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Journal Articles

Circulating tumor DNA reveals genetics, clonal evolution, and residual disease in classical Hodgkin lymphoma

Blood (2018) 131 (22): 2413–2425.

https://doi.org/10.1182/blood-2017-11-812073

Published: 2018

Includes: Supplemental data

Journal Articles

Genotyping of Classical Hodgkin Lymphoma on the Liquid Biopsy

Blood (2017) 130 (Supplement 1): 307.

https://doi.org/10.1182/blood.V130.Suppl_1.307.307

Published: 2017

Journal Articles

Primary Trombocythemia in Children and Adolescents Includes Different Subtypes Compared to Adult Essential Thrombocythemia

Fiorina Giona, MD, Marica Laurino, Luciana Teofili, MD PhD, Sara Capodimonti, BSc, PhD, Maurizio Martini, MD PhD, Giovanna Palumbo, MD, Maria Luisa Moleti, MD, Deborah Marzella, MD, Daniela Diverio, Maria Grazia Mascolo, Luigi Maria Larocca, MD, Robin Foà, MD

Blood (2014) 124 (21): 1865.

https://doi.org/10.1182/blood.V124.21.1865.1865

Published: 2014

Journal Articles

Prognostic Role of the CD68+ Cell Count and Early Response Evaluation with Interim-PET and Levels of Plasma Thymus and Activation-Regulated Chemokine (TARC) in ABVD-Treated Classical Hodgkin Lymphoma

Stefan Hohaus, MD, Annarosa Cuccaro, MD, Elisa Cupelli, PhD, Salvatore Annunziata, MD, Manuela Giachelia, PhD, Eugenio Galli, Francesca Bartolomei, MD, Marika Picardi, PhD, Maurizio Martini, MD PhD, Francesco D'Alo', MD, Maria Teresa Voso, MD, Maria Lucia Calcagni, MD, Vittoria Rufini, MD, Alessandro Giordano, MD, Giuseppe Leone, MD, Luigi M. Maria Larocca, MD

Blood (2014) 124 (21): 138.

https://doi.org/10.1182/blood.V124.21.138.138

Published: 2014

Journal Articles

Abnormal Mirna Expression Profile and Cytokine Production in Myelodysplastic Vascular Niche

Maurizio Martini, MD PhD, Luciana Teofili, MD PhD, Sara Capodimonti, BSc, PhD, Eugenia Rosa Nuzzolo, BSc, PhD, Maria Grazia Iachininoto, BSc, PhD, Alessandra Cocomazzi, BSc, Maria Teresa Voso, MD PhD, Luigi Maria Larocca, MD

Blood (2014) 124 (21): 1890.

https://doi.org/10.1182/blood.V124.21.1890.1890

Published: 2014

Journal Articles

CALR mutations in patients with essential thrombocythemia diagnosed in childhood and adolescence

Fiorina Giona, Luciana Teofili, Sara Capodimonti, Marica Laurino, Maurizio Martini, Deborah Marzella, Giovanna Palumbo, Daniela Diverio, Robin Foà, Luigi Maria Larocca

Blood (2014) 123 (23): 3677–3679.

https://doi.org/10.1182/blood-2014-04-572040

Published: 2014

Journal Articles

EBV-DNA In Peripheral Blood Of Patients With Diffuse Large B Cell Lymphoma: Associations With Patient Characteristics and Outcome

Stefan Hohaus, MD, Maria Chiara Tisi, M.D., Elisa Cupelli, Ph.D, Manuela Giachelia, Ph.D., Valentina Bozzoli, MD, Elena Maiolo, M.D., Rosaria Santangelo, M.D., Maurizio Martini, M.D., Francesco D'Alo', M.D., Maria Teresa Voso, M.D., Luigi M. Larocca, M.D., Giuseppe Leone, MD

Blood (2013) 122 (21): 4243.

https://doi.org/10.1182/blood.V122.21.4243.4243

Published: 2013

Journal Articles

Defective WNT Signaling and Genetic Profile Of Endothelial Cells In Patients With Low Risk Myelodysplastic Syndromes Suggest a Contribution Of Vascular Niches To Myelodysplasia

Luciana Teofili, Maurizio Martini, M.D., Eugenia Rosa Nuzzolo, Sara Capodimonti, Alessandra Cocomazzi, Maria Grazia Iachininoto, Maria Teresa Voso, M.D., Gina Zini, Luigi M. Larocca, M.D.

