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Myositis is inflammation especially of the voluntary muscles, characterized by localized or diffuse pain, tenderness on movement or palpation, swelling, and/or weakness. The two main categories of myositis include non‐infectious and infectious. Infective
G. Narayanappa, B. Nandeesh
semanticscholar +3 more sources
ZusammenfassungUnter der Federführung der Deutschen Gesellschaft für Neurologie und Beteiligung vieler weiterer Fachgesellschaften wurde die S2k-Leitlinie zu Myositissyndromen vollständig aktualisiert und überarbeitet. Bei der Klassifikation der Myositiden werden nun die immunmediierte nekrotisierende Myopathie und das Antisynthetasesyndrom als ...
Peter Korsten, Eugen Feist
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Resistin Expression Is Associated With Interstitial Lung Disease in Dermatomyositis
ObjectiveIn the current study, we aimed to assess resistin mRNA levels in the peripheral blood mononuclear cells (PBMCs) of dermatomyositis patients with interstitial lung disease (DM-ILD) and their correlation with disease activity.MethodsWe detected ...
Lifang Ye+15 more
doaj +1 more source
Objectives The purpose was to clarify the characteristics of interstitial lung disease (ILD) in immune-mediated necrotizing myopathy (IMNM) patients with anti-signal recognition particle (SRP) antibodies.
Yongpeng Ge+5 more
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Rheumatoid Myositis: A Rare Case Report [PDF]
Rheumatoid Arthritis (RA) and inflammatory myositis are distinct clinical syndromes. Muscle involvement in RA is frequently secondary to therapy with steroids or immune-modulators medication.
Satish Kumar+2 more
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Pneumatosis cystoides intestinalis in dermatomyositis: a case series report and literature review
Pneumatosis cystoides intestinalis (PCI) in adult dermatomyositis (DM) is rarely described. This report aimed to describe the clinical features and prognosis of PCI in six adult patients with DM (four with anti-MDA5 antibodies, one with anti-SAE ...
Jianwen Liu+4 more
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[West J Emerg Med. 2011;12(4):371.]
Chuah, Tyng Yu+3 more
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The role of interferons type I, II and III in myositis: A review
The classification of idiopathic inflammatory myopathies (IIM) is based on clinical, serological and histological criteria. The identification of myositis‐specific antibodies has helped to define more homogeneous groups of myositis into four dominant ...
L. Bolko+6 more
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Background Perifascicular atrophy is a unique pathological hallmark in dermatomyositis (DM)-affected muscles; however, the mechanism underlying this process remains unclear.
Lu Zhang+8 more
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Myositis-associated interstitial lung disease: a comprehensive approach to diagnosis and management.
Interstitial lung disease (ILD) frequently complicates the inflammatory myopathies and at times is the most prominent clinical feature. Over the years, there has been a growing recognition for the strong association between seropositivity of several ...
R. Hallowell, Julie J. Paik
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