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  • Sakata H, Taketazu G, Nagaya K, Shirai M, Sugai R, Ikegami K, Maruyama S : Outbreak of severe infection due to adenovirus type 7 in a paediatric ward in Japan. J Hosp Infect39(3),207-11,1998
  • Sakata H, Ikegami K, Nagaya K, Shirai M, Maruyama S : Thrombocytopenia caused by acquired cytomegalovirus infection in children. Pediatr Int 41(1),113-4,1999
  • 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 Hum Dev 83,285-291, 2007
  • Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K: Increased matrix metalloproteinase-9 activity in the cerebrospinal fluid of infants with posthemorrhagic hydrocephalus. Early Hum Dev 84(2):137-139, 2008
  • Nagaya K, Okamoto T, Nakamura E, Hayashi T, Fujieda K. Airway humidification with a heated wire humidifier during high-frequency ventilation using Babylog 8000 plusR in neonates. Pediatr Pulmonol, 44: 260-266, 2009
  • Nagaya K, Makita Y, Taketazu G, Okamoto T, Nakamura E, Hayashi T, Fujieda K:Paternal allele of IGF2 gene haplotype CTG is associated with fetal and placental growth in Japanese. Pediatr Res, 66: 135-139, 2009
  • Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Fujieda K:Transforming growth factor-beta1 induces matrix metallpproteinase-9 expression in human meningeal cells via ERK and Smad pathways. BBRC, 383: 475-479, 2009
  • Nakamura E, Makita Y, Okamoto T, Nagaya K, Hayashi T, Sugimoto M, Manabe H, Taketazu G, Kajino H, Fujieda K : 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects. Eur J Med Genet. 54(3):354-6. 2011
  • Nagamori T, Koyano S, Asai Y, Nohara F, Okamoto T, Nagaya K, Hayashi T, Miura Y, Tsuda N, Iseki K, Azuma H. Sequential changes in pathophysiology of systemic inflammatory response in a disseminated neonatal herpes simplex virus (HSV) infection. J Clin. Virol. In Press
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