Simultaneous development of IgA vasculitis and eosinophilic granulomatosis with polyangiitis-Reference-Cited by-同舟云学术

Simultaneous development of IgA vasculitis and eosinophilic granulomatosis with polyangiitis

Published:2019-10-23 Issue:1 Volume:4 Page:63-69
ISSN:2472-5625
Container-title:Modern Rheumatology Case Reports
language:en
Short-container-title:Modern Rheumatology Case Reports

Author:

Asano Yosuke¹,Matsumoto Yoshinori¹,Miyazaki Tatsuhiko²,Ishizu Akihiro³,Morizane Shin⁴,Hayashi Keigo¹,Yamamura Yuriko¹,Hiramatsu Sumie¹,Miyawaki Yoshia¹,Morishita Michiko¹,Ohashi Keiji¹,Watanabe Haruki¹,Watanabe Katsue Sunahori¹,Kawabata Tomoko¹,Sada Ken-Ei¹,Makino Hirofumi¹,Wada Jun¹

Affiliation:

1. Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan;

2. Division of Pathology, Gifu University Hospital, Gifu, Japan;

3. Faculty of Health Sciences, Hokkaido University, Sapporo, Japan;

4. Department of Dermatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/24725625.2019.1673528

Reference32 articles.

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2. 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides

3. Characteristics and Management of IgA Vasculitis (Henoch-Schönlein) in Adults: Data From 260 Patients Included in a French Multicenter Retrospective Survey

4. Incidence of Henoch-Schonlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins

5. A nationwide survey on epidemiological characteristics of childhood Henoch–Schönlein purpura in Taiwan