-
1
-
-
84887373344
-
Evaluation of WHO criteria for diagnosis of polycythemia vera: a prospective analysis
-
Silver RT, Chow W, Orazi A, Arles SP, Goldsmith SJ. Evaluation of WHO criteria for diagnosis of polycythemia vera: a prospective analysis. Blood 2013;122:1881–6.
-
(2013)
Blood
, vol.122
, pp. 1881-1886
-
-
Silver, R.T.1
Chow, W.2
Orazi, A.3
Arles, S.P.4
Goldsmith, S.J.5
-
2
-
-
84890372480
-
Somatic mutations of calreticulin in myeloproliferative neoplasms
-
Klampfl T, Gisslinger H, Harutyunyan AS, Nivarthi H, Rumi E, Milosevic JD, Them NC, Berg T, Gisslinger B, Pietra D, Chen D, Vladimer GI, Bagienski K, Milanesi C, Casetti IC, Sant'Antonio E, Ferretti V, Elena C, Schischlik F, Cleary C, Six M, Schalling M, Schonegger A, Bock C, Malcovati L, Pascutto C, Superti-Furga G, Cazzola M, Kralovics R. Somatic mutations of calreticulin in myeloproliferative neoplasms. N Engl J Med 2013;369:2379–90.
-
(2013)
N Engl J Med
, vol.369
, pp. 2379-2390
-
-
Klampfl, T.1
Gisslinger, H.2
Harutyunyan, A.S.3
Nivarthi, H.4
Rumi, E.5
Milosevic, J.D.6
Them, N.C.7
Berg, T.8
Gisslinger, B.9
Pietra, D.10
Chen, D.11
Vladimer, G.I.12
Bagienski, K.13
Milanesi, C.14
Casetti, I.C.15
Sant'Antonio, E.16
Ferretti, V.17
Elena, C.18
Schischlik, F.19
Cleary, C.20
Six, M.21
Schalling, M.22
Schonegger, A.23
Bock, C.24
Malcovati, L.25
Pascutto, C.26
Superti-Furga, G.27
Cazzola, M.28
Kralovics, R.29
more..
-
3
-
-
84908147447
-
Long-term survival and blast transformation in molecularly annotated essential thrombocythemia, polycythemia vera, and myelofibrosis
-
quiz 615
-
Tefferi A, Guglielmelli P, Larson DR, Finke C, Wassie EA, Pieri L, Gangat N, Fjerza R, Belachew AA, Lasho TL, Ketterling RP, Hanson CA, Rambaldi A, Finazzi G, Thiele J, Barbui T, Pardanani A, Vannucchi AM. Long-term survival and blast transformation in molecularly annotated essential thrombocythemia, polycythemia vera, and myelofibrosis. Blood 2014;124:2507–13; quiz 615.
-
(2014)
Blood
, vol.124
, pp. 2507-2513
-
-
Tefferi, A.1
Guglielmelli, P.2
Larson, D.R.3
Finke, C.4
Wassie, E.A.5
Pieri, L.6
Gangat, N.7
Fjerza, R.8
Belachew, A.A.9
Lasho, T.L.10
Ketterling, R.P.11
Hanson, C.A.12
Rambaldi, A.13
Finazzi, G.14
Thiele, J.15
Barbui, T.16
Pardanani, A.17
Vannucchi, A.M.18
-
4
-
-
84890328032
-
Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2
-
Nangalia J, Massie CE, Baxter EJ, Nice FL, Gundem G, Wedge DC, Avezov E, Li J, Kollmann K, Kent DG, Aziz A, Godfrey AL, Hinton J, Martincorena I, Van Loo P, Jones AV, Guglielmelli P, Tarpey P, Harding HP, Fitzpatrick JD, Goudie CT, Ortmann CA, Loughran SJ, Raine K, Jones DR, Butler AP, Teague JW, O'Meara S, McLaren S, Bianchi M, Silber Y, Dimitropoulou D, Bloxham D, Mudie L, Maddison M, Robinson B, Keohane C, Maclean C, Hill K, Orchard K, Tauro S, Du MQ, Greaves M, Bowen D, Huntly BJ, Harrison CN, Cross NC, Ron D, Vannucchi AM, Papaemmanuil E, Campbell PJ, Green AR. Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2. N Engl J Med 2013;369:2391–405.
