Results 11 to 20 of about 20,247 (257)

Idiopathic inflammatory myopathies [PDF]

open access: greenNature Reviews Disease Primers, 2021
Idiopathic inflammatory myopathies (IIM), also known as myositis, are a heterogeneous group of autoimmune disorders with varying clinical manifestations, treatment responses and prognoses. Muscle weakness is usually the classical clinical manifestation but other organs can be affected, including the skin, joints, lungs, heart and gastrointestinal tract,
Lundberg, Ingrid E.   +7 more
  +9 more sources

Idiopathic inflammatory myopathies

open access: goldBest Practice & Research Clinical Rheumatology, 2012
Inflammatory myopathies are chronic, immune-mediated diseases characterised by progressive proximal muscle weakness. They encompass a variety of syndromes with protean manifestations. The diagnosis is based on Bohan and Peter's classification criteria, which nowadays seem to be obsolete.
Dominique Figarella‐Branger   +4 more
  +7 more sources

Idiopathic Inflammatory Myopathies [PDF]

open access: yesSeminars in Neurology, 2009
The idiopathic inflammatory myopathies are a group of rare disorders including polymyositis (PM), dermatomyositis (DM), and autoimmune necrotizing myopathies (NMs). The idiopathic inflammatory myopathies share many similarities. They present acutely, subacutely, or chronically with marked proximal and symmetric muscle weakness, except for associated ...
Mazen M, Dimachkie, Richard J, Barohn
openaire   +6 more sources

Idiopathic inflammatory myopathies [PDF]

open access: yesNeurologic Clinics, 2014
Idiopathic inflammatory myopathies (IIMs), except for sporadic inclusion body myositis (sIBM), present with subacute symmetrical weakness of the limb girdle muscles, an elevated serum creatine kinase activity, and inflammatory cells in the muscle biopsy (necrotizing autoimmune myopathy being an exception).
van der Kooi, A. J., de Visser, M.
openaire   +5 more sources

Idiopathic inflammatory myopathies [PDF]

open access: yesVnitřní lékařství, 2018
Idiopathic inflammatory myopathies form a heterogeneous group of acquired inflammatory diseases afflicting striated muscles. The disease is frequently accompanied by systemic and organ involvement. Dermatomyositis, polymyositis, cancer associated myositis, immune mediated necrotizing myopathy, myositis in overlap syndromes, juvenile myositis and ...
Parker, Matthew   +3 more
openaire   +4 more sources

Murine models of idiopathic inflammatory myopathy

open access: yesImmunological Medicine, 2023
Idiopathic inflammatory myopathies (IIMs) are characterized by inflammation of muscles and other organs. Several myositis-specific autoantibodies (MSAs) have been identified in IIMs and were found to be associated with distinct clinical features ...
Risa Konishi   +2 more
doaj   +1 more source

Myositis after SARS-CoV-2 vaccination occurs more frequently than assumed and is probably causally related

open access: yesReumatismo, 2023
We read with interest the article by Camargo-Coronel et al. reporting on a systematic review of patients with idiopathic, inflammatory myopathy developing after anti-SARS-CoV-2 vaccinations.
J. Finsterer   +2 more
doaj   +1 more source

Patient-reported outcome for physical function in idiopathic inflammatory myopathy. [PDF]

open access: greenRheumatology (Oxford)
Keret S   +6 more
europepmc   +3 more sources

Emerging therapeutics in idiopathic inflammatory myopathy

open access: yesIndian Journal of Rheumatology, 2020
Idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of systemic autoimmune diseases characterized mainly by inflammation of muscle tissue.
Shinji Sato
doaj   +1 more source

Home - About - Disclaimer - Privacy