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- W2114966100 abstract "of the skin and muscle. However, systemic findings characterized by vasculitis and vasculopathy are also observed in the early phases (1). The incidence of this idiopathic inflammatory myositis (IIM) that presents with acute or chronic multisystemic destruction is 4/1,000,000 with a predominance of females and Caucasians (2). Diagnosis is suggested by clinical presentation accompanied by increased muscle enzymes and muscle MRI findings as well as a negative (-) rheumatoid factor, SS-A, SS-B, Sm, RNP and DNA (3). The frequency of calcinosis and functional deterioration that developed in 23%-70% of patients treated with historical techniques decreased significantly with high dose steroid therapy (4)." @default.
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- W2114966100 date "2005-04-01" @default.
- W2114966100 modified "2023-10-17" @default.
- W2114966100 title "Juvenile Dermatomyositis Resistant to Steroids" @default.
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