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Journal Articles

Genetic Variants Associated with High Plasma Levels of Factor VIII and Von Willebrand Factor in a Family with Thrombotic Episodes

Silvia Spena, Andrea Cairo, Francesca Gianniello, Emanuela Pappalardo, Mimosa Mortarino, Isabella Garagiola, Ida Martinelli, Flora Peyvandi

Blood (2023) 142 (Supplement 1): 5402.

https://doi.org/10.1182/blood-2023-189383

Published: 2023

Journal Articles

The Histopathological Landscape of Synovitis in Hemophilic Arthropathy

Roberta Gualtierotti, Chiara Suffritti, Carlo Pescia, Andrea Giachi, Silvia Spena, Federico Molfino, Stanislao Lavorato, Eleonora Semproni, Addolorata Truma, Sara Arcudi, Alessandro Ciavarella, Marco Maggioni, Umberto Gianelli, Simona Maria Siboni, Jacopo Acquati Lozej, Luigi Piero Solimeno, Flora Peyvandi

Blood (2023) 142 (Supplement 1): 5481.

https://doi.org/10.1182/blood-2023-173554

Published: 2023

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

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

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Genetic Variants Associated with High Plasma Levels of Factor VIII and Von Willebrand Factor in a Family with Thrombotic Episodes

The Histopathological Landscape of Synovitis in Hemophilic Arthropathy

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

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

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ASH Publications

American Society of Hematology

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Genetic Variants Associated with High Plasma Levels of Factor VIII and Von Willebrand Factor in a Family with Thrombotic Episodes

The Histopathological Landscape of Synovitis in Hemophilic Arthropathy

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

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

Email alerts

ASH Publications

American Society of Hematology

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