Hidekawa C, Kaoru Minegishi, Kouji Kobayashi, Ryusuke Yoshimi, Yohei Kirino, Shigeru Ohno, Mitsuhiro Takeno, Hideaki Nakajima: Successful treatment of extensive venous thrombosis with combination of immunosuppressants and a direct Xa inhibitor in Behçet’s disease. Mod Rheumatol Case Reports. 2(2):204-208, 2018.
Kamiyama R, Yoshimi R, Takeno M, Iribe Y, Tsukahara T, Kishimoto D, Kunishita Y, Sugiyama Y, Tsuchida N, Nakano H, Minegishi K, Tamura M, Asami Y, Kirino Y, Ishigatsubo Y, Ozato K, Nakajima H. : Dysfunction of TRIM21 in interferon signature of systemic lupus erythematosus. Mod Rheumatol, 2018, e-pub.
Kirino Y, Kawaguchi Y, Tada Y, Tsukamoto H, Ota T, Iwamoto M, Takahashi H, Nagasawa K, Takei S, Horiuchi T, Ichida H, Minota S, Ueda A, Ohta A, Ishigatsubo Y. : Beneficial use of serum ferritin and heme oxygenase 1 as biomarkers in adult-onset Still’s disease: a multicenter retrospective study. Mod Rheumatol, 2018, e-pub.
Kishimoto D, Kirino Y, Tamura M, Takeno M, Kunishita Y, Takase-Minegishi K, Nakano H, Kato I, Nagahama K, Yoshimi R, Igarashi K, Aoki I, Nakajima H. : Dysregulated heme oxygenase-1-low M2-like macrophages augment lupus nephritis via Bach1 induced by type-I interferons. Arthritis Res Ther, 2018, 20(1):64.
Kondo K, Kenji Yanishi, Ryo Hayashida, Satoshi Shintani, Rei Shibata, Kenta Murotani, Masahiko Ando, Masaaki Mizuno, Tadami Fujiwara, Toyoaki Murohara, Satoaki Matoba, TACT Follow-up Study Investigators: Long-term clinical outcomes survey of bone marrow-derived cell therapy in critical limb ischemia in Japan. Circ J. 82(4): 1168-1178, 2018.
Mizuguchi T, Nakashima M, Kato M, Okamoto N, Kurahashi H, Ekhilevitch N, Shiina M, Nishimura G, Shibata T, Matsuo M, Ikeda T, Ogata K, Tsuchida N, Mitsuhashi S, Miyatake S, Takata A, Miyake N, Hata K, Kaname T, Matsubara Y, Saitsu H, Matsumoto N.: Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders. Hum Mol Genet. 27(8):1421-1433. 2018.
Nakano H, Kirino Y, Takeno M, Higashitani K, Nagai H, Yoshimi R,Yamaguchi Y, Kato I, Aoki I, Nakajima H. : GWAS-identified CCR1 and IL10 loci contribute to M1-macrophage predominant Inflammation in Behçet’s disease. Arthritis Res Ther, 20(1):124, 2018. *Corresponding author.
Osada A, Yamada H, Takehara S, Tozuka Y, Fukushima T, Oka H, Okazaki H, Nagaoka S.: Gastrocnemius Myalgia as a Rare Initial Manifestation of Crohn’s Disease. Inten Med, 2018, 57(14), 2001-2006．
Sugiyama Y, Yoshimi R, Tamura M, Takeno M, Kunishita Y, Kishimoto D, Yoshioka Y, Kobayashi K, Takase-Minegishi K, Watanabe T, Hamada N, Nagai H, Tsuchida N, Soejima Y, Nakano H, Kamiyama R, Uehara T, Kirino Y, Sekiguchi A, Ihata A, Ohno S, Nagaoka S, Nakajima H. : The predictive prognostic factors for polymyositis / dermatomyositis-associated interstitial lung disease. Arthritis Res Ther, 2018, 20(1):7.
Suzuki T, Horita N, Takeuchi M, Ishido T, Mizuki Y, Mizuki R, Kawagoe T, Shibuya E, Yuta K, Yamane T, Hayashi T, Meguro A, Ishido M, Minegishi K, Yoshimi R, Kirino Y, Kato S, Arimoto J, Fukumoto T, Ishigatsubo Y, Kurosawa M, Takeno M, Kaneko T, Mizuki N. : Mod Rheumatol, 2018, e-pub.
Takase-Minegishi K, Horita N, Kobayashi K, Yoshimi R, Kirino Y, Ohno S, Kaneko T, Nakajima H, Wakefield RJ, Emery P. : Diagnostic test accuracy of ultrasonography for synovitis in rheumatoid arthritis: systematic review and meta-analysis. Rheumatology, 2018, 57(1):49-58.
Terao C, Yoshifuji H, Matsumura T, Naruse TK, Ishii T, Nakaoka Y, Kirino Y, Matsuo K, Origuchi T, Shimizu M, Maejima Y, Amiya E, Tamura N, Kawaguchi T, Takahashi M, Setoh K, Ohmura K, Watanabe R, Horita T, Atsumi T, Matsukura M, Miyata T, Kochi Y, Suda T, Tanemoto K, Meguro A, Okada Y, Ogimoto A, Yamamoto M,, Takahashi H, Nakayamada S, Saito K, Kuwana M, Mizuki N, Tabara Y, Ueda A, Komuro I, Kimura A, Isobe M, Mimori T, Matsuda F. : Novel genetic determinants and an epistasis of LILRA3 and HLA-B*52 in Takayasu arteritis. Proc Natl Acad Sci USA, 2018, e-pub.
Tsuchida N, Nakashima M, Miyauchi A, Yoshitomi S, Kimizu T, Ganesan V, Teik KW, Ch’ng GS, Kato M, Mizuguchi T, Takata A, Miyatake S, Miyake N, Osaka H, Yamagata T, Nakajima H, Saitsu H, Matsumoto N.: Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathy. Clin Genet. 93(2):266-274. 2018.
Tsuchida N, Nakashima M, Kato M, Heyman E, Inui T, Haginoya K, Watanabe S, Chiyonobu T, Morimoto M, Ohta M, Kumakura A, Kubota M, Kumagai Y, Hamano SI, Lourenco CM, Yahaya NA, Ch’ng GS, Ngu LH, Fattal-Valevski A, Weisz Hubshman M, Orenstein N, Marom D, Cohen L, Goldberg-Stern H, Uchiyama Y, Imagawa E, Mizuguchi T, Takata A, Miyake N, Nakajima H, Saitsu H, Miyatake S, Matsumoto N.: Detection of copy number variations in epilepsy using exome data. Clin Genet. 93(3):577-587. 2018.
Tsuchida N, Hamada K, Shiina M, Kato M, Kobayashi Y, Tohyama J, Kimura K, Hoshino K, Ganesan V, Teik KW, Nakashima M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Saitsu H, Ogata K, Miyatake S, Matsumoto N.: GRIN2D variants in three cases of developmental and epileptic encephalopathy. Clin Genet. 94(6):538-547. 2018.
Yamanaka Y, Baba T, Hagiwara E, Yanagawa N, Takemura T, Nagaoka S, Sakai F, Kuwano K, Ogura T.: Radiological Images of Interstitial Pneumonia in Mixed Connective Tissue Disease Compared with Scleroderma and Polymyositis / Dermatomyositis. Eur J Radiol, 107;26-32,2018.
