1 - 28 of about 28
English: Imanishi R, Nakau K , Shimada S, Oka H, Takeguchi R, Tanaka R, Sugiyama T, Nii M, Okamoto T, Nagaya K, Makita Y, Yanagi K, Kaname T, Takahashi S., A novel HECW2 variant in an infant with congenital long QT syndrome. , Human Genome Variation , vol.10 (1) (p.17 - ) , 2023 , (IF:1.5)
English: Nii M, Okamoto T, Sugiyama T, Aoyama A, Nagaya K, Reticulocyte hemoglobin content changes after treatment of anemia of prematurity , Pediatrics International , 2022 , (IF:1.617)
English: Nii M, Asai H, Nohara F, Okamoto T, Nagaya K., Severe hyponatremia in a neonate with Costello syndrome and CoA during PGE1 infusion , Pediatrics International , 2022 , (IF:1.524)
English: Asai H, Okamoto T, Nii M, Nohara F, Nagaya K., Neurally adjusted ventilatory assist in an infant with tracheobronchomalacia. , Pediatrics International , 2021 , (IF:1.524)
English: Okamoto T, Nagaya K, Toriumi N, Sarashina T, Azuma H., Retrospective diagnosis of transient abnormal myelopoiesis by using preserved dried umbilical cord , Pediatrics International , 2021 , (IF:1.524)
English: Okamoto T, Nagaya K, Sugiyama T, Aoyama A, Nii M, Azuma H., Two patients of trisomy 21 with transient abnormal myelopoiesis with hypereosinophilia without blasts in peripheral blood smears. , Pediatric Hematology and Oncology , vol.38 (2) (p.168 - 173) , 2021 , (IF:1.969)
English: Shibata Y, Okamoto T, Saruta T, Matsuoka F, Fujieda M, Sano S, A de novo novel splice-site mutation in FLT4/VEGFR3 is associated with Milroy disease. , The Journal of Dermatology , 2021 , (IF:3.072)
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. , Journal of Oncology Pharmacy Practice , 2020 , (IF:1.85)
English: Okano S, Tanaka R, Okayama A, Tsuchida E, Nohara F, Suzuki N, Okamoto T, Nagaya K, Takahashi S, Azuma H, Congenital basal meningoceles with different outcomes: a case series. , Journal of Medical Case Reports , vol.11 (1) (p.359 - ) , 2017
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:1.083)
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 , (IF:2.375)
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:1.409)
English: Nohara F, Nagaya K, Asai H, Tsuchida E, Okamoto T, 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:0.875)
English: Suzuki S, Koga M, Niizeki N, Furuya A, Matsuo K, Tanahashi Y, Tsuchida E, Nohara F, Okamoto T, Nagaya K, Azuma H, Evaluation of glycated hemoglobin and fetal hemoglobin-adjusted HbA1c measurements in infants , Pediatric Diabetes , vol.14 (4) (p.267 - 272) , 2013
English: Suzuki S, Koga M, Niizeki N, Furuya A, Takahashi H, Matsuo K, Tanahashi Y, Kawata Y, Asai H, Tsuchida E, Nohara F, Okamoto T, Nagaya K, Azuma H., Glycated albumin is lower in infants than in adults and correlated with both age and serum albumin , Pediatric Diabetes , vol.14 (1) (p.25 - 30) , 2013
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 , American Journal of Medical Genetics Part A , vol.158A (8) (p.1953 - 1956) , 2012 , (IF:2.391)
English: Nakamura E, Okamoto T, Nagaya K, Hayashi T., Maternal deletion allele of angiotensin-converting enzyme gene is associated with fetal growth restriction , Pediatric and Developmental Pathology , vol.15 (2) (p.114 - 117) , 2012 , (IF:0.986)
English: 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 , Journal of Clinical Virology , vol.53 (3) (p.265 - 267) , 2012 , (IF:3.453)
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 , European Journal of Medical Genetics , vol.15 (3) (p.114 - 117) , 2011 , (IF:1.568)
English: Okamoto T, Nakamura E, Nagaya K, Hayashi T, Mukai T, Fujieda K, Patient reports: 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 (11) (p.1189 - 1194) , 2010 , (IF:0.738)
English: Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K, Increased expression of matrix metalloproteinase-9 and hepatocyte growth factor in the cerebrospinal fluid of infants with posthemorrhagic hydrocephalus , Early Human Development , vol.86 (4) (p.251 - 254) , 2010 , (IF:2.122)
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 , Pediatric Research , vol.66 (2) (p.135 - 139) , 2009 , (IF:2.604)
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 , Biochemical and Biophysical Research Communications , vol.383 (4) (p.475 - 479) , 2009 , (IF:2.548)
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 plusR in neonates , Pediatric Pulmonology , vol.44 (3) (p.260 - 266) , 2009 , (IF:1.816)
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 Human Development , vol.84 (2) (p.137 - 139) , 2008 , (IF:2.122)
English: Okamoto T, Shirai M, Kokubo M, Takahashi S, Kajino M, Takase M, Sakata H, Oki J, Human milk reduces the risk of retinal detachment in extremely low birth weight infants , Pediatrics International , vol.49 (6) (p.894 - 897) , 2007 , (IF:0.707)
Japanese: Severe tricuspid insufficiency with rupture of the papillary muscle secondary to premature closure of ductus arterioles: a case report , vol.59 (1) (p.77 - 81) , 2023
Japanese: Toshio Okamoto, Yumi Kawata, Hiroko Asai, Etsushi Tsuchida, Fumikatsu Nohara, Hiroyuki Kitamura, Yoshiaki Sasaki, Ken Nagaya, Hiroshi Azuma, Clinical courses of five patients with various "lethal" skeletal dysplasias , The Journal of the Japanese Pediatric Society , vol.118 (8) (p.1229 - 1236) , 2014
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