1 - 20 of about 30
English: Nagaya K, Okamoto T, Nii M, Aoyama-Hashimoto A, Sugiyama T, Takahashi K, Sato T, Shirai M, Impact of visitation restrictions in neonatal intensive care units during the COVID‐19 pandemic on parents in northern Hokkaido, Japan. , Journal of Paediatrics and Child Health , 2024 , (IF:1.6)
English: Okamoto T, Nagaya K, Nii M, Takahashi S, Non-progressive hepatic tumor with high levels of serum alpha-fetoprotein in two infants with trisomy 18 , Congenital Anomalies , 2024 , (IF:1.3)
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: 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, 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)
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