-
2
-
-
77954463374
-
Splenic diffuse red pulp small B-cell lymphoma: Revision of a series of cases reveals characteristic clinico-pathological features
-
Kanellis G, Mollejo M, Montes-Moreno S, et al. Splenic diffuse red pulp small B-cell lymphoma: revision of a series of cases reveals characteristic clinico-pathological features. Haematologica. 2010;95:1122-1129.
-
(2010)
Haematologica.
, vol.95
, pp. 1122-1129
-
-
Kanellis, G.1
Mollejo, M.2
Montes-Moreno, S.3
-
3
-
-
0036153733
-
Splenic small B-cell lymphoma with predominant red pulp involvement: A diffuse variant of splenic marginal zone lymphoma?
-
Mollejo M, Algara P, Mateo MS, et al. Splenic small B-cell lymphoma with predominant red pulp involvement: a diffuse variant of splenic marginal zone lymphoma? Histopathology. 2002;40:22-30.
-
(2002)
Histopathology.
, vol.40
, pp. 22-30
-
-
Mollejo, M.1
Algara, P.2
Mateo, M.S.3
-
4
-
-
41449095195
-
Splenic red pulp lymphoma with numerous basophilic villous lymphocytes: A distinct clinicopathologic and molecular entity?
-
Traverse-Glehen A, Baseggio L, Bauchu EC, et al. Splenic red pulp lymphoma with numerous basophilic villous lymphocytes: a distinct clinicopathologic and molecular entity? Blood. 2008;111:2253-2260.
-
(2008)
Blood.
, vol.111
, pp. 2253-2260
-
-
Traverse-Glehen, A.1
Baseggio, L.2
Bauchu, E.C.3
-
6
-
-
84866392764
-
Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma
-
Kiel MJ, Velusamy T, Betz BL, et al. Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma. J Exp Med. 2012;209:1553-1565.
-
(2012)
J Exp Med.
, vol.209
, pp. 1553-1565
-
-
Kiel, M.J.1
Velusamy, T.2
Betz, B.L.3
-
7
-
-
84902121064
-
Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation
-
Martinez N, Almaraz C, Vaque JP, et al. Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation. Leukemia. 2014;28: 1334-1340.
-
(2014)
Leukemia.
, vol.28
, pp. 1334-1340
-
-
Martinez, N.1
Almaraz, C.2
Vaque, J.P.3
-
8
-
-
84866429139
-
The coding genome of splenic marginal zone lymphoma: Activation of NOTCH2 and other pathways regulating marginal zone development
-
Rossi D, Trifonov V, Fangazio M, et al. The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone development. J Exp Med. 2012; 209:1537-1551.
-
(2012)
J Exp Med.
, vol.209
, pp. 1537-1551
-
-
Rossi, D.1
Trifonov, V.2
Fangazio, M.3
-
9
-
-
84891371044
-
High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias
-
Waterfall JJ, Arons E, Walker RL, et al. High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias. Nat Genet. 2014;46:8-10.
-
(2014)
Nat Genet.
, vol.46
, pp. 8-10
-
-
Waterfall, J.J.1
Arons, E.2
Walker, R.L.3
-
10
-
-
84875382111
-
Distinguishing hairy cell leukemia variant from hairy cell leukemia: Development and validation of diagnostic criteria
-
Shao H, Calvo KR, Gronborg M, et al. Distinguishing hairy cell leukemia variant from hairy cell leukemia: development and validation of diagnostic criteria. Leuk Res. 2013;37:401-409.
-
(2013)
Leuk Res.
, vol.37
, pp. 401-409
-
-
Shao, H.1
Calvo, K.R.2
Gronborg, M.3
-
11
-
-
84859576293
-
Both variant and IGHV4-34-expressing hairy cell leukemia lack the BRAF V600E mutation
-
Xi L, Arons E, Navarro W, et al. Both variant and IGHV4-34-expressing hairy cell leukemia lack the BRAF V600E mutation. Blood. 2012;119:3330-3332.
-
(2012)
Blood.
