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The first case of adult-onset PFAPA syndrome in Japan.
Kutsuna S, Ohmagari N, Tanizaki R, Hagino N, Nishikomori R, Ujiie M, Takeshita N, Hayakawa K, Kato Y, Kanagawa S. Kutsuna S, et al. Among authors: nishikomori r. Mod Rheumatol. 2016;26(2):286-7. doi: 10.3109/14397595.2013.857801. Epub 2013 Dec 2. Mod Rheumatol. 2016. PMID: 24289199
MEFV Variants in Patients with PFAPA Syndrome in Japan.
Taniuchi S, Nishikomori R, Iharada A, Tuji S, Heike T, Kaneko K. Taniuchi S, et al. Among authors: nishikomori r. Open Rheumatol J. 2013 Apr 19;7:22-5. doi: 10.2174/1874312901307010022. Print 2013. Open Rheumatol J. 2013. PMID: 23847694 Free PMC article.
National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics.
Tanaka T, Yoshioka K, Nishikomori R, Sakai H, Abe J, Yamashita Y, Hiramoto R, Morimoto A, Ishii E, Arakawa H, Kaneko U, Ohshima Y, Okamoto N, Ohara O, Hata I, Shigematsu Y, Kawai T, Yasumi T, Heike T. Tanaka T, et al. Among authors: nishikomori r. Mod Rheumatol. 2019 Jan;29(1):181-187. doi: 10.1080/14397595.2018.1442639. Epub 2018 Mar 2. Mod Rheumatol. 2019. PMID: 29451047
186 results