Results 11 to 20 of about 1,609,796 (235)
G-Protein-Coupled Estrogen Receptor (GPER) in Inflammatory Myopathies [PDF]
Neurology InternationalBackground/Objectives: Given the multifaceted role of estrogen hormones in skeletal muscle pathophysiology and their well-established immunomodulatory properties, this study aimed to characterize the expression of the G-protein-coupled estrogen receptor (
Delia Righi +9 more
doaj +2 more sources
Biomarkers in Inflammatory Myopathies—An Expanded Definition
Frontiers in Neurology, 2019 Biomarkers as parameters of pathophysiological conditions can be of outmost relevance for inflammatory myopathies. They are particularly warranted to inform about diagnostic, prognostic, and therapeutic questions.
Olivier Benveniste +3 more
doaj +2 more sources
Cardiovascular manifestations in idiopathic inflammatory myopathies
Clinical Rheumatology, 2023 Cardiovascular involvement in idiopathic inflammatory myopathies (IIM) is an understudied area which is gaining increasing recognition in recent times.
Meera Shah, S. Shinjo, J. Day, L. Gupta
semanticscholar +1 more source
Targeting necroptosis in muscle fibers ameliorates inflammatory myopathies
Nature Communications, 2022 Muscle cell death in polymyositis is induced by CD8 + cytotoxic T lymphocytes. We hypothesized that the injured muscle fibers release pro-inflammatory molecules, which would further accelerate CD8 + cytotoxic T lymphocytes-induced muscle injury, and ...
M. Kamiya +9 more
semanticscholar +1 more source
Optimizing Cardiac Assessment in Idiopathic Inflammatory Myopathies [PDF]
Annals of Indian Academy of NeurologySruthi S Nair
doaj +2 more sources
Biological Therapies in Inflammatory Myopathies
Rambam Maimonides Medical Journal, 2023 Idiopathic inflammatory myopathies (IIM) are a rare group of disorders that feature progressive immune-mediated skeletal muscle destruction along with skin, lung, and joint involvement.
Abd El Haleem Natour, Shaye Kivity
doaj +1 more source
Idiopathic Inflammatory Myopathies [PDF]
Seminars 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
MRI and muscle imaging for idiopathic inflammatory myopathies
Brain Pathology, 2021 Although idiopathic inflammatory myopathies (IIM) are a heterogeneous group of diseases nearly all patients display muscle inflammation. Originally, muscle biopsy was considered as the gold standard for IIM diagnosis.
Samuel Malartre +6 more
semanticscholar +1 more source
Idiopathic Inflammatory Myopathies [PDF]
Neurologic Clinics, 2014 The idiopathic inflammatory myopathies (IIM) consist of rare heterogeneous autoimmune disorders that present with marked proximal and symmetric muscle weakness, except for distal and asymmetric weakness in inclusion body myositis. Despite many similarities, the IIM are fairly heterogeneous from the histopathologic and pathogenetic standpoints, and also
Mazen M, Dimachkie +2 more
openaire +5 more sources