, vol.119
, pp. 3330-3332
-
-
Xi, L.1
Arons, E.2
Navarro, W.3
-
12
-
-
84891690579
-
BRAF V600E is also seen in unclassifiable splenic B-cell lymphoma/leukemia, a potential mimic of hairy cell leukemia
-
Raess PW, Mintzer D, Husson M, et al. BRAF V600E is also seen in unclassifiable splenic B-cell lymphoma/leukemia, a potential mimic of hairy cell leukemia. Blood. 2013;122:3084-3085.
-
(2013)
Blood.
, vol.122
, pp. 3084-3085
-
-
Raess, P.W.1
Mintzer, D.2
Husson, M.3
-
13
-
-
33744516644
-
FISH analysis for the detection of lymphoma-associated chromosomal abnormalities in routine paraffin-embedded tissue
-
Ventura RA, Martin-Subero JI, Jones M, et al. FISH analysis for the detection of lymphoma-associated chromosomal abnormalities in routine paraffin-embedded tissue. J Mol Diagn. 2006;8: 141-151.
-
(2006)
J Mol Diagn.
, vol.8
, pp. 141-151
-
-
Ventura, R.A.1
Martin-Subero, J.I.2
Jones, M.3
-
14
-
-
84874407720
-
CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma
-
Salaverria I, Royo C, Carvajal-Cuenca A, et al. CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma. Blood. 2013;121:1394-1402.
-
(2013)
Blood.
, vol.121
, pp. 1394-1402
-
-
Salaverria, I.1
Royo, C.2
Carvajal-Cuenca, A.3
-
15
-
-
33947496614
-
Revised response criteria for malignant lymphoma
-
Cheson BD, Pfistner B, Juweid ME, et al. Revised response criteria for malignant lymphoma. J Clin Oncol. 2007;25:579-586.
-
(2007)
J Clin Oncol.
, vol.25
, pp. 579-586
-
-
Cheson, B.D.1
Pfistner, B.2
Juweid, M.E.3
-
16
-
-
64549150146
-
Among 157 marginal zone lymphomas DBA.44(CD76) expression is restricted to tumour cells infiltrating the red pulp of the spleen with a diffuse architectural pattern
-
Petit B, Parrens M, Soubeyran I, et al. Among 157 marginal zone lymphomas, DBA.44(CD76) expression is restricted to tumour cells infiltrating the red pulp of the spleen with a diffuse architectural pattern. Histopathology. 2009;54:626-631.
-
(2009)
Histopathology.
, vol.54
, pp. 626-631
-
-
Petit, B.1
Parrens, M.2
Soubeyran, I.3
-
17
-
-
19944429608
-
Splenic lymphoma with villous lymphocytes, associated with type II cryoglobulinemia and HCV infection: A new entity?
-
Saadoun D, Suarez F, Lefrere F, et al. Splenic lymphoma with villous lymphocytes, associated with type II cryoglobulinemia and HCV infection: a new entity? Blood. 2005;105:74-76.
-
(2005)
Blood.
, vol.105
, pp. 74-76
-
-
Saadoun, D.1
Suarez, F.2
Lefrere, F.3
-
18
-
-
84865545078
-
Malignant lymphoma of the spleen in Japan: A clinicopathological analysis of 115 cases
-
Shimizu-Kohno K, Kimura Y, Kiyasu J, et al. Malignant lymphoma of the spleen in Japan: a clinicopathological analysis of 115 cases. Pathol Int. 2012;62:577-582.
-
(2012)
Pathol Int.
, vol.62
, pp. 577-582
-
-
Shimizu-Kohno, K.1
Kimura, Y.2
Kiyasu, J.3
-
19
-
-
79960036578
-
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
-
Puente XS, Pinyol M, Quesada V, et al. Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature. 2011;475:101-105.
-
(2011)
Nature.
, vol.475
, pp. 101-105
-
-
Puente, X.S.1
Pinyol, M.2
Quesada, V.3
-
20
-
-
77956592193
-
Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: A multicenter study of the Splenic B-Cell Lymphoma Group
-
Salido M, Baro C, Oscier D, et al. Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group. Blood. 2010;116:1479-1488.
-
(2010)
Blood.
