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资源简介：
Polyautoimmunity in APS.
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创建时间：
2015-12-02
相关数据集
Supplementary Material for: Retinal Pigment Epithelial Proliferation Secondary to Retinal Ischemia: A Case Report and Literature Review
Introduction: Antiphospholipid syndrome is one of the most common causes of acquired hypercoagulable conditions which is correlated with ocular conditions not least of which is retinal ischaemia due t
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Supplementary Material for: Prevalence and outcome of cerebral microbleeds in antiphospholipid syndrome
Introduction: Antiphospholipid syndrome (APS) is an acquired autoimmune disease characterized by arterial and venous thrombosis. Acute ischemic stroke (AIS) and transient ischemic attack (TIA) are com
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Demographic and clinical characteristics of APS and non-APS patients.
Demographic and clinical characteristics of APS and non-APS patients.
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ROMAS study: An intestinal microbiome intervention affects biochemical disease activity in patients with antiphospholipid syndrome
Aim of this study was to evaluate whether the gut microbiome affects disease activity in human APS. 15 APS patients with stable disease received oral vancomycin, 500mg four times daily for seven days.
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Nephropathy in Pparg -null mice highlights PPARγ systemic activities in metabolism and in the immune system
Peroxisome proliferator-activated receptor γ (PPARγ) is a ligand-dependent transcription factor involved in many aspects of metabolism, immune response, and development. Total-body deletion of the two
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