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List of works by Sonia Caccia

A transcriptomics study of hereditary angioedema attacks

scientific article published on 04 May 2018

Acid Sphingomyelinase Downregulation Enhances Mitochondrial Fusion and Promotes Oxidative Metabolism in a Mouse Model of Melanoma ⬇️

scientific article published on 31 March 2020

Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency

scientific article published on 01 September 2009

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

scientific article published on 01 July 2006

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

scientific article published on 20 November 2003

C1-inhibitor deficiency and angioedema: molecular mechanisms and clinical progress

scientific article published on 21 January 2009

Current and emerging biologics for the treatment of hereditary angioedema

scientific article published on 26 March 2019

Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency

scientific article

Embelin binds to human neuroserpin and impairs its polymerisation.

scientific article

First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family.

scientific article published on 10 December 2015

Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.

scientific article

Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain

scientific article published in March 2016

Human neuroserpin: structure and time-dependent inhibition

scientific article

Interaction of C1 inhibitor with thrombin on the endothelial surface

Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight

scientific article published on 17 January 2018

Modulation of the Association Reaction between Hemoglobin and Carbon Monoxide by Proton and Chloride†

scientific article published in February 1998

Molecular bases of neuroserpin function and pathology

scientific article published in August 2010

Molecular dissection of Na+ binding to thrombin.

scientific article published on 19 May 2004

Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.

scientific article

Novelties in the Diagnosis and Treatment of Angioedema

scientific article

Pathophysiology of Hereditary Angioedema

scientific article published in December 2014

Recombinant human C1 esterase inhibitor (Conestat alfa) for prophylaxis to prevent attacks in adult and adolescent patients with hereditary angioedema

scientific article published on 13 September 2018

The Anticoagulant Thrombin Mutant W215A/E217A Has a Collapsed Primary Specificity Pocket

scientific article published on 13 July 2004

The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.

scientific article

The kinetics of the reaction between NO and O2 as studied by a novel approach

scientific article published on 01 January 1999

The spectrum of factor XI deficiency in Italy.

scientific article published on 24 September 2013

The stability and activity of human neuroserpin are modulated by a salt bridge that stabilises the reactive centre loop.

scientific article published on 2 September 2015

Unexpected crucial role of residue 225 in serine proteases

scientific article

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