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S

Sonia Caccia

university of milan

H指数:24

被引数:1,767

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Patterns of C1-Inhibitor Plasma Levels and Kinin-Kallikrein System Activation in Relation to COVID-19 Severity

IF3.4

2024-11-210

OAAI

Alpha-synuclein dynamics bridge Type-I Interferon response and SARS-CoV-2 replication in peripheral cells

BIOLOGICAL RESEARCH

IF4.6

2024-01-096

OAAI

Efficacy of lanadelumab in angioedema due to acquired C1 inhibitor deficiency

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE

IF6.6

2023-03-014

PRE

An Atypical Case of Idiopathic Nonhistaminergic Angioedema With Anti-C1-INH Antibodies

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY

IF4.8

2022-12-160

OA

IgM Autoantibodies to Complement Factor H in Atypical Hemolytic Uremic Syndrome

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

IF9.4

2021-05-0316

OA

Circulating endothelial progenitors are increased in COVID-19 patients and correlate with SARS-CoV-2 RNA in severe cases

JOURNAL OF THROMBOSIS AND HAEMOSTASIS

IF5

2020-10-0133

OAAI

The central role of endothelium in hereditary angioedema due to C1 inhibitor deficiency

INTERNATIONAL IMMUNOPHARMACOLOGY

IF4.7

2020-05-0117

OAAI

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

IF5.2

2020-03-3113

OAAI

Current and emerging biologics for the treatment of hereditary angioedema

用于治疗遗传性血管性水肿的当前和新兴生物制剂

EXPERT OPINION ON BIOLOGICAL THERAPY

IF4

2019-03-2619

OAAI

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

EXPERT REVIEW OF CLINICAL IMMUNOLOGY

IF3.7

2018-09-139

OAAI

A transcriptomics study of hereditary angioedema attacks

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

IF11.2

2018-09-0117

OAAI

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

SCIENTIFIC REPORTS

IF3.9

2018-01-1723

OAAI

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

THROMBOSIS AND HAEMOSTASIS

IF4.3

2017-11-223

PREAI

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

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE

IF6.6

2017-09-0173

PREAI

Novelties in the Diagnosis and Treatment of Angioedema

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY

IF4.8

2016-08-0262

OAAI

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

MOLECULAR IMMUNOLOGY

IF3

2016-03-015

PREAI

Embelin binds to human neuroserpin and impairs its polymerisation

Embelin与人类神经丝氨酸蛋白结合并削弱其聚合

SCIENTIFIC REPORTS

IF3.9

2016-01-0616

OAAI

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

SCIENTIFIC REPORTS

IF3.9

2015-09-029

OAAI

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

JOURNAL OF THROMBOSIS AND HAEMOSTASIS

IF5

2015-08-0133

OAAI

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

PRPS1-associated表型的扩展范围: 与X连锁听力损失和轻度周围神经病变分离的三种新突变

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2014-09-0324

OAAI