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by Watanabe, Haruki and Sada, Ken-Ei and Matsumoto, Yoshinori and Harigai, Masayoshi and Amano, Koichi and Dobashi, Hiroaki and Fujimoto, Shouichi and Usui, Joichi and Yamagata, Kunihiro and Atsumi, Tatsuya and Banno, Shogo and Sugihara, Takahiko and Arimura, Yoshihiro and Matsuo, Seiichi and Makino, Hirofumi and Sugiyama, Hitoshi and Takasaki, Yoshinari and Ishizu, Akihiro and Fujii, Takao and Okada, Yasunori and Homma, Sakae and Tsuboi, Naotake and Kumagai, Shunichi and Muso, Eri and Murakawa, Yohko and Hasegawa, Hitoshi and Yumura, Wako and Matsubara, Hiroaki and Yoshida, Masaharu and Katsuoka, Kensei and Ogawa, Noriyoshi and Komatsuda, Atsushi and Ito, Satoshi and Kawakami, Atsushi and Nakaya, Izaya and Saito, Takao and Ito, Takafumi and Hirawa, Nobuhito and Yamamura, Masahiro and Nakano, Masaaki and Nitta, Kosaku and Ogura, Makoto and Naniwa, Taio and Ozaki, Shoichi and Hirahashi, Junichi and Hosoya, Tatsuo and Wada, Takashi and Horikoshi, Satoshi and Kawaguchi, Yasushi and Hayashi, Taichi and Watanabe, Tsuyoshi and Inaguma, Daijo and Tsuruya, Kazuhiko and Homma, Noriyuki and Takeuchi, Tsutomu and Nakagawa, Naoki and Takeda, Shinichi and Katabuchi, Ritsuko and Iwano, Masayuki and Kobayashi, Masaki and Res Comm Intractable Renal Dis Min and Japan Research Committee of the Ministry of Health, Labour, and Welfare for Intractable Vasculitis, and the Research Committee of Intractable Renal Disease of the Ministry of Health, Labour, and Welfare of Japan and the Japan Research Committee of the Ministry of Health, Labour, and Welfare for Intractable Vasculitis, and the Research Committee of Intractable Renal Disease of the Ministry of Health, Labour, and Welfare of Japan
Arthritis and Rheumatology, ISSN 2326-5191, 10/2018, Volume 70, Issue 10, pp. 1626 - 1633
Journal Article
Arthritis & Rheumatology, ISSN 2326-5191, 12/2016, Volume 68, Issue 12, pp. 2945 - 2952
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Arthritis & Rheumatology, ISSN 2326-5191, 07/2018, Volume 70, Issue 7, pp. 1114 - 1121
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Annals of Internal Medicine, ISSN 0003-4819, 05/2009, Volume 150, Issue 10, pp. 670 - W120
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Medicine, ISSN 0025-7974, 12/2018, Volume 97, Issue 51, p. e13805
Rationale: Familial Mediterranean fever (FMF) is a genetic autoinflammatory disorder characterized by serositis and recurrent fever. Previous reports... 
MEDICINE, GENERAL & INTERNAL | NEUTROPHIL EXTRACELLULAR TRAPS | propylthiouracil | familial Mediterranean fever | antineutrophil cytoplasmic antibody | periodic fever | pleurisy | Case studies | Care and treatment | Familial Mediterranean fever | Diagnosis | Hyperthyroidism
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