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BMJ Case Reports|October 13, 2019
Nutcracker syndrome complicated with intestinal malrotationYosuke Nishio, Yoshihiko Kawano, Shinya Hara
Frontiers in Oncology|June 17, 2024
MYCN in human development and diseasesYosuke Nishio, Kohji Kato, Hisashi Oishi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|July 14, 2018
A case of refractory cytomegalovirus-related thrombocytopenia that achieved complete remission without antiviral therapyYosuke Nishio, Yoshihiko Kawano, Jun-Ichi Kawada, et al.
Brain & Development|May 8, 2004
Clinical and electroencephalographic characteristics of children with febrile seizures plusKatsuhiro Kobayashi, Yoko Ohtsuka, Iori Ohmori, et al.
Human Genome Variation|February 21, 2024
A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variantHiromi Nyuzuki, Junichi Ozawa, Keisuke Nagasaki, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 29, 2025
Gerstmann-Sträussler-Scheinker disease mimicking primary progressive multiple sclerosis: A case with positive oligoclonal bandsMiwa Ito, Hiroki Masuda, Marie Morooka, et al.
Journal of Human Genetics|February 12, 2025
Novel FBN1 intron variant causes isolated ectopia lentis via in-frame exon skippingNorihiro Shimizu, Yoichi Mashimo, Hirotaka Yokouchi, et al.
Biochemical and Biophysical Research Communications|February 8, 2012
O-linked-N-acetylglucosamine modification of mammalian Notch receptors by an atypical O-GlcNAc transferase Eogt1Yuta Sakaidani, Naoki Ichiyanagi, Chika Saito, et al.
Journal of Biotechnology|March 12, 2010
Dynamic modeling of Escherichia coli metabolic and regulatory systems for amino-acid productionYoshihiro Usuda, Yosuke Nishio, Shintaro Iwatani, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 22, 2024
Pathophysiological significance of the p.E31G variant in RAC1 responsible for a neurodevelopmental disorder with microcephalyMasashi Nishikawa, Shin Hayashi, Atsushi Nakayama, et al.
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