CACCIA, SONIA
CACCIA, SONIA
Dipartimento di Scienze Biomediche e Cliniche
A case of remittent C1-inhibitor deficiency
2015 S. Caccia, C. Suffritti, T. Carzaniga, R. Berardelli, A. Fra, C. Drouet, M. Cicardi
A SERPING1 variant that causes C1-inhibitor deficiency without hereditary angioedema
2019 S. Berra, C. Suffritti, A. Zanichelli, D. Parolin, M.A. Wu, F. Perego, M. Cicardi, S. Caccia
A transcriptomics study of hereditary angioedema attacks
2018 G. Castellano, C. Divella, F. Sallustio, V. Montinaro, C. Curci, A. Zanichelli, E. Bonanni, C. Suffritti, S. Caccia, F. Bossi, A. Gallone, F.P. Schena, L. Gesualdo, M. Cicardi
Acid Sphingomyelinase Downregulation Enhances Mitochondrial Fusion and Promotes Oxidative Metabolism in a Mouse Model of Melanoma
2020 M. Coazzoli, A. Napoli, P. Roux-Biejat, C.D. Palma, C. Moscheni, E. Catalani, S. Zecchini, V. Conte, M. Giovarelli, S. Caccia, P. Procacci, D. Cervia, E. Clementi, C. Perrotta
An atypical case of idiopathic nonhistaminergic angioedema with anti-C1-INH antibodies
2022 M. Bova, C. Suffritti, J. Kusumam, S. Caccia, K.A. Gelderman, S. Berra, S. Loffredo, R. Santacroce, A. Petraroli, D. Roem-Haagsma, M. Margaglione, G. Spadaro, A.P. Kaplan
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency
2009 S. Spena, R. Asselta, S. Caccia, V. Rimoldi, S.H. Giacomelli, A. Tagliaferri, F. Peyvandi, G. Castaman, S. Duga
Anti-C1-Inhibitor Autoantibody Detection by ELISA
2021 C. Suffritti, S. Caccia, S. Berra, D. Parolin, M. Cicardi
Antibodies to tissue-type plasminogen activator (t-PA) in patients with inflammatory bowel disease : high prevalence, interactions with functional domains of t-PA and possible implications in thrombosis
2006 S. Saibeni, C. Ciscato, M. Vecchi, M. Boscolo Anzoletti, E. Kaczmarek, S. Caccia, R. de Franchis, M. Cugno
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 patients
2004 M. Cugno, M. Cabibbe, M. Galli, P.L. Meroni, S. Caccia, R. Russo, B. Bottasso, P.M. Mannucci
C1 esterase inhibitor and the kinin-kallikrein system in COVID-19
2022 S. Caccia, S. Berra, D. Parolin, C. Suffritti, A. Folcia, A. Zanichelli, C.B. Cogliati, A. Riva, A. Gidaro
C1-inhibitor deficiency and angioedema : molecular mechanisms and clinical progress
2009 M. Cugno, A. Zanichelli, F. Foieni, S. Caccia, M. Cicardi
Circulating endothelial progenitors are increased in Covid‐19 patients and correlate with SARS‐CoV‐2 RNA in severe cases
2020 P. Mancuso, A. Gidaro, G. Gregato, A. Raveane, P. Cremonesi, J. Quarna, S. Caccia, L. Gusso, S. Rusconi, A. Giacomelli, C. Cogliati, F. Bertolini
Cleaved human neuroserpin
2009 S. Ricagno, G. Sorrentino, S. Caccia, M. Bolognesi
Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop)
2019 T. Simurda, S. Caccia, R. Asselta, J. Zolkova, J. Stasko, I. Skornova, Z. Snahnicanova, D. Loderer, Z. Lasabova, P. Kubisz
Crystal structure of the potent anticoagulant thrombin mutant W215A/E217A in free form
2004 A.O. Pineda, Z.-. Chen, S. Caccia, S.N. Savvides, G. Waksman, F.S. Mathews, E. Di Cera
Current and emerging biologics for the treatment of hereditary angioedema
2019 F. Perego, M.A. Wu, A. Valerieva, S. Caccia, C. Suffritti, A. Zanichelli, L. Bergamaschini, M. Cicardi
Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency
2017 A. Zanichelli, G.M. Azin, M.A. Wu, C. Suffritti, L. Maggioni, S. Caccia, F. Perego, R. Vacchini, M. Cicardi
Donor complement gene abnormalities cause transplant associated microangiopathy after allogeneic bone marrow transplantation
2017 M. Parma, E. Terruzzi, E. Diral, S. Salardi, S. Berra, M. Sgarbanti, S. Caccia, G. Colussi, M. Cugno, F. Giglio, T. Mina, J. Peccatori, M. Zecca, A. Clivio, S. Tedeschi, P. Pioltelli, G. Ardissino
Effect of mutations within the coding region of C1-INH gene on protein function in families with HAE
2005 S. Caccia, E. Pappalardo, L. Maggioni, M. Cicardi
Effects of mutations within the coding region of C1-INH gene on disease manifestation and protein function in families with HAE
2004 S. Caccia, E. Pappalardo, A. Folcioni, L.C. Zingalea, A. Zanichellia, M. Cicardi