Results 31 to 40 of about 2,106 (149)
Clinical Images: Sporadic inclusion body myositis in American Indian/Alaska Native patient with overlap of rheumatoid arthritis and Sjögren disease [PDF]
ACR Open Rheumatology, 2023 Prashant Kaushik +2 more
doaj +2 more sources
Macroautophagy as a Pathomechanism in Sporadic Inclusion Body Myositis [PDF]
Autophagy, 2007 Skeletal muscle fibers show a high level of constitutive and starvation-induced macroautophagy. Sporadic Inclusion Body Myositis (sIBM) is the most common acquired skeletal muscle disease in patients above the age of 50 years and is characterized by inflammation and intracellular accumulation of aggregate-prone proteins such as amyloid precursor ...
Lunemann, Jan D. +3 more
openaire +3 more sources
On the role of anti-cN1A antibodies in sporadic inclusion body myositis and beyond: a challenging task full of surprises [PDF]
Rheumatology, 2023 Eleni Patrikiou +2 more
doaj +2 more sources
Update on sporadic inclusion body myositis [PDF]
Brain, 2011 Sporadic inclusion body myositis (IBM) is the most frequent acquired myopathy seen in adults aged over 50 years. Despite the presence of conspicuous inflammatory infiltrates, sporadic IBM is essentially resistant to immunosuppressive treatment and carries an ominous prognosis.
openaire +2 more sources
Inclusion body myositis – pathomechanism and lessons from genetics
Open Medicine, 2015 Inclusion body myositis is a rare, late-onset myopathy. Both inflammatory and myodegenerative features play an important role in their pathogenesis.
Murnyák Balázs +8 more
doaj +1 more source
Современная ревматология, 2023 The article presents a review of the literature and a clinical observation of a patient with long-term anamnesis of primary Sjögren's syndrome (SS) in combination with sporadic inclusion body myositis (sIBM).
Yu. I. Khvan +1 more
doaj +1 more source
Evolving classification and role of muscle biopsy in diagnosis of inflammatory myopathies
Indian Journal of Pathology and Microbiology, 2022 Idiopathic inflammatory myopathy (IIM) is a broad term that includes dermatomyositis, polymyositis, overlap myositis, sporadic inclusion body myositis, and immune-mediated necrotizing myopathy.
Meenakshi Swain, Megha Uppin
doaj +1 more source
International Journal of Physiotherapy, 2017 Background: Sporadic inclusion body myositis is an autoimmune and degenerative disorder of skeletal muscle that affects people at random. It most commonly begins as progressive weakness and atrophy of lower extremity musculature, beginning with the ...
Tyler Harrigfeld, Trent Jackman
doaj +1 more source
Cardiac Involvement in Sporadic Inclusion-Body Myositis [PDF]
Circulation, 2010 A 36-year-old man came to the emergency department with acute onset of exertional chest pain. He had had no recent infections, and no cardiovascular risk factors were present. However, the patient had used a wheelchair since his mid-20s because of sporadic inclusion-body myositis, as established by muscle biopsy.
Wolfgang, Utz +4 more
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Sporadic inclusion body myositis: overreliance on histology may lead to misdiagnosis [PDF]
Folia MedicaWe describe a 57-year-old man who had initial isolated weakness in the deep finger flexors of his non-dominant hand, followed by quadriceps weakness and wasting a year later.
Behidzhe Sadarzanska-Terzieva +2 more
doaj +3 more sources