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Mitochondrial DNA depletion in sporadic inclusion body myositis [PDF]
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial changes such as cytochrome oxidase deficient fibres are a well recognised feature and mitochondrial DNA (mtDNA) deletions have also been reported, but not consistently.
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Sporadic Inclusion Body Myositis
2008Sporadic inclusion body myositis (sIBM) is the most common acquired muscle disease in elderly individuals, particularly men. Its prevalence varies among ethnic groups, but it is estimated at 35 per one million people over 50 years. Genetic as well as environmental factors and autoimmune processes might both have a role in its pathogenesis. Unlike other
Josep M. Grau +1 more
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Genetic advances in sporadic inclusion body myositis
Current Opinion in Rheumatology, 2015To describe recent developments in the genetics of sporadic inclusion body myositis (sIBM).Genes located within major histocompatibility complex regions remain the strongest genetic association with sIBM. The rs10527454 polymorphism in the TOMM40 gene seems to have a disease modifying effect on sIBM by delaying the onset of symptoms, and this effect ...
Qiang, Gang +4 more
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ANT1 is reduced in sporadic inclusion body myositis
Neurological Sciences, 2012To investigate ANT1 and NF-κB expression in inclusion body myositis (IBM) muscle and to verify their possible roles in the pathogenesis of the disease, we collected muscle samples from five patients with IBM, polimyositis (PM) and controls. p65 form of NF-κB was analyzed using immunocytochemistry, Western blot and EMSA.
BARCA, EMANUELE +8 more
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Sporadic inclusion body myositis: a continuing puzzle
Neuromuscular Disorders, 2008There is now compelling evidence that sporadic inclusion body myositis (sIBM) is a muscle-specific autoimmune disease in which both T and B-cells play a part and in which both cytotoxic muscle fibre necrosis and degeneration occur. However the factors responsible for breakdown of immune tolerance and the nature of the target antigens expressed by ...
Needham, M., Mastaglia, F.L.
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McArdle disease and sporadic inclusion body myositis
Neuropathology and Applied Neurobiology, 2009No abstract ...
Scarpelli M. +6 more
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Electromyographic findings in sporadic inclusion body myositis
Journal of Electromyography and Kinesiology, 2018Clinically oriented diagnostic criteria can be as specific for diagnosis of sporadic inclusion body myositis (sIBM) as pathological criteria, especially at the time of presentation. EMG may provide an convincing proof that a muscle biopsy should be performed.To compare the EMG results in patients with sIBM divided into subgroups based on the newest ...
Monika Magdalena Nojszewska +7 more
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Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
Hector Chinoy +2 more
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Sporadic inclusion body myositis: Pathogenic considerations
Annals of Neurology, 2009AbstractSporadic inclusion body myositis is the commonest acquired disease of skeletal muscles after 50 years of age, and as such it has commanded a great deal of attention of investigators over the past 25 years. As a result, a large amount of information has accumulated concerning its clinical profile, myopathology, and immunopathology.
George, Karpati, Erin K, O'Ferrall
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Controlling autoimmunity in sporadic inclusion-body myositis
Neurology, 2006Sporadic inclusion-body myositis (s-IBM) spans two areas of interest in my research lab, the role of protein aggregation in neurodegenerative disease1–4 and the role of secondary autoimmunity in degenerative conditions in the nervous system5–10 and in muscle.11,12 After some comments on the potential pathologic role of inclusion bodies themselves, I ...
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