A5069524192- Systemic Lupus Erythematosus Research
- Rheumatoid Arthritis Research and Therapies
- Inflammatory Myopathies and Dermatomyositis
- Vasculitis and related conditions
- Systemic Sclerosis and Related Diseases
- Musculoskeletal synovial abnormalities and treatments
- Pregnancy and Medication Impact
- Fibromyalgia and Chronic Fatigue Syndrome Research
- Retinal and Optic Conditions
- Hematological disorders and diagnostics
- Ocular Diseases and Behçet’s Syndrome
- Eosinophilic Esophagitis
- Nutrition, Genetics, and Disease
- Genetic Neurodegenerative Diseases
- Autoimmune and Inflammatory Disorders Research
- Science, Research, and Medicine
- Inflammasome and immune disorders
- Biotechnology and Related Fields
- Hepatitis C virus research
- Cytokine Signaling Pathways and Interactions
- Eosinophilic Disorders and Syndromes
- Diabetes and associated disorders
- Health and Well-being Studies
- Connective Tissue Growth Factor Research
- Peripheral Neuropathies and Disorders
Luigi Sacco Hospital
2021
Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda
2019-2020
University of Pavia
1988-2015
Istituto Dermopatico dell'Immacolata
1974
Antisynthetase syndrome (ASSD) is a rare clinical condition that characterized by the occurrence of classic triad, encompassing myositis, arthritis, and interstitial lung disease (ILD), along with specific autoantibodies are addressed to different aminoacyl tRNA synthetases (ARS). Until now, it has been unknown whether presence ARS might affect presentation, evolution, outcome ASSD. In this study, we retrospectively recorded time onset, characteristics, clustering triad findings, survival...
The increased number of childbearing women with autoimmune diseases leads to a growing interest in studying relationship among maternal disease, therapy, pregnancy and off-spring. aim this study was determine the impact disease on neonatal outcome, taking into account treatment transplacental autoantibodies passage. We studied 70 infants born pregnant attended Fondazione IRCCS Policlinico San Matteo, Pavia, Italy from June 2005 2012. Maternal characteristics were collected relevant clinical,...
<h3>Background:</h3> Mixed Cryoglobuminaemia(MC) is a small vessel vasculitis characterized by the presence of monoclonal rheumatoid factor(RF) and polyclonal immunoglobulins that precipitate at cold temperature, with large spectrum clinical manifestations. MC strongly associated hepatitis C(HCV) infection>90%. The new direct–acting antivirals(DAA) against HCV, which can eradicate virus in >95% patients, are supposed to have benefits on manifestations MC, nonetheless amount data still...
<h3>Background</h3> Systemic sclerosis (SSc) is a chronic autoimmune connective tissue disorder of not fully understood aetiology characterized by vascular and fibrotic abnormalities in the skin internal organs. Musculoskeletal involvement, mainly affecting hands feet, frequent SSc represents major cause disability. Ultrasonography non-invasive, cost-effective imaging modality which able to detect presence joint involvement SSc. <h3>Methods</h3> 61 consecutive patients (60 women) were...
<h3>Background</h3> Digital health innovations have opened up several opportunities to help patients with rheumatologic conditions and their treating clinicians in improving routine healthcare. <h3>Objectives</h3> To evaluate the applicability of a wearable smartwatch for monitoring hip osteoarthritis who received viscosupplementation. Samsung Electronics Italia MDApp srl supported present study. <h3>Methods</h3> Consecutive viscosupplementation jaluronic acid between November 2017 May 2018...
Background: Behcet disease is a rare inflammatory disorder with the unique ability to affect vessels of any size. The could be associated thrombosis in both venous and arterial compartment, often aneurysms. In particular, presence aneurysms pulmonary artery rarely, if ever, seen conditions other than Behcet. Cardiac involvement, albeit uncommon, also described severe prognosis. treatment based on immunosuppressants, meanwhile use anticoagulants -especially when are present- debated....
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Remitting seronegative symmetric synovitis with pitting edema (RS3PE) is a rare syndrome characterised by acute onset of symmetrical distal and tenosynovitis, associated severe the dorsum hands feet, seronegativity for autoimmunity dramatic response to glucocorticoids. First described McCarty et al. in 1985, RS3PE reported mostly elderly males, but it can also rarely occur young people. Although was initially regarded as form rheumatoid arthritis (RA), now considered clinical distinct entity...