-
1
-
-
19944427850
-
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
-
DOI 10.1056/NEJMoa041974
-
Falini B, Mecucci C, Tiacci E, Alcalay M, Rosati R, Pasqualucci L, La Starza R, Diverio D, Colombo E, Santucci A, Bigerna B, Pacini R, Pucciarini A, Liso A, Vignetti M, Fazi P, Meani N, Pettirossi V, Saglio G, Mandelli F, Lo-Coco F, Pelicci PG, Martelli MF (2005) Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med 352:254-266 (Pubitemid 40110814)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.3
, pp. 254-266
-
-
Falini, B.1
Mecucci, C.2
Tiacci, E.3
Alcalay, M.4
Rosati, R.5
Pasqualucci, L.6
La Starza, R.7
Diverio, D.8
Colombo, E.9
Santucci, A.10
Bigerna, B.11
Pacini, R.12
Pucciarini, A.13
Liso, A.14
Vignetti, M.15
Fazi, P.16
Meani, N.17
Pettirossi, V.18
Saglio, G.19
Mandelli, F.20
Lo-Coco, F.21
Pelicci, P.-G.22
Martelli, M.F.23
more..
-
2
-
-
0035093813
-
Dominant-negative mutations of CEBPA, encoding CCAAT/ enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia
-
Pabst T, Mueller BU, Zhang P, Radomska HS, Narravula S, Schnittger S, Behre G, Hiddemann W, Tenen DG (2001) Dominant-negative mutations of CEBPA, encoding CCAAT/ enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia. Nat Genet 27:263-270
-
(2001)
Nat Genet
, vol.27
, pp. 263-270
-
-
Pabst, T.1
Mueller, B.U.2
Zhang, P.3
Radomska, H.S.4
Narravula, S.5
Schnittger, S.6
Behre, G.7
Hiddemann, W.8
Tenen, D.G.9
-
3
-
-
53249123632
-
-
4th edn. WHO press, Lyon
-
Swerdlow S, Campo E, Lee Harris N, Jaffe E, Pileri S, Stein H, Thiele J, Vardiman J (2008) WHO classification of tumours of haematopoietic and lymphoid tissues, 4th edn. WHO press, Lyon
-
(2008)
WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues
-
-
Swerdlow, S.1
Campo, E.2
Lee Harris, N.3
Jaffe, E.4
Pileri, S.5
Stein, H.6
Thiele, J.7
Vardiman, J.8
-
4
-
-
42949083345
-
MicroRNA expression in cytogenetically normal acute myeloid leukemia
-
Marcucci G, Radmacher MD, Maharry K, Mrozek K, Ruppert AS, Paschka P, Vukosavljevic T, Whitman SP, Baldus CD, Langer C, Liu CG, Carroll AJ, Powell BL, Garzon R, Croce CM, Kolitz JE, Caligiuri MA, Larson RA, Bloomfield CD (2008) MicroRNA expression in cytogenetically normal acute myeloid leukemia. N Engl J Med 358:1919-1928
-
(2008)
N Engl J Med
, vol.358
, pp. 1919-1928
-
-
Marcucci, G.1
Radmacher, M.D.2
Maharry, K.3
Mrozek, K.4
Ruppert, A.S.5
Paschka, P.6
Vukosavljevic, T.7
Whitman, S.P.8
Baldus, C.D.9
Langer, C.10
Liu, C.G.11
Carroll, A.J.12
Powell, B.L.13
Garzon, R.14
Croce, C.M.15
Kolitz, J.E.16
Caligiuri, M.A.17
Larson, R.A.18
Bloomfield, C.D.19
-
5
-
-
15644380236
-
Long-term survival of patients with acute myeloid leukemia: A third follow-up of the Fourth International Workshop on Chromosomes in Leukemia
-
Bloomfield CD, Shuma C, Regal L, Philip PP, Hossfeld DK, Hagemeijer AM, Garson OM, Peterson BA, Sakurai M, Alimena G, Berger R, Rowley JD, Ruutu T, Mitelman F, Dewald GW, Swansbury J (1997) Long-term survival of patients with acute myeloid leukemia: A third follow-up of the Fourth International Workshop on Chromosomes in Leukemia. Cancer 80(11 Suppl):2191-2198
-
(1997)
Cancer
, vol.80
, Issue.11 SUPPL.
