Results 11 to 20 of about 3,762 (157)

Pediatric immune-mediated necrotizing myopathy [PDF]

open access: yesFrontiers in Neurology, 2023
Immune-mediated necrotizing myopathy (IMNM) is a type of inflammatory myopathy. Most patients with IMNM produce anti-3-hydroxy-3-methylglutaryl coenzyme A reductase or anti-signal-recognition particle autoantibodies.
Chen-Hua Wang   +4 more
doaj   +6 more sources

Treatment of refractory immune-mediated necrotizing myopathy with efgartigimod [PDF]

open access: yesFrontiers in Immunology
ObjectiveWe aimed to explore the efficacy and safety of efgartigimod in patients with refractory immune-mediated necrotizing myopathy (IMNM).MethodsThis open-label pilot observational study included seven patients with refractory IMNM, all of whom ...
MengTing Yang   +11 more
doaj   +6 more sources

Immune-Mediated Necrotizing Myopathy (IMNM): A Story of Antibodies [PDF]

open access: yesAntibodies
Immune-mediated necrotizing myopathy (IMNM) is a rare and severe disease that corresponds to a specific entity of idiopathic inflammatory myopathy. Patients with IMNM suffer from proximal muscle weakness, and present high levels of creatine kinase and ...
Sarah Julien   +5 more
doaj   +6 more sources

Characteristics of cardiac involvement in immune-mediated necrotizing myopathy

open access: yesFrontiers in Immunology, 2023
ObjectiveTo investigate the characteristics of cardiac involvement due to Immune-mediated Necrotizing Myopathy (IMNM).MethodsPatients diagnosed with Immune-mediated Necrotizing Myopathy (IMNM) who attended the Department of Neurology and the Department ...
Mengyang Liu   +5 more
doaj   +5 more sources

Treatment of Immune-Mediated Necrotizing Myopathy. [PDF]

open access: yesCurr Treatm Opt Rheumatol, 2023
Immune-mediated necrotizing myositis (IMNM) is a rare autoimmune disorder characterized by proximal muscle weakness, elevated creatine kinase levels, and necrosis of muscle fibers. While the exact pathogenesis of IMNM remains unknown, anti-HMGCR and anti-SRP autoantibodies are associated with different predisposing factors, clinical manifestations, and
Ogbonnaya-Whittlesey SA   +4 more
europepmc   +4 more sources

Etiopathogenesis of Immune-Mediated Necrotizing Myopathy: A Comprehensive Review of Recent Advances. [PDF]

open access: yesCNS Neurosci Ther
This review systematically clarifies that the core of IMNM begins with specific autoantibodies, which in turn trigger complement activation, immune cell infiltration, and a storm of inflammatory factors. Together, these processes induce regulatory cell death and mitochondrial dysfunction, ultimately leading to muscle fiber necrosis. Genetic factors and
Gao C, Li W, Liu Q, Wang G, Peng Q.
europepmc   +2 more sources

Prominent Asymmetric Muscle Weakness and Atrophy in Seronegative Immune-Mediated Necrotizing Myopathy

open access: yesDiagnostics, 2021
Immune-mediated necrotizing myopathy, a new subgroup of inflammatory myopathies, usually begins with subacute onset of symmetrical proximal muscle weakness.
Sunha Park   +3 more
doaj   +3 more sources

Statins and Immune-Mediated Necrotizing Myopathy

open access: yesClinical Management Issues, 2018
Statins are a well-recognized cause of a variety of skeletal myopathic effects, which generally resolve when discontinuing the treatment. Among autoimmune manifestations associated with statins, there is immune-mediated necrotizing myopathy (IMNM).
Mauro Turrin
doaj   +4 more sources

Statin-associated anti-HMGCR immune-mediated necrotizing myopathy with dermatomyositis-like features: A case report

open access: yesSAGE Open Medical Case Reports, 2020
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) immune-mediated necrotizing myopathy is a subtype of idiopathic inflammatory myopathy which may be associated with statin exposure.
Darosa Lim   +6 more
doaj   +2 more sources

MRI patterns of thigh muscle involvement in immune-mediated necrotizing myopathy and dermatomyositis [PDF]

open access: yesBMC Rheumatology
Background Immune-mediated necrotizing myopathy (IMNM) and dermatomyositis (DM) are characterized by weakness, hyperCKemia, associated autoantibodies, and varying extramuscular manifestations.
Anson W. Wilks   +5 more
doaj   +2 more sources

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