Results 31 to 40 of about 9,523 (188)
COVID-19 Vaccination in Autoimmune Diseases (COVAD) study: Vaccine safety in idiopathic inflammatory myopathies [PDF]
, 2022 We studied COVID-19 vaccination-related adverse events (ADEs) 7-days post-vaccination in patients with idiopathic inflammatory myopathies (IIMs) and other systemic autoimmune and inflammatory disorders (SAIDs)
Selva-O'Callaghan A. +32 more
core +1 more source
Case of Polymyositis Associated with Celiac Disease: A Case Report
Pakistan Armed Forces Medical Journal, 2023 Polymyositis is an important subtype of idiopathic inflammatory myopathies characterized by muscle inflammation andweakness, often associated with other systemic diseases and malignancies.
Abdul Rehman Azeem +4 more
doaj +1 more source
Evolving classification and role of muscle biopsy in diagnosis of inflammatory myopathies
Indian Journal of Pathology and Microbiology, 2022 Idiopathic inflammatory myopathy (IIM) is a broad term that includes dermatomyositis, polymyositis, overlap myositis, sporadic inclusion body myositis, and immune-mediated necrotizing myopathy.
Meenakshi Swain, Megha Uppin
doaj +1 more source
Polymyositis and dermatomyositis: Disease spectrum and classification
Indian Journal of Dermatology, 2012 Muscle inflammation and weakness are the key features of idiopathic inflammatory myopathies (IIMs). In addition IIMs are frequently associated with cutaneous and pulmonary involvement. In clinical practice the three common inflammatory myopathies we come
Siba P Raychaudhuri, Anupam Mitra
doaj +1 more source
Management of the idiopathic inflammatory myopathies [PDF]
, 2019 The idiopathic inflammatory myopathies (IIMs) – comprising polymyositis, dermatomyositis and inclusion body myositis – are a rare group of disorders characterised by muscle inflammation.
Ashraful Haque +7 more
core +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
Predictors of cardiac involvement in idiopathic inflammatory myopathies
Frontiers in Immunology, 2023 ObjectivesIdiopathic inflammatory myopathies (IIM) are a group of rare disorders that can affect the heart. This work aimed to find predictors of cardiac involvement in IIM.MethodsMulticenter, open cohort study, including patients registered in the IIM ...
Matilde Bandeira +43 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
Cardiac Manifestations in Idiopathic Inflammatory Myopathies: An Overview [PDF]
, 2019 Idiopathic inflammatory myopathies are a group of autoimmune diseases that are characterized by muscle inflammation resulting in elevated muscle enzyme release and distinctive biopsy findings.
Divya Jayakumar +7 more
core +1 more source