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Genetics of the idiopathic inflammatory myopathies
Current Opinion in Rheumatology, 1996Genetic predisposition to development of the idiopathic inflammatory myopathies is probably multifactorial. Major histocompatibility complex associations with these diseases provide the strongest evidence for a genetic component. In Caucasoids, haplotypes marked by B8/DR3 are associated with each of the clinical subgroups, except mixed connective ...
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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 myopathy
Medicina Clínica (English Edition)Albert, Selva-O'Callaghan +2 more
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Single‐cell profiling of muscle‐infiltrating T cells in idiopathic inflammatory myopathies
EMBO Molecular Medicine, 2023Begum Horuluoglu +2 more
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Systematic review of physical exercise for patients with idiopathic inflammatory myopathies
Australian Journal of Cancer Nursing, 2021Huan Zhang, Yuanfei Liu, Jingya Ma
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Relapses in idiopathic inflammatory myopathies
Muscle & Nerve, 1999O, Miró, M, Laguno, J M, Grau
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[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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Implications of glucocorticoid therapy in idiopathic inflammatory myopathies
Nature Reviews Rheumatology, 2012BEATRIZ Y Hanaoka +2 more
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