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Brain & Development|April 8, 2021
SCN8A-related developmental and epileptic encephalopathy with ictal asystole requiring cardiac pacemaker implantationYutaka Negishi, Yusuke Aoki, Kazuya Itomi, et al.
Pediatrics and Neonatology|March 26, 2019
Visual function scale for identification of infants with low respiratory complianceEimei Harada, Masahiro Kinoshita, Sachiko Iwata, et al.
Brain & Development|January 4, 2020
Novel compound heterozygous MCOLN1 mutations identified in a Japanese girl with severe developmental delay and thin corpus callosumNaoya Yamaguchi, Kyoko Ban, Atsushi Suzuki, et al.
Neuropediatrics|December 17, 2013
Fulminant encephalopathy with marked brain edema and bilateral thalamic lesionsNaoki Ando, Akihisa Okumura, Satoru Kobayashi, et al.
The Journal of Pediatrics|March 4, 2018
Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in JapanTakao Togawa, Tatsuki Mizuochi, Tokio Sugiura, et al.
Japanese Journal of Clinical Oncology|December 15, 2019
Reliability and validity of a Japanese version of the psychosocial assessment tool for families of children with cancerAkemi Tsumura, Toru Okuyama, Yoshinori Ito, et al.
Nutrients|December 11, 2022
Influence of Intrauterine Inflammation, Delivery, and Postnatal Feeding on the Temporal Changes of Serum Alpha 1 Acid Glycoprotein Levels in Extremely-Low-Birth-Weight InfantsYasuhisa Nakamura, Sachiko Iwata, Kyoko Yokoi, et al.
Epilepsy Research|July 8, 2010
The applications of time-frequency analyses to ictal magnetoencephalography in neocortical epilepsyKazuyori Yagyu, Fumiya Takeuchi, Hideaki Shiraishi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 5, 2016
Effects of 4-phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosisShogo Ito, Hisamitsu Hayashi, Tokio Sugiura, et al.
Plos One|August 18, 2020
Two mouse models carrying truncating mutations in Magel2 show distinct phenotypesDaisuke Ieda, Yutaka Negishi, Tomomi Miyamoto, et al.
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