-
1
-
-
38349060667
-
The history of myeloproliferative disorders: Before and after Dameshek
-
Tefferi A: The history of myeloproliferative disorders: Before and after Dameshek. Leukemia 22: 3-13, 2008
-
(2008)
Leukemia
, vol.22
, pp. 3-13
-
-
Tefferi, A.1
-
2
-
-
0001639195
-
Some speculations on the myeloproliferative syndromes
-
Dameshek W: Some speculations on the myeloproliferative syndromes. Blood 6: 372-375, 1951
-
(1951)
Blood
, vol.6
, pp. 372-375
-
-
Dameshek, W.1
-
3
-
-
70349256226
-
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: Rationale and important changes
-
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: 937-951, 2009
-
(2009)
Blood
, vol.114
, pp. 937-951
-
-
Vardiman, J.W.1
Thiele, J.2
Arber, D.A.3
-
4
-
-
77954581139
-
Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1
-
Tefferi A: Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1. Leukemia 24: 1128-1138, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1128-1138
-
-
Tefferi, A.1
-
5
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
DOI 10.1038/nature03546
-
James C, Ugo V, Le Couedic JP, et al: A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 434: 1144-1148, 2005 (Pubitemid 40663494)
-
(2005)
Nature
, vol.434
, Issue.7037
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le, C.J.-P.3
Staerk, J.4
Delhommeau, F.5
Lacout, C.6
Garcon, L.7
Raslova, H.8
Berger, R.9
Bennaceur-Griscelli, A.10
Villeval, J.L.11
Constantinescu, S.N.12
Casadevall, N.13
Vainchenker, W.14
-
6
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
DOI 10.1056/NEJMoa051113
-
Kralovics R, Passamonti F, Buser AS, et al: A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 352: 1779-1790, 2005 (Pubitemid 40570926)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.17
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
Teo, S.-S.4
Tiedt, R.5
Passweg, J.R.6
Tichelli, A.7
Cazzola, M.8
Skoda, R.C.9
-
7
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
DOI 10.1016/j.ccr.2005.03.023
-
Levine RL, Wadleigh M, Cools J, et al: Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 7: 387-397, 2005 (Pubitemid 40544655)
-
(2005)
Cancer Cell
, vol.7
, Issue.4
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
Ebert, B.L.4
Wernig, G.5
Huntly, B.J.P.6
Boggon, T.J.7
Wlodarska, I.8
Clark, J.J.9
Moore, S.10
Adelsperger, J.11
Koo, S.12
Lee, J.C.13
Gabriel, S.14
Mercher, T.15
D'Andrea, A.16
Frohling, S.17
Dohner, K.18
Marynen, P.19
Vandenberghe, P.20
Mesa, R.A.21
Tefferi, A.22
Griffin, J.D.23
Eck, M.J.24
Sellers, W.R.25
Meyerson, M.26
Golub, T.R.27
Lee, S.J.28
Gilliland, D.G.29
more..
-
8
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
DOI 10.1016/S0140-6736(05)71142-9
-
Baxter EJ, Scott LM, Campbell PJ, et al: Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 365: 1054-1061, 2005 (Pubitemid 40386783)
-
(2005)
Lancet
, vol.365
, Issue.9464
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
East, C.4
Fourouclas, N.5
Swanton, S.6
Vassiliou, G.S.7
Bench, A.J.8
Boyd, E.M.9
Curtin, N.10
Scott, M.A.11
Erber, W.N.12
Avis, T.13
Barthorpe, A.14
Bignell, G.15
Blow, M.16
Brackenbury, L.17
Buck, G.18
Clegg, S.19
Clements, J.20
Cole, J.21
Davies, H.22
Edkins, S.23
Gray, K.24
Gorton, M.25
O'Meara, S.26
Halliday, K.27
Harrison, R.28
Haynes, W.29
Hills, K.30
Hunter, C.31
Jones, D.32
Kosmidou, V.33
Laman, R.34
Lugg, R.35
Parker, A.36
Perry, J.37
Petty, R.38
Small, A.39
Solomon, H.40
Stephens, P.41
Stephens, Y.42
Stevens, C.43
Smith, R.44
Tarpey, P.45
Tofts, C.46
Varian, J.47
West, S.48
Widaa, S.49
Bamford, S.50
Butler, A.51
Dawson, E.52
Dicks, E.53
Edwards, K.54
Forbes, S.55
Greenman, C.56
Hinton, J.57
Menzies, A.58
Raine, K.59
Shepherd, R.60
Teague, J.61
Yates, A.62
Wooster, R.63
Futreal, A.64
Stratton, M.65
Green, A.R.66
more..
-
9
-
-
33846660947
-
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
-
DOI 10.1056/NEJMoa065202
-
Scott LM, Tong W, Levine RL, et al: JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med 356: 459-468, 2007 (Pubitemid 46193073)
-
(2007)
New England Journal of Medicine
, vol.356
, Issue.5
, pp. 459-468
-
-
Scott, L.M.1
Tong, W.2
Levine, R.L.3
Scott, M.A.4
Beer, P.A.5
Stratton, M.R.6
Futreal, P.A.7
Erber, W.N.8
McMullin, M.F.9
Harrison, C.N.10
Warren, A.J.11
Gilliland, D.G.12
Lodish, H.F.13
Green, A.R.14
-
10
-
-
33746437130
-
MPLW515L Is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia
-
Pikman Y, Lee BH, Mercher T, et al: MPLW515L Is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med 3: e270, 2006
-
(2006)
PLoS Med
, vol.3
-
-
Pikman, Y.1
Lee, B.H.2
Mercher, T.3
-
11
-
-
33750534561
-
MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients
-
Pardanani AD, Levine RL, Lasho T, et al: MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients. Blood 108: 3472-3476, 2006
-
(2006)
Blood
, vol.108
, pp. 3472-3476
-
-
Pardanani, A.D.1
Levine, R.L.2
Lasho, T.3
-
13
-
-
70450239681
-
Mutations of ASXL1 gene in myeloproliferative neoplasms
-
Carbuccia N, Murati A, Trouplin V, et al: Mutations of ASXL1 gene in myeloproliferative neoplasms. Leukemia 23:2183-2186, 2009
-
(2009)
Leukemia
, vol.23
, pp. 2183-2186
-
-
Carbuccia, N.1
Murati, A.2
Trouplin, V.3
-
14
-
-
75449119103
-
Somatic mutations of IDH1 and IDH2 in the leukemic transformation of myeloproliferative neoplasms
-
Green A, Beer P: Somatic mutations of IDH1 and IDH2 in the leukemic transformation of myeloproliferative neoplasms. N Engl J Med 362: 369-370, 2010