-
(2013)
N Engl J Med
, vol.369
, pp. 2391-2405
-
-
Nangalia, J.1
Massie, C.E.2
Baxter, E.J.3
Nice, F.L.4
Gundem, G.5
Wedge, D.C.6
Avezov, E.7
Li, J.8
Kollmann, K.9
Kent, D.G.10
Aziz, A.11
Godfrey, A.L.12
Hinton, J.13
Martincorena, I.14
Van Loo, P.15
Jones, A.V.16
Guglielmelli, P.17
Tarpey, P.18
Harding, H.P.19
Fitzpatrick, J.D.20
Goudie, C.T.21
Ortmann, C.A.22
Loughran, S.J.23
Raine, K.24
Jones, D.R.25
Butler, A.P.26
Teague, J.W.27
O'Meara, S.28
McLaren, S.29
Bianchi, M.30
Silber, Y.31
Dimitropoulou, D.32
Bloxham, D.33
Mudie, L.34
Maddison, M.35
Robinson, B.36
Keohane, C.37
Maclean, C.38
Hill, K.39
Orchard, K.40
Tauro, S.41
Du, M.Q.42
Greaves, M.43
Bowen, D.44
Huntly, B.J.45
Harrison, C.N.46
Cross, N.C.47
Ron, D.48
Vannucchi, A.M.49
Papaemmanuil, E.50
Campbell, P.J.51
Green, A.R.52
more..
-
5
-
-
47649121826
-
The revised World Health Organization diagnostic criteria for polycythemia vera, essential thrombocytosis, and primary myelofibrosis: an alternative proposal
-
Spivak JL, Silver RT. The revised World Health Organization diagnostic criteria for polycythemia vera, essential thrombocytosis, and primary myelofibrosis: an alternative proposal. Blood 2008;112:231–9.
-
(2008)
Blood
, vol.112
, pp. 231-239
-
-
Spivak, J.L.1
Silver, R.T.2
-
6
-
-
33846660947
-
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
-
Scott LM, Tong W, Levine RL, Scott MA, Beer PA, Stratton MR, Futreal PA, Erber WN, McMullin MF, Harrison CN, Warren AJ, Gilliland DG, Lodish HF, Green AR. JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med 2007;356:459–68.
-
(2007)
N Engl J Med
, vol.356
, 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
-
7
-
-
55149092331
-
The classification and diagnosis of erythrocytosis
-
McMullin MF. The classification and diagnosis of erythrocytosis. Int J Lab Hematol 2008;30:447–59.
-
(2008)
Int J Lab Hematol
, vol.30
, pp. 447-459
-
-
McMullin, M.F.1
-
8
-
-
34548152255
-
Amendment to the guideline for diagnosis and investigation of polycythaemia/erythrocytosis
-
McMullin MF, Reilly JT, Campbell P, Bareford D, Green AR, Harrison CN, Conneally E, Ryan K. Amendment to the guideline for diagnosis and investigation of polycythaemia/erythrocytosis. Br J Haematol 2007;138:821–2.
-
(2007)
Br J Haematol
, vol.138
, pp. 821-822
-
-
McMullin, M.F.1
Reilly, J.T.2
Campbell, P.3
Bareford, D.4
Green, A.R.5
Harrison, C.N.6
Conneally, E.7
Ryan, K.8
-
9
-
-
84886575906
-
The new genetics of chronic neutrophilic leukemia and atypical CML: implications for diagnosis and treatment
-
Gotlib J, Maxson JE, George TI, Tyner JW. The new genetics of chronic neutrophilic leukemia and atypical CML: implications for diagnosis and treatment. Blood 2013;122:1707–11.