, pp. 2191-2198
-
-
Bloomfield, C.D.1
Shuma, C.2
Regal, L.3
Philip, P.P.4
Hossfeld, D.K.5
Hagemeijer, A.M.6
Garson, O.M.7
Peterson, B.A.8
Sakurai, M.9
Alimena, G.10
Berger, R.11
Rowley, J.D.12
Ruutu, T.13
Mitelman, F.14
Dewald, G.W.15
Swansbury, J.16
-
6
-
-
0028182306
-
Long-term survival in acute myelogenous leukemia: A second follow-up of the Fourth International Workshop on Chromosomes in Leukemia
-
Swansbury GJ, Lawler SD, Alimena G, Arthur D, Berger R, Van den Berghe H, Bloomfield CD, de la Chappelle A, Dewald G, Garson OM (1994) Long-term survival in acute myelogenous leukemia: A second follow-up of the Fourth International Workshop on Chromosomes in Leukemia. Cancer Genet Cytogenet 73:1-7
-
(1994)
Cancer Genet Cytogenet
, vol.73
, pp. 1-7
-
-
Swansbury, G.J.1
Lawler, S.D.2
Alimena, G.3
Arthur, D.4
Berger, R.5
Van Den Berghe, H.6
Bloomfield, C.D.7
De La Chappelle, A.8
Dewald, G.9
Garson, O.M.10
-
7
-
-
0034672269
-
Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: A Southwest Oncology Group/Eastern Cooperative Oncology Group Study
-
Slovak ML, Kopecky KJ, Cassileth PA, Harrington DH, Theil KS, Mohamed A, Paietta E, Willman CL, Head DR, Rowe JM, Forman SJ, Appelbaum FR (2000) Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: A Southwest Oncology Group/Eastern Cooperative Oncology Group Study. Blood 96:4075-4083
-
(2000)
Blood
, vol.96
, pp. 4075-4083
-
-
Slovak, M.L.1
Kopecky, K.J.2
Cassileth, P.A.3
Harrington, D.H.4
Theil, K.S.5
Mohamed, A.6
Paietta, E.7
Willman, C.L.8
Head, D.R.9
Rowe, J.M.10
Forman, S.J.11
Appelbaum, F.R.12
-
8
-
-
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, Loffler H, Sauerland CM, Serve H, Buchner T, Haferlach T, Hiddemann W (2002) 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 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
Loffler, H.7
Sauerland, C.M.8
Serve, H.9
Buchner, T.10
Haferlach, T.11
Hiddemann, W.12
-
9
-
-
0036720398
-
The roles of FLT3 in hematopoiesis and leukemia
-
Gilliland DG, Griffin JD (2002) The roles of FLT3 in hematopoiesis and leukemia. Blood 100:1532-1542
-
(2002)
Blood
, vol.100
, pp. 1532-1542
-
-
Gilliland, D.G.1
Griffin, J.D.2
-
10
-
-
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
-
Christiansen DH, Andersen MK, Pedersen-Bjergaard J (2004) 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 104:1474-1481
-
(2004)
Blood
, vol.104
, pp. 1474-1481
-
-
Christiansen, D.H.1
Andersen, M.K.2
Pedersen-Bjergaard, J.3
-
11
-
-
34347236177
-
A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia
-
Bacher U, Haferlach T, Kern W, Haferlach C, Schnittger S (2007) A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia. Haematologica 92:744-752
-
(2007)
Haematologica
, vol.92
, pp. 744-752
-
-
Bacher, U.1
Haferlach, T.2
Kern, W.3
Haferlach, C.4
Schnittger, S.5
-
13
-
-
33646475438
-
Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations
-
Niimi H, Harada H, Harada Y, Ding Y, Imagawa J, Inaba T, Kyo T, Kimura A (2006) Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations. Leukemia 20:635-644
-
(2006)
Leukemia
, vol.20
, pp. 635-644
-
-
Niimi, H.1
Harada, H.2
Harada, Y.3
Ding, Y.4
Imagawa, J.5
Inaba, T.6
Kyo, T.7
Kimura, A.8
-
14
-
-
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, Pfeilstocker M, Nosslinger T, Hildebrandt B, Kundgen A, Lubbert M, Kunzmann R, Giagounidis AA, Aul C, Trumper L, Krieger O, Stauder R, Muller TH, Wimazal F, Valent P, Fonatsch C, Steidl C (2007) New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: Evidence from a core dataset of 2124 patients. Blood 110:4385-4395
-
(2007)
Blood
, vol.110
, 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.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
-
15
-
-
25444516768
-
JAK2 mutations in myeloproliferative disorders
-
Tefferi A, Lasho TL, Gilliland G (2005) JAK2 mutations in myeloproliferative disorders. N Engl J Med 353:1416-1417
-
(2005)
N Engl J Med
, vol.353
, pp. 1416-1417
-
-
Tefferi, A.1
Lasho, T.L.2
Gilliland, G.3
-
16
-
-
33845355846
-
JAK-2 mutations and their relevance to myeloproliferative disease
-
Levine RL, Gilliland DG (2007) JAK-2 mutations and their relevance to myeloproliferative disease. Curr Opin Hematol 14:43-47
-
(2007)
Curr Opin Hematol
, vol.14
, pp. 43-47
-
-
Levine, R.L.1
Gilliland, D.G.2
-
17
-
-
33750534561
-
MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients
-
Pardanani AD, Levine RL, Lasho T, Pikman Y, Mesa RA, Wadleigh M, Steensma DP, Elliott MA, Wolanskyj AP, Hogan WJ, McClure RF, Litzow MR, Gilliland DG, Tefferi A (2006) MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients. Blood 108:3472-3476
-
(2006)
Blood
, vol.108
, pp. 3472-3476
-
-
Pardanani, A.D.1
Levine, R.L.2
Lasho, T.3
Pikman, Y.4
Mesa, R.A.5
Wadleigh, M.6
Steensma, D.P.7
Elliott, M.A.8
Wolanskyj, A.P.9
Hogan, W.J.10
McClure, R.F.11
Litzow, M.R.12
Gilliland, D.G.13
Tefferi, A.14
-
18
-
-
38949160429
-
Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders
-
Pietra D, Li S, Brisci A, Passamonti F, Rumi E, Theocharides A, Ferrari M, Gisslinger H, Kralovics R, Cremonesi L, Skoda R, Cazzola M (2008) Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 111:1686-1689
-
(2008)
Blood
, vol.111
, 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
-
19
-
-
66249137734
-
Mutation in TET2 in myeloid cancers
-
Delhommeau F, Dupont S, Della Valle V, James C, Trannoy S, Masse A, Kosmider O, Le Couedic JP, Robert F, Alberdi A, Lecluse Y, Plo I, Dreyfus FJ, Marzac C, Casadevall N, Lacombe C, Romana SP, Dessen P, Soulier J, Viguie F, Fontenay M, Vainchenker W, Bernard OA (2009) Mutation in TET2 in myeloid cancers. N Engl J Med 360:2289-2301
-
(2009)
N Engl J Med
, vol.360
, pp. 2289-2301
-
-
Delhommeau, F.1
Dupont, S.2
Della Valle, V.3
James, C.4
Trannoy, S.5
Masse, A.6
Kosmider, O.7
Le Couedic, J.P.8
Robert, F.9
Alberdi, A.10
Lecluse, Y.11
Plo, I.12
Dreyfus, F.J.13
Marzac, C.14
Casadevall, N.15
Lacombe, C.16
Romana, S.P.17
Dessen, P.18
Soulier, J.19
Viguie, F.20
Fontenay, M.21
Vainchenker, W.22
Bernard, O.A.23
more..
