Results 311 to 320 of about 1,622,130 (371)

Recognition of Idiopathic Inflammatory Myopathies Underlying Interstitial Lung Diseases. [PDF]

Diagnostics (Basel)
Morina G, Sambataro D, Libra A, Palmucci S, Colaci M, La Rocca G, Ferro F, Carli L, Baldini C, Liuzzo SV, Vancheri C, Sambataro G.   +11 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Epidemiology of the idiopathic inflammatory myopathies

Nature Reviews Rheumatology, 2023
James B Lilleker, Bernard Yu-Hor Thong, Janine A Lamb   +2 more
exaly   +2 more sources

Inflammatory Myopathies

Continuum, 2006
To discuss the clinical, laboratory, and histopathologic features and presumed pathogenic mechanisms of the four major categories of idiopathic inflammatory myopathy, namely dermatomyositis, polymyositis, immune-mediated necrotizing myopathy, and inclusion body myositis.Dermatomyositis, polymyositis, necrotizing myopathy, and inclusion body myositis ...
Anthony A, Amato, Steven A, Greenberg
openaire   +4 more sources

INFLAMMATORY MYOPATHIES

Acta Clinica Belgica, 2004
Primary myositis (or inflammatory myopathies) comprises three main groups of diseases, based on clinical and immunohistochemical characteristics: polymyositis (PM), dermatomyositis (DM) and inclusion body myositis. Their clinical presentation and course are disparate, but a common characteristic is immune dysfunction-related inflammation of the ...
Patrick M., Grogan, Jonathan S., Katz
openaire   +5 more sources

Contribution of Necroptosis to Myofiber Death in Idiopathic Inflammatory Myopathies

Arthritis & Rheumatology, 2022
Myofiber necrosis is a significant pathologic characteristic of idiopathic inflammatory myopathies (IIMs), and its molecular mechanism is largely unknown.
Q. Peng, Yamei Zhang, Yan-Chun Liu, Lin Liang, Wen-li Li, X. Tian, Lu Zhang, Hongxia Yang, Xin Lu, Guo-chun Wang   +9 more
semanticscholar   +1 more source

Long‐Term Outcomes and Prognosis Factors in Patients With Idiopathic Inflammatory Myopathies Based on Myositis‐Specific Autoantibodies: A Single Cohort Study

Arthritis care & research, 2022
This study was undertaken to investigate the long‐term survival rates and prognostic factors in patients with idiopathic inflammatory myopathies (IIMs) based on myositis‐specific antibody (MSA) stratification.
Wei Jiang, Jingli Shi, Hongxia Yang, X. Tian, Hanbo Yang, Qingning Chen, Lining Zhang, Q. Peng, Guochun Wang, Xin Lu   +9 more
semanticscholar   +1 more source

Defining cardiac involvement in idiopathic inflammatory myopathies: a systematic review.

Rheumatology, 2021
OBJECTIVE Recent advances in cardiac magnetic resonance imaging (CMR) and other diagnostic techniques have made it easier to identify subclinical cardiac inflammation and dysfunction in the idiopathic inflammatory myopathies (IIM).
J. Fairley, I. Wicks, S. Peters, J. Day
semanticscholar   +1 more source

Classification and management of adult inflammatory myopathies

Lancet Neurology, The, 2018
Albert Selva-O'Callaghan, Iago Pinal-Fernandez, Ernesto Trallero-Araguás   +2 more
exaly   +2 more sources

Idiopathic Inflammatory Myopathies

Indian Journal of Pediatrics, 2023
Idiopathic inflammatory myopathies (IIMs) are a diverse group of diseases characterized by proximal muscle weakness and inflammation in skeletal muscle. Phenotypically, the subtypes include dermatomyositis, polymyositis, inclusion body myositis, and amyopathic dermatomyositis. The most common IIM in children is juvenile dermatomyositis (JDM).
Suma Balan, Sumanth Madan
openaire   +2 more sources