-
(2013)
Blood
, vol.122
, pp. 1707-1711
-
-
Gotlib, J.1
Maxson, J.E.2
George, T.I.3
Tyner, J.W.4
-
10
-
-
51649120030
-
Atypical chronic myeloid leukemia as defined in the WHO classification is a JAK2 V617F negative neoplasm
-
Fend F, Horn T, Koch I, Vela T, Orazi A. Atypical chronic myeloid leukemia as defined in the WHO classification is a JAK2 V617F negative neoplasm. Leuk Res 2008;32:1931–5.
-
(2008)
Leuk Res
, vol.32
, pp. 1931-1935
-
-
Fend, F.1
Horn, T.2
Koch, I.3
Vela, T.4
Orazi, A.5
-
11
-
-
84893964717
-
Luigia Randi M, Vannucchi AM, Gisslinger B, Mullauer L, Ruggeri M, Rambaldi A, Tefferi A. Masked polycythemia vera diagnosed according to WHO and BCSH classification
-
Barbui T, Thiele J, Carobbio A, Gisslinger H, Finazzi G, Rumi E. Luigia Randi M, Vannucchi AM, Gisslinger B, Mullauer L, Ruggeri M, Rambaldi A, Tefferi A. Masked polycythemia vera diagnosed according to WHO and BCSH classification. Am J Hematol 2014;89:199–202.
-
(2014)
Am J Hematol
, vol.89
, pp. 199-202
-
-
Barbui, T.1
Thiele, J.2
Carobbio, A.3
Gisslinger, H.4
Finazzi, G.5
Rumi, E.6
-
12
-
-
84899652823
-
Atypical chronic myeloid leukemia is clinically distinct from unclassifiable myelodysplastic/myeloproliferative neoplasms
-
Wang SA, Hasserjian RP, Fox PS, Rogers HJ, Geyer JT, Chabot-Richards D, Weinzierl E, Hatem J, Jaso J, Kanagal-Shamanna R, Stingo FC, Patel KP, Mehrotra M, Bueso-Ramos C, Young KH, Dinardo CD, Verstovsek S, Tiu RV, Bagg A, Hsi ED, Arber DA, Foucar K, Luthra R, Orazi A. Atypical chronic myeloid leukemia is clinically distinct from unclassifiable myelodysplastic/myeloproliferative neoplasms. Blood 2014;123:2645–51.
-
(2014)
Blood
, vol.123
, pp. 2645-2651
-
-
Wang, S.A.1
Hasserjian, R.P.2
Fox, P.S.3
Rogers, H.J.4
Geyer, J.T.5
Chabot-Richards, D.6
Weinzierl, E.7
Hatem, J.8
Jaso, J.9
Kanagal-Shamanna, R.10
Stingo, F.C.11
Patel, K.P.12
Mehrotra, M.13
Bueso-Ramos, C.14
Young, K.H.15
Dinardo, C.D.16
Verstovsek, S.17
Tiu, R.V.18
Bagg, A.19
Hsi, E.D.20
Arber, D.A.21
Foucar, K.22
Luthra, R.23
Orazi, A.24
more..
-
13
-
-
84892882972
-
Masked polycythemia vera (mPV): results of an international study
-
Barbui T, Thiele J, Gisslinger H, Finazzi G, Carobbio A, Rumi E, LuigiaRandi M, Betozzi I, Vannucchi AM, Pieri L, Carrai V, Gisslinger B, Mullauer L, Ruggeri M, Rambaldi A, Tefferi A. Masked polycythemia vera (mPV): results of an international study. Am J Hematol 2014;89:52–4.