-
(2010)
N Engl J Med
, vol.362
, pp. 369-370
-
-
Green, A.1
Beer, P.2
-
15
-
-
76549109434
-
Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias
-
Abdel-Wahab O, Manshouri T, Patel J, et al: Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias. Cancer Res 70: 447-452, 2010
-
(2010)
Cancer Res
, vol.70
, pp. 447-452
-
-
Abdel-Wahab, O.1
Manshouri, T.2
Patel, J.3
-
16
-
-
77954573304
-
IDH1 and IDH2 mutation analysis in chronic and blast phase myeloproliferative neoplasms
-
Pardanani A, Lasho T, Finke C, et al: IDH1 and IDH2 mutation analysis in chronic and blast phase myeloproliferative neoplasms. Leukemia 24:1146-1151, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1146-1151
-
-
Pardanani, A.1
Lasho, T.2
Finke, C.3
-
17
-
-
67650401377
-
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
-
Grand FH, Hidalgo-Curtis CE, Ernst T, et al: Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms. Blood 113: 6182-6192, 2009
-
(2009)
Blood
, vol.113
, pp. 6182-6192
-
-
Grand, F.H.1
Hidalgo-Curtis, C.E.2
Ernst, T.3
-
18
-
-
77954661062
-
Deletions of the transcription factor Ikaros in myeloproliferative neoplasms
-
Jager R, Gisslinger H, Berg T, et al: Deletions of the transcription factor Ikaros in myeloproliferative neoplasms. Leukemia 24:1290-1298, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1290-1298
-
-
Jager, R.1
Gisslinger, H.2
Berg, T.3
-
19
-
-
77953485892
-
Novel mutations in the inhibitory adaptor protein LNK drive JAK-STAT signaling in patients with myeloproliferative neoplasms
-
Oh ST, Simonds EF, Jones C, et al: Novel mutations in the inhibitory adaptor protein LNK drive JAK-STAT signaling in patients with myeloproliferative neoplasms. Blood 116:988-992, 2010
-
(2010)
Blood
, vol.116
, pp. 988-992
-
-
Oh, S.T.1
Simonds, E.F.2
Jones, C.3
-
20
-
-
77955085750
-
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
-
Ernst T, Chase AJ, Score J, et al: Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat Genet 42: 722-726, 2010
-
(2010)
Nat Genet
, vol.42
, pp. 722-726
-
-
Ernst, T.1
Chase, A.J.2
Score, J.3
-
21
-
-
43249084493
-
Ratio of mutant JAK2-V617F to wild-type Jak2 determines the MPD phenotypes in transgenic mice
-
Tiedt R, Hao-Shen H, Sobas MA, et al: Ratio of mutant JAK2-V617F to wild-type Jak2 determines the MPD phenotypes in transgenic mice. Blood 111: 3931-3940, 2008
-
(2008)
Blood
, vol.111
, pp. 3931-3940
-
-
Tiedt, R.1
Hao-Shen, H.2
Sobas, M.A.3
-
22
-
-
33749358349
-
Progenitors homozygous for the V617F mutation occur in most patients with polycythemia vera, but not essential thrombocythemia
-
DOI 10.1182/blood-2006-04-018259
-
Scott LM, Scott MA, Campbell PJ, et al: Progenitors homozygous for the V617F mutation occur in most patients with polycythemia vera, but not essential thrombocythemia. Blood 108:2435-2437, 2006 (Pubitemid 44497530)
-
(2006)
Blood
, vol.108
, Issue.7
, pp. 2435-2437
-
-
Scott, L.M.1
Scott, M.A.2
Campbell, P.J.3
Green, A.R.4
-
23
-
-
47649123488
-
Clinical correlates of JAK2V617F presence or allele burden in myeloproliferative neoplasms: A critical reappraisal
-
Vannucchi AM, Antonioli E, Guglielmelli P, et al: Clinical correlates of JAK2V617F presence or allele burden in myeloproliferative neoplasms: A critical reappraisal. Leukemia 22: 1299-1307, 2008
-
(2008)
Leukemia
, vol.22
, pp. 1299-1307
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
-
24
-
-
77956439565
-
A prospective study of 338 patients with polycythemia vera: The impact of JAK2 (V617F) allele burden and leukocytosis on fibrotic or leukemic disease transformation and vascular complications
-
Passamonti F, Rumi E, Pietra D, et al: A prospective study of 338 patients with polycythemia vera: The impact of JAK2 (V617F) allele burden and leukocytosis on fibrotic or leukemic disease transformation and vascular complications. Leukemia 24: 1574-1579, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1574-1579
-
-
Passamonti, F.1
Rumi, E.2
Pietra, D.3
-
25
-
-
42449124578
-
Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival
-
DOI 10.1038/sj.leu.2405097, PII 2405097
-
Tefferi A, Lasho TL, Huang J, et al: Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival. Leukemia 22:756-761, 2008 (Pubitemid 351559282)
-
(2008)
Leukemia
, vol.22
, Issue.4
, pp. 756-761
-
-
Tefferi, A.1
Lasho, T.L.2
Huang, J.3
Finke, C.4
Mesa, R.A.5
Li, C.Y.6
Wu, W.7
Hanson, C.A.8
Pardanani, A.9
-
26
-
-
70349580685
-
Identification of patients with poorer survival in primary myelofibrosis based on the burden of JAK2V617F mutated allele
-
Guglielmelli P, Barosi G, Specchia G, et al: Identification of patients with poorer survival in primary myelofibrosis based on the burden of JAK2V617F mutated allele. Blood 114: 1477-1483, 2009
-
(2009)
Blood
, vol.114
, pp. 1477-1483
-
-
Guglielmelli, P.1
Barosi, G.2
Specchia, G.3
-
27
-
-
34548128326
-
Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera
-
Pardanani A, Lasho TL, Finke C, et al: Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera. Leukemia 21:1960-1963, 2007
-
(2007)
Leukemia
, vol.21
, pp. 1960-1963
-
-
Pardanani, A.1
Lasho, T.L.2
Finke, C.3
-
28
-
-
38949160429
-
Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders
-
DOI 10.1182/blood-2007-07-101576
-
Pietra D, Li S, Brisci A, et al: Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 111: 1686-1689, 2008 (Pubitemid 351213460)
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1686-1689
-
-