Blood (2013) 122 (21): 860.

https://doi.org/10.1182/blood.V122.21.860.860

Published: 2013

Journal Articles

The Contact with MDS Endothelial Cells Alters the Pattern of Lineage-Specific Gene Expression During Normal Hematopoietic Differentiation

Luciana Teofili, Eugenia Rosa Nuzzolo, Maurizio Martini, Maria Teresa Voso, Sara Capodimonti, Valeriana Cocomazzi, Maria Grazia Iachininoto, Gina Zini, Hematology Professor, Luigi M. Larocca

Blood (2012) 120 (21): 1718.

https://doi.org/10.1182/blood.V120.21.1718.1718

Published: 2012

Journal Articles

Thrombocythemia and polycythemia in patients younger than 20 years at diagnosis: clinical and biologic features, treatment, and long-term outcome

Fiorina Giona, Luciana Teofili, Maria Luisa Moleti, Maurizio Martini, Giovanna Palumbo, Angela Amendola, Maria Gabriella Mazzucconi, Anna Maria Testi, Patrizia Pignoloni, Sonia Maria Orlando, Sara Capodimonti, Mauro Nanni, Giuseppe Leone, Luigi Maria Larocca, Robin Foà

Blood (2012) 119 (10): 2219–2227.

https://doi.org/10.1182/blood-2011-08-371328

Published: 2012

Includes: Supplemental data

Journal Articles

Endothelial progenitor cells are clonal and exhibit the JAK2 V617F mutation in a subset of thrombotic patients with Ph-negative myeloproliferative neoplasms

Luciana Teofili, Maurizio Martini, Maria Grazia Iachininoto, Sara Capodimonti, Eugenia Rosa Nuzzolo, Lorenza Torti, Tonia Cenci, Luigi Maria Larocca, Giuseppe Leone

Blood (2011) 117 (9): 2700–2707.

https://doi.org/10.1182/blood-2010-07-297598

Published: 2011

Journal Articles

Quantitation of EBV-DNA In Peripheral Blood In Hodgkin Lymphoma: Associations with Other Biomarkers and Patient Characteristics

Stefan Hohaus, Manuela Giachelia, Barabara Vannata, Rosaria Santangelo, Maurizio Martini, Tonia Cenci, Giuseppina Massini, Annarosa Cuccaro, D'Alo Francesco, Maria Teresa Voso, Giovanni Fadda, Luigi Larocca, Giuseppe Leone, MD

Blood (2010) 116 (21): 2678.

https://doi.org/10.1182/blood.V116.21.2678.2678

Published: 2010

Journal Articles

Molecular History of Richter Syndrome: Origin From a Common Ancestor Cell Already Present at Chronic Lymphocytic Leukemia Diagnosis

Davide Rossi, Valeria Spina, Daniela Capello, Francesco Forconi, Maurizio Martini, Silvia Rasi, Marco Fangazio, Valter Gattei, Luigi M. Larocca, Francesco Bertoni, Gianluca Gaidano

Blood (2010) 116 (21): 2425.

https://doi.org/10.1182/blood.V116.21.2425.2425

Published: 2010

Journal Articles

Usage of IGHV4-39 with Stereotypic B Cell Receptor Is An Independent Risk Factor of Chronic Lymphocytic Leukemia Transformation to Richter Syndrome

Blood (2008) 112 (11): 778.

https://doi.org/10.1182/blood.V112.11.778.778

Published: 2008

Journal Articles

Hereditary Thrombocythemia: Clinical Characteristics, Biological Markers and Long-Term Follow-up in 4 Families Observed in a Single Hematologic Pediatric Center

Fiorina Giona, Angela Amendola, Luciana Teofili, MD, Giovanna Palumbo, Francesca Mancini, Vittorio Nunes, Massimiliano Rea, Maurizio Martini, Robert Foa

Blood (2008) 112 (11): 5226.

https://doi.org/10.1182/blood.V112.11.5226.5226

Published: 2008

Journal Articles

The revised WHO diagnostic criteria for Ph-negative myeloproliferative diseases are not appropriate for the diagnostic screening of childhood polycythemia vera and essential thrombocythemia

Luciana Teofili, Fiorina Giona, Maurizio Martini, Tonia Cenci, Francesco Guidi, Lorenza Torti, Giovanna Palumbo, Angela Amendola, Giuseppe Leone, Robin Foà, Luigi M. Larocca

Blood (2007) 110 (9): 3384–3386.

https://doi.org/10.1182/blood-2007-06-094276

Published: 2007

Journal Articles

Different STAT-3 and STAT-5 phosphorylation discriminates among Ph-negative chronic myeloproliferative diseases and is independent of the V617F JAK-2 mutation

Luciana Teofili, Maurizio Martini, Tonia Cenci, Giovanna Petrucci, Lorenza Torti, Sergio Storti, Francesco Guidi, Giuseppe Leone, Luigi Maria Larocca

Blood (2007) 110 (1): 354–359.

https://doi.org/10.1182/blood-2007-01-069237

Published: 2007

Journal Articles

Polymorphism in Cytokine Genes as Prognostic Marker in Hodgkin’s Lymphoma.