-
(2014)
Am J Hematol
, vol.89
, pp. 52-54
-
-
Barbui, T.1
Thiele, J.2
Gisslinger, H.3
Finazzi, G.4
Carobbio, A.5
Rumi, E.6
LuigiaRandi, M.7
Betozzi, I.8
Vannucchi, A.M.9
Pieri, L.10
Carrai, V.11
Gisslinger, B.12
Mullauer, L.13
Ruggeri, M.14
Rambaldi, A.15
Tefferi, A.16
-
14
-
-
45149121653
-
Prognostic interaction between thrombocytosis and JAK2 V617F mutation in the WHO subcategories of myelodysplastic/myeloproliferative disease-unclassifiable and refractory anemia with ringed sideroblasts and marked thrombocytosis
-
Atallah E, Nussenzveig R, Yin CC, Bueso-Ramos C, Tam C, Manshouri T, Pierce S, Kantarjian H, Verstovsek S. Prognostic interaction between thrombocytosis and JAK2 V617F mutation in the WHO subcategories of myelodysplastic/myeloproliferative disease-unclassifiable and refractory anemia with ringed sideroblasts and marked thrombocytosis. Leukemia 2008;22:1295–8.
-
(2008)
Leukemia
, vol.22
, pp. 1295-1298
-
-
Atallah, E.1
Nussenzveig, R.2
Yin, C.C.3
Bueso-Ramos, C.4
Tam, C.5
Manshouri, T.6
Pierce, S.7
Kantarjian, H.8
Verstovsek, S.9
-
15
-
-
77956237515
-
Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1
-
Kohlmann A, Grossmann V, Klein HU, Schindela S, Weiss T, Kazak B, Dicker F, Schnittger S, Dugas M, Kern W, Haferlach C, Haferlach T. Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1. J Clin Oncol 2010;28:3858–65.
-
(2010)
J Clin Oncol
, vol.28
, pp. 3858-3865
-
-
Kohlmann, A.1
Grossmann, V.2
Klein, H.U.3
Schindela, S.4
Weiss, T.5
Kazak, B.6
Dicker, F.7
Schnittger, S.8
Dugas, M.9
Kern, W.10
Haferlach, C.11
Haferlach, T.12
-
16
-
-
84900852237
-
Discriminating between essential thrombocythemia and masked polycythemia vera in JAK2 mutated patients
-
Barbui T, Thiele J, Carobbio A, Guglielmelli P, Rambaldi A, Vannucchi AM, Tefferi A. Discriminating between essential thrombocythemia and masked polycythemia vera in JAK2 mutated patients. Am J Hematol 2014;89:588–90.
-
(2014)
Am J Hematol
, vol.89
, pp. 588-590
-
-
Barbui, T.1
Thiele, J.2
Carobbio, A.3
Guglielmelli, P.4
Rambaldi, A.5
Vannucchi, A.M.6
Tefferi, A.7
-
17
-
-
39749120756
-
Clinical and prognostic features of patients with myelodysplastic/myeloproliferative syndrome categorized as unclassified (MDS/MPD-U) by WHO classification
-
Cannella L, Breccia M, Latagliata R, Frustaci A, Alimena G. Clinical and prognostic features of patients with myelodysplastic/myeloproliferative syndrome categorized as unclassified (MDS/MPD-U) by WHO classification. Leuk Res 2008;32:514–6.
-
(2008)
Leuk Res
, vol.32
, pp. 514-516
-
-
Cannella, L.1
Breccia, M.2
Latagliata, R.3
Frustaci, A.4
Alimena, G.5
-
18
-
-
73149094518
-
TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia
-
Kosmider O, Gelsi-Boyer V, Ciudad M, Racoeur C, Jooste V, Vey N, Quesnel B, Fenaux P, Bastie JN, Beyne-Rauzy O, Stamatoulas A, Dreyfus F, Ifrah N, de Botton S, Vainchenker W, Bernard OA, Birnbaum D, Fontenay M, Solary E. TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia. Haematologica 2009;94:1676–81.