, vol.116
, pp. 1479-1488
-
-
Salido, M.1
Baro, C.2
Oscier, D.3
-
21
-
-
79960285663
-
High-resolution genomic profiling in hairy cell leukemia-variant compared with typical hairy cell leukemia
-
Hockley SL, Morgan GJ, Leone PE, et al. High-resolution genomic profiling in hairy cell leukemia-variant compared with typical hairy cell leukemia. Leukemia. 2011;25:1189-1192.
-
(2011)
Leukemia.
, vol.25
, pp. 1189-1192
-
-
Hockley, S.L.1
Morgan, G.J.2
Leone, P.E.3
-
22
-
-
0033069482
-
T(9;14)(p13;q32) involving the PAX-5 gene: A unique subtype of 14q32 translocation in B cell non-Hodgkin's lymphoma
-
Amakawa R, Ohno H, Fukuhara S. t(9;14)(p13;q32) involving the PAX-5 gene: a unique subtype of 14q32 translocation in B cell non-Hodgkin's lymphoma. Int J Hematol. 1999;69:65-69.
-
(1999)
Int J Hematol.
, vol.69
, pp. 65-69
-
-
Amakawa, R.1
Ohno, H.2
Fukuhara, S.3
-
23
-
-
24944550194
-
PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements
-
Poppe B, De PP, Michaux L, et al. PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements. Genes Chromosomes Cancer. 2005;44: 218-223.
-
(2005)
Genes Chromosomes Cancer.
, vol.44
, pp. 218-223
-
-
Poppe, B.1
De Pp Michaux, L.2
-
24
-
-
0028587370
-
Identification of the TCL1 gene involved in T-cell malignancies
-
Virgilio L, Narducci MG, Isobe M, et al. Identification of the TCL1 gene involved in T-cell malignancies. Proc Natl Acad Sci USA. 1994;91:12530-12534.
-
(1994)
Proc Natl Acad Sci USA.
, vol.91
, pp. 12530-12534
-
-
Virgilio, L.1
Narducci, M.G.2
Isobe, M.3
-
25
-
-
59149093632
-
TCL1A expression delineates biological and clinical variability in B-cell lymphoma
-
Aggarwal M, Villuendas R, Gomez G, et al. TCL1A expression delineates biological and clinical variability in B-cell lymphoma. Mod Pathol. 2009;22:206-215.
-
(2009)
Mod Pathol.
, vol.22
, pp. 206-215
-
-
Aggarwal, M.1
Villuendas, R.2
Gomez, G.3
-
26
-
-
79957445887
-
Molecular variant of hairy cell leukemia with poor prognosis
-
Arons E, Kreitman RJ. Molecular variant of hairy cell leukemia with poor prognosis. Leuk Lymphoma. 2011;52(suppl 2):99-102.
-
(2011)
Leuk Lymphoma.
, vol.52
, pp. 99-102
-
-
Arons, E.1
Kreitman, R.J.2
-
27
-
-
84863785935
-
Over 30% of patients with splenic marginal zone lymphoma express the same immunoglobulin heavy variable gene: Ontogenetic implications
-
Bikos V, Darzentas N, Hadzidimitriou A, et al. Over 30% of patients with splenic marginal zone lymphoma express the same immunoglobulin heavy variable gene: ontogenetic implications. Leukemia. 2012;26:1638-1646.
-
(2012)
Leukemia.
, vol.26
, pp. 1638-1646
-
-
Bikos, V.1
Darzentas, N.2
Hadzidimitriou, A.3
-
28
-
-
75149189505
-
Insight into the molecular pathogenesis of hairy cell leukaemia, hairy cell leukaemia variant and splenic marginal zone lymphoma, provided by the analysis of their IGH rearrangements and somatic hypermutation patterns
-
Hockley SL, Giannouli S, Morilla A, et al. Insight into the molecular pathogenesis of hairy cell leukaemia, hairy cell leukaemia variant and splenic marginal zone lymphoma, provided by the analysis of their IGH rearrangements and somatic hypermutation patterns. Br J Haematol. 2010;148:666-669.
-
(2010)
Br J Haematol.
, vol.148
, pp. 666-669
-
-
Hockley, S.L.1
Giannouli, S.2
Morilla, A.3
-
29
-
-
84867513141
-
Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features
-
Navarro A, Clot G, Royo C, et al. Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features. Cancer Res. 2012;72:5307-5316.
