セッション詳細
[IO1]International Session(Platform Presentation)1
2025年6月5日(木) 14:35 〜 15:35
第8会場
Chair：Yuko Shimizu-Motohashi(Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan),Kit Yan Leung(Department of Paediatrics and Adolescent Medicine, Princess Margaret Hospital, Hong Kong. )
[IO1-01]The Impact of Simulation-Based Training on Self-Efficacy in Sedation for Pediatric Magnetic Resonance Imaging
○Yuto Arai, Kento Ohta, Go Yoshino, Tohru Okanishi, Yoshihiro Maegaki (Division of Child Neurology, Department of Brain and Neurosciences, School of Medicine, Faculty of Medicine, Tottori University, Tottori, Japan.)
[IO1-02]Two cases of Phelan-McDermid syndrome showing ventriculomegaly with deformity of the lateral ventricles on head MRI
○Ken Imai1,2, Eri Takeshita2, Haruna Yokoyama3, Aki kawakami4, Kenatarou Fukuda5, Sahoko Miyama1 (1.Department of Neurology, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan, 2.Department of Neuropediatrics, National Center of Neurology and Psychiatry, Tokyo, Japan, 3.Department of Pediatrics, Japanese Red Cross Musashino Hospital, Tokyo, Japan, 4.Department of Home Medical Care, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan, 5.Department of Clinical Genetics, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan)
[IO1-03]The number of individuals with genetic neuromuscular disorders in Japan: A study using the National Database
○Yuko Shimizu-Motohashi1, Takashi Furuno2,3, Kentaro Usuda2, Naoaki Kuroda2, Kenjiro Imai3, Takehiro Sugiyama3, Hiroyasu Iso3, Hirofumi Komaki1,4 (1.Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan, 2.Department of Public Mental Health Research, National Center of Neurology and Psychiatry, Tokyo, Japan, 3.Bureau of International Health Cooperation, National Center for Global Health and Medicine, Tokyo, Japan, 4.Translational Medical Center, National Center of Neurology and Psychiatry, Tokyo, Japan)
[IO1-04]Imaging analysis of masticatory muscles to detect disease-specific abnormalities in hereditary muscle diseases
○Yoshihiko Saito1,2, Wakako Yoshioka1, Nobuyuki Eura1,3, Shinichiro Hayashi1, Satoru Noguchi1, Ichizo Nishino1 (1.Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan, 2.Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan, 3.Department of Neurology, Nara Medical University School of Medicine, Nara, Japan)
[IO1-05]Exploration of strategies to convert human microglia to neurons
○Eriko Hatai1,2, Kanae Matsuda1, Taito Matsuda1, Ikumi Katano3, Riichi Takahashi3, Mamoru Ito3, Yasunari Sakai2, Shouichi Ohga2, Kinichi Nakashima1 (1.Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan, 2.Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan, 3.Central Institute for Experimental Medicine and Life Science, Kanagawa, Japan)
[IO1-06]A Case Report of a 6-Year-Old Boy with Cerebellar Ataxia and Mild Intellectual Disability Due to COQ8A Gene Mutation
○Hirotaka Motoi1, Yusuke Sakata1, Yuki Minamisawa1, Yukiko Kuroda2, Yoshihiro Watanabe1 (1.Department of Pediatrics, Yokohama city university, Kanagawa, Japan, 2.Department of Genetics, Kanagawa children’s medical center, Kanagawa, Japan)