Pietra, D.1
Li, S.2
Brisci, A.3
Passamonti, F.4
Rumi, E.5
Theocharides, A.6
Ferrari, M.7
Gisslinger, H.8
Kralovics, R.9
Cremonesi, L.10
Skoda, R.11
Cazzola, M.12
-
29
-
-
77953183876
-
Molecular and clinical features of the myeloproliferative neoplasm associated with JAK2 exon 12 mutations: A European Multicenter Study
-
Passamonti F, Schnittger S, Girodon F, et al: Molecular and clinical features of the myeloproliferative neoplasm associated with JAK2 exon 12 mutations: A European Multicenter Study. Blood 114: 3904, 2009
-
(2009)
Blood
, vol.114
, pp. 3904
-
-
Passamonti, F.1
Schnittger, S.2
Girodon, F.3
-
30
-
-
50949127379
-
Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemia
-
Vannucchi AM, Antonioli E, Guglielmelli P, et al: Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemia. Blood 112: 844-847, 2009
-
(2009)
Blood
, vol.112
, pp. 844-847
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
-
31
-
-
47249092413
-
MPL mutations in myeloproliferative disorders: Analysis of the PT-1 cohort
-
Beer PA, Campbell PJ, Scott LM, et al: MPL mutations in myeloproliferative disorders: Analysis of the PT-1 cohort. Blood 112: 141-149, 2008
-
(2008)
Blood
, vol.112
, pp. 141-149
-
-
Beer, P.A.1
Campbell, P.J.2
Scott, L.M.3
-
32
-
-
34047211223
-
W515L/K mutation
-
DOI 10.1111/j.1365-2141.2007.06565.x
-
Guglielmelli P, Pancrazzi A, Bergamaschi G, et al: Anaemia characterises patients with myelofibrosis harbouring Mpl mutation. Br J Haematol 137: 244-247, 2007 (Pubitemid 46537640)
-
(2007)
British Journal of Haematology
, vol.137
, Issue.3
, pp. 244-247
-
-
Guglielmelli, P.1
Pancrazzi, A.2
Bergamaschi, G.3
Rosti, V.4
Villani, L.5
Antonioli, E.6
Bosi, A.7
Barosi, G.8
Vannucchi, A.M.9
-
33
-
-
67349124376
-
TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis
-
Tefferi A, Pardanani A, Lim KH, et al: TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia 23: 905-911, 2009
-
(2009)
Leukemia
, vol.23
, pp. 905-911
-
-
Tefferi, A.1
Pardanani, A.2
Lim, K.H.3
-
34
-
-
77950388949
-
Clonal analysis of TET2 and JAK2 mutations suggests that TET2 can be a late event in the progression of myeloproliferative neoplasms
-
Schaub FX, Looser R, Li S, et al: Clonal analysis of TET2 and JAK2 mutations suggests that TET2 can be a late event in the progression of myeloproliferative neoplasms. Blood 115:2003-2007, 2010
-
(2010)
Blood
, vol.115
, pp. 2003-2007
-
-
Schaub, F.X.1
Looser, R.2
Li, S.3
-
35
-
-
66849124925
-
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
-
Gelsi-Boyer V, Trouplin V, Adelaide J, et al: Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. Br J Haematol 145: 788-800, 2009
-
(2009)
Br J Haematol
, vol.145
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adelaide, J.3
-
36
-
-
76749084667
-
Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias
-
Carbuccia N, Trouplin V, Gelsi-Boyer V, et al: Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias. Leukemia 24:469-473, 2010
-
(2010)
Leukemia
, vol.24
, pp. 469-473
-
-
Carbuccia, N.1
Trouplin, V.2
Gelsi-Boyer, V.3
-
37
-
-
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 24:1370-1372, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1370-1372
-
-
Pardanani, A.1
Patnaik, M.M.2
Lasho, T.L.3
-
38
-
-
77954658823
-
IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fibrotic- or blast-phase essential thrombocythemia, polycythemia vera or myelofibrosis
-
Tefferi A, Lasho TL, Abdel-Wahab O, et al: IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fibrotic- or blast-phase essential thrombocythemia, polycythemia vera or myelofibrosis. Leukemia 24:1302-1309, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1302-1309
-
-
Tefferi, A.1
Lasho, T.L.2
Abdel-Wahab, O.3
-
39
-
-
70349249988
-
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia
-
Loh ML, Sakai DS, Flotho C, et al: Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. Blood 114: 1859-1863, 2009
-
(2009)
Blood
, vol.114
, pp. 1859-1863
-
-
Loh, M.L.1
Sakai, D.S.2
Flotho, C.3
-
40
-
-
43049139905
-
BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros
-
DOI 10.1038/nature06866, PII NATURE06866
-
Mullighan CG, Miller CB, Radtke I, et al: BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. Nature 453: 110-114, 2008 (Pubitemid 351630327)
-
(2008)
Nature
, vol.453
, Issue.7191
, pp. 110-114
-
-
Mullighan, C.G.1
Miller, C.B.2
Radtke, I.3
Phillips, L.A.4
Dalton, J.5
Ma, J.6
White, D.7
Hughes, T.P.8
Le, B.M.M.9
Pui, C.-H.10
Relling, M.V.11
Shurtleff, S.A.12
Downing, J.R.13
-
41
-
-
67149083222
-
Lnk inhibits myeloproliferative disorder-associated JAK2 mutant, JAK2V617F
-
Gery S, Cao Q, Gueller S, et al: Lnk inhibits myeloproliferative disorder-associated JAK2 mutant, JAK2V617F. J Leukoc Biol 85: 957-965, 2009
-
(2009)
J Leukoc Biol
, vol.85
, pp. 957-965
-
-
Gery, S.1
Cao, Q.2
Gueller, S.3
-
42
-
-
77958021645
-
LNK mutation studies in blast-phase myeloproliferative neoplasms, and in chronic-phase disease with TET2, IDH, JAK2 or MPL mutations
-
Pardanani A, Lasho T, Finke C, et al: LNK mutation studies in blast-phase myeloproliferative neoplasms, and in chronic-phase disease with TET2, IDH, JAK2 or MPL mutations. Leukemia 24:1713-1718, 2010
-
(2010)
Leukemia
, vol.24
, pp. 1713-1718
-
-
Pardanani, A.1
Lasho, T.2
Finke, C.3
-
43
-
-
77956670899
-
LNK mutations in JAK2 mutation-negative erythrocytosis
-
Lasho TL, Pardanani A, Tefferi A: LNK mutations in JAK2 mutation-negative erythrocytosis. N Engl J Med 363: 1189-1190, 2010