-
20
-
-
67649876132
-
Acquired mutations in TET2 are common in myelodysplastic syndromes
-
Langemeijer SM, Kuiper RP, Berends M, Knops R, Aslanyan MG, Massop M, Stevens-Linders E, van Hoogen P, van Kessel AG, Raymakers RA, Kamping EJ, Verhoef GE, Verburgh E, Hagemeijer A, Vandenberghe P, de Witte T, van der Reijden BA, Jansen JH (2009) Acquired mutations in TET2 are common in myelodysplastic syndromes. Nat Genet 41:838-842
-
(2009)
Nat Genet
, vol.41
, pp. 838-842
-
-
Langemeijer, S.M.1
Kuiper, R.P.2
Berends, M.3
Knops, R.4
Aslanyan, M.G.5
Massop, M.6
Stevens-Linders, E.7
Van Hoogen, P.8
Van Kessel, A.G.9
Raymakers, R.A.10
Kamping, E.J.11
Verhoef, G.E.12
Verburgh, E.13
Hagemeijer, A.14
Vandenberghe, P.15
De Witte, T.16
Van Der Reijden, B.A.17
Jansen, J.H.18
-
21
-
-
67650924270
-
Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML
-
Tefferi A, Lim KH, Abdel-Wahab O, Lasho TL, Patel J, Patnaik MM, Hanson CA, Pardanani A, Gilliland DG, Levine RL (2009) Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML. Leukemia 23:1343-1345
-
(2009)
Leukemia
, vol.23
, pp. 1343-1345
-
-
Tefferi, A.1
Lim, K.H.2
Abdel-Wahab, O.3
Lasho, T.L.4
Patel, J.5
Patnaik, M.M.6
Hanson, C.A.7
Pardanani, A.8
Gilliland, D.G.9
Levine, R.L.10
-
22
-
-
57749114621
-
250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies
-
Dunbar AJ, Gondek LP, O'Keefe CL, Makishima H, Rataul MS, Szpurka H, Sekeres MA, Wang XF, McDevitt MA, Maciejewski JP (2008) 250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies. Cancer Res 68:10349-10357
-
(2008)
Cancer Res
, vol.68
, pp. 10349-10357
-
-
Dunbar, A.J.1
Gondek, L.P.2
O'Keefe, C.L.3
Makishima, H.4
Rataul, M.S.5
Szpurka, H.6
Sekeres, M.A.7
Wang, X.F.8
McDevitt, M.A.9
Maciejewski, J.P.10
-
23
-
-
34547946211
-
Flt3-dependent transformation by inactivating c-Cbl mutations in AML
-
Sargin B, Choudhary C, Crosetto N, Schmidt MH, Grundler R, Rensinghoff M, Thiessen C, Tickenbrock L, Schwable J, Brandts C, August B, Koschmieder S, Bandi SR, Duyster J, Berdel WE, Muller-Tidow C, Dikic I, Serve H (2007) Flt3-dependent transformation by inactivating c-Cbl mutations in AML. Blood 110:1004-1012
-
(2007)
Blood
, vol.110
, pp. 1004-1012
-
-
Sargin, B.1
Choudhary, C.2
Crosetto, N.3
Schmidt, M.H.4
Grundler, R.5
Rensinghoff, M.6
Thiessen, C.7
Tickenbrock, L.8
Schwable, J.9
Brandts, C.10
August, B.11
Koschmieder, S.12
Bandi, S.R.13
Duyster, J.14
Berdel, W.E.15
Muller-Tidow, C.16
Dikic, I.17
Serve, H.18
-
24
-
-
67349124376
-
TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis
-
Tefferi A, Pardanani A, Lim KH, bdel-Wahab O, Lasho TL, Patel J, Gangat N, Finke CM, Schwager S, Mullally A, Li CY, Hanson CA, Mesa R, Bernard O, Delhommeau F, Vainchenker W, Gilliland DG, Levine RL (2009) TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia 23:905-911
-
(2009)
Leukemia
, vol.23
, pp. 905-911
-
-
Tefferi, A.1
Pardanani, A.2
Lim, K.H.3
Bdel-Wahab, O.4
Lasho, T.L.5
Patel, J.6
Gangat, N.7
Finke, C.M.8
Schwager, S.9
Mullally, A.10
Li, C.Y.11
Hanson, C.A.12
Mesa, R.13
Bernard, O.14
Delhommeau, F.15
Vainchenker, W.16
Gilliland, D.G.17
Levine, R.L.18
-
25
-
-
0037350661
-
TET1, a member of a novel protein family, is fused to MLL in acute myeloid leukemia containing the t(10;11) (q22;q23
-
Lorsbach RB, Moore J, Mathew S, Raimondi SC, Mukatira ST, Downing JR (2003) TET1, a member of a novel protein family, is fused to MLL in acute myeloid leukemia containing the t(10;11) (q22;q23). Leukemia 17:637-641
-
(2003)
Leukemia
, vol.17
, pp. 637-641
-
-
Lorsbach, R.B.1
Moore, J.2
Mathew, S.3
Raimondi, S.C.4
Mukatira, S.T.5
