與「Giacomo Emmi」相符的使用者個人學術檔案
 | Giacomo EmmiDepartment of Medical Science, University of Trieste, Italy 在 units.it 的電子郵件地址已通過驗證 被引用 11318 次 |
Evidence-Based Guideline for the diagnosis and management of eosinophilic granulomatosis with polyangiitis
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare anti-neutrophil cytoplasmic
antibody (ANCA)-associated vasculitis, characterized by asthma, eosinophilia and …
antibody (ANCA)-associated vasculitis, characterized by asthma, eosinophilia and …
SARS-CoV-2 infection among patients with systemic autoimmune diseases
G Emmi, A Bettiol, I Mattioli, E Silvestri, G Di Scala… - Autoimmunity …, 2020 - Elsevier
Objectives This study aimed to evaluate the prevalence of clinically overt SARS-CoV-2
infection (COVID-19) among patients with systemic autoimmune diseases residing in Tuscany, …
infection (COVID-19) among patients with systemic autoimmune diseases residing in Tuscany, …
Sjögren's syndrome: a systemic autoimmune disease
S Negrini, G Emmi, M Greco, M Borro… - Clinical and …, 2022 - Springer
Sjögren’s syndrome is a chronic autoimmune disease characterized by ocular and oral
dryness resulting from lacrimal and salivary gland dysfunction. Besides, a variety of systemic …
dryness resulting from lacrimal and salivary gland dysfunction. Besides, a variety of systemic …
[HTML][HTML] Interleukin 1α: a comprehensive review on the role of IL-1α in the pathogenesis and treatment of autoimmune and inflammatory diseases
The interleukin (IL)-1 family member IL-1α is a ubiquitous and pivotal pro-inflammatory
cytokine. The IL-1α precursor is constitutively present in nearly all cell types in health, but is …
cytokine. The IL-1α precursor is constitutively present in nearly all cell types in health, but is …
[HTML][HTML] Behçet's syndrome patients exhibit specific microbiome signature
Background and aims Behçet syndrome is a systemic inflammatory condition characterized
by muco-cutaneous and ocular manifestations, with central nervous system, vascular and/or …
by muco-cutaneous and ocular manifestations, with central nervous system, vascular and/or …
Central vein sign differentiates Multiple Sclerosis from central nervous system inflammatory vasculopathies
Objectives In multiple sclerosis (MS), magnetic resonance imaging (MRI) is a sensitive tool
for detecting white matter lesions, but its diagnostic specificity is still suboptimal; ambiguous …
for detecting white matter lesions, but its diagnostic specificity is still suboptimal; ambiguous …
Mepolizumab for eosinophilic granulomatosis with polyangiitis: a European multicenter observational study
Objective Mepolizumab proved to be an efficacious treatment for eosinophilic granulomatosis
with polyangiitis (EGPA) at a dose of 300 mg every 4 weeks in the randomized, controlled …
with polyangiitis (EGPA) at a dose of 300 mg every 4 weeks in the randomized, controlled …
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status
…, C Baldini, F Bonatti, MC Cid, H Elding, G Emmi… - Nature …, 2019 - nature.com
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare inflammatory disease of unknown
cause. 30% of patients have anti-neutrophil cytoplasmic antibodies (ANCA) specific for …
cause. 30% of patients have anti-neutrophil cytoplasmic antibodies (ANCA) specific for …
Vascular Behçet syndrome: from pathogenesis to treatment
Behçet syndrome is a rare, chronic inflammatory disease of unknown aetiopathogenesis,
most commonly presenting with mucocutaneous and ocular manifestations. Vascular …
most commonly presenting with mucocutaneous and ocular manifestations. Vascular …
Thrombosis in vasculitis: from pathogenesis to treatment
In recent years, the relationship between inflammation and thrombosis has been deeply
investigated and it is now clear that immune and coagulation systems are functionally …
investigated and it is now clear that immune and coagulation systems are functionally …