-
(2010)
N Engl J Med
, vol.363
, pp. 1189-1190
-
-
Lasho, T.L.1
Pardanani, A.2
Tefferi, A.3
-
44
-
-
34548042964
-
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel
-
DOI 10.1182/blood-2007-04-083501
-
Tefferi A, Thiele J, Orazi A, et al: Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel. Blood 110: 1092-1097, 2007 (Pubitemid 47281402)
-
(2007)
Blood
, vol.110
, Issue.4
, pp. 1092-1097
-
-
Tefferi, A.1
Thiele, J.2
Orazi, A.3
Kvasnicka, H.M.4
Barbui, T.5
Hanson, C.A.6
Barosi, G.7
Verstovsek, S.8
Birgegard, G.9
Mesa, R.10
Reilly, J.T.11
Gisslinger, H.12
Vannucchi, A.M.13
Cervantes, F.14
Finazzi, G.15
Hoffman, R.16
Gilliland, D.G.17
Bloomfield, C.D.18
Vardiman, J.W.19
-
45
-
-
32944477304
-
V617F mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia
-
DOI 10.1111/j.1365-2141.2005.05743.x
-
Tefferi A, Sirhan S, Lasho TL, et al: Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia. Br J Haematol 131: 166-171, 2005 (Pubitemid 43899681)
-
(2005)
British Journal of Haematology
, vol.131
, Issue.2
, pp. 166-171
-
-
Tefferi, A.1
Sirhan, S.2
Lasho, T.L.3
Schwager, S.M.4
Li, C.-Y.5
Dingli, D.6
Wolanskyj, A.P.7
Steensma, D.P.8
Mesa, R.9
Gilliland, D.G.10
-
46
-
-
31444439623
-
Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis [1]
-
DOI 10.1038/sj.leu.2404069, PII 2404069
-
James C, Delhommeau F, Marzac C, et al: Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis. Leukemia 20: 350-353, 2006 (Pubitemid 43148676)
-
(2006)
Leukemia
, vol.20
, Issue.2
, pp. 350-353
-
-
James, C.1
Delhommeau, F.2
Marzac, C.3
Teyssandier, I.4
Le, C.J.-P.5
Giraudier, S.6
Roy, L.7
Saulnier, P.8
Lacroix, L.9
Maury, S.10
Tulliez, M.11
Vainchenker, W.12
Ugo, V.13
Casadevall, N.14
-
47
-
-
19644392085
-
Diagnostic value of serum erythropoietin level in patients with absolute erythrocytosis
-
Mossuz P, Girodon F, Donnard M, et al: Diagnostic value of serum erythropoietin level in patients with absolute erythrocytosis. Haematologica 89:1194-1198, 2004
-
(2004)
Haematologica
, vol.89
, pp. 1194-1198
-
-
Mossuz, P.1
Girodon, F.2
Donnard, M.3
-
48
-
-
70449520449
-
Myeloproliferative neoplasms: Contemporary diagnosis using histology and genetics
-
Tefferi A, Skoda R, Vardiman JW: Myeloproliferative neoplasms: Contemporary diagnosis using histology and genetics. Nat Rev Clin Oncol 6: 627-637, 2009
-
(2009)
Nat Rev Clin Oncol
, vol.6
, pp. 627-637
-
-
Tefferi, A.1
Skoda, R.2
Vardiman, J.W.3
-
49
-
-
34250792174
-
Classification of Ph-negative chronic myeloproliferative disorders - Morphology as the yardstick of classification
-
DOI 10.1159/000101706
-
Kvasnicka HM, Thiele J: Classification of Ph-negative chronic myeloproliferative disorders-morphology as the yardstick of classification. Pathobiology 74: 63-71, 2007 (Pubitemid 46985278)
-
(2007)
Pathobiology
, vol.74
, Issue.2
, pp. 63-71
-
-
Kvasnicka, H.M.1
Thiele, J.2
-
50
-
-
39149105615
-
Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: A consensus statement from the international working group for myelofibrosis research and treatment [6]
-
DOI 10.1038/sj.leu.2404914, PII 2404914
-
Barosi G, Mesa RA, Thiele J, et al: Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: A consensus statement from the International Working Group for Myelofibrosis Research and Treatment. Leukemia 22: 437-438, 2008 (Pubitemid 351250553)
-
(2008)
Leukemia
, vol.22
, Issue.2
, pp. 437-438
-
-
Barosi, G.1
Mesa, R.A.2
Thiele, J.3
Cervantes, F.4
Campbell, P.J.5
Verstovsek, S.6
Dupriez, B.7
Levine, R.L.8
Passamonti, F.9
Gotlib, J.10
Reilly, J.T.11
Vannucchi, A.M.12
Hanson, C.A.13
Solberg, L.A.14
Orazi, A.15
Tefferi, A.16
-
51
-
-
49449089516
-
Evidence and expertise in the management of polycythemia vera and essential thrombocythemia
-
Finazzi G, Barbui T: Evidence and expertise in the management of polycythemia vera and essential thrombocythemia. Leukemia 22: 1494-1502, 2008
-
(2008)
Leukemia
, vol.22
, pp. 1494-1502
-
-
Finazzi, G.1
Barbui, T.2
-
52
-
-
79952087335
-
DIPSS Plus: A refined Dynamic International Prognostic Scoring System for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count, and transfusion status
-
Gangat N, Caramazza D, Vaidya R, et al: DIPSS Plus: A refined Dynamic International Prognostic Scoring System for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count, and transfusion status. J Clin Oncol 29:392-397, 2011
-
(2011)
J Clin Oncol
, vol.29
, pp. 392-397
-
-
Gangat, N.1
Caramazza, D.2
Vaidya, R.3
-
53
-
-
55549099571
-
Prognostic factors for thrombosis, myelofibrosis, and leukemia in essential thrombocythemia: A study of 605 patients
-
Passamonti F, Rumi E, Arcaini L, et al: Prognostic factors for thrombosis, myelofibrosis, and leukemia in essential thrombocythemia: A study of 605 patients. Haematologica 93:1645-1651, 2008
-
(2008)
Haematologica
, vol.93
, pp. 1645-1651
-
-
Passamonti, F.1
Rumi, E.2
Arcaini, L.3
-
54
-
-
8344229870
-
Life expectancy and prognostic factors for survival in patients with polycythemia vera and essential thrombocythemia
-
DOI 10.1016/j.amjmed.2004.06.032, PII S0002934304005315
-
Passamonti F, Rumi E, Pungolino E, et al: Life expectancy and prognostic factors for survival in patients with polycythemia vera and essential thrombocythemia. Am J Med 117: 755-761, 2004 (Pubitemid 39482529)
-
(2004)
American Journal of Medicine
, vol.117
, Issue.10
, pp. 755-761
-
-
Passamonti, F.1
Rumi, E.2
Pungolino, E.3
