Zobrazeno 1 - 10
of 1 558
pro vyhledávání: '"Idiopathic inflammatory myopathy"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Idiopathic inflammatory myopathy (IIM) with autoantibodies recognizing the signal recognition particle (SRP) is characterized by prominent proximal weakness, infrequent extramuscular involvement, dramatically elevated creatine kinase levels,
Externí odkaz:
https://doaj.org/article/30b17c21ca864659a75d959a3aef38d3
Autor:
Mariko Ogawa-Momohara, Yoshinao Muro
Publikováno v:
Immunological Medicine, Pp 1-13 (2024)
In recent years, various myositis-specific and myositis-associated autoantibodies have been identified in idiopathic inflammatory myopathies, including dermatomyositis (DM), anti-synthetase syndrome (ASS), immune-mediated necrotizing myopathy (IMNM),
Externí odkaz:
https://doaj.org/article/26650075af5948d2856f9a568dfda342
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-11 (2024)
Abstract Background Anti-Ro-52 antibodies have been associated with interstitial lung disease (ILD) in various autoimmune diseases. However, their role in ILD among patients with idiopathic inflammatory myopathies (IIMs) is relatively underexplored.
Externí odkaz:
https://doaj.org/article/2b80548ec4814d7988bce52699dade94
Publikováno v:
Rheumatology, Vol 62, Iss 3, Pp 196-206 (2024)
Magnetic resonance imaging (MRI) of the musculoskeletal system is an examination increasingly performed for suspected juvenile idiopathic arthritis, chronic nonbacterial osteomyelitis and juvenile idiopathic inflammatory myopathies, as well as other
Externí odkaz:
https://doaj.org/article/2e5883372c064467851d88812f8f0af6
Autor:
Chao Huang, Xuelian Dai, Jiacheng Liu, Yunting Zhang, Bianli Yin, Chao Liu, Xiangyang Ren, Zhihui Duan, Huan Yang
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Myasthenia gravis (MG) and idiopathic inflammatory myopathy (IIM) are autoimmune diseases of the nervous system, and their main clinical manifestation is muscle weakness. The concurrent presence of both conditions in the same patient is clinically ra
Externí odkaz:
https://doaj.org/article/b0604a95bb0e43e893d4958529abcc34
Autor:
LI Xingjun, LI Shuangrong, WANG Nan, WANG Xiangyu, CUI Ruomei, XU Jian, GUO Yulong, LIU Shuang
Publikováno v:
Zhongguo quanke yixue, Vol 27, Iss 13, Pp 1623-1629 (2024)
Background Idiopathic inflammatory myopathy (IIM) is a group of connective tissue diseases characterized by muscle inflammation and muscle weakness, lung involvement is an important factor affecting the prognosis of patients. IIM can be classified in
Externí odkaz:
https://doaj.org/article/6f6a0669abbd4e81a58602047a60608c
Publikováno v:
Tomography, Vol 10, Iss 3, Pp 368-377 (2024)
(1) Background: The intravoxel incoherent motion (IVIM) model can provide information about both molecular diffusion and blood flow for the evaluation of skeletal muscle inflammation. MRI-based fat quantification is advantageous for assessing fat inf
Externí odkaz:
https://doaj.org/article/5f1e16364ece4c5ca8a243f97bb015e5
Publikováno v:
ImmunoTargets and Therapy, Vol Volume 13, Pp 151-172 (2024)
Lydia Cassard,1 Noelle Seraly,2 Maureen Riegert,3 Aditi Patel,4 Anthony P Fernandez5 1Cleveland Clinic Lerner College of Medicine at Case Western Reserve University, Cleveland, OH, USA; 2Department of Dermatology, Cleveland Clinic, Cleveland, OH, USA
Externí odkaz:
https://doaj.org/article/d301ae4f51f14fae90de8d5a74057e0e
Publikováno v:
Annals of Medicine, Vol 56, Iss 1 (2024)
Objective Rapidly progressive interstitial lung disease (RP-ILD) is a frequent and serious manifestation of idiopathic inflammatory myopathy (IIM) associated with poor outcomes. Plasma exchange (PE) can quickly remove pathogenic substances from the b
Externí odkaz:
https://doaj.org/article/e56c320dfefa43feb20a169e9dcc9e30
Autor:
Masaru Takeshita, Katsuya Suzuki, Maho Nakazawa, Hirofumi Kamata, Makoto Ishii, Yoshitaka Oyamada, Hisaji Oshima, Satoshi Usuda, Kazuyuki Tsunoda, Tsutomu Takeuchi
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Interstitial lung disease is a common complication of anti-synthetase syndrome (ASS), and lymphocytic infiltration is often observed in the lesion. We have recently reported that disease-specific autoantibodies are produced by infiltrating lymphocyte
Externí odkaz:
https://doaj.org/article/d7f67e22fa9f430da443f477468e3e06