Downing, J.R.6
-
26
-
-
67651065502
-
Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies
-
Abdel-Wahab O, Mullally A, Hedvat C, Garcia-Manero G, Patel J, Wadleigh M, Malinge S, Yao J, Kilpivaara O, Bhat R, Huberman K, Thomas S, Dolgalev I, Heguy A, Paietta E, Le Beau MM, Beran M, Tallman MS, Ebert BL, Kantarjian HM, Stone RM, Gilliland DG, Crispino JD, Levine RL (2009) Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies. Blood 114:144-147
-
(2009)
Blood
, vol.114
, pp. 144-147
-
-
Abdel-Wahab, O.1
Mullally, A.2
Hedvat, C.3
Garcia-Manero, G.4
Patel, J.5
Wadleigh, M.6
Malinge, S.7
Yao, J.8
Kilpivaara, O.9
Bhat, R.10
Huberman, K.11
Thomas, S.12
Dolgalev, I.13
Heguy, A.14
Paietta, E.15
Le Beau, M.M.16
Beran, M.17
Tallman, M.S.18
Ebert, B.L.19
Kantarjian, H.M.20
Stone, R.M.21
Gilliland, D.G.22
Crispino, J.D.23
Levine, R.L.24
more..
-
27
-
-
70350438115
-
TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDS
-
Kosmider O, Gelsi-Boyer V, Cheok M, Grabar S, la-Valle V, Picard F, Viguie F, Quesnel B, Beyne-Rauzy O, Solary E, Vey N, Hunault-Berger M, Fenaux P, Mansat-De Mas V, Delabesse E, Guardiola P, Lacombe C, Vainchenker W, Preudhomme C, Dreyfus F, Bernard OA, Birnbaum D, Fontenay M (2009) TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDS). Blood 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
Viguie, F.7
Quesnel, B.8
Beyne-Rauzy, O.9
Solary, E.10
Vey, N.11
Hunault-Berger, M.12
Fenaux, P.13
Mansat-De Mas, V.14
Delabesse, E.15
Guardiola, P.16
Lacombe, C.17
Vainchenker, W.18
Preudhomme, C.19
Dreyfus, F.20
Bernard, O.A.21
Birnbaum, D.22
Fontenay, M.23
more..
-
28
-
-
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 (2009) TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia. Haematologica 94:1676-1681
-
(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
-
29
-
-
70149101696
-
Analysis of the teneleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms
-
Saint-Martin C, Leroy G, Delhommeau F, Panelatti G, Dupont S, James C, Plo I, Bordessoule D, Chomienne C, Delannoy A, Devidas A, Gardembas-Pain M, Isnard F, Plumelle Y, BernardO, Vainchenker W, Najman A, Bellanne-Chantelot C (2009) Analysis of the teneleven translocation 2 (TET2) gene in familial myeloproliferative neoplasms. Blood 114:1628-1632
-
(2009)
Blood
, vol.114
, pp. 1628-1632
-
-
Saint-Martin, C.1
Leroy, G.2
Delhommeau, F.3
Panelatti, G.4
Dupont, S.5
James, C.6
Plo, I.7
Bordessoule, D.8
Chomienne, C.9
Delannoy, A.10
Devidas, A.11
Gardembas-Pain, M.12
Isnard, F.13
Plumelle, Y.14
Bernard, O.15
Vainchenker, W.16
Najman, A.17
Bellanne-Chantelot, C.18
-
30
-
-
67349124376
-
TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis
-
Tefferi A, Pardanani A, Lim KH, Abdel-Wahab O, Lasho TL, Patel J, Gangat N, Finke CM, Schwager S, Mullally A, Li CY, Hanson CA, Mesa R, Bernard O, Delhommeau F, Vainchenker W, Gilliland DG, Levine RL (2009) TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia 23:905-911
-
(2009)
Leukemia
, vol.23
, pp. 905-911
-
-
Tefferi, A.1
Pardanani, A.2
Lim, K.H.3
Abdel-Wahab, O.4
Lasho, T.L.5
Patel, J.6
Gangat, N.7
Finke, C.M.8
Schwager, S.9
Mullally, A.10
Li, C.Y.11
Hanson, C.A.12
Mesa, R.13
Bernard, O.14
Delhommeau, F.15
Vainchenker, W.16
Gilliland, D.G.17
Levine, R.L.18
-
31
-
-
67650588639
-
Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms
-
Jankowska AM, Szpurka H, Tiu RV, Makishima H, Afable M, Huh J, O'Keefe CL, Ganetzky R, McDevitt MA, Maciejewski JP (2009) Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms. Blood 113:6403-6410
-
(2009)
Blood
, vol.113
, pp. 6403-6410
-
-
