CACCIA, SONIA
CACCIA, SONIA
Dipartimento di Scienze Biomediche e Cliniche
Acid Sphingomyelinase Downregulation Enhances Mitochondrial Fusion and Promotes Oxidative Metabolism in a Mouse Model of Melanoma
2020-03-31 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
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency
2009-09-01 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
2021-01-01 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
2006-01-01 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
2004-01-01 M. Cugno, M. Cabibbe, M. Galli, P.L. Meroni, S. Caccia, R. Russo, B. Bottasso, P.M. Mannucci
The anticoagulant thrombin mutant W215A/E217A has a collapsed primary specificity pocket
2004-09-17 A.O. Pineda, Z.W. Chen, S. Caccia, A.M. Cantwell, S.N. Savvides, G. Waksman, F.S. Mathews, E. Di Cera
An atypical case of idiopathic nonhistaminergic angioedema with anti-C1-INH antibodies
2022-02-11 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
C1 esterase inhibitor and the kinin-kallikrein system in COVID-19
2022-01-01 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
2009-01-01 M. Cugno, A. Zanichelli, F. Foieni, S. Caccia, M. Cicardi
A case of remittent C1-inhibitor deficiency
2015-09-01 S. Caccia, C. Suffritti, T. Carzaniga, R. Berardelli, A. Fra, C. Drouet, M. Cicardi
The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency
2020-05-01 M.A. Wu, M. Bova, S. Berra, R. Senter, D. Parolin, S. Caccia, M. Cicardi
Circulating endothelial progenitors are increased in Covid‐19 patients and correlate with SARS‐CoV‐2 RNA in severe cases
2020-01-01 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
2009-01-01 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)
2019-01-01 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
2004-01-01 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
2019-03-26 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
2017-01-01 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
2017-07-01 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
2005-04-29 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
2004-06-01 S. Caccia, E. Pappalardo, A. Folcioni, L.C. Zingalea, A. Zanichellia, M. Cicardi