-
(2012)
Cancer Res.
, vol.72
, pp. 5307-5316
-
-
Navarro, A.1
Clot, G.2
Royo, C.3
-
30
-
-
84887285547
-
Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
-
Bea S, Valdes-Mas R, Navarro A, et al. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma. Proc Natl Acad Sci USA. 2013;110:18250-18255.
-
(2013)
Proc Natl Acad Sci USA.
, vol.110
, pp. 18250-18255
-
-
Bea, S.1
Valdes-Mas, R.2
Navarro, A.3
-
31
-
-
79960353160
-
Analysis of the chronic lymphocytic leukemia coding genome: Role of NOTCH1 mutational activation
-
Fabbri G, Rasi S, Rossi D, et al. Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation. J Exp Med. 2011;208:1389-1401.
-
(2011)
J Exp Med.
, vol.208
, pp. 1389-1401
-
-
Fabbri, G.1
Rasi, S.2
Rossi, D.3
-
32
-
-
84857763426
-
Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma
-
Kridel R, Meissner B, Rogic S, et al. Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. Blood. 2012;119:1963-1971.
-
(2012)
Blood.
, vol.119
, pp. 1963-1971
-
-
Kridel, R.1
Meissner, B.2
Rogic, S.3
-
33
-
-
84877635463
-
NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome
-
Villamor N, Conde L, Martinez-Trillos A, et al. NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome. Leukemia. 2013;27:1100-1106.
-
(2013)
Leukemia.
, vol.27
, pp. 1100-1106
-
-
Villamor, N.1
Conde, L.2
Martinez-Trillos, A.3
-
34
-
-
84925547095
-
Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours
-
Karube K, Martinez D, Royo C, et al. Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours. J Pathol. 2014;234:423-430.
-
(2014)
J Pathol.
, vol.234
, pp. 423-430
-
-
Karube, K.1
Martinez, D.2
Royo, C.3
-
35
-
-
84878411259
-
Clonal evolution, genomic drivers, and effects of therapy in chronic lymphocytic leukemia
-
Ouillette P, Saiya-Cork K, Seymour E, et al. Clonal evolution, genomic drivers, and effects of therapy in chronic lymphocytic leukemia. Clin Cancer Res. 2013;19:2893-2904.
-
(2013)
Clin Cancer Res.
, vol.19
, pp. 2893-2904
-
-
Ouillette, P.1
Saiya-Cork, K.2
Seymour, E.3
-
36
-
-
37249018491
-
Notch-1 mutations are secondary events in some patients with T-cell acute lymphoblastic leukemia
-
Mansour MR, Duke V, Foroni L, et al. Notch-1 mutations are secondary events in some patients with T-cell acute lymphoblastic leukemia. Clin Cancer Res. 2007;13:6964-6969.
-
(2007)
Clin Cancer Res.
, vol.13
, pp. 6964-6969
-
-
Mansour, M.R.1
Duke, V.2
Foroni, L.3
-
37
-
-
84909609809
-
Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis
-
Chakraborty R, Hampton OA, Shen X, et al. Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis. Blood. 2014;124:3007-3015.
-
(2014)
Blood.
, vol.124
, pp. 3007-3015
-
-
Chakraborty, R.1
Hampton, O.A.2
Shen, X.3
-
38
-
-
84907009615
-
High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis
-
Brown NA, Furtado LV, Betz BL, et al. High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis. Blood. 2014;124:1655-1658.
-
(2014)
Blood.
, vol.124
, pp. 1655-1658
-
-
Brown, N.A.1
Furtado, L.V.2
Betz, B.L.3
-
39
-
-
84863835270
-
The prognostic impact of clinical and molecular features in hairy cell leukaemia variant and splenic marginal zone lymphoma
-
Hockley SL, Else M, Morilla A, et al. The prognostic impact of clinical and molecular features in hairy cell leukaemia variant and splenic marginal zone lymphoma. Br J Haematol. 2012; 158:347-354.
-
(2012)
Br J Haematol.
, vol.158
, pp. 347-354
-
-
Hockley, S.L.1
Else, M.2
Morilla, A.3
|