Idiopathic inflammatory myopathies (IIMs) are a group of chronic autoimmune systemic diseases affecting the skeletal muscle and other organs. IIMs are also a complex group of diseases, in some cases, difficult to manage. Literature on IIMs has been growing fairly rapidly and keeping up-to-date on such a topic is of utmost importance for any rheumatologist who looks after IIM patients. Thus, the aim of this review is to summarise the most relevant literature contributions published over the last year on the pathogenesis, serology, diagnosis and treatment of IIMs.

One year in review 2018: idiopathic inflammatory myopathies

Marasco, Emiliano
Writing – Original Draft Preparation
;
Zanframundo, Giovanni
Writing – Original Draft Preparation
;
Cavagna, Lorenzo
Supervision
;
2018-01-01

Abstract

Idiopathic inflammatory myopathies (IIMs) are a group of chronic autoimmune systemic diseases affecting the skeletal muscle and other organs. IIMs are also a complex group of diseases, in some cases, difficult to manage. Literature on IIMs has been growing fairly rapidly and keeping up-to-date on such a topic is of utmost importance for any rheumatologist who looks after IIM patients. Thus, the aim of this review is to summarise the most relevant literature contributions published over the last year on the pathogenesis, serology, diagnosis and treatment of IIMs.
2018
The Rheumatology category covers resources on clinical, laboratory, and therapeutic research in all aspects of rheumatology including arthritis and rheumatism.
Esperti anonimi
Inglese
Internazionale
ELETTRONICO
36
6
937-947
Animals; Anti-Inflammatory Agents; Autoantibodies; Autoimmunity; Biomarkers; Humans; Predictive Value of Tests; Risk Factors; Serologic Tests; Treatment Outcome; Myositis
no
8
info:eu-repo/semantics/article
262
Marasco, Emiliano; Cioffi, Elisa; Cometi, Laura; Valentini, Valentina; Zanframundo, Giovanni; Neri, Rossella; Cavagna, Lorenzo; Barsotti, Simone...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1277866
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