Αποτελέσματα Αναζήτησης
24 Φεβ 2022 · Dermatomyositis (DM) and polymyositis (PM) are idiopathic inflammatory myopathies, characterized by the shared features of proximal skeletal muscle weakness and evidence of muscle inflammation . DM, unlike PM, is associated with a variety of characteristic skin manifestations.
8 Οκτ 2019 · Polymyositis (PM) and dermatomyositis (DM) are different disease subtypes of idiopathic inflammatory myopathies (IIMs). The main clinical features of PM and DM include progressive symmetric, predominantly proximal muscle weakness.
Dermatomyositis (DM), polymyositis (PM) and inclusion body myositis (IBM) belong to the heterogeneous group of the inflammatory myopathies and are characterized by muscle cell infiltrations and specific alterations of the muscle fibers.
19 Απρ 2024 · Dermatomyositis (DM) and polymyositis (PM) are immune-mediated myopathies, characterized by the shared features of proximal skeletal muscle weakness and evidence of muscle inflammation . DM, unlike PM, is associated with a variety of characteristic skin manifestations.
4 Φεβ 2014 · Dermatomyositis (DM), polymyositis (PM), necrotizing myopathy (NM) and inclusion body myositis (IBM) are four distinct subtypes of idiopathic inflammatory myopathies – in short myositis. Recent studies have shed some light on the unique pathogenesis of each entity.
Polymyositis (PM) and Dermatomyositis (DM) are autoimmune myopathies characterized by inflammation and weakness of proximal muscles with extra muscular manifestations. In DM there is muscle weakness associated with skin rash.
Polymyositis (PM) and dermatomyositis (DM) are ‘autoimmune’ conditions. This means that the immune system – which usually protects the body against infection/germs – becomes overactive and starts attacking the body’s own tissues rather than protecting them.
