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Pediatrics International : Official Journal of the Japan Pediatric Society|November 22, 2023
Medical records as screening tools for child death review in JapanAtsushi Numaguchi, Akira Ishii, Jun Natsume, et al.
Peerj|May 6, 2021
Temporal inversion of the acid-base equilibrium in newborns: an observational studyYuko Mizutani, Masahiro Kinoshita, Yung-Chieh Lin, et al.
Environmental Pollution (Barking, Essex : 1987)|November 8, 2025
Associations of PFAS exposure with obstetric and birth outcomes in the Japan Environment and Children's Study (JECS): Is maternal endometriosis an effect modifier?Joselyn Dionisio, Yuki Ito, Sayaka Kato, et al.
Pediatrics and Neonatology|December 28, 2020
Promoting sound development of preterm infants in the name of developmental neuroscience: Beyond advanced life support and neuroprotectionOsuke Iwata, Sachiko Iwata, Yung-Chieh Lin, et al.
Environmental Health and Preventive Medicine|August 13, 2024
Oral hygiene status and vascular aging in schoolchildren and their mothersShogo Nakane, Yuki Ito, Kayo Kaneko, et al.
Scientific Reports|January 14, 2026
Brain organoid models of SZT2-related disease reveal an overproduction of outer radial glial cells through mTORC1 activationEmi Sato, Yuji Nakamura, Masanori Fujimoto, et al.
Brain & Development|May 14, 2014
Advantageous information provided by magnetoencephalography for patients with neocortical epilepsyTomoshiro Ito, Hiroshi Otsubo, Hideaki Shiraishi, et al.
Medicine|December 23, 2022
A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant in the ARL6 gene who was initially diagnosed with retinitis punctata albescens: A case reportKeitaro Mizumoto, Kumiko Kato, Kaoru Fujinami, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|April 30, 2013
Effect of Japanese cedar specific immunotherapy on allergen-specific T(H)2 cells in peripheral bloodTakayasu Nomura, Ikuya Tsuge, Chisato Inuo, et al.
Brain & Development|December 17, 2021
Hemorrhagic shock and encephalopathy syndrome in a patient with a de novo heterozygous variant in KIF1AKouji Isobe, Daisuke Ieda, Fuyuki Miya, et al.
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