Betekintés az idiopathiás inflammatorikus myopathiában szenvedő betegek gyógytornájába | Insight into the training of patients with idiopathic inflammatory myopathy [PDF]
, 2016 Absztrakt Idiopathiás inflammatorikus myopathiában szenvedő betegeknél a jelenleg alkalmazott gyógyszeres kezelés mellett izomkárosodás és egészségromlás alakul ki.
Váncsa, Andrea
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Clinicopathological Reclassification of Idiopathic Inflammatory Myopathy to Match the Serological Results of Myositis-Specific Antibodies. [PDF]
J Clin NeurolPark YE, Kim DS, Kang M, Shin JH.
europepmc +2 more sources
Incidence and Prevalence of Idiopathic Inflammatory Myopathies in Korea: a Nationwide Population-based Study [PDF]
, 2019 Background: This study aimed to estimate the incidence and prevalence of idiopathic inflammatory myopathies (IIM) and associated comorbidities in Korea from 2006 to 2015.
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Review paper Polymyositis and dermatomyositis as a risk of developing cancer
Rheumatology, 2015 Polymyositis (PM) is an idiopathic inflammatory myopathy that affects striated muscles. Dermatomyositis (DM) is an idiopathic inflammatory myopathy with presence of skin symptoms.
Michał Jakubaszek +2 more
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Idiopathic inflammatory myopathy: From muscle biopsy to serology
Indian Journal of Rheumatology, 2020 Idiopathic inflammatory myopathies (IIMs) are heterogeneous group of muscle disorders characterized by variable degree of muscle weakness and muscle inflammation. Various classification systems have been proposed for myositis.
Ritu Verma, Vimal Kumar Paliwal
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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
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Elevated serum levels of macrophage migration inhibitory factor and stem cell growth factor β in patients with idiopathic and systemic sclerosis associated pulmonary arterial hypertension. [PDF]
, 2015 Pulmonary arterial hypertension (PAH) can be idiopathic or secondary to autoimmune diseases, and it represents one of the most threatening complications of systemic sclerosis (SSc).
Alessandri, Cristiano +9 more
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Alu Overexpression Leads to an Increased Double‐stranded RNA Signature in Dermatomyositis
Arthritis &Rheumatology, Accepted Article.Objective Dermatomyositis is an autoimmune condition characterized by a high interferon signature of unknown etiology. Because coding sequences constitute <1.2% of our genomes, there is a need to explore the role of the non‐coding genome in disease pathogenesis.
Rayan Najjar +2 more
wiley +1 more source
Coexistence of Axial Spondyloarthritis and Idiopathic Inflammatory Myopathy
Case Reports in Rheumatology, 2020 Both axial spondyloarthritis (axSpA) and idiopathic inflammatory myopathy (IIM) are infrequent, and their coexistence is even rarer; there are a few reported cases in the literature.
Yongpeng Ge, Linrong He
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Polymyositis And Dermatomyositis - Inflammation, Muscle Structure & Immunosuppressive Treatment [PDF]
, 2012 Polymyositis and dermatomyositis are chronic, inflammatory disorders characterized by muscle weakness, low muscle endurance and by inflammation in skeletal muscle tissues.
Loell, Ingela
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