Showing results (11-20 of 65) with videos related to
Sort By:
Pageof 7
BMC Medicine|March 3, 2026
Early childhood weight gain and alanine aminotransferase at age 8: an adjunct study of the Japan Environment and Children's StudyNaw Awn J-P, Keiko Yamasaki, Naomi Mitsuda, et al.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.Plos Genetics|May 27, 2020
Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophyShigefumi Morioka, Hirofumi Sakaguchi, Hiroaki Mohri, 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.Clinical and Experimental Nephrology|November 20, 2015
X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 geneXue Jun Fu, Kandai Nozu, Aya Eguchi, et al.Pageof 7