Jankowska, A.M.1
Szpurka, H.2
Tiu, R.V.3
Makishima, H.4
Afable, M.5
Huh, J.6
O'Keefe, C.L.7
Ganetzky, R.8
McDevitt, M.A.9
Maciejewski, J.P.10
-
32
-
-
77950388949
-
Clonal analysis of TET2 and JAK2 mutations suggests that TET2 can be a late event in the progression ofmyeloproliferative neoplasms
-
online prepublished, Jan 8, doi:10.1182/ blood-2009-09-245381
-
Schaub FX, Looser R, Li S, Hao-Shen H, Lehmann T, Tichelli A, Skoda RC: Clonal analysis of TET2 and JAK2 mutations suggests that TET2 can be a late event in the progression ofmyeloproliferative neoplasms. Blood; online prepublished, Jan 8, 2010. doi:10.1182/ blood-2009-09-245381
-
(2010)
Blood
-
-
Schaub, F.X.1
Looser, R.2
Li, S.3
Hao-Shen, H.4
Lehmann, T.5
Tichelli, A.6
Skoda, R..C.7
-
33
-
-
76549109434
-
Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias
-
Abdel-Wahab O, Manshouri T, Patel J, Harris K, Yao J, Hedvat C, Heguy A, Bueso-Ramos C, Kantarjian H, Levine RL, Verstovsek S (2010) Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias. Cancer Res 70:447-452
-
(2010)
Cancer Res
, vol.70
, pp. 447-452
-
-
Abdel-Wahab, O.1
Manshouri, T.2
Patel, J.3
Harris, K.4
Yao, J.5
Hedvat, C.6
Heguy, A.7
Bueso-Ramos, C.8
Kantarjian, H.9
Levine, R.L.10
Verstovsek, S.11
-
34
-
-
77955662987
-
RUNX1 mutations play a major role in the progression of MDS to s-AML following MDS: A genetic and cytogenetic analysis of sequential samples
-
abstract #3634
-
Dicker F, Haferlach C, Kern W, Haferlach T, Schnittger S (2008) RUNX1 mutations play a major role in the progression of MDS to s-AML following MDS: A genetic and cytogenetic analysis of sequential samples. Annual Meeting of the Society of Hematology Blood 112. abstract #3634
-
(2008)
Annual Meeting of the Society of Hematology Blood
, pp. 112
-
-
Dicker, F.1
Haferlach, C.2
Kern, W.3
Haferlach, T.4
Schnittger, S.5
-
35
-
-
67349145955
-
Frequent TET2 mutations in systemic mastocytosis: Clinical, KITD816V and FIP1L1-PDGFRA correlates
-
Tefferi A, Levine RL, Lim KH, Abdel-Wahab O, Lasho TL, Patel J, Finke CM, Mullally A, Li CY, Pardanani A, Gilliland DG (2009) Frequent TET2 mutations in systemic mastocytosis: Clinical, KITD816V and FIP1L1-PDGFRA correlates. Leukemia 23:900-904
-
(2009)
Leukemia
, vol.23
, pp. 900-904
-
-
Tefferi, A.1
Levine, R.L.2
Lim, K.H.3
Abdel-Wahab, O.4
Lasho, T.L.5
Patel, J.6
Finke, C.M.7
Mullally, A.8
Li, C.Y.9
Pardanani, A.10
Gilliland, D.G.11
-
36
-
-
12044256844
-
Tumour induction by activated abl involves tyrosine phosphorylation of the product of the cbl oncogene
-
Andoniou CE, Thien CB, Langdon WY (1994) Tumour induction by activated abl involves tyrosine phosphorylation of the product of the cbl oncogene. EMBO J 13:4515-4523
-
(1994)
EMBO J
, vol.13
, pp. 4515-4523
-
-
Andoniou, C.E.1
Thien, C.B.2
Langdon, W.Y.3
-
37
-
-
0026020985
-
Relationship of the human protooncogene CBL2 on 11q23 to the t (4;11), t(11;22), and t(11;14) breakpoints
-
Savage PD, Shapiro M, Langdon WY, Geurts van Kessel AD, Seuanez HN, Akao Y, Croce C, Morse HC III, Kersey JH (1991) Relationship of the human protooncogene CBL2 on 11q23 to the t (4;11), t(11;22), and t(11;14) breakpoints. Cytogenet Cell Genet 56:112-115
-
(1991)
Cytogenet Cell Genet
, vol.56
, pp. 112-115
-
-
Savage, P.D.1
Shapiro, M.2
Langdon, W.Y.3
Geurts Van Kessel, A.D.4
Seuanez, H.N.5
Akao, Y.6
Croce, C.7
Morse III, H.C.8
Kersey, J.H.9
-
38
-
-
0037732866
-
Identification of CBL, a proto-oncogene at 11q23.3, as a novel MLL fusion partner in a patient with de novo acute myeloid leukemia
-
