CACCIA, SONIA
CACCIA, SONIA
Dipartimento di Scienze Biomediche e Cliniche
A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia
2025 M. Drotarova, R. Asselta, S. Caccia, I. Skornova, J. Zolkova, Z. Kolkova, D. Loderer, V. Podusel, J. Stasko, T. Simurda
Elevated serum levels of interleukin-18 discriminate Still's disease from other autoinflammatory conditions: results from the European ImmunAID cohort
2025 G. Charlotte, R. Emiliana, M. Yvonne M, C. Assunta, K. Peter D, G. Cem, S. Caccia
Alpha-synuclein dynamics bridge Type-I Interferon response and SARS-CoV-2 replication in peripheral cells
2024 F. Limanaqi, S. Zecchini, I. Saulle, S. Strizzi, C. Vanetti, M. Garziano, G. Cappelletti, D. Parolin, S. Caccia, D. Trabattoni, C. Fenizia, M. Clerici, M. Biasin
Patterns of C1-Inhibitor Plasma Levels and Kinin–Kallikrein System Activation in Relation to COVID-19 Severity
2024 S. Berra, D. Parolin, C. Suffritti, A. Folcia, A. Zanichelli, L. Gusso, C. Cogliati, A. Riva, A. Gidaro, S. Caccia
Efficacy of Lanadelumab in angioedema due to acquired C1 inhibitor deficiency
2023 C. Suffritti, S. Sartorio, S. Berra, V. Popescu Janu, S. Caccia, A. Zanichelli
Platelet Microvesicles, Inflammation, and Coagulation Markers: A Pilot Study
2023 A. Gidaro, A.P. Delitala, R. Manetti, S. Caccia, M.J. Soloski, G. Lambertenghi Deliliers, D. Castro, M. Donadoni, A. Bartoli, G. Sanna, L. Bergamaschini, R. Castelli
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
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
Hereditary angioedema due to C1 inhibitor deficiency in Belarus : epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene
2021 I. Guryanova, C. Suffritti, D. Parolin, A. Zanichelli, N. Ishchanka, E. Polyakova, M. Belevtsev, F. Perego, M. Cicardi, Y. Zharankova, N. Konoplya, S. Caccia, A. Gidaro
Anti-C1-Inhibitor Autoantibody Detection by ELISA
2021 C. Suffritti, S. Caccia, S. Berra, D. Parolin, M. Cicardi
IgM Autoantibodies to Complement Factor H in Atypical Hemolytic Uremic Syndrome
2021 M. Cugno, S. Berra, F. Depetri, S. Tedeschi, S. Griffini, E. Grovetti, S. Caccia, D. Cresseri, P. Messa, S. Testa, F. Giglio, F. Peyvandi, G. Ardissino
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
The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency
2020 M.A. Wu, M. Bova, S. Berra, R. Senter, D. Parolin, S. Caccia, M. Cicardi
Genetic variants in the fgb and fgg genes mapping in the beta and gamma nodules of the fibrinogen molecule in congenital quantitative fibrinogen disorders associated with a thrombotic phenotype
2020 T. Simurda, M. Brunclikova, R. Asselta, S. Caccia, J. Zolkova, Z. Kolkova, D. Loderer, I. Skornova, J. Hudecek, Z. Lasabova, J. Stasko, P. Kubisz
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
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
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
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
Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight
2018 S. Caccia, C. Suffritti, T. Carzaniga, R. Berardelli, S. Berra, V. Martorana, A. Fra, C. Drouet, M. Cicardi
Novel SERPING1 mutations in bulgarian patients revealed by a targeted next generation sequencing platform
2018 A. Valerieva, M. Staevska, M. Zamanakou, G. Loules, S. Caccia, M. Cicardi, A. Germenis