Results 21 to 30 of about 7,670 (175)
Idiopathic inflammatory myopathies [PDF]
Vnitřní lékařství, 2018 Idiopathic inflammatory myopathies form a heterogeneous group of acquired inflammatory diseases afflicting striated muscles. The disease is frequently accompanied by systemic and organ involvement. Dermatomyositis, polymyositis, cancer associated myositis, immune mediated necrotizing myopathy, myositis in overlap syndromes, juvenile myositis and ...
Parker, Matthew +3 more
openaire +4 more sources
Idiopathic inflammatory myopathies: a review [PDF]
Internal Medicine Journal, 2021 AbstractIdiopathic inflammatory myopathy (IIM) is the umbrella term including dermatomyositis (DM), polymyositis (PM), overlap myositis (OM), sporadic inclusion body myositis (IBM) and necrotising autoimmune myopathy (NAM), also known as immune‐mediated necrotising myopathy.
Catherine Ashton +4 more
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Idiopathic inflammatory myopathies: Contributions from India
Indian Journal of Rheumatology, 2020 A careful literature search would reveal significant contributions by Indian clinicians and basic researchers in the field of Idiopathic inflammatory myopathies (IIMs).
Anand Narayan Malaviya
doaj +1 more source
Idiopathic inflammatory myopathies linked to vaccination against SARS-CoV-2: a systematic review
Reumatismo, 2023 The COVID-19 pandemic represents a global health problem, which has been mitigated by the opportune introduction of vaccination programs. Although we already know the benefit that vaccines provide, these are not exempt from adverse events which can be ...
A. Camargo-Coronel +4 more
doaj +1 more source
Clinical characteristics of patients with anti-TIF1-γ antibodies
Rheumatology, 2016 Objectives : Inflammatory myopathies are a group of idiopathic, heterogeneous systemic diseases affecting predominantly skeletal muscles, though they can also involve the skin and internal organs.
Anna Masiak +3 more
doaj +1 more source
POLYMYOSITIS/DERMATOMIOSITIS: DIFFERENTIAL DIAGNOSIS
Научно-практическая ревматология, 2016 The lecture considers the problem of rare systemic connective tissue diseases, such as idiopathic inflammatory myopathies (IIMs). It underlines the clinical and immunological heterogeneity of their subtypes, which defines therapeutic tactics and ...
O. A. Antelava
doaj +1 more source
Polymyositis and dermatomyositis – challenges in diagnosis and management
Journal of Translational Autoimmunity, 2019 Polymyositis (PM) and dermatomyositis (DM) are different disease subtypes of idiopathic inflammatory myopathies (IIMs). The main clinical features of PM and DM include progressive symmetric, predominantly proximal muscle weakness.
Shu-Han Yang +2 more
doaj +1 more source
Malignancy and idiopathic inflammatory myopathies
North American Journal of Medical Sciences, 2013 Association between idiopathic inflammatory myopathies (IIMs) and malignancy is well known and has been extensively reported in the literature. However, in the recent years, several new studies were published allowing us to better understand the clinical characteristics and pathophysiology of cancer-associated IIMs.
Ungprasert, Patompong +2 more
openaire +3 more sources
Annals of Noninvasive Electrocardiology, 2022 Background Inflammatory cardiomyopathy (IC) is a syndrome with chronic myocarditis and cardiac remodeling. This study aimed to explore predicting factors of adverse outcomes in patients with IC secondary to idiopathic inflammatory myopathy (IIM‐IC ...
Yingxian Liu +9 more
doaj +1 more source
An update on the pathogenesis of idiopathic inflammatory myopathies. [PDF]
Curr Opin RheumatolPurpose of review As the question of the pathogenesis of inflammatory myopathies remains unanswered, there has been a significant effort in recent years to investigate various components of the innate and adaptive immune systems, with evidence pointing that they work together to initiate and propagate the autoimmune response ...
Tiniakou E.
europepmc +4 more sources