Reply to the Letter: ‘Thrombotic microangiopathy in adult-onset Still’s disease: the story is just beginning’-Reference-Cited by-同舟云学术

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Reply to the Letter: ‘Thrombotic microangiopathy in adult-onset Still’s disease: the story is just beginning’

Published:2019-10-31 Issue:11 Volume:15 Page:1125-1126
ISSN:1744-666X
Container-title:Expert Review of Clinical Immunology
language:en
Short-container-title:Expert Review of Clinical Immunology

Author:

Mitrovic Stéphane¹²^ORCID,Hertig Alexandre³^ORCID,Fautrel Bruno¹⁴⁵^ORCID

Affiliation:

1. Department of Rheumatology, AP-HP, Hôpital de La Pitié Salpêtrière, Sorbonne Université, Paris, France

2. Department of Internal Medicine, Institut Mutualiste Montsouris, Paris, France

3. Department of Renal Transplantation, AP-HP, Hôpital de La Pitié Salpêtrière, Sorbonne Université, Paris, France

4. Faculté de Médecine et Institut Pierre Louis d’Epidémiologie et Santé publique, Sorbonne Université, Paris, France

5. CRI-IMIDIATE, a FCRIN Clinical Research Network, France

Publisher

Informa UK Limited

Subject

Immunology,Immunology and Allergy

Link

https://www.tandfonline.com/doi/pdf/10.1080/1744666X.2019.1682893

Reference12 articles.

1. Thrombotic microangiopathy in adult-onset Still’s disease: the story is just beginning

2. Complications of adult-onset Still’s disease and their management

3. Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura in the setting of adult-onset Still's disease

4. Risk Factors for Autoimmune Diseases Development After Thrombotic Thrombocytopenic Purpura

5. Predictive Features of Severe Acquired ADAMTS13 Deficiency in Idiopathic Thrombotic Microangiopathies: The French TMA Reference Center Experience

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