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Juvenile Idiopathic Inflammatory Myopathies
Pediatric Clinics of North America, 2018The juvenile idiopathic inflammatory myopathies (JIIM) are a group of rare, chronic, autoimmune illnesses that affect muscle and, to a lesser extent, skin. The presence of new-onset weakness and, in juvenile dermatomyositis, typical rahes, should lead to consideration of these diagnoses.
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Idiopathic Inflammatory Myopathies
2008The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of disorders characterized by symmetric proximal muscle weakness and elevated serum levels of enzymes derived from skeletal muscle. These include creatine phosphokinase (CPK), aldolase, aspartate, and alanine aminotransferases (AST and ALT), and lactate dehydrogenase (LDH).
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Idiopathic inflammatory myopathy
Medicina Clínica (English Edition)Albert, Selva-O'Callaghan +2 more
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Relapses in idiopathic inflammatory myopathies
Muscle & Nerve, 1999O, Miró, M, Laguno, J M, Grau
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The Role of Immune Cells in the Pathogenesis of Idiopathic Inflammatory Myopathies
2021Honglin Zhu
exaly
Implications of glucocorticoid therapy in idiopathic inflammatory myopathies
Nature Reviews Rheumatology, 2012Charlotte Peterson +2 more
exaly
[Idiopathic inflammatory myopathies].
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego, 2005The following disease entities are being included into the idiopathic inflammatory myopathy group (IIM): dermatomyositis (DM), polymyositis (PM), inclusion body myositis (IBM). These are primary inflammatory muscle diseases with substantial muscle weakening in their course. Everyone of the entities belonging to IIM is possessed of a particular clinical
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