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原著
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- Kagami-Takasugi M, Katsumata N, Tanaka T, Tajima T, Fujieda K:Molecular genetic analysis of MODY candidate genes in Japanese patients with non-obese juvenile onset diabetes mellitus.J Pediatr Endocrinol Metab 19:143-148, 2006
- Tanaka T, Fujieda K, Yokoya S, Shimatsu A, Tachibana K, Tanaka H, Tanizawa T, Teramoto A, Nagai T, Nishi Y, Hasegawa Y, Hanew K, Fujita K, Horikawa R, Takada G, Hasegawa Y, Ohno T, Komatsu K:No improvement of adult height in non-growth hormone (GH) deficient short children with GH treatment. Clin Pediatr Endocrinol 15:15-21, 2006
- Saito T, Tachibana K, Shimazu A, Katsumata N, Hizuka N, Fujieda K, Yokoya S, Tanaka T:Standardization of blood growth hormone levels measured by different kits using linear structural relationship. Clin Pediatr Endocrinol, 15:79-84, 2006
- Hanew K, Tachibana K, Yokoya S, Fujieda K, Tanaka T, Igarashi Y, Shimatsu A, Tanaka H, Tanizawa T, Teramoto A, Nishi Y, Hasegawa Y, Hizuka N, Hirano T, Fujita K:Clinical characteristics, etiologies and pathophysiology of patients with severe short stature with severe GH deficiency:Questionnaire study on the data registered with the foundation for growth science, Japan, Endocrine J 53:259-265, 2006
- Tajima T, Nawate M, Takahashi Y, Mizoguchi Y, Sugihara S, Yoshimoto M, Murakami M, Adachi M, Tachibana K, Mochizuki H, Fujieda K:Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome.Endocr J 53:647-652, 2006
- Ito Y, Fujieda K, Tanaka T, Takano K, Chihara K, Seino Y, Irie M:Low-dose growth hormone treatment (0.175 mg/kg/week) for short stature in patients with Turner syndrome: Data from KIGS Japan. Endocr J 53:699-703, 2006
- Savage MO, Cassorla FG, Gluckman PD, Gruters-Kieslich A, Raghupathy P, Silink M, Czernichow P, Chiarelli F, Rogol AD, Crock PA, Cowell CT, Fujieda K, Arnhold IJ: International Societies for Paediatric Endocrinology: Global inequalities in paediatric endocrine practice:statement of minimal acceptable care. Statement from the International Societies for Paediatric Endocrinology.Horm Res 65:111-113, 2006
- Tanaka H, Amamiya S, Miura N, Araki A, Ohinata J, Fujieda K: Postnatal development of brainstem serotonin-containing neurons projecting to lumbar spinal cord in rats.Brain Dev 28: 586-591, 2006.
- Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES/ESPE Consensus Group (Fujieda K, et al):Consensus statement on management of intersex disorders, Arch Dis Child 91:554-563, 2006
- Okamoto T, Shirai M, Kokubo M, Takahashi S, Kajino M, Takase M, Sakata H, and Oki J:Human milk reduces the risk of retinal detachment in extremely low birth weight infants. Pediatrics International (in press)
- Nagaya K, Tanaka S, Kitajima H, Fujimura M: The corrected blood urea nitrogen predicts the developmental quotient of extremely low-birth-weight infants at the corrected age of 36 months, Early Human Development2006 ( in press)
- Hiroshi Ogawa, Tatsuo Suzutani, Yohko Baba, Shin Koyano, Naoki Nozawa, Kei Ishibashi, Kenji Fujieda, Naoki Inoue, Koichi Omori: Etiology of severe sensorineural hearing loss in children: independent impact of congenital cytomegalovirus infection and GJB2 mutations.J. Infect. Dis. (in press)
- Ohsaki Y, Koyano S, Tachibana M, Shibukawa K, Kuroki M, Yoshida I, Ito Y:Undetected Bacillus pseudo-outbreak after renovation work in a teaching hospital. J. Infect. 2006 (in press)
- Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Kurosawa K, Kawame H, Iwakoshi M, Kosho T, Fukushima Y, Makita Y, Yokoyama Y, Yamagata T, Kato M, Hiraki Y, Nomura M, Yoshiura K, Kishino T, Ohta T, Mizuguchi T, Niikawa N, Matsumoto N: BAC array CGH reveals genomic aberrations in idiopathic mental retardation, Am J Med Genet A 140:205-11, 2006
- Osaki M, Makita Y, Miura J, Abe N, Noguchi S, Miyamoto A. A Japanese boywith apparent Bohring-Opitz or "C-like" syndrome: Am J Med Genet A 140: 897-899, 2006
- Takikawa K, Haga N, Maruyama T, Nakatomi A, Kondoh T, Makita Y, Hata A, Kawabata H, Ikegawa S: Spine and rib abnormalities and stature in spondylocostal dysostosis, Spine 31:E192-7, 200
- Nakayama T, Kuroi N, Sano M, Tabara Y, Katsuya T, Ogihara T, Makita Y, Hata A, Yamada M, Takahashi N, Hirawa N, Umemura S, Miki T, Soma M: Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension, Hypertension 48:512-8, 2006
- Aramaki M, Udaka T, Kosaki R, Makita Y, Okamoto N, Yoshihashi H, Oki H, Nanao K, Moriyama N, Oku S, Hasegawa T, Tahahashi T, Fukushima Y, Kawame H, Kosaki K: Phenotypic spectrum of CHARGE syndrome with CHD7 mutations, J Pediatr 148:410-414, 2006
- Puvabanditsin S, Garrow E, Snider ZG, Akahira-Azuma M: Tavaria A, Cerefice M Dandy-Walker malformation in mosaic Klinefelter syndrome, Genet Couns,17(2):245-8,2006
- 長屋 建、中村英記、竹田津原野、林時仲、藤枝憲二： 臍帯潰瘍を合併した先天性上部消化管閉鎖症の２例、日本周産期新生児学会誌 42:37-41,2006:HLH)の一例、未熟児新生児学会誌(in press)
- 長森恒久，岡本年男，梶野真弓，高瀬雅史，白井 勝，坂田 宏，沖 順一，丸山静男：胎児期に発症した血球貪食症候群(Hemophagocytic lymphohistiocytosis)の一例 (in press)
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