7月の掲載論文・受賞
・循環器グループ
・著書
武田 充人、須藤 章
日本臨床 新領域別症候群シリーズ
骨格筋症候群（第２版）下 「Barth症候群」p.130-134
・内分泌グループ
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)
Mass Screening Committee, Japanese Society for Pediatric Endocrinology, and Japanese Society for Mass Screening, T.Ishii, M.Anzo, M.Adachi, K.Onigata, S.Kusuda, K.Nagasaki, S.Harada, R.Horikawa, M.Minagawa, K.Minamitani, H.Mizuno1, Y.Yamakami, M.Fukushi, T.Tajima
Clinical Pediatric EndocrinologyVol. Vol.24 (2015) No.3 p.77-105
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)
Mass Screening Committee, Japanese Society for Pediatric Endocrinology, and Japanese Society for Mass Screening, K.Nagasaki, K.Minamitani, M.Anzo, M.Adachi, T.Ishii, K.Onigata, S.Kusuda, S.Harada, R.Horikawa, M.Minagawa, H.Mizuno, Y.Yamakami, M.Fukushi, T.Tajima
Clinical Pediatric Endocrinology. Vol.24 (2015) No.3 p.107-133
Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2
S.Morikawa, N.Komatsu, S.Sakata, A.Nakamura-Utsunomiya, S.Okada, T.Tajima
Clinical Pediatric Endocrinology. Vol.24 (2015) No.3 p.135-138