems in myelodysplastic syndromes: a retrospective analysis of 311 patients. Leuk Res 2005, 30:971-977.
-
(2005)
Leuk Res
, vol.30
, pp. 971-977
-
-
Navarro, I.1
Ruiz, M.2
Cabello, A.3
Collado, R.4
Ferrer, R.5
Hueso, J.6
-
19
-
-
28844463547
-
Usefulness and prognostic impact on survival of WHO reclassification in FAB low risk myelodysplastic syndromes
-
Breccia M., Carmosino I., Biondo F., Mancini M., Russo E., Latagliata R., et al. Usefulness and prognostic impact on survival of WHO reclassification in FAB low risk myelodysplastic syndromes. Leuk Res 2005, 30:178-182.
-
(2005)
Leuk Res
, vol.30
, pp. 178-182
-
-
Breccia, M.1
Carmosino, I.2
Biondo, F.3
Mancini, M.4
Russo, E.5
Latagliata, R.6
-
20
-
-
36148993604
-
Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
-
Mohamedali A., Gaken J., Twine N.A., Ingram W., Westwood N., Lea N.C., et al. Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes. Blood 2007, 110:3365-3373.
-
(2007)
Blood
, vol.110
, pp. 3365-3373
-
-
Mohamedali, A.1
Gaken, J.2
Twine, N.A.3
Ingram, W.4
Westwood, N.5
Lea, N.C.6
-
21
-
-
83455234787
-
Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms
-
Malcovati L., Papaemmanuil E., Bowen D., Boultwood J., Della-Porta M., Pascutto C., et al. Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms. Blood 2011, 118:6239-6246.
-
(2011)
Blood
, vol.118
, pp. 6239-6246
-
-
Malcovati, L.1
Papaemmanuil, E.2
Bowen, D.3
Boultwood, J.4
Della-Porta, M.5
Pascutto, C.6
-
22
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar R., Stevenson K., Abdel-Wahab O., Galili N., Nilsson B., Garcia-Manero G., et al. Clinical effect of point mutations in myelodysplastic syndromes. N Engl J Med 2011, 364:2496-2506.
-
(2011)
N Engl J Med
, vol.364
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
Abdel-Wahab, O.3
Galili, N.4
Nilsson, B.5
Garcia-Manero, G.6
-
23
-
-
70350438115
-
TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs)
-
Kosmider O., Gelsi-Boyer V., Cheok M., Grabar S., La-Valle V., Picard F., et al. TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs). Blood 2009, 114:3285-3291.
-
(2009)
Blood
, vol.114
, pp. 3285-3291
-
-
Kosmider, O.1
Gelsi-Boyer, V.2
Cheok, M.3
Grabar, S.4
La-Valle, V.5
Picard, F.6
|