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Journal Articles

Clinical relevance of clonal hematopoiesis in persons aged ≥80 years

Marianna Rossi, Manja Meggendorfer, Matteo Zampini, Mauro Tettamanti, Emma Riva, Erica Travaglino, Matteo Bersanelli, Sara Mandelli, Alessia Antonella Galbussera, Ettore Mosca, Elena Saba, Chiara Chiereghin, Nicla Manes, Chiara Milanesi, Marta Ubezio, Lucio Morabito, Clelia Peano, Giulia Soldà, Rosanna Asselta, Stefano Duga, Carlo Selmi, Maria De Santis, Karolina Malik, Giulia Maggioni, Marilena Bicchieri, Alessia Campagna, Cristina A. Tentori, Antonio Russo, Efrem Civilini, Paola Allavena, Rocco Piazza, Giovanni Corrao, Claudia Sala, Alberto Termanini, Laura Giordano, Paolo Detoma, Aurelio Malabaila, Luca Sala, Stefano Rosso, Roberto Zanetti, Claudia Saitta, Elena Riva, Gianluigi Condorelli, Francesco Passamonti, Armando Santoro, Francesc Sole, Uwe Platzbecker, Pierre Fenaux, Niccolò Bolli, Gastone Castellani, Wolfgang Kern, George S. Vassiliou, Torsten Haferlach, Ugo Lucca, Matteo G. Della Porta

Blood (2021) 138 (21): 2093–2105.

https://doi.org/10.1182/blood.2021011320

Published: 2021

Includes: Supplemental data

Journal Articles

Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study

Blood (2018) 132 (Supplement 1): 750.

https://doi.org/10.1182/blood-2018-99-114717

Published: 2018

Journal Articles

Exploring the global landscape of genetic variation in coagulation factor XI deficiency

Rosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, Marzia Menegatti, Flora Peyvandi, Ophira Salomon, Stefano Duga

Blood (2017) 130 (4): e1–e6.

https://doi.org/10.1182/blood-2017-04-780148

Published: 2017

Journal Articles

Response: Further thoughts on the “phantom” Δ6/7 FXI isoform

Rosanna Asselta, Valeria Rimoldi, Ilaria Guella, Giulia Soldà, Raimondo De Cristofaro, Flora Peyvandi, Stefano Duga

Blood (2010) 116 (7): 1186–1187.

https://doi.org/10.1182/blood-2010-06-287284

Published: 2010

Journal Articles

Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA

Rosanna Asselta, Valeria Rimoldi, Ilaria Guella, Giulia Soldà, Raimondo De Cristofaro, Flora Peyvandi, Stefano Duga

Blood (2010) 115 (10): 2065–2072.

https://doi.org/10.1182/blood-2009-09-245092

Published: 2010

Includes: Supplemental data

Journal Articles

The Use of High Resolution Melting (HRM) Analysis for Molecular Gene Defects of Type 3 Von Willebrand Disease: Studies of An Italian Cohort of 10 Patients.

Maria Solimando, Augusto B. Federici, Luciano Baronciani, Alberto Mussetti, Margherita Punzo, Silvia La Marca, Manuela Platè, Rosanna Asselta, Pier Mannuccio Mannucci

Blood (2009) 114 (22): 3498.

https://doi.org/10.1182/blood.V114.22.3498.3498

Published: 2009

Journal Articles

Factor V Leiden Is Associated with Premature Myocardial Infarction.

Flora Peyvandi, Marta Spreafico, Luisa Foco, Luisa Bernardinelli, Stefano Duga, Rosanna Asselta, Diego Ardissino, Sekar Kathiresan, Pierangelica Merlini, Pier M. Mannucci, MD

Blood (2008) 112 (11): 1817.

https://doi.org/10.1182/blood.V112.11.1817.1817

Published: 2008

Journal Articles

Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia

Rosanna Asselta, Stefano Duga, Silvia Spena, Flora Peyvandi, Giancarlo Castaman, Massimo Malcovati, Pier Mannuccio Mannucci, Maria Luisa Tenchini

Blood (2004) 103 (8): 3051–3054.

https://doi.org/10.1182/blood-2003-10-3725

Published: 2004

Journal Articles

Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations

Maria Claudia Montefusco, Stefano Duga, Rosanna Asselta, Massimo Malcovati, Flora Peyvandi, Elena Santagostino, Pier Mannuccio Mannucci, Maria Luisa Tenchini

Blood (2003) 102 (9): 3210–3216.

https://doi.org/10.1182/blood-2003-03-0922

Published: 2003

Journal Articles

Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant protein

Stefano Duga, Maria Claudia Montefusco, Rosanna Asselta, Massimo Malcovati, Flora Peyvandi, Elena Santagostino, Pier Mannuccio Mannucci, Maria Luisa Tenchini

Blood (2003) 101 (1): 173–177.

https://doi.org/10.1182/blood-2002-06-1928

Published: 2003

Journal Articles

Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bβ-chain gene causing activation of cryptic splice sites

Silvia Spena, Stefano Duga, Rosanna Asselta, Massimo Malcovati, Flora Peyvandi, Maria Luisa Tenchini

Blood (2002) 100 (13): 4478–4484.

https://doi.org/10.1182/blood-2002-06-1647

Published: 2002

Journal Articles

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs

Rosanna Asselta, Stefano Duga, Silvia Spena, Elena Santagostino, Flora Peyvandi, Gavino Piseddu, Roberto Targhetta, Massimo Malcovati, Pier Mannuccio Mannucci, Maria Luisa Tenchini

Blood (2001) 98 (13): 3685–3692.

https://doi.org/10.1182/blood.V98.13.3685

Published: 2001

Journal Articles

Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation

Rosanna Asselta, Stefano Duga, Tatjana Simonic, Massimo Malcovati, Elena Santagostino, Paul L. F. Giangrande, Pier Mannuccio Mannucci, Maria Luisa Tenchini

Blood (2000) 96 (7): 2496–2500.

https://doi.org/10.1182/blood.V96.7.2496

Published: 2000

Journal Articles

Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion

Stefano Duga, Rosanna Asselta, Elena Santagostino, Sirous Zeinali, Tatjana Simonic, Massimo Malcovati, Pier Mannuccio Mannucci, Maria Luisa Tenchini

Blood (2000) 95 (4): 1336–1341.

https://doi.org/10.1182/blood.V95.4.1336.004k16_1336_1341

Published: 2000

NARROW

Clinical relevance of clonal hematopoiesis in persons aged ≥80 years

Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study

Exploring the global landscape of genetic variation in coagulation factor XI deficiency

Response: Further thoughts on the “phantom” Δ6/7 FXI isoform

Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA

The Use of High Resolution Melting (HRM) Analysis for Molecular Gene Defects of Type 3 Von Willebrand Disease: Studies of An Italian Cohort of 10 Patients.

Factor V Leiden Is Associated with Premature Myocardial Infarction.

Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia

Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations

Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant protein

Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bβ-chain gene causing activation of cryptic splice sites

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs

Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation

Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion

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American Society of Hematology

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ASH Publications

American Society of Hematology

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