Titlebook: Immunology and Rheumatology in Questions; Haralampos M. Moutsopoulos,Evangelia Zampeli Book 2021Latest edition The Editor(s) (if applicabl

敌意

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

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

Inflated

宫殿般

atopic-rhinitis

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

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, thrombocy

ASTER

Spartan

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 minor

Melodrama

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

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