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International Immunopharmacology|March 2, 2020
The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiencyMaddalena Alessandra Wu, Maria Bova, Silvia Berra, et al.
Journal of Human Genetics|December 15, 2015
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian familyGiulia Soldà, Sonia Caccia, Michela Robusto, et al.
Molecular Immunology|February 20, 2016
Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domainSaied A Jaradat, Sonia Caccia, Rifaat Rawashdeh, et al.
Scientific Reports|September 3, 2015
The stability and activity of human neuroserpin are modulated by a salt bridge that stabilises the reactive centre loopRosina Noto, Loredana Randazzo, Samuele Raccosta, et al.
Expert Opinion on Biological Therapy|March 27, 2019
Current and emerging biologics for the treatment of hereditary angioedemaFrancesca Perego, Maddalena A Wu, Anna Valerieva, et al.
Blood|November 25, 2003
Antibodies to tissue-type plasminogen activator (tPA) in patients with antiphospholipid syndrome: evidence of interaction between the antibodies and the catalytic domain of tPA in 2 patientsMassimo Cugno, Mara Cabibbe, Monica Galli, et al.
Scientific Reports|January 19, 2018
Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural InsightSonia Caccia, Chiara Suffritti, Thomas Carzaniga, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 13, 2017
Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor DeficiencyAndrea Zanichelli, Giulia Maria Azin, Maddalena Alessandra Wu, et al.
Life (Basel, Switzerland)|January 8, 2025
Patterns of C1-Inhibitor Plasma Levels and Kinin-Kallikrein System Activation in Relation to COVID-19 SeveritySilvia Berra, Debora Parolin, Chiara Suffritti, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 1, 2025
A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemiaMiroslava Drotarova, Rosanna Asselta, Sonia Caccia, et al.
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