Fu JF, Hsu JJ, Tang TC, Shih LY (2003) Identification of CBL, a proto-oncogene at 11q23.3, as a novel MLL fusion partner in a patient with de novo acute myeloid leukemia. Genes Chromosomes Cancer 37:214-219
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 214-219
-
-
Fu, J.F.1
Hsu, J.J.2
Tang, T.C.3
Shih, L.Y.4
-
39
-
-
65249132999
-
CBL exon 8/9 mutants activate the FLT3 pathway and cluster in core binding factor/11q deletion acute myeloid leukemia/myelodysplastic syndrome subtypes
-
Reindl C, Quentmeier H, Petropoulos K, Greif PA, Benthaus T, Argiropoulos B, Mellert G, Vempati S, Duyster J, Buske C, Bohlander SK, Humphries KR, Hiddemann W, Spiekermann K (2009) CBL exon 8/9 mutants activate the FLT3 pathway and cluster in core binding factor/11q deletion acute myeloid leukemia/myelodysplastic syndrome subtypes. Clin Cancer Res 15:2238-2247
-
(2009)
Clin Cancer Res
, vol.15
, pp. 2238-2247
-
-
Reindl, C.1
Quentmeier, H.2
Petropoulos, K.3
Greif, P.A.4
Benthaus, T.5
Argiropoulos, B.6
Mellert, G.7
Vempati, S.8
Duyster, J.9
Buske, C.10
Bohlander, S.K.11
Humphries, K.R.12
Hiddemann, W.13
Spiekermann, K.14
-
40
-
-
34547950568
-
Novel c-CBL and CBL-b ubiquitin ligase mutations in human acute myeloid leukemia
-
Caligiuri MA, Briesewitz R, Yu J, Wang L, Wei M, Arnoczky KJ, Marburger TB, Wen J, Perrotti D, Bloomfield CD, Whitman SP (2007) Novel c-CBL and CBL-b ubiquitin ligase mutations in human acute myeloid leukemia. Blood 110:1022-1024
-
(2007)
Blood
, vol.110
, pp. 1022-1024
-
-
Caligiuri, M.A.1
Briesewitz, R.2
Yu, J.3
Wang, L.4
Wei, M.5
Arnoczky, K.J.6
Marburger, T.B.7
Wen, J.8
Perrotti, D.9
Bloomfield, C.D.10
Whitman, S.P.11
-
41
-
-
67650401377
-
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
-
Grand FH, Hidalgo-Curtis CE, Ernst T, Zoi K, Zoi C, McGuire C, Kreil S, Jones A, Score J, Metzgeroth G, Oscier D, Hall A, Brandts C, Serve H, Reiter A, Chase AJ, Cross NC (2009) Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms. Blood 113:6182-6192
-
(2009)
Blood
, vol.113
, pp. 6182-6192
-
-
Grand, F.H.1
Hidalgo-Curtis, C.E.2
Ernst, T.3
Zoi, K.4
Zoi, C.5
McGuire, C.6
Kreil, S.7
Jones, A.8
Score, J.9
Metzgeroth, G.10
Oscier, D.11
Hall, A.12
Brandts, C.13
Serve, H.14
Reiter, A.15
Chase, A.J.16
Cross, N.C.17
-
42
-
-
54349105660
-
Exon 8 splice site mutations in the gene encoding the E3-ligase CBL are associated with core binding factor acute myeloid leukemias
-
Abbas S, Rotmans G, Lowenberg B, Valk PJ (2008) Exon 8 splice site mutations in the gene encoding the E3-ligase CBL are associated with core binding factor acute myeloid leukemias. Haematologica 93:1595-1597
-
(2008)
Haematologica
, vol.93
, pp. 1595-1597
-
-
Abbas, S.1
Rotmans, G.2
Lowenberg, B.3
Valk, P.J.4
-
43
-
-
68949124841
-
Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms
-
Sanada M, Suzuki T, Shih LY, Otsu M, Kato M, Yamazaki S, Tamura A, Honda H, Sakata-Yanagimoto M, Kumano K, Oda H, Yamagata T, Takita J, Gotoh N, Nakazaki K, Kawamata N, Onodera M, Nobuyoshi M, Hayashi Y, Harada H, Kurokawa M, Chiba S,Mori H, Ozawa K, OmineM,Hirai H, Nakauchi H, Koeffler HP, Ogawa S (2009) Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms. Nature 460:904-908
-
(2009)
Nature
, vol.460
, pp. 904-908
-
-
Sanada, M.1
Suzuki, T.2
Shih, L.Y.3
Otsu, M.4
Kato, M.5
Yamazaki, S.6
Tamura, A.7
Honda, H.8
Sakata-Yanagimoto, M.9
Kumano, K.10
Oda, H.11
Yamagata, T.12
Takita, J.13
Gotoh, N.14
Nakazaki, K.15
Kawamata, N.16
Onodera, M.17
Nobuyoshi, M.18
Hayashi, Y.19
Harada, H.20
Kurokawa, M.21
Chiba, S.22
Mori, H.23
Ozawa, K.24
Omine, M.25
Hirai, H.26
Nakauchi, H.27
Koeffler, H.P.28
Ogawa, S.29
more..