-
(2009)
Haematologica
, vol.94
, pp. 1676-1681
-
-
Kosmider, O.1
Gelsi-Boyer, V.2
Ciudad, M.3
Racoeur, C.4
Jooste, V.5
Vey, N.6
Quesnel, B.7
Fenaux, P.8
Bastie, J.N.9
Beyne-Rauzy, O.10
Stamatoulas, A.11
Dreyfus, F.12
Ifrah, N.13
de Botton, S.14
Vainchenker, W.15
Bernard, O.A.16
Birnbaum, D.17
Fontenay, M.18
Solary, E.19
-
19
-
-
84898916955
-
Bone marrow fibrosis in 66 patients with immune thrombocytopenia treated with thrombopoietin-receptor agonists: a single-center, long-term follow-up
-
Ghanima W, Geyer JT, Lee CS, Boiocchi L, Imahiyerobo AA, Orazi A, Bussel JB. Bone marrow fibrosis in 66 patients with immune thrombocytopenia treated with thrombopoietin-receptor agonists: a single-center, long-term follow-up. Haematologica 2014;99:937–44.
-
(2014)
Haematologica
, vol.99
, pp. 937-944
-
-
Ghanima, W.1
Geyer, J.T.2
Lee, C.S.3
Boiocchi, L.4
Imahiyerobo, A.A.5
Orazi, A.6
Bussel, J.B.7
-
20
-
-
79953074952
-
Recent advances in diagnosis, molecular pathology and therapy of chronic myelomonocytic leukaemia
-
Bacher U, Haferlach T, Schnittger S, Kreipe H, Kroger N. Recent advances in diagnosis, molecular pathology and therapy of chronic myelomonocytic leukaemia. Br J Haematol 2011;153:149–67.
-
(2011)
Br J Haematol
, vol.153
, pp. 149-167
-
-
Bacher, U.1
Haferlach, T.2
Schnittger, S.3
Kreipe, H.4
Kroger, N.5
-
21
-
-
33747610392
-
Refractory anemia with ringed sideroblasts associated with marked thrombocytosis harbors JAK2 mutation and shows overlapping myeloproliferative and myelodysplastic features
-
Wang SA, Hasserjian RP, Loew JM, Sechman EV, Jones D, Hao S, Liu Q, Zhao W, Mehdi M, Galili N, Woda B, Raza A. Refractory anemia with ringed sideroblasts associated with marked thrombocytosis harbors JAK2 mutation and shows overlapping myeloproliferative and myelodysplastic features. Leukemia 2006;20:1641–4.
-
(2006)
Leukemia
, vol.20
, pp. 1641-1644
-
-
Wang, S.A.1
Hasserjian, R.P.2
Loew, J.M.3
Sechman, E.V.4
Jones, D.5
Hao, S.6
Liu, Q.7
Zhao, W.8
Mehdi, M.9
Galili, N.10
Woda, B.11
Raza, A.12
-
22
-
-
84955194034
-
Chronic myelomonocytic leukemia with nucleophosmin (NPM1) mutation
-
Peng J, Zuo Z, Fu B, Oki Y, Tang G, Goswami M, Priyanka P, Muzzafar T, Medeiros LJ, Luthra R, Wang SA. Chronic myelomonocytic leukemia with nucleophosmin (NPM1) mutation. Eur J Haematol 2016;96:65–71.
-
(2016)
Eur J Haematol
, vol.96
, pp. 65-71
-
-
Peng, J.1
Zuo, Z.2
Fu, B.3
Oki, Y.4
Tang, G.5
Goswami, M.6
Priyanka, P.7
Muzzafar, T.8
Medeiros, L.J.9
Luthra, R.10
Wang, S.A.11
-
23
-
-
84857775547
-
European Bone Marrow Working Group trial on reproducibility of World Health Organization criteria to discriminate essential thrombocythemia from prefibrotic primary myelofibrosis–comment. Haematologica 2012;97(3):360–5--comment
-
discussion 8
-
Thiele J, Orazi A, Kvasnicka HM, Franco V, Boveri E, Gianelli U, Gisslinger H, Passamonti F, Tefferi A, Barbui T. European Bone Marrow Working Group trial on reproducibility of World Health Organization criteria to discriminate essential thrombocythemia from prefibrotic primary myelofibrosis–comment. Haematologica 2012;97(3):360–5--comment. Haematologica 2012;97:e5–6; discussion e7-8.
