Results 41 to 50 of about 16,326 (177)

Diagnosis of Polymyositis

, 1990
The criteria for the diagnosis of polymyositis, the differential diagnosis, and treatment are reported from the Division of Rheumatology and Internal Medicine, Mayo Clinic, Rochester ...
J Gordon Millichap
core   +1 more source

Polymyositis Initiation Involving Amlodipine Besylate [PDF]

, 2006
© 2006 R. M. Golding, L. G.F. Giles and E. M. Sokoya. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Golding, Raymund M, Giles, Lynton G F, Sokoya, Elke Marion   +2 more
core   +1 more source

Improved Detection of Myositis‐Specific Autoantibodies Using Luciferase Immunoprecipitation Systems Assay: Comparison With Line Blot and Conventional Immunoprecipitation

Arthritis &Rheumatology, EarlyView.
Objective Myositis‐specific autoantibodies guide the diagnosis and classification of idiopathic inflammatory myopathies, but current immunoassays vary in accuracy, particularly for autoantibodies associated with interstitial lung disease. To compare the performance of the luciferase immunoprecipitation systems (LIPS) assay with line blot and ...
Peter D. Burbelo, Iago Pinal‐Fernandez, Maria Casal‐Dominguez, Xin Tian, Shijinqiu Gao, Neha Gupta, Eric W. Robbins, John A. Chiorini, Christopher A. Mecoli, Lisa Christopher‐Stine, Livia Casciola‐Rosen, Andrew L. Mammen, Sonye K. Danoff, Anthony F. Suffredini, Julio A. Huapaya   +14 more
wiley   +1 more source

Polymyositis as a manifestation of chronic graft‐versus‐host disease after allo‐HSCT

Clinical Case Reports, 2018
Key Clinical Message Patients who received allogeneic haematopoietic stem cell transplantation (allo‐HSCT) may develop T cell‐mediated immunologic injury to muscles, recapitulating the characteristics of polymyositis clinically and pahtologically ...
Lijuan Meng, Suqiong Ji, Qiong Wang, Bitao Bu   +3 more
doaj   +1 more source

Interleukin‐2 Deprived State of Regulatory T cells and Their Recovery by Low‐Dose Interleukin‐2 in Patients With Inflammatory Myopathies

Arthritis &Rheumatology, EarlyView.
Objective Regeneration and expansion of Treg by low‐dose interleukin‐2 (IL‐2) therapy is considered a potential treatment strategy for a wide range of autoimmune diseases. To provide a pathophysiologically‐based rationale for low‐dose IL‐2 therapy, we investigated whether reversible defects in the Treg–IL‐2 axis emerge in inflammatory myopathies ...
Justus Ohmes, Luisa R. Monne, Sara Comdühr, Fynn Gerlach, Hanna Grasshoff, Alexander Dübbers, Antje Müller, Alexander Scheffold, Gabriela Riemekasten, Reza Akbarzadeh, Jens Y. Humrich   +10 more
wiley   +1 more source

Early prediction of acute kidney injury in traumatic and non‐traumatic rhabdomyolysis using an interpretable machine learning model: A multicenter study with external validation

Journal of Intelligent Medicine, EarlyView.
Abstract Acute kidney injury (AKI) is a common and severe complication of rhabdomyolysis (RM), and early risk stratification remains challenging because of its multifactorial and heterogeneous nature. We developed and externally validated an interpretable machine learning (ML) model for early prediction of AKI in RM across traumatic and non‐traumatic ...
Chunli Liu, Jie Shi, Fengjuan Wang, Liang Ma, Huangang Hu, Li Zhang, Jie Song, Heng Jin, Dingwei Yang, Xiaoqin Guo, Haojun Fan, Qi Lv   +11 more
wiley   +1 more source

Monocyte/macrophage differentiation in dermatomyositis and polymyositis

, 2004
Recent advances have revealed significant differences in the pathogenesis of inflammatory myopathies. To determine whether different patterns of macrophage differentiation are a useful tool to delineate the major groups of inflammatory myopathies, the ...
Rostasy, Kevin, Schulz-Schaeffer, Walter J., Goebel, Hans H., Menck, S., Piepkorn, M., Hanefeld, Folker   +5 more
core   +1 more source

Dermatomyositis, polymyositis and immune-mediated necrotising myopathies [PDF]

, 2015
Dermatomyositis, polymyositis and immune-mediated necrotising myopathy are major forms of idiopathic inflammatory myopathy. We review here recent developments in understanding the pathology and pathogenesis of these diseases, and characterisation of ...
Mastaglia, F.L., Luo, Yue-Bei, Frank L. Mastaglia, Yue-Bei Luo, Luo, Y-B, Mastaglia, Frank L.   +5 more
core   +1 more source

Type I interferon overactivation in sera of patients with anti‐MDA5‐positive dermatomyositis‐associated interstitial lung disease

Rheumatology &Autoimmunity, EarlyView.
Sera from patients with anti‐MDA5‐positive dermatomyositis‐associated interstitial lung disease (ILD) exhibit significantly higher type I interferon (IFN‐I) bioactivity and interferon‐stimulated gene‐inducing activity compared to anti‐ARS‐positive ILD and healthy controls.
Shohei Nakamura, Yasuhiro Katsumata, Yuko Okamoto, Masayoshi Harigai   +3 more
wiley   +1 more source

Magnetic Resonance Imaging Characteristics of Hereditary Polymyositis in the Dutch Kooiker Dog

Pets
Background: Hereditary immune-mediated polymyositis has been reported in the Kooiker dog breed, associated with a 39 kb deletion and low penetrance.
Yvet Opmeer, Stefanie Veraa, Simon Platt, Paul Mandigers   +3 more
doaj   +1 more source