Malabarba, L.4
Bertazzoni, P.5
Valentini, M.6
Orlandi, E.7
Arcaini, L.8
Brusamolino, E.9
Pascutto, C.10
Cazzola, M.11
Morra, E.12
Lazzarino, M.13
-
55
-
-
34447132275
-
Leucocytosis in polycythaemia vera predicts both inferior survival and leukaemic transformation
-
DOI 10.1111/j.1365-2141.2007.06674.x
-
Gangat N, Strand J, Li CY, et al: Leucocytosis in polycythaemia vera predicts both inferior survival and leukaemic transformation. Br J Haematol 138: 354-358, 2007 (Pubitemid 47035399)
-
(2007)
British Journal of Haematology
, vol.138
, Issue.3
, pp. 354-358
-
-
Gangat, N.1
Strand, J.2
Li, C.-Y.3
Wu, W.4
Pardanani, A.5
Tefferi, A.6
-
56
-
-
33845900474
-
The haematocrit and platelet target in polycythemia vera
-
DOI 10.1111/j.1365-2141.2006.06430.x
-
Di Nisio M, Barbui T, Di Gennaro L, et al: The haematocrit and platelet target in polycythemia vera. Br J Haematol 136: 249-259, 2007 (Pubitemid 46020752)
-
(2007)
British Journal of Haematology
, vol.136
, Issue.2
, pp. 249-259
-
-
Di, N.M.1
Barbui, T.2
Di, G.L.3
Borrelli, G.4
Finazzi, G.5
Landolfi, R.6
Leone, G.7
Marfisi, R.8
Porreca, E.9
Ruggeri, M.10
Rutjes, A.W.S.11
Tognoni, G.12
Vannucchi, A.M.13
Marchioli, R.14
-
57
-
-
0021683781
-
Acquired von Willebrand's disease in the myeloproliferative syndrome
-
Budde U, Schaefer G, Mueller N, et al: Acquired von Willebrand's disease in the myeloproliferative syndrome. Blood 64: 981-985, 1984 (Pubitemid 15212036)
-
(1984)
Blood
, vol.64
, Issue.5
, pp. 981-985
-
-
Budde, U.1
Schaefer, G.2
Mueller, N.3
-
58
-
-
33846540216
-
Risk stratification for survival and leukemic transformation in essential thrombocythemia: A single institutional study of 605 patients
-
DOI 10.1038/sj.leu.2404500, PII 2404500
-
Gangat N, Wolanskyj AP, McClure RF, et al: Risk stratification for survival and leukemic transformation in essential thrombocythemia: A single institutional study of 605 patients. Leukemia 21: 270-276, 2007 (Pubitemid 46158119)
-
(2007)
Leukemia
, vol.21
, Issue.2
, pp. 270-276
-
-
Gangat, N.1
Wolanskyj, A.P.2
McClure, R.F.3
Li, C.-Y.4
Schwager, S.5
Wu, W.6
Tefferi, A.7
-
59
-
-
75449101962
-
Leukocytosis as a risk factor for thrombosis in myeloproliferative neoplasmsbiologically plausible but clinically uncertain
-
Tefferi A: Leukocytosis as a risk factor for thrombosis in myeloproliferative neoplasmsbiologically plausible but clinically uncertain. Am J Hematol 85: 93-94, 2009
-
(2009)
Am J Hematol
, vol.85
, pp. 93-94
-
-
Tefferi, A.1
-
60
-
-
67649402606
-
Perspectives on thrombosis in essential thrombocythemia and polycythemia vera: Is leukocytosis a causative factor?
-
Barbui T, Carobbio A, Rambaldi A, et al: Perspectives on thrombosis in essential thrombocythemia and polycythemia vera: Is leukocytosis a causative factor? Blood 114: 759-763, 2009
-
(2009)
Blood
, vol.114
, pp. 759-763
-
-
Barbui, T.1
Carobbio, A.2
Rambaldi, A.3
-
61
-
-
70349479426
-
Essential thrombocythemia and pregnancy: Observations from recent studies and management recommendations
-
Tefferi A, Passamonti F: Essential thrombocythemia and pregnancy: Observations from recent studies and management recommendations. Am J Hematol 84:629-630, 2009
-
(2009)
Am J Hematol
, vol.84
, pp. 629-630
-
-
Tefferi, A.1
Passamonti, F.2
-
62
-
-
63849328927
-
New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment
-
Cervantes F, Dupriez B, Pereira A, et al: New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment. Blood 113: 2895-2901, 2009
-
(2009)
Blood
, vol.113
, pp. 2895-2901
-
-
Cervantes, F.1
Dupriez, B.2
Pereira, A.3
-
63
-
-
77950352432
-
A dynamic prognostic model to predict survival in primary myelofibrosis: A study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment)
-
Passamonti F, Cervantes F, Vannucchi AM, et al: A dynamic prognostic model to predict survival in primary myelofibrosis: A study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment). Blood 115: 1703-1708, 2010
-
(2010)
Blood
, vol.115
, pp. 1703-1708
-
-
Passamonti, F.1
Cervantes, F.2
Vannucchi, A.M.3
-
64
-
-
85044556540
-
Refined cytogenetic risk categorization for overall and leukemia-free survival in primary myelofibrosis: A single center study of 433 patients
-
in press
-
Caramazza D, Begna KH, Gangat N, et al: Refined cytogenetic risk categorization for overall and leukemia-free survival in primary myelofibrosis: A single center study of 433 patients. Leukemia (in press)
-
Leukemia
-
-
Caramazza, D.1
Begna, K.H.2
Gangat, N.3
-
65
-
-
74249123815
-
JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: Nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival
-
Tefferi A, Lasho TL, Patnaik MM, et al: JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: Nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival. Leukemia 24:105-109, 2010
-
(2010)
Leukemia
, vol.24
, pp. 105-109
-
-
Tefferi, A.1
Lasho, T.L.2
Patnaik, M.M.3
-
66
-
-
73949151305
-
Dynamic model for predicting death within 12 months in patients with primary or post-polycythemia vera/ essential thrombocythemia myelofibrosis
-
Tam CS, Kantarjian H, Cortes J, et al: Dynamic model for predicting death within 12 months in patients with primary or post-polycythemia vera/ essential thrombocythemia myelofibrosis. J Clin Oncol 27: 5587-5593, 2009
-
(2009)
J Clin Oncol
, vol.27
, pp. 5587-5593
-
-
Tam, C.S.1
Kantarjian, H.2
Cortes, J.3
-
67
-
-
46049106196
-
Risk factors for leukemic transformation in patients with primary myelofibrosis
