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Pediatric Emergency Care|April 15, 2016
Current Situation of Treatment for Anaphylaxis in a Japanese Pediatric Emergency CenterTakeshi Ninchoji, Sota Iwatani, Masahiro Nishiyama, et al.
Brain & Development|October 12, 2013
Leigh syndrome with Fukuyama congenital muscular dystrophy: a case reportHidehito Kondo, Koichi Tanda, Chihiro Tabata, et al.
Scientific Reports|February 26, 2025
Urinary prostaglandin D2 and E2 metabolites are elevated with disease severity in patients with Fukuyama congenital muscular dystrophyKeiko Ishigaki, Atsuko Takeuchi, Mariko Taniguchi-Ikeda, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 28, 2015
Association of HMOX1 gene promoter polymorphisms with hyperbilirubinemia in the early neonatal periodYoshinori Katayama, Tomoyuki Yokota, Hui Zhao, et al.
Journal of Human Genetics|June 1, 2012
Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytesMakiko Tsutsumi, Hiroe Kowa-Sugiyama, Hasbaira Bolor, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 7, 2016
Mitochondrial respiratory chain complex IV deficiency complicated with chronic intestinal pseudo-obstruction in a neonateYuya Hashimura, Ichiro Morioka, Chieko Hisamatsu, et al.
Minerva Pediatrica|June 9, 2016
Clinical factors associated with prehospital exacerbation of anaphylaxis in childrenTakeshi Ninchoji, Sota Iwatani, Masahiro Nishiyama, et al.
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