Results 11 to 20 of about 27,152 (204)

Characteristics and risk of interstitial lung disease in dermatomyositis and polymyositis: a retrospective cohort study in Japan

open access: yesScientific Reports, 2023
Dermatomyositis and polymyositis are rare, idiopathic inflammatory myopathies. Interstitial lung disease is one of the most common and potentially severe extra-muscular manifestations of dermatomyositis and polymyositis and is strongly linked to poor ...
Qingqing Hu   +5 more
doaj   +1 more source

Association between a C8orf13-BLK polymorphism and polymyositis/dermatomyositis in the Japanese population: an additive effect with STAT4 on disease susceptibility. [PDF]

open access: yesPLoS ONE, 2014
BACKGROUND:Accumulating evidence has shown that several non-HLA genes are involved in the susceptibility to polymyositis/dermatomyositis. This study aimed to investigate the involvement of C8orf13-BLK, one of the strongest candidate genes for autoimmune ...
Tomoko Sugiura   +7 more
doaj   +1 more source

Case of Polymyositis Associated with Celiac Disease: A Case Report

open access: yesPakistan 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

Anti-RuvBL1/2 Antibodies in Scleromyositis: A Clinicopathological Report of Two Cases. [PDF]

open access: yesACR Open Rheumatol
We report two patients with scleromyositis with anti‐RuvBL1/2 antibodies, recently identified rare autoantibodies associated with older age at onset, diffuse sclerodactyly, skeletal and cardiac myositis, and interstitial lung disease (ILD). Both patients showed sclerodactyly and skeletal myositis.
Imai Y   +6 more
europepmc   +2 more sources

The relationship between platelet distribution width and disease activity in patients with polymyositis

open access: yesRheumatology, 2022
Introduction Muscle enzymes are an indicator of ongoing muscle damage and disease activity in patients with idiopathic inflammatory myopathy. Although platelet-related parameters have been shown to be useful as markers of disease activity in autoimmune ...
Gokhan Sargin   +3 more
doaj   +1 more source

IL‐15 is a biomarker involved in the development of rapidly progressive interstitial lung disease complicated with polymyositis/dermatomyositis

open access: yesJournal of Internal Medicine, 2020
Polymyositis/dermatomyositis (PM/DM) is an autoimmune disease that is sometimes complicated with rapidly progressive interstitial lung disease (RPILD). However, serum and lung biomarkers that can predict RPILD development remain unclear.
T. Shimizu   +23 more
semanticscholar   +1 more source

Risk Factors of Progression to Active Tuberculosis in Rheumatic Patients With Latent Tuberculosis: A Retrospective Study. [PDF]

open access: yesImmun Inflamm Dis
ABSTRACT Background In rheumatism patients, the immune system erroneously attacks the body′s own tissues. This impairs the body′s defense against external pathogens and is a contributing factor to the occurrence of tuberculosis infection. The primary objective of this investigation was to examine the risk factors for the progression from latent ...
Wang F, Zhou L, Hao X, Liu J.
europepmc   +2 more sources

An electrophysiological investigation of skeletal muscles in polymyositis

open access: yesArquivos de Neuro-Psiquiatria, 1976
An electrophysiological study has been made of the extensor digitorum brevis, thenar and hypothenar muscles in 25 patients with chronic and acute polymyositis.
R. E. P. Sica   +3 more
doaj   +1 more source

Diffuse alveolar hemorrhage, a rare presentation of polymyositis

open access: yesRespiratory Medicine Case Reports, 2020
Background: Diffuse alveolar hemorrhage is a medical emergency caused by persistent and recurrent pulmonary hemorrhage [1]. It is an uncommon presentation of polymyositis.
Sharoon Samuel   +3 more
doaj   +1 more source

Acute respiratory distress syndrome relapsing in 10 months with an initial manifestation of polymyositis

open access: yesClinical Case Reports, 2021
Autoimmune disorders are an important cause of acute respiratory distress syndrome (ARDS). We report a case of a patient with steroid‐responsive ARDS that relapsed in 10 months with an initial manifestation of seronegative polymyositis.
Yukihisa Takeda   +7 more
doaj   +1 more source

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