Results 11 to 20 of about 751 (90)

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

open access: yesPLoS ONE, 2014
BackgroundAccumulating 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

Identification of Palmitoleic Acid Controlled by mTOR Signaling as a Biomarker of Polymyositis

open access: yesJournal of Immunology Research, 2017
Polymyositis (PM) is a chronic disease characterized by muscle pain, weakness, and increase in muscle-related enzymes, accompanied with inflammations in lymphocytes.
Geng Yin   +5 more
doaj   +1 more source

Roles of macrophage migration inhibitory factor in polymyositis: Inflammation and regeneration

open access: yesJournal of International Medical Research, 2018
Objective To elucidate the clinical significance of macrophage migration inhibitory factor (MIF) serum concentration in patients with polymyositis. Methods Thirty-six patients with polymyositis were enrolled.
Yu-Qiong Zou, Wei-Dong Jin, Ya-Song Li
doaj   +1 more source

The clinical application of tumor markers in the screening of malignancies and interstitial lung disease of dermatomyositis/polymyositis patients: A retrospective study

open access: yesSAGE Open Medicine, 2018
Objective: To examine the clinical utility of tumor markers in dermatomyositis/polymyositis patients in Taiwan. Method: Data were collected retrospectively from the database of Taichung Veterans General Hospital in Taiwan from 1998 to 2014.
Chong Hong Lim   +6 more
doaj   +1 more source

Bilateral leg pain and unilateral calf atrophy caused by polymyositis accompanying lumbar spinal stenosis and disc herniation: a case report

open access: yesJournal of International Medical Research, 2022
Polymyositis is a subgroup of idiopathic inflammatory myopathies characterized by symmetric proximal limb weakness and chronic skeletal muscle inflammation.
In-Hwa Baek   +3 more
doaj   +1 more source

Polymyositis following varicella and mumps infection in adults: report of two cases

open access: yesReumatismo, 2023
Idiopathic immune myopathies (IIMs) are autoimmune diseases caused by immune-mediated muscle damage. The etiology remains unclear. Epidemiological and experimental studies, both in animals and humans, hint at viruses as major environmental factors able ...
F. Masini   +5 more
doaj   +1 more source

Severe myopathy in a patient with chronic neurological disease – diagnostic challenges [PDF]

open access: yesRomanian Journal of Rheumatology, 2023
Polymyositis is a rare disease that belongs to the idiopathic inflammatory myopathies (IIMs) group, characterized by chronic muscle inflammation, and in rare cases a life-threatening condition due to extra-muscular involvement.
Cristian-Mihai Ilie   +7 more
doaj   +1 more source

High-Dose Subcutaneous Immunoglobulins for the Treatment of Severe Treatment-Resistant Polymyositis

open access: yesCase Reports in Rheumatology, 2014
Polymyositis is a rare debilitating condition characterized by chronic inflammation and muscle weakness. Standard treatments include corticosteroids and immunosuppressants; however, resistance to these regimens may develop.
Cherin Patrick   +3 more
doaj   +1 more source

Chronic-graft-versus-host-disease-related polymyositis: a 17-months-old child with a rare and late complication of haematopoietic stem cell transplantation.

open access: yesMediterranean Journal of Hematology and Infectious Diseases, 2020
Background: Chronic graft versus host disease (cGVHD) occurs in 20-30% of paediatric patients receiving haemopoietic stem cell transplantation (HSCT). Neuromuscular disorders such as polymyositis are considered a rare and distinctive but non-diagnostic ...
Matteo Chinello   +9 more
doaj   +1 more source

Severe Rhabdomyolysis without Systemic Involvement: A Rare Case of Idiopathic Eosinophilic Polymyositis

open access: yesCase Reports in Rheumatology, 2015
Introduction. Eosinophilic polymyositis (EPM) is a rare cause of rhabdomyolysis characterized by eosinophilic infiltrates in the muscle. We describe the case of a young patient with eosinophilic polymyositis causing isolated severe rhabdomyolysis without
Ayesha Farooq   +6 more
doaj   +1 more source

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