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Aberrant T-cell antigen expression in classical Hodgkin lymphoma is associated with decreased event-free survival and overall survival

Blood, 2013-03, Vol.121 (10), p.1795-1804

2013

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Clonal evolution leading to ibrutinib resistance in chronic lymphocytic leukemia

Blood, 2017-03, Vol.129 (11), p.1469-1479

2017

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Mutations in the JAK/STAT and RAS signaling pathways are common in intestinal T-cell lymphomas

Leukemia, 2016-11, Vol.30 (11), p.2245-2247

2016

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Blastic plasmacytoid dendritic cell neoplasm in children: diagnostic features and clinical implications

Haematologica (Roma), 2010-11, Vol.95 (11), p.1873-1879

2010

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Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications

Haematologica (Roma), 2011-08, Vol.96 (8), p.1221-1225

2011

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Age-related EBV-associated lymphoproliferative disorders in the Western population: a spectrum of reactive lymphoid hyperplasia and lymphoma

Blood, 2011-05, Vol.117 (18), p.4726-4735

2011

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Genomic profiling of primary histiocytic sarcoma reveals two molecular subgroups

Haematologica (Roma), 2020-04, Vol.105 (4), p.951

2020

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Recurrent somatic JAK3 mutations in NK-cell enteropathy

Blood, 2019-09, Vol.134 (12), p.986-991

2019

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The impact of cyclin D1 mRNA isoforms, morphology and p53 in mantle cell lymphoma: p53 alterations and blastoid morphology are strong predictors of a high proliferation index

Haematologica (Roma), 2012-09, Vol.97 (9), p.1422-1430

2012

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Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea

Blood, 2017-02, Vol.129 (5), p.650-653

2017

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Modeling tumor-host interactions of chronic lymphocytic leukemia in xenografted mice to study tumor biology and evaluate targeted therapy

Leukemia, 2013-12, Vol.27 (12), p.2311-2321

2013

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Clonally related follicular lymphomas and histiocytic/dendritic cell sarcomas: evidence for transdifferentiation of the follicular lymphoma clone

Blood, 2008-06, Vol.111 (12), p.5433-5439

2008

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Episodic angioedema with eosinophilia (Gleich syndrome) is a multilineage cell cycling disorder

Haematologica (Roma), 2015-03, Vol.100 (3), p.300

2015

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EBV-positive large B-cell lymphomas in young patients: a nodal lymphoma with evidence for a tolerogenic immune environment

Blood, 2015-08, Vol.126 (7), p.863-872

2015

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Eradication of B-lineage cells and regression of lymphoma in a patient treated with autologous T cells genetically engineered to recognize CD19

Blood, 2010-11, Vol.116 (20), p.4099-4102

2010

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Molecular assessment of clonality in lymphoid neoplasms

Seminars in hematology, 2019-01, Vol.56 (1), p.37-45

2019

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Both variant and IGHV4-34–expressing hairy cell leukemia lack the BRAF V600E mutation

Blood, 2012-04, Vol.119 (14), p.3330-3332

2012

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Constitutive activation of Akt contributes to the pathogenesis and survival of mantle cell lymphoma

Blood, 2006-09, Vol.108 (5), p.1668-1676

2006

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In situ localization of follicular lymphoma: description and analysis by laser capture microdissection

Blood, 2002-05, Vol.99 (9), p.3376-3382

2002

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Peripheral T‐cell lymphomas expressing CD30 and CD15 expand the spectrum of anaplastic large cell lymphoma, ALK‐negative

British journal of haematology, 2024-05, Vol.204 (5), p.1862-1871

2024

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CREBBP gene mutations are frequently detected in in situ follicular neoplasia

Blood, 2018-12, Vol.132 (25), p.2687-2690

2018

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Bone marrow findings in autoimmune lymphoproliferative syndrome with germline FAS mutation

Haematologica (Roma), 2017-02, Vol.102 (2), p.364

2017

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Highly effective treatment of acquired immunodeficiency syndrome–related lymphoma with dose-adjusted EPOCH: impact of antiretroviral therapy suspension and tumor biology

Blood, 2003-06, Vol.101 (12), p.4653-4659

2003

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Aberrant T-cell antigen expression in classical Hodgkin lymphoma is associated with decreased event-free survival and overall survival

Clonal evolution leading to ibrutinib resistance in chronic lymphocytic leukemia

Mutations in the JAK/STAT and RAS signaling pathways are common in intestinal T-cell lymphomas

Blastic plasmacytoid dendritic cell neoplasm in children: diagnostic features and clinical implications

Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications

Age-related EBV-associated lymphoproliferative disorders in the Western population: a spectrum of reactive lymphoid hyperplasia and lymphoma

Genomic profiling of primary histiocytic sarcoma reveals two molecular subgroups

Recurrent somatic JAK3 mutations in NK-cell enteropathy

The impact of cyclin D1 mRNA isoforms, morphology and p53 in mantle cell lymphoma: p53 alterations and blastoid morphology are strong predictors of a high proliferation index

Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea

Modeling tumor-host interactions of chronic lymphocytic leukemia in xenografted mice to study tumor biology and evaluate targeted therapy

Clonally related follicular lymphomas and histiocytic/dendritic cell sarcomas: evidence for transdifferentiation of the follicular lymphoma clone

Episodic angioedema with eosinophilia (Gleich syndrome) is a multilineage cell cycling disorder

EBV-positive large B-cell lymphomas in young patients: a nodal lymphoma with evidence for a tolerogenic immune environment

Eradication of B-lineage cells and regression of lymphoma in a patient treated with autologous T cells genetically engineered to recognize CD19

Molecular assessment of clonality in lymphoid neoplasms

Both variant and IGHV4-34–expressing hairy cell leukemia lack the BRAF V600E mutation

Constitutive activation of Akt contributes to the pathogenesis and survival of mantle cell lymphoma

The lymph node microenvironment promotes B-cell receptor signaling, NF-κB activation, and tumor proliferation in chronic lymphocytic leukemia

In situ localization of follicular lymphoma: description and analysis by laser capture microdissection

Peripheral T‐cell lymphomas expressing CD30 and CD15 expand the spectrum of anaplastic large cell lymphoma, ALK‐negative

CREBBP gene mutations are frequently detected in in situ follicular neoplasia

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome

Bone marrow findings in autoimmune lymphoproliferative syndrome with germline FAS mutation

Highly effective treatment of acquired immunodeficiency syndrome–related lymphoma with dose-adjusted EPOCH: impact of antiretroviral therapy suspension and tumor biology

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