-
DOI 10.1002/cncr.23505
-
Huang J, Li CY, Mesa RA, et al: Risk factors for leukemic transformation in patients with primary myelofibrosis. Cancer 112: 2726-2732, 2008 (Pubitemid 351969217)
-
(2008)
Cancer
, vol.112
, Issue.12
, pp. 2726-2732
-
-
Huang, J.1
Li, C.-Y.2
Mesa, R.A.3
Wu, W.4
Hanson, C.A.5
Pardanani, A.6
Tefferi, A.7
-
68
-
-
30844463437
-
Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis
-
Dingli D, Schwager SM, Mesa RA, et al: Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis. Cancer 106: 1985-1989, 2006
-
(2006)
Cancer
, vol.106
, pp. 1985-1989
-
-
Dingli, D.1
Schwager, S.M.2
Mesa, R.A.3
-
69
-
-
43549125836
-
A dynamic prognostic model to predict survival in post-polycythemia vera myelofibrosis
-
Passamonti F, Rumi E, Caramella M, et al: A dynamic prognostic model to predict survival in post-polycythemia vera myelofibrosis. Blood 111: 3383-3387, 2008
-
(2008)
Blood
, vol.111
, pp. 3383-3387
-
-
Passamonti, F.1
Rumi, E.2
Caramella, M.3
-
70
-
-
0346727336
-
Efficacy and Safety of Low-Dose Aspirin in Polycythemia Vera
-
DOI 10.1056/NEJMoa035572
-
Landolfi R, Marchioli R, Kutti J, et al: Efficacy and safety of low-dose aspirin in polycythemia vera. N Engl J Med 350: 114-124, 2004 (Pubitemid 38056222)
-
(2004)
New England Journal of Medicine
, vol.350
, Issue.2
, pp. 114-124
-
-
Landolfi, R.1
Marchioli, R.2
Kutti, J.3
Gisslinger, H.4
Tognoni, G.5
Patrono, C.6
Barbui, T.7
-
71
-
-
0028913012
-
Hydroxyurea for patients with essential thrombocythemia and a high risk of thrombosis
-
Cortelazzo S, Finazzi G, Ruggeri M, et al: Hydroxyurea for patients with essential thrombocythemia and a high risk of thrombosis. N Engl J Med 332: 1132-1136, 1995
-
(1995)
N Engl J Med
, vol.332
, pp. 1132-1136
-
-
Cortelazzo, S.1
Finazzi, G.2
Ruggeri, M.3
-
72
-
-
21444434751
-
Hydroxyurea compared with anagrelide in high-risk essential thrombocythemia
-
DOI 10.1056/NEJMoa043800
-
Harrison CN, Campbell PJ, Buck G, et al: Hydroxyurea compared with anagrelide in high-risk essential thrombocythemia. N Engl J Med 353: 33-45, 2005 (Pubitemid 41007805)
-
(2005)
New England Journal of Medicine
, vol.353
, Issue.1
, pp. 33-45
-
-
Harrison, C.N.1
Campbell, P.J.2
Buck, G.3
Wheatley, K.4
East, C.L.5
Bareford, D.6
Wilkins, B.S.7
Van, D.W.J.D.8
Reilly, J.T.9
Grigg, A.P.10
Revell, P.11
Woodcock, B.E.12
Green, A.R.13
-
73
-
-
0002596838
-
Treatment of polycythemia vera: A summary of clinical trials conducted by the polycythemia vera study group
-
Wasserman LR, Berk PD, Berlin NI (eds): Philadelphia, PA, W.B. Saunders
-
Berk PD, Wasserman LR, Fruchtman SM, et al: Treatment of polycythemia vera: A summary of clinical trials conducted by the polycythemia vera study group, in Wasserman LR, Berk PD, Berlin NI (eds): Polycythemia Vera and the Myeloproliferative Disorders. Philadelphia, PA, W.B. Saunders, 1995, pp 166-194
-
(1995)
Polycythemia Vera and the Myeloproliferative Disorders
, pp. 166-194
-
-
Berk, P.D.1
Wasserman, L.R.2
Fruchtman, S.M.3
-
74
-
-
77956524019
-
Observation versus antiplatelet therapy as primary prophylaxis for thrombosis in low-risk essential thrombocythemia
-
Alvarez-Larran A, Cervantes F, Pereira A, et al: Observation versus antiplatelet therapy as primary prophylaxis for thrombosis in low-risk essential thrombocythemia. Blood 116: 1205-1210, 2010
-
(2010)
Blood
, vol.116
, pp. 1205-1210
-
-
Alvarez-Larran, A.1
Cervantes, F.2
Pereira, A.3
-
75
-
-
0027227873
-
Elevated platelet count as a cause of abnormal von Willebrand factor multimer distribution in plasma
-
Budde U, Scharf RE, Franke P, et al: Elevated platelet count as a cause of abnormal von Wille-brand factor multimer distribution in plasma. Blood 82:1749-1757, 1993 (Pubitemid 23278765)
-
(1993)
Blood
, vol.82
, Issue.6
, pp. 1749-1757
-
-
Budde, U.1
Scharf, R.E.2
Franke, P.3
Hartmann-Budde, K.4
Dent, J.5
Ruggeri, Z.M.6
-
76
-
-
73949090770
-
Pegylated interferon alfa-2a yields high rates of hematologic and molecular response in patients with advanced essential thrombocythemia and polycythemia vera
-
Quintas-Cardama A, Kantarjian H, Manshouri T, et al: Pegylated interferon alfa-2a yields high rates of hematologic and molecular response in patients with advanced essential thrombocythemia and polycythemia vera. J Clin Oncol 27: 5418-5424, 2009
-
(2009)
J Clin Oncol
, vol.27
, pp. 5418-5424
-
-
Quintas-Cardama, A.1
Kantarjian, H.2
Manshouri, T.3
-
77
-
-
54049141336
-
Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera
-
Kiladjian JJ, Cassinat B, Chevret S, et al: Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera. Blood 112: 3065-3072, 2008
-
(2008)
Blood
, vol.112
, pp. 3065-3072
-
-
Kiladjian, J.J.1
Cassinat, B.2
Chevret, S.3
-
78
-
-
34548125318
-
Busulphan is safe and efficient treatment in elderly patients with essential thrombocythemia [15]
-
DOI 10.1038/sj.leu.2404743, PII 2404743
-
Shvidel L, Sigler E, Haran M, et al: Busulphan is safe and efficient treatment in elderly patients with essential thrombocythemia. Leukemia 21: 2071-2072, 2007 (Pubitemid 47299992)
-
(2007)
Leukemia
, vol.21
, Issue.9
, pp. 2071-2072
-
-
Shvidel, L.1
Sigler, E.2
Haran, M.3
Klepfish, A.4
Duek, A.5
Berrebi, A.6
Shtalrid, M.7
-
79
-
-
0019488158
-
Treatment of polycythaemia vera by radiophosphorus or busulphan: A randomized trial
-
"Leukemia and Hematosarcoma" Cooperative Group, European Organization for Research on Treatment of Cancer (E.O.R.T.C.)