-
(2012)
Haematologica
, vol.97
, pp. e5-6
-
-
Thiele, J.1
Orazi, A.2
Kvasnicka, H.M.3
Franco, V.4
Boveri, E.5
Gianelli, U.6
Gisslinger, H.7
Passamonti, F.8
Tefferi, A.9
Barbui, T.10
-
24
-
-
64249155712
-
Refractory anemia with ringed sideroblasts associated with thrombocytosis: comparative analysis of marked with non-marked thrombocytosis, and relationship with JAK2 V617F mutational status
-
Raya JM, Arenillas L, Domingo A, Bellosillo B, Gutierrez G, Luno E, Pinan MA, Barbon M, Perez-Sirvent ML, Muruzabal MJ, Yanez L, Garcia L, Lemes A, Navarro JT, Elosegi A, Cortes MA, Villegas A, Duran MA, Ardanaz M, Florensa L. Refractory anemia with ringed sideroblasts associated with thrombocytosis: comparative analysis of marked with non-marked thrombocytosis, and relationship with JAK2 V617F mutational status. Int J Hematol 2008;88:387–95.
-
(2008)
Int J Hematol
, vol.88
, pp. 387-395
-
-
Raya, J.M.1
Arenillas, L.2
Domingo, A.3
Bellosillo, B.4
Gutierrez, G.5
Luno, E.6
Pinan, M.A.7
Barbon, M.8
Perez-Sirvent, M.L.9
Muruzabal, M.J.10
Yanez, L.11
Garcia, L.12
Lemes, A.13
Navarro, J.T.14
Elosegi, A.15
Cortes, M.A.16
Villegas, A.17
Duran, M.A.18
Ardanaz, M.19
Florensa, L.20
more..
-
25
-
-
84878574439
-
Clinicopathologic analysis of acute myeloid leukemia arising from chronic myelomonocytic leukemia
-
Courville EL, Wu Y, Kourda J, Roth CG, Brockmann J, Muzikansky A, Fathi AT, de Leval L, Orazi A, Hasserjian RP. Clinicopathologic analysis of acute myeloid leukemia arising from chronic myelomonocytic leukemia. Mod Pathol 2013;26:751–61.
-
(2013)
Mod Pathol
, vol.26
, pp. 751-761
-
-
Courville, E.L.1
Wu, Y.2
Kourda, J.3
Roth, C.G.4
Brockmann, J.5
Muzikansky, A.6
Fathi, A.T.7
de Leval, L.8
Orazi, A.9
Hasserjian, R.P.10
-
26
-
-
84908065771
-
The prognostic advantage of calreticulin mutations in myelofibrosis might be confined to type 1 or type 1-like CALR variants
-
Tefferi A, Lasho TL, Tischer A, Wassie EA, Finke CM, Belachew AA, Ketterling RP, Hanson CA, Pardanani AD. The prognostic advantage of calreticulin mutations in myelofibrosis might be confined to type 1 or type 1-like CALR variants. Blood 2014;124:2465–6.
-
(2014)
Blood
, vol.124
, pp. 2465-2466
-
-
Tefferi, A.1
Lasho, T.L.2
Tischer, A.3
Wassie, E.A.4
Finke, C.M.5
Belachew, A.A.6
Ketterling, R.P.7
Hanson, C.A.8
Pardanani, A.D.9
-
27
-
-
70449486011
-
Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
-
Malcovati L, Della Porta MG, Pietra D, Boveri E, Pellagatti A, Galli A, Travaglino E, Brisci A, Rumi E, Passamonti F, Invernizzi R, Cremonesi L, Boultwood J, Wainscoat JS, Hellstrom-Lindberg E, Cazzola M. Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Blood 2009;114:3538–45.