Stefan Hohaus, MD, Manuela Giachelia, Annalaura Di Febo, MD, Maurizio Martini, MD, Giuseppina Massini, MD, Barbara Vanata, Giovanna Mansueto, MD, Francesco Guidi, MD, Luigi M. Larocca, MD, Maria Teresa Voso, MD, Giuseppe Leone, MD

Blood (2005) 106 (11): 21.

https://doi.org/10.1182/blood.V106.11.21.21

Published: 2005

Journal Articles

Combined Muliparameter Approach to the Diagnosis of Polycythemia Vera and Essential Thrombocythemia.

Luciana Teofili, MD, Maurizio Martini, MD, Tonia Cenci, PhD, Luigi M. Larocca, MD, Giuseppe Leone, MD

Blood (2005) 106 (11): 4950.

https://doi.org/10.1182/blood.V106.11.4950.4950

Published: 2005

Journal Articles

The PRV-1 gene expression in essential thrombocythemia

Luciana Teofili, Maurizio Martini, Francesco Guidi, Daniela Venditti, Giuseppe Leone, M. Luigi Larocca

Blood (2004) 104 (9): 2995–2996.

https://doi.org/10.1182/blood-2004-06-2160

Published: 2004

NARROW

Circulating tumor DNA reveals genetics, clonal evolution, and residual disease in classical Hodgkin lymphoma

Genotyping of Classical Hodgkin Lymphoma on the Liquid Biopsy

Primary Trombocythemia in Children and Adolescents Includes Different Subtypes Compared to Adult Essential Thrombocythemia

Prognostic Role of the CD68+ Cell Count and Early Response Evaluation with Interim-PET and Levels of Plasma Thymus and Activation-Regulated Chemokine (TARC) in ABVD-Treated Classical Hodgkin Lymphoma

Abnormal Mirna Expression Profile and Cytokine Production in Myelodysplastic Vascular Niche

CALR mutations in patients with essential thrombocythemia diagnosed in childhood and adolescence

EBV-DNA In Peripheral Blood Of Patients With Diffuse Large B Cell Lymphoma: Associations With Patient Characteristics and Outcome

Defective WNT Signaling and Genetic Profile Of Endothelial Cells In Patients With Low Risk Myelodysplastic Syndromes Suggest a Contribution Of Vascular Niches To Myelodysplasia

The Contact with MDS Endothelial Cells Alters the Pattern of Lineage-Specific Gene Expression During Normal Hematopoietic Differentiation

Thrombocythemia and polycythemia in patients younger than 20 years at diagnosis: clinical and biologic features, treatment, and long-term outcome

Endothelial progenitor cells are clonal and exhibit the JAK2 V617F mutation in a subset of thrombotic patients with Ph-negative myeloproliferative neoplasms

Quantitation of EBV-DNA In Peripheral Blood In Hodgkin Lymphoma: Associations with Other Biomarkers and Patient Characteristics

Molecular History of Richter Syndrome: Origin From a Common Ancestor Cell Already Present at Chronic Lymphocytic Leukemia Diagnosis

Usage of IGHV4-39 with Stereotypic B Cell Receptor Is An Independent Risk Factor of Chronic Lymphocytic Leukemia Transformation to Richter Syndrome

Hereditary Thrombocythemia: Clinical Characteristics, Biological Markers and Long-Term Follow-up in 4 Families Observed in a Single Hematologic Pediatric Center

The revised WHO diagnostic criteria for Ph-negative myeloproliferative diseases are not appropriate for the diagnostic screening of childhood polycythemia vera and essential thrombocythemia

Different STAT-3 and STAT-5 phosphorylation discriminates among Ph-negative chronic myeloproliferative diseases and is independent of the V617F JAK-2 mutation

Polymorphism in Cytokine Genes as Prognostic Marker in Hodgkin’s Lymphoma.

Combined Muliparameter Approach to the Diagnosis of Polycythemia Vera and Essential Thrombocythemia.

The PRV-1 gene expression in essential thrombocythemia

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American Society of Hematology

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American Society of Hematology

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