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Titlebook: Challenging Cases in Rheumatology and Diseases of the Immune System; Massoud Mahmoudi Book 2013 Springer Science+Business Media, LLC 2013

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https://doi.org/10.1007/978-3-030-74768-8y arterial involvement from giant cell arteritis has also been described. Clinicians should be aware of the different presenting manifestations of large-vessel vasculitis like giant cell arteritis and its evaluation and treatment.
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Systemic Lupus Erythematosus, course, and prognosis characterized by remissions and flares. The extreme heterogeneity of the disease has led some investigators to propose that SLE represents a syndrome rather than a single disease. Here we present two cases describing the complexity and heterogeneity of the disease.
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Systemic Sclerosistasias) syndrome. There are several illnesses that might mimic SSc like morphea, nephrogenic systemic fibrosis, and eosinophilic fasciitis. This is a case based review of SSc, diffuse and limited phenotypes.
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Chromatography of Phenolic Antioxidantsanding the signs and symptoms, laboratory findings, and biopsy results are key to making the diagnosis of Granulomatosis with Polyangiitis. A heightened degree of clinical suspicion for this rare disease will often lead to the correct diagnosis.
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Osteoarthritisd disability. The symptoms of osteoarthritis, specifically joint pain, are a common presenting complaint to primary care and rheumatology clinics. Osteoarthritis is a clinical diagnosis whose management requires a multidisciplinary approach to make use of the wide range of appropriate therapies. Her
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Goutn the United States (Zhu et al. Arthritis Rheum 63(10):3136–41, 2011). Gout is a multifactorial disease characterized by hyperuricemia and monosodium urate monohydrate crystal deposition in the joint and soft tissue. Classically, gout presents as recurrent, acute, monoarticular, or oligoarticular ar
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