37 件中 1 - 20 件目
英語 ：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）
英語 ：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）
英語 ：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, 10 (1) （17 - ） , 2023 , （IF:1.5）
英語 ：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）
英語 ：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）
英語 ：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）
英語 ：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）
英語 ：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, 38 (2) （168 - 173） , 2021 , （IF:1.969）
英語 ：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）
英語 ：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）
英語 ：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, 11 (1) （359 - ） , 2017
英語 ：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, 55 (3) （155 - 157） , 2015 , （IF:1.083）
英語 ：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, 50 (2) （173 - 178） , 2015 , （IF:2.375）
英語 ：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, 24 (6) （603 - 606） , 2014 , （IF:1.409）
英語 ：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, 55 (4) （519 - 521） , 2013 , （IF:0.875）
英語 ：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, 14 (4) （267 - 272） , 2013
英語 ：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, 14 (1) （25 - 30） , 2013
英語 ：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, 158A (8) （1953 - 1956） , 2012 , （IF:2.391）
英語 ：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, 53 (3) （265 - 267） , 2012 , （IF:3.453）
英語 ：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, 15 (2) （114 - 117） , 2012 , （IF:0.986）
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