5' exonucleases. Genes Dev 13, 2148-2158. , and Boyer, O. (2011). Anti-signal recognition particle auto-antibody levels correlate with creatine kinase activity in patients with necrotizing myopathy. Arthritis Rheum. , and McHugh, N. (2007). Anti-synthetase syndrome: a new autoantibody to phenylalanyl transfer RNA synthetase (anti-Zo) 38 Idiopathic Inflammatory Myopathies – Recent Developments associated with polymyositis and interstitial pneumonia.
A 83, 9507-9511. , and Trowsdale, J. (2002). The 52 000 MW Ro/SS-A autoantigen in Sjogren's syndrome/systemic lupus erythematosus (Ro52) is an interferon-gamma inducible tripartite motif protein associated with membrane proximal structures. Immunology 106, 246-256. , and Kveder, T. (2000). Immunoserological aspects of idiopathic inflammatory muscle disease. Wien. Klin. Wochenschr. 112, 722-727. J. (1997). Anti-Ro52 antibodies frequently co-occur with anti-Jo-1 antibodies in sera from patients with idiopathic inflammatory myopathy.
2011). Pathogenesis, classification and treatment of inflammatory myopathies. Nature Reviews Rheumatology, Vol. 7, No. 5, (May, 2011), pp. (297-306), ISSN: 1759-4790 2 Serological Aspects of Myositis Johannes Schulte-Pelkum Dr. Fooke Laboratorien GmbH, Neuss Germany 1. Introduction Idiopathic polymyositis is a chronic inflammatory systemic disease with preponderant infestation of the musculature. , 2001c; Kalovidouris, 1992; Mimori, 1996). Idiopathic, secondary and paraneoplastic forms of the disease can also be observed.
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