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Haralampos M. Moutsopoulos,Evangelia Zampelickle a multi-dimensional problem of this size and nature. This book is the first broad attempt to address the issue of leadership by one of the major parties to978-90-481-5524-8978-94-017-1049-7Series ISSN 1383-5130 Series E-ISSN 2215-0110神刊 发表于 2025-3-25 09:36:24
Haralampos M. Moutsopoulos,Evangelia Zampelickle a multi-dimensional problem of this size and nature. This book is the first broad attempt to address the issue of leadership by one of the major parties to978-90-481-5524-8978-94-017-1049-7Series ISSN 1383-5130 Series E-ISSN 2215-0110Inflated 发表于 2025-3-25 15:32:48
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Inflammatory ArthritidesType and location of articular involvement, extra-articular and systemic manifestations, as well as findings from joint imaging are important in distinguishing different types of arthritis. Sacroiliac joint and spine involvement alone or accompanied by asymmetrical arthritis of large peripheral join露天历史剧 发表于 2025-3-26 02:29:17
Systemic Lupus Erythematosus, Mixed Connective Tissue Disease and Antiphospholipid SyndromedsDNA antibodies with SLE nephritis, anti-ribosomal P with psychosis, antiphospholipids with thromboses and recurrent abortions, and anti-histones with drug-induced SLE. IgG anti-Ro/SSA or anti-La/SSB antibodies cross the placenta and affect the fetus which develops anti-Ro-related rashes, thrombocyASTER 发表于 2025-3-26 04:39:57
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Sjögren’s Syndrome, IgG4-Related Disorderstial manifestations of SS. After excluding other causes of sicca symptomatology, patients should be assessed for lacrimal and salivary gland function (ocular staining with lissamine green or rose Bengal, Schirmer’s test, and unstimulated saliva secretion, respectively), and a biopsy of labial minorMelodrama 发表于 2025-3-26 13:28:35
Systemic Sclerosisnon and arthritis, presence of anti-topoisomerase I and anti-RNA polymerase III antibodies, a higher risk for interstitial lung disease, and scleroderma renal crisis development; and (c) systemic sclerosis sine scleroderma which refers to patients who develop internal organ involvement without skin芳香一点 发表于 2025-3-26 19:53:24
Vasculitides and Related Diseasesitis (GPA, formerly known as Wegener’s granulomatosis), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA, formerly known as Churg-Strauss syndrome). Other non-ANCA-associated small-vessel vasculitides are typically characterized by either the presence of immune