1 - 15 of about 15
English: Terao R, Nii M, Asai H, Nohara F, Okamoto T, Nagaya K, Azuma H, Breastfeeding in a patient with chronic myeloid leukemia during tyrosine kinase inhibitor therapy , J Oncol Pharm Practice , vol.27 (p.756 - 760) , 2021
English: Nagaya K, Tsuchida E, Nohara F, Okamoto T, Azuma H., The temperature change in an endotracheal tube during high frequency ventilation using an artificial neonatal lung model with Babylog® 8000 plus , Pediatric Pulmonology , vol.50 (2) (p.173 - 178) , 2015
English: Okamoto T, Nagaya K, Kawata Y, Asai H, Tsuchida E, Nohara F, Okajima K, Azuma H, Novel compound heterozygous mutations in DYNC2H1 in a patient with severe short-rib polydactyly syndrome type III phenotype , Congenital Anomalies , vol.55 (3) (p.155 - 157) , 2015 , (IF:0.985)
English: Asai H, Okamoto T, Tsuchida E, Nohara F, Nagaya K, Azuma H , Thrombosed Dural Sinus Malformation in a Fetus: A Case Report , Journal of Neuroimaging , vol.24 (6) (p.603 - 606) , 2014 , (IF:1.734)
English: Nohara F, Nagaya K, Asai H, Tsuchida E, OkamotoT, Hayashi T, Sakata H, Terao Y, Azuma H , Neonatal pleural empyema caused by emm type 6 group A streptococcus , Pediatrics International , vol.55 (4) (p.519 - 521) , 2013 , (IF:0.731)
English: Okamoto T, Nagaya K, Asai H, Tsuchida E, Nohara F, Hayashi T, Yamashita A, Nishimura G, Azuma H., Platyspondylic lethal dysplasia torrance type with a heterozygous mutation in the triple helical domain of COL2A1 in two sibs from phenotypically normal parents. , Am J Med Genet A. , vol.158 (8) (p.1953 - 1956) , 2012
English: 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 , vol.54 (3) (p.354 - 356) , 2011
English: Okamoto T, Nakamura E, Nagaya K, Hayashi T, Mukai T, Fujieda K, Two novel frameshift mutations in the SOX9 gene in two patients with campomelic dysplasia who showed long-term survival , Journal of Pediatric Endocrinology and Metabolism , vol.23 (p.1189 - 1194) , 2010
English: 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 , vol.66 (p.135 - 139) , 2009 , (IF:2.604)
English: Nagaya K, Okamoto T, Nakamura E, Hayashi T, Fujieda K., Airway humidification with a heated wire humidifier during high-frequency ventilation using Babylog 8000 plus® in neonates. , Pediatr Pulmonol , vol.44 (p.260 - 266) , 2009 , (IF:1.883)
English: Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Fujieda K, Transforming growth factor-b1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways , BBRC , vol.383 (p.475 - 479) , 2009 , (IF:2.648)
English: 7. Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Fujieda K, Transforming growth factor-b1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways , BBRC , vol.383 (p.475 - 479) , 2009
English: 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 , vol.84 ((2)) (p.137 - 139) , 2008 , (IF:2.12)
English: 4. 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 , Ear Hum Dev , vol.84 (p.137 - 139) , 2008
English: 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 Development , vol.83 (p.285 - 291) , 2007 , (IF:2.12)
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