-
44
-
-
77955657303
-
AML with CBFB-MYH11 rearrangement is characterized by RAS pathway alterations in 92% of cases and demonstrates a high frequency of NF1 deletions
-
in press
-
Haferlach C, Dicker F, Kohlmann A, Schindela S, Weiss T, Kern W, Schnittger S, Haferlach T (2010) AML with CBFB-MYH11 rearrangement is characterized by RAS pathway alterations in 92% of cases and demonstrates a high frequency of NF1 deletions. Leukemia, in press
-
(2010)
Leukemia
-
-
Haferlach, C.1
Dicker, F.2
Kohlmann, A.3
Schindela, S.4
Weiss, T.5
Kern, W.6
Schnittger, S.7
Haferlach, T.8
-
45
-
-
74949108515
-
Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies
-
Makishima H, Cazzolli H, Szpurka H, Dunbar A, Tiu R, Huh J, Muramatsu H, O'Keefe C, Hsi E, Paquette RL, Kojima S, List AF, Sekeres MA, McDevitt MA, Maciejewski JP (2009) Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies. J Clin Oncol 27:6109-6116
-
(2009)
J Clin Oncol
, vol.27
, pp. 6109-6116
-
-
Makishima, H.1
Cazzolli, H.2
Szpurka, H.3
Dunbar, A.4
Tiu, R.5
Huh, J.6
Muramatsu, H.7
O'Keefe, C.8
Hsi, E.9
Paquette, R.L.10
Kojima, S.11
List, A.F.12
Sekeres, M.A.13
McDevitt, M.A.14
Maciejewski, J.P.15
-
46
-
-
77955653966
-
Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 75% of chronic myelomonocytic leukemia (CMML) by detecting frequent alterations in TET2, RUNX1, CBL, and RAS Annual Meeting of the American Society of Hematology
-
abstract #417
-
Kohlmann A, Grossmann V, Haferlach C, Kazak B, Schindela S, Klein H-U, Weiss T, Dicker F, Schnittger S, Dugas M, Kern W, Haferlach T (2009) Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 75% of chronic myelomonocytic leukemia (CMML) by detecting frequent alterations in TET2, RUNX1, CBL, and RAS. Annual Meeting of the American Society of Hematology. Blood 114. abstract #417
-
(2009)
Blood
, pp. 114
-
-
Kohlmann, A.1
Grossmann, V.2
Haferlach, C.3
Kazak, B.4
Schindela, S.5
Klein, H.-U.6
Weiss, T.7
Dicker, F.8
Schnittger, S.9
Dugas, M.10
Kern, W.11
Haferlach, T.12
-
47
-
-
77950382457
-
Mutations of E3 ubiquitin ligase Cbl family members but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia
-
online prepublished, Dec 11, doi:10.1182/blood-2009-06-226340
-
Muramatsu H,Makishima H, Jankowska AM, Cazzolli H, O'Keefe C, Yoshida N, Xu Y, Nishio N, Hama A, Yagasaki H, Takahashi Y, Kato K, Manabe A, Kojima S, Maciejewski JP. Mutations of E3 ubiquitin ligase Cbl family members but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia. Blood, online prepublished, Dec 11, 2009. doi:10.1182/blood-2009-06-226340
-
(2009)
Blood
-
-
Muramatsu, H.1
Makishima, H.2
Jankowska, A.M.3
Cazzolli, H.4
O'Keefe, C.5
Yoshida, N.6
Xu, Y.7
Nishio, N.8
Hama, A.9
Yagasaki, H.10
Takahashi, Y.11
Kato, K.12
Manabe, A.13
Kojima, S.14
Maciejewski, J.P.15
-
48
-
-
70349249988
-
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia
-
Loh ML, Sakai DS, Flotho C, Kang M, Fliegauf M, Archambeault S, Mullighan CG, Chen L, Bergstraesser E, Bueso-Ramos CE, Emanuel PD, Hasle H, Issa JP, van den Heuvel-Eibrink MM, Locatelli F, Stary J, Trebo M, Wlodarski M, Zecca M, Shannon KM, Niemeyer CM (2009) Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. Blood 114:1859-1863
-
(2009)
Blood
, vol.114
, pp. 1859-1863
-
-
Loh, M.L.1
Sakai, D.S.2
Flotho, C.3
Kang, M.4
Fliegauf, M.5
Archambeault, S.6
Mullighan, C.G.7
Chen, L.8
Bergstraesser, E.9
Bueso-Ramos, C.E.10
Emanuel, P.D.11
Hasle, H.12
Issa, J.P.13
Van Den Heuvel-Eibrink, M.M.14
Locatelli, F.15
Stary, J.16
Trebo, M.17
Wlodarski, M.18
Zecca, M.19
Shannon, K.M.20
Niemeyer, C.M.21
more..