-
Treatment of polycythaemia vera by radiophosphorus or busulphan: A randomized trial. "Leukemia and Hematosarcoma" Cooperative Group, European Organization for Research on Treatment of Cancer (E.O.R.T.C.). Br J Cancer 44: 75-80, 1981
-
(1981)
Br J Cancer
, vol.44
, pp. 75-80
-
-
-
80
-
-
20144389274
-
Acute leukemia in polycythemia vera. An analysis of 1,638 patients enrolled in a prospective observational study
-
Finazzi G, Caruso V, Marchioli R, et al: Acute leukemia in polycythemia vera. An analysis of 1,638 patients enrolled in a prospective observational study. Blood 105:2664-2670, 2005
-
(2005)
Blood
, vol.105
, pp. 2664-2670
-
-
Finazzi, G.1
Caruso, V.2
Marchioli, R.3
-
81
-
-
0030784247
-
Treatment of polycythemia vera: The use of hydroxyurea and pipobroman in 292 patients under the age of 65 years
-
Najean Y, Rain JD: Treatment of polycythemia vera: The use of hydroxyurea and pipobroman in 292 patients under the age of 65 years. Blood 90: 3370-3377, 1997 (Pubitemid 27473405)
-
(1997)
Blood
, vol.90
, Issue.9
, pp. 3370-3377
-
-
Najean, Y.1
Rain, J.-D.2
-
82
-
-
33846540216
-
Risk stratification for survival and leukemic transformation in essential thrombocythemia: A single institutional study of 605 patients
-
DOI 10.1038/sj.leu.2404500, PII 2404500
-
Gangat N, Wolanskyj AP, McClure RF, et al: Risk stratification for survival and leukemic transformation in essential thrombocythemia: A single institutional study of 605 patients. Leukemia 21: 270-276, 2007 (Pubitemid 46158119)
-
(2007)
Leukemia
, vol.21
, Issue.2
, pp. 270-276
-
-
Gangat, N.1
Wolanskyj, A.P.2
McClure, R.F.3
Li, C.-Y.4
Schwager, S.5
Wu, W.6
Tefferi, A.7
-
83
-
-
77950622293
-
The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: Results of a 17-year, single-center trial (LaSHS)
-
Voskaridou E, Christoulas D, Bilalis A, et al: The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: Results of a 17-year, single-center trial (LaSHS). Blood 115: 2354-2363, 2010
-
(2010)
Blood
, vol.115
, pp. 2354-2363
-
-
Voskaridou, E.1
Christoulas, D.2
Bilalis, A.3
-
84
-
-
0022400901
-
Treatment of primary proliferative polycythaemia by venesection and low dose busulphan: Retrospective study from one centre
-
Messinezy M, Pearson TC, Prochazka A, et al: Treatment of primary proliferative polycythaemia by venesection and low dose busulphan: Retrospective study from one centre. Br J Haematol 61: 657-666, 1985 (Pubitemid 16231518)
-
(1985)
British Journal of Haematology
, vol.61
, Issue.4
, pp. 657-666
-
-
Messinezy, M.1
Pearson, T.C.2
Prochazka, A.3
Wetherley-Mein, G.4
-
85
-
-
79951899119
-
Anahydret: A European Multicenter Prospective phase 3-study: Non-inferiority of anagrelide compared to hydroxyurea in newly who-diagnosed et patients
-
Petrides E, Gotic M, Penka M, et al: Anahydret: A European Multicenter Prospective phase 3-study: Non-inferiority of anagrelide compared to hydroxyurea in newly who-diagnosed ET patients. Haematologica 94:440, 2009
-
(2009)
Haematologica
, vol.94
, pp. 440
-
-
Petrides, E.1
Gotic, M.2
Penka, M.3
-
86
-
-
39749167036
-
New and old treatment modalities in primary myelofibrosis
-
Cervantes F, Mesa R, Barosi G: New and old treatment modalities in primary myelofibrosis. Cancer J 13:377-383, 2007
-
(2007)
Cancer J
, vol.13
, pp. 377-383
-
-
Cervantes, F.1
Mesa, R.2
Barosi, G.3
-
87
-
-
67650766311
-
Erythropoiesis stimulating agents have limited therapeutic activity in transfusion-dependent patients with primary myelofibrosis regardless of serum erythropoietin level
-
Huang J, Tefferi A: Erythropoiesis stimulating agents have limited therapeutic activity in transfusion-dependent patients with primary myelofibrosis regardless of serum erythropoietin level. Eur J Haematol 83:154-155, 2009
-
(2009)
Eur J Haematol
, vol.83
, pp. 154-155
-
-
Huang, J.1
Tefferi, A.2
-
88
-
-
0036243117
-
Thalidomide treatment in myelofibrosis with myeloid metaplasia
-
DOI 10.1046/j.1365-2141.2002.03443.x
-
Elliott MA, Mesa RA, Li CY, et al: Thalidomide treatment in myelofibrosis with myeloid metaplasia. Br J Haematol 117: 288-296, 2002 (Pubitemid 34451143)
-
(2002)
British Journal of Haematology
, vol.117
, Issue.2
, pp. 288-296
-
-
Elliott, M.A.1
Mesa, R.A.2
Li, C.-Y.3
Hook, C.C.4
Ansell, S.M.5
Levitt, R.M.6
Geyer, S.M.7
Tefferi, A.8
-
89
-
-
33646336631
-
Thalidomide therapy for myelofibrosis with myeloid metaplasia
-
Thomas DA, Giles FJ, Albitar M, et al: Thalidomide therapy for myelofibrosis with myeloid metaplasia. Cancer 106: 1974-1984, 2006
-
(2006)
Cancer
, vol.106
, pp. 19741984
-
-
Thomas, D.A.1
Giles, F.J.2
Albitar, M.3
-
90
-
-
0012889254
-
A phase 2 trial of combination low-dose thalidomide and prednisone for the treatment of myelofibrosis with myeloid metaplasia
-
DOI 10.1182/blood-2002-09-2928
-
Mesa RA, Steensma DP, Pardanani A, et al: A phase 2 trial of combination low-dose thalidomide and prednisone for the treatment of myelofibrosis with myeloid metaplasia. Blood 101: 2534-2541, 2003 (Pubitemid 36857609)
-
(2003)
Blood
, vol.101
, Issue.7
, pp. 2534-2541
-
-
Mesa, R.A.1
Steensma, D.P.2
Pardanani, A.3
Li, C.-Y.4
Elliott, M.5
Kaufmann, S.H.6
Wiseman, G.7
Gray, L.A.8
Schroeder, G.9
Reeder, T.10
Zeldis, J.B.11
Tefferi, A.12
-
91
-
-
33747167338
-
Lenalidomide therapy in myelofibrosis with myeloid metaplasia