-
(2009)
Blood
, vol.114
, pp. 3538-3545
-
-
Malcovati, L.1
Della Porta, M.G.2
Pietra, D.3
Boveri, E.4
Pellagatti, A.5
Galli, A.6
Travaglino, E.7
Brisci, A.8
Rumi, E.9
Passamonti, F.10
Invernizzi, R.11
Cremonesi, L.12
Boultwood, J.13
Wainscoat, J.S.14
Hellstrom-Lindberg, E.15
Cazzola, M.16
-
28
-
-
84877608004
-
Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML
-
Maxson JE, Gotlib J, Pollyea DA, Fleischman AG, Agarwal A, Eide CA, Bottomly D, Wilmot B, McWeeney SK, Tognon CE, Pond JB, Collins RH, Goueli B, Oh ST, Deininger MW, Chang BH, Loriaux MM, Druker BJ, Tyner JW. Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML. N Engl J Med 2013;368:1781–90.
-
(2013)
N Engl J Med
, vol.368
, pp. 1781-1790
-
-
Maxson, J.E.1
Gotlib, J.2
Pollyea, D.A.3
Fleischman, A.G.4
Agarwal, A.5
Eide, C.A.6
Bottomly, D.7
Wilmot, B.8
McWeeney, S.K.9
Tognon, C.E.10
Pond, J.B.11
Collins, R.H.12
Goueli, B.13
Oh, S.T.14
Deininger, M.W.15
Chang, B.H.16
Loriaux, M.M.17
Druker, B.J.18
Tyner, J.W.19
-
29
-
-
79958244398
-
Characterization of NPM1-mutated AML with a history of myelodysplastic syndromes or myeloproliferative neoplasms
-
Schnittger S, Bacher U, Haferlach C, Alpermann T, Dicker F, Sundermann J, Kern W, Haferlach T. Characterization of NPM1-mutated AML with a history of myelodysplastic syndromes or myeloproliferative neoplasms. Leukemia 2011;25:615–21.
-
(2011)
Leukemia
, vol.25
, pp. 615-621
-
-
Schnittger, S.1
Bacher, U.2
Haferlach, C.3
Alpermann, T.4
Dicker, F.5
Sundermann, J.6
Kern, W.7
Haferlach, T.8
-
30
-
-
38549176801
-
JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
-
Schmitt-Graeff AH, Teo SS, Olschewski M, Schaub F, Haxelmans S, Kirn A, Reinecke P, Germing U, Skoda RC. JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Haematologica 2008;93:34–40.
-
(2008)
Haematologica
, vol.93
, pp. 34-40
-
-
Schmitt-Graeff, A.H.1
Teo, S.S.2
Olschewski, M.3
Schaub, F.4
Haxelmans, S.5
Kirn, A.6
Reinecke, P.7
Germing, U.8
Skoda, R.C.9
-
31
-
-
84883743018
-
CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia
-
Pardanani A, Lasho TL, Laborde RR, Elliott M, Hanson CA, Knudson RA, Ketterling RP, Maxson JE, Tyner JW, Tefferi A. CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia. Leukemia 2013;27:1870–3.
-
(2013)
Leukemia
, vol.27
, pp. 1870-1873
-
-
Pardanani, A.1
Lasho, T.L.2
Laborde, R.R.3
Elliott, M.4
Hanson, C.A.5
Knudson, R.A.6
Ketterling, R.P.7
Maxson, J.E.8
Tyner, J.W.9
Tefferi, A.10
-
32
-
-
84871988651
-
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
-
Piazza R, Valletta S, Winkelmann N, Redaelli S, Spinelli R, Pirola A, Antolini L, Mologni L, Donadoni C, Papaemmanuil E, Schnittger S, Kim DW, Boultwood J, Rossi F, Gaipa G, De Martini GP, di Celle PF, Jang HG, Fantin V, Bignell GR, Magistroni V, Haferlach T, Pogliani EM, Campbell PJ, Chase AJ, Tapper WJ, Cross NC, Gambacorti-Passerini C. Recurrent SETBP1 mutations in atypical chronic myeloid leukemia. Nat Genet 2013;45:18–24.