-
49
-
-
66249123891
-
A common genetic mechanism in malignant bone marrow diseases
-
Levine RL, Carroll M (2009) A common genetic mechanism in malignant bone marrow diseases. N Engl J Med 360:2355-2357
-
(2009)
N Engl J Med
, vol.360
, pp. 2355-2357
-
-
Levine, R.L.1
Carroll, M.2
-
50
-
-
67649872341
-
TET2 mutations in myelodysplasia and myeloid malignancies
-
Mullighan CG (2009) TET2 mutations in myelodysplasia and myeloid malignancies. Nat Genet 41:766-767
-
(2009)
Nat Genet
, vol.41
, pp. 766-767
-
-
Mullighan, C.G.1
-
51
-
-
69849110150
-
Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome
-
Mohamedali AM, Smith AE, Gaken J, Lea NC, Mian SA, Westwood NB, Strupp C, Gattermann N, Germing U, Mufti GJ (2009) Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome. J Clin Oncol 27:4002-4006
-
(2009)
J Clin Oncol
, vol.27
, pp. 4002-4006
-
-
Mohamedali, A.M.1
Smith, A.E.2
Gaken, J.3
Lea, N.C.4
Mian, S.A.5
Westwood, N.B.6
Strupp, C.7
Gattermann, N.8
Germing, U.9
Mufti, G.J.10
-
52
-
-
66149146320
-
Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1
-
Tahiliani M, Koh KP, Shen Y, Pastor WA, Bandukwala H, Brudno Y, Agarwal S, Lyer LM, Liu DR, Aravind L, Rao A (2009) Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1. Science 324:930-935
-
(2009)
Science
, vol.324
, pp. 930-935
-
-
Tahiliani, M.1
Koh, K.P.2
Shen, Y.3
Pastor, W.A.4
Bandukwala, H.5
Brudno, Y.6
Agarwal, S.7
Lyer, L.M.8
Liu, D.R.9
Aravind, L.10
Rao, A.11
-
53
-
-
76749084667
-
Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias
-
online prepublished, Oct 29, doi: 10.1038/leu.2009.218
-
Carbuccia N, Trouplin V, Gelsi-Boyer V, Murati A, Rocquain J, Adelaide J, Olschwang S, Xerri L, Vey N, Chaffanet M, Birnbaum D, Mozziconacci MJ. Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias. Leukemia, online prepublished, Oct 29, 2009. doi: 10.1038/leu.2009.218
-
(2009)
Leukemia
-
-
Carbuccia, N.1
Trouplin, V.2
Gelsi-Boyer, V.3
Murati, A.4
Rocquain, J.5
Adelaide, J.6
Olschwang, S.7
Xerri, L.8
Vey, N.9
Chaffanet, M.10
Birnbaum, D.11
Mozziconacci, M.J.12
-
54
-
-
77950529536
-
E3 ligase-defective Cbl mutants lead to a generalized mastocytosis and a myeloproliferative disease
-
Bandi SR, Brandts C, Rensinghoff M, Grundler R, Tickenbrock L, Kohler G, Duyster J, Berdel WE, Muller-Tidow C, Serve H, Sargin B (2009) E3 ligase-defective Cbl mutants lead to a generalized mastocytosis and a myeloproliferative disease. Blood 114:14197-14208
-
(2009)
Blood
, vol.114
, pp. 14197-14208
-
-
Bandi, S.R.1
Brandts, C.2
Rensinghoff, M.3
Grundler, R.4
Tickenbrock, L.5
Kohler, G.6
Duyster, J.7
Berdel, W.E.8
Muller-Tidow, C.9
Serve, H.10
Sargin, B.11
-
55
-
-
61849150985
-
High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients
-
Tyner JW, Erickson H, Deininger MW, Willis SG, Eide CA, Levine RL, Heinrich MC, Gattermann N, Gilliland DG, Druker BJ, Loriaux MM (2009) High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients. Blood 113:1749-1755
-
(2009)
Blood
, vol.113
, pp. 1749-1755
-
-
Tyner, J.W.1
Erickson, H.2
Deininger, M.W.3
Willis, S.G.4
Eide, C.A.5
Levine, R.L.6
Heinrich, M.C.7
Gattermann, N.8
Gilliland, D.G.9
Druker, B.J.10
Loriaux, M.M.11
-
56
-
-
47049105417
-
Highthroughput sequence analysis of the tyrosine kinome in acute myeloid leukemia
-
Loriaux MM, Levine RL, Tyner JW, Frohling S, Scholl C, Stoffregen EP, Wernig G, Erickson H, Eide CA, Berger R, Bernard OA, Griffin JD, Stone RM, Lee B, Meyerson M, Heinrich MC, Deininger MW, Gilliland DG, Druker BJ (2008) Highthroughput sequence analysis of the tyrosine kinome in acute myeloid leukemia. Blood 111:4788-4796
-
(2008)
Blood
, vol.111
, pp. 4788-4796
-
-
Loriaux, M.M.1
Levine, R.L.2
Tyner, J.W.3
Frohling, S.4
Scholl, C.5
Stoffregen, E.P.6
Wernig, G.7
Erickson, H.8
Eide, C.A.9
Berger, R.10
Bernard, O.A.11
Griffin, J.D.12
Stone, R.M.13
Lee, B.14
Meyerson, M.15
Heinrich, M.C.16
Deininger, M.W.17
Gilliland, D.G.18
Druker, B.J.19
-
57
-
-
74249096163
-
Analyses of TET2 mutations in post-myeloproliferative neoplasm acute myeloid leukemias
-
Couronne L, Lippert E, Andrieux J, Kosmider O, Radford-Weiss I, Penther D, Dastugue N, Mugneret F, Lafage M, Gachard N, Nadal N, Bernard OA, Nguyen-Khac F (2010) Analyses of TET2 mutations in post-myeloproliferative neoplasm acute myeloid leukemias. Leukemia 24:201-203
-
(2010)
Leukemia
, vol.24
, pp. 201-203
-
-
Couronne, L.1
Lippert, E.2
Andrieux, J.3
Kosmider, O.4
Radford-Weiss, I.5
Penther, D.6
Dastugue, N.7
Mugneret, F.8
Lafage, M.9
Gachard, N.10
Nadal, N.11
Bernard, O.A.12
Nguyen-Khac, F.13
|