-
DOI 10.1182/blood-2006-02-004572
-
Tefferi A, Cortes J, Verstovsek S, et al: Lenalidomide therapy in myelofibrosis with myeloid metaplasia. Blood 108: 1158-1164, 2006 (Pubitemid 44232010)
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1158-1164
-
-
Tefferi, A.1
Cortes, J.2
Verstovsek, S.3
Mesa, R.A.4
Thomas, D.5
Lasho, T.L.6
Hogan, W.J.7
Litzow, M.R.8
Allred, J.B.9
Jones, D.10
Byrne, C.11
Zeldis, J.B.12
Ketterling, R.P.13
McClure, R.F.14
Giles, F.15
Kantarjian, H.M.16
-
92
-
-
78649475876
-
Lenalidomide and prednisone for myelofibrosis: Eastern Cooperative Oncology Group (ECOG) phase-2 trial E4903
-
Mesa RA, Yao X, Cripe LD, et al: Lenalidomide and prednisone for myelofibrosis: Eastern Cooperative Oncology Group (ECOG) phase-2 trial E4903. Blood 116:4436-4438, 2010
-
(2010)
Blood
, vol.116
, pp. 4436-4438
-
-
Mesa, R.A.1
Yao, X.2
Cripe, L.D.3
-
93
-
-
70350439432
-
Lenalidomide plus prednisone results in durable clinical, histopathologic, and molecular responses in patients with myelofibrosis
-
Quintas-Cardama A, Kantarjian HM, Manshouri T, et al: Lenalidomide plus prednisone results in durable clinical, histopathologic, and molecular responses in patients with myelofibrosis. J Clin Oncol 27:4760-4766, 2009
-
(2009)
J Clin Oncol
, vol.27
, pp. 4760-4766
-
-
Quintas-Cardama, A.1
Kantarjian, H.M.2
Manshouri, T.3
-
94
-
-
34447634117
-
Lenalidomide therapy in del(5)(q31)-associated myelofibrosis: Cytogenetic and JAK2V617F molecular remissions
-
Tefferi A, Lasho TL, Mesa RA, et al: Lenalidomide therapy in del(5)(q31)-associated myelofibrosis: Cytogenetic and JAK2V617F molecular remissions. Leukemia 21: 1827-1828, 2007
-
(2007)
Leukemia
, vol.21
, pp. 1827-1828
-
-
Tefferi, A.1
Lasho, T.L.2
Mesa, R.A.3
-
95
-
-
77955828956
-
Treatment options for hydroxyurea-refractory disease complications in myeloproliferative neoplasms: JAK2 inhibitors, radiotherapy, splenectomy and transjugular intrahepatic portosystemic shunt
-
Mishchenko E, Tefferi A: Treatment options for hydroxyurea-refractory disease complications in myeloproliferative neoplasms: JAK2 inhibitors, radiotherapy, splenectomy and transjugular intrahepatic portosystemic shunt. Eur J Haematol 85: 192-199, 2010
-
(2010)
Eur J Haematol
, vol.85
, pp. 192-199
-
-
Mishchenko, E.1
Tefferi, A.2
-
96
-
-
71949121402
-
Pomalidomide is active in the treatment of anemia associated with myelofibrosis
-
Tefferi A, Verstovsek S, Barosi G, et al: Pomalidomide is active in the treatment of anemia associated with myelofibrosis. J Clin Oncol 27: 4563-4569, 2009
-
(2009)
J Clin Oncol
, vol.27
, pp. 4563-4569
-
-
Tefferi, A.1
Verstovsek, S.2
Barosi, G.3
-
97
-
-
79751533175
-
A phase-2 trial of low-dose pomalidomide in myelofibrosis with anemia
-
in press
-
Begna KH, Mesa RA, Pardanani A, et al: A phase-2 trial of low-dose pomalidomide in myelofibrosis with anemia. Leukemia (in press)
-
Leukemia
-
-
Begna, K.H.1
Mesa, R.A.2
Pardanani, A.3
-
98
-
-
79952333359
-
Safety and efficacy of TG101348, a selective JAK2 inhibitor, in myelofibrosis
-
in press
-
Pardanani A, Gotlib JR, Jamieson C, et al: Safety and efficacy of TG101348, a selective JAK2 inhibitor, in myelofibrosis. J Clin Oncol (in press)
-
J Clin Oncol
-
-
Pardanani, A.1
Gotlib, J.R.2
Jamieson, C.3
-
99
-
-
77956696835
-
Safety and efficacy of INCB018424, a JAK1 and JAK2 inhibitor, in myelofibrosis
-
Verstovsek S, Kantarjian H, Mesa RA, et al: Safety and efficacy of INCB018424, a JAK1 and JAK2 inhibitor, in myelofibrosis. N Engl J Med 363:1117-1127, 2010
-
(2010)
N Engl J Med
, vol.363
, pp. 1117-1127
-
-
Verstovsek, S.1
Kantarjian, H.2
Mesa, R.A.3
-
100
-
-
77953225534
-
A phase 2 study of INCB018424, an oral, selective JAK1/JAK2 inhibitor, in patients with advanced polycythemia vera (PV) and essential thrombocythemia (ET) refractory to hydroxyurea
-
Verstovsek S, Passamonti F, Rambaldi A, et al: A phase 2 study of INCB018424, an oral, selective JAK1/JAK2 inhibitor, in patients with advanced polycythemia vera (PV) and essential thrombocythemia (ET) refractory to hydroxyurea. Blood 114:311, 2009
-
(2009)
Blood
, vol.114
, pp. 311
-
-
Verstovsek, S.1
Passamonti, F.2
Rambaldi, A.3
-
101
-
-
79551585770
-
A phase I/II study of CYT387, an oral JAK-1/2 inhibitor, in myelofibrosis: Significant response rates in anemia, splenomegaly, and constitutional symptoms
-
in press
-
Pardanani A, George G, Lasho T, et al: A phase I/II study of CYT387, an oral JAK-1/2 inhibitor, in myelofibrosis: Significant response rates in anemia, splenomegaly, and constitutional symptoms. Blood (in press)
-
Blood
-
-
Pardanani, A.1
George, G.2
Lasho, T.3
-
103
-
-
73949084969
-
Allogeneic stem cell transplantation after reduced-intensity conditioning in patients with myelofibrosis: A prospective, multicenter study of the Chronic Leukemia Working Party of the European Group for Blood and Marrow Transplantation
-
Kroger N, Holler E, Kobbe G, et al: Allogeneic stem cell transplantation after reduced-intensity conditioning in patients with myelofibrosis: A prospective, multicenter study of the Chronic Leukemia Working Party of the European Group for Blood and Marrow Transplantation. Blood 114: 5264-5270, 2009
-
(2009)
Blood
, vol.114
, pp. 5264-5270
-
-
Kroger, N.1
Holler, E.2
Kobbe, G.3
|