-
(2013)
Nat Genet
, vol.45
, pp. 18-24
-
-
Piazza, R.1
Valletta, S.2
Winkelmann, N.3
Redaelli, S.4
Spinelli, R.5
Pirola, A.6
Antolini, L.7
Mologni, L.8
Donadoni, C.9
Papaemmanuil, E.10
Schnittger, S.11
Kim, D.W.12
Boultwood, J.13
Rossi, F.14
Gaipa, G.15
De Martini, G.P.16
di Celle, P.F.17
Jang, H.G.18
Fantin, V.19
Bignell, G.R.20
Magistroni, V.21
Haferlach, T.22
Pogliani, E.M.23
Campbell, P.J.24
Chase, A.J.25
Tapper, W.J.26
Cross, N.C.27
Gambacorti-Passerini, C.28
more..
-
33
-
-
84900810119
-
Chronic neutrophilic leukemia 2014: Update on diagnosis, molecular genetics, and management
-
Elliott MA, Tefferi A. Chronic neutrophilic leukemia 2014: Update on diagnosis, molecular genetics, and management. Am J Hematol 2014;89:651–8.
-
(2014)
Am J Hematol
, vol.89
, pp. 651-658
-
-
Elliott, M.A.1
Tefferi, A.2
-
34
-
-
84922213806
-
Recurrent ETNK1 mutations in atypical chronic myeloid leukemia
-
Gambacorti-Passerini CB, Donadoni C, Parmiani A, Pirola A, Redaelli S, Signore G, Piazza V, Malcovati L, Fontana D, Spinelli R, Magistroni V, Gaipa G, Peronaci M, Morotti A, Panuzzo C, Saglio G, Usala E, Kim DW, Rea D, Zervakis K, Viniou N, Symeonidis A, Becker H, Boultwood J, Campiotti L, Carrabba M, Elli E, Bignell GR, Papaemmanuil E, Campbell PJ, Cazzola M, Piazza R. Recurrent ETNK1 mutations in atypical chronic myeloid leukemia. Blood 2015;125:499–503.
-
(2015)
Blood
, vol.125
, pp. 499-503
-
-
Gambacorti-Passerini, C.B.1
Donadoni, C.2
Parmiani, A.3
Pirola, A.4
Redaelli, S.5
Signore, G.6
Piazza, V.7
Malcovati, L.8
Fontana, D.9
Spinelli, R.10
Magistroni, V.11
Gaipa, G.12
Peronaci, M.13
Morotti, A.14
Panuzzo, C.15
Saglio, G.16
Usala, E.17
Kim, D.W.18
Rea, D.19
Zervakis, K.20
Viniou, N.21
Symeonidis, A.22
Becker, H.23
Boultwood, J.24
Campiotti, L.25
Carrabba, M.26
Elli, E.27
Bignell, G.R.28
Papaemmanuil, E.29
Campbell, P.J.30
Cazzola, M.31
Piazza, R.32
more..
-
35
-
-
83455234787
-
Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms
-
Malcovati L, Papaemmanuil E, Bowen DT, Boultwood J, Della Porta MG, Pascutto C, Travaglino E, Groves MJ, Godfrey AL, Ambaglio I, Galli A, Da Via MC, Conte S, Tauro S, Keenan N, Hyslop A, Hinton J, Mudie LJ, Wainscoat JS, Futreal PA, Stratton MR, Campbell PJ, Hellstrom-Lindberg E, Cazzola M. Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms. Blood 2011;118:6239–46.
-
(2011)
Blood
, vol.118
, pp. 6239-6246
-
-
Malcovati, L.1
Papaemmanuil, E.2
Bowen, D.T.3
Boultwood, J.4
Della Porta, M.G.5
Pascutto, C.6
Travaglino, E.7
Groves, M.J.8
Godfrey, A.L.9
Ambaglio, I.10
Galli, A.11
Da Via, M.C.12
Conte, S.13
Tauro, S.14
Keenan, N.15
Hyslop, A.16
Hinton, J.17
Mudie, L.J.18
Wainscoat, J.S.19
Futreal, P.A.20
Stratton, M.R.21
Campbell, P.J.22
Hellstrom-Lindberg, E.23
Cazzola, M.24
more..
|