Thrombotic microangiopathy in adult-onset Still’s disease: the story is just beginning
Author:
Affiliation:
1. Urgences Néphrologiques et Transplantation Rénale, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Tenon, Paris, France
2. Sorbonne Université, Inserm, Paris, France
Publisher
Informa UK Limited
Subject
Immunology,Immunology and Allergy
Link
https://www.tandfonline.com/doi/pdf/10.1080/1744666X.2019.1682892
Reference19 articles.
1. Complications of adult-onset Still’s disease and their management
2. Purtscher-like retinopathy in a patient with Adult-onset Still's disease and concurrent thrombotic thrombocytopenic purpura
3. Acute renal failure is prevalent in patients with thrombotic thrombocytopenic purpura associated with low plasma ADAMTS13 activity
4. Thrombotic thrombocytopenic purpura and acute renal failure in adult Still's disease
5. Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Adult‐onset Still's disease with concurrent thrombotic microangiopathy: Observations from pooled analysis for an uncommon finding;European Journal of Haematology;2023-11-23
2. Reply to the Letter: ‘Thrombotic microangiopathy in adult-onset Still’s disease: the story is just beginning’;Expert Review of Clinical Immunology;2019-10-31
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