CACCIA, SONIA

CACCIA, SONIA

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Pubblicazioni

Risultati 1 - 20 di 58 (tempo di esecuzione: 0.0 secondi).

TitoloData di pubblicazioneAutoriTipoFile Abstract
1Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiencyset-2009SPENA, SILVIA  ; ASSELTA, ROSANNA  ; CACCIA, SONIA  ; RIMOLDI, VALERIA  ; PAYVANDI, FLORA  ; DUGA, STEFANO  Article (author)--
2Antibodies 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 thrombosis2006VECCHI, MAURIZIO  ; CACCIA, SONIA  ; DE FRANCHIS, ROBERTO  ; CUGNO, MASSIMO  Article (author)-
3Antibodies 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 patients2004CUGNO, MASSIMO  ; MERONI, PIERLUIGI  ; CACCIA, SONIA  ; RUSSO, ROSARIA  ; BOTTASSO, BIANCAMARIA  ; MANNUCCI, PIER MANNUCCIO  Article (author)-
4The anticoagulant thrombin mutant W215A/E217A has a collapsed primary specificity pocket17-set-2004CACCIA, SONIA  ; Article (author)-
5C1-inhibitor deficiency and angioedema : molecular mechanisms and clinical progress2009CUGNO, MASSIMO  ; ZANICHELLI, ANDREA  ; FOIENI, FABRIZIO  ; CACCIA, SONIA  ; CICARDI, MARCO  Article (author)-
6A case of remittent C1-inhibitor deficiencyset-2015CACCIA, SONIA  ; SUFFRITTI, CHIARA  ; CARZANIGA, THOMAS  ; CICARDI, MARCO  Article (author)-
7Cleaved human neuroserpin2009RICAGNO, STEFANO  ; SORRENTINO, GRAZIELLA  ; CACCIA, SONIA  ; BOLOGNESI, MARTINO  Dataset--
8Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop)2019CACCIA, SONIA  ; Article (author)  Solo autorizzati-
9Crystal structure of the potent anticoagulant thrombin mutant W215A/E217A in free form2004CACCIA, SONIA  ; Dataset--
10Current and emerging biologics for the treatment of hereditary angioedema26-mar-2019WU, MADDALENA ALESSANDRA  ; CACCIA, SONIA  ; SUFFRITTI, CHIARA  ; BERGAMASCHINI, LUIGI CESARE  ; CICARDI, MARCO  Article (author)  Open Access dal 6/3/20
11Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency2017ZANICHELLI, ANDREA  ; WU, MADDALENA ALESSANDRA  ; SUFFRITTI, CHIARA  ; MAGGIONI, LORENA MARIA  ; CACCIA, SONIA  ; PEREGO, FRANCESCA  ; CICARDI, MARCO  Article (author)  riservati
12Donor complement gene abnormalities cause transplant associated microangiopathy after allogeneic bone marrow transplantationlug-2017BERRA, SILVIA  ; CACCIA, SONIA  ; CUGNO, MASSIMO  ; CLIVIO, ALBERTO  ; ARDISSINO, GIAN LUIGI  Article (author)  riservati-
13Effect of mutations within the coding region of C1-INH gene on protein function in families with HAE29-apr-2005CACCIA, SONIA  ; PAPPALARDO, EMANUELA  ; CICARDI, MARCO  Book Part (author)-
14Effects of mutations within the coding region of C1-INH gene on disease manifestation and protein function in families with HAEgiu-2004CACCIA, SONIA  ; PAPPALARDO, EMANUELA  ; FOLCIONI, ANNA  ; ZINGALE, LORENZA CHIARA  ; ZANICHELLI, ANDREA  ; CICARDI, MARCO  Article (author)-
15Embelin binds to human neuroserpin and impairs its polymerisation6-gen-2016BARBIROLI, ALBERTO GIUSEPPE  ; RUSSO, ROSARIA  ; CACCIA, SONIA  ; BOLOGNESI, MARTINO  ; RICAGNO, STEFANO  Article (author)  Open Access
16Exome sequencing identifies PRPS1 as a major locus for X-linked nonsyndromic hearing loss in the Italian populationgiu-2012ROBUSTO, MICHELA  ; ASSELTA, ROSANNA  ; CACCIA, SONIA  ; AMBROSETTI, UMBERTO  ; DUGA, STEFANO  ; SOLDA', GIULIA MARIA EMILIA ANTONIETTA  Conference Object-
17The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathygiu-2015CACCIA, SONIA  ; CESARANI, ANTONIO  ; AMBROSETTI, UMBERTO  ; Article (author)  riservati
18Fast form of thrombin mutant R(77a)A bound to PPACK2004CACCIA, SONIA  ; Dataset--
19First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family2015CACCIA, SONIA  ; ROBUSTO, MICHELA  ; AMBROSETTI, UMBERTO  ; Article (author)  riservati
20Gene regulation in the pathogenesis of angioedema due to inherited c1 inhibitor deficiency (hereditary angioedema)7-mar-2009CICARDI, MARCO  ; ZANICHELLI, ANDREA  ; SUFFRITTI, CHIARA  ; MAGGIONI, LORENA MARIA  ; CACCIA, SONIA  ; RUSSO, ROSARIA  ; ZHI, YUXIANG  ; DUGA, STEFANO  ; ASSELTA, ROSANNA  ; RIMOLDI, VALERIA  ; Conference Object-

Dettaglio

CACCIA, SONIA 

Dipartimento di Scienze Biomediche e Cliniche L. Sacco 

 
 
 
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