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Hiroyuki Torisu

Showing results (61-70 of 67) with videos related to

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Neurology. Clinical Practice|November 29, 2021
Neurodevelopmental Outcomes of High-Risk Preterm Infants: A Prospective Study in JapanMichiko Torio, Mariko Iwayama, Toru Sawano, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|July 4, 2024
An N-terminal and ankyrin repeat domain interactome of Shank3 identifies the protein complex with the splicing regulator Nono in miceSayaka Okuzono, Fumihiko Fujii, Daiki Setoyama, et al.
Epilepsia Open|March 29, 2018
Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in <i>NF1</i> and <i>MAGEL2</i>Satoshi Akamine, Noriaki Sagata, Yasunari Sakai, et al.
Brain & Development|November 28, 2009
Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, JapanHiroyuki Torisu, Ryutaro Kira, Yoshito Ishizaki, et al.
Clinical Immunology (Orlando, Fla.)|September 7, 2023
Heterogeneity and mitochondrial vulnerability configurate the divergent immunoreactivity of human induced microglia-like cellsKousuke Yonemoto, Fumihiko Fujii, Ryoji Taira, et al.
Seizure|June 3, 2019
PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesiaAkihisa Okumura, Keiko Shimojima, Hirokazu Kurahashi, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Neurology. Clinical Practice|November 29, 2021
Neurodevelopmental Outcomes of High-Risk Preterm Infants: A Prospective Study in JapanMichiko Torio, Mariko Iwayama, Toru Sawano, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|July 4, 2024
An N-terminal and ankyrin repeat domain interactome of Shank3 identifies the protein complex with the splicing regulator Nono in miceSayaka Okuzono, Fumihiko Fujii, Daiki Setoyama, et al.
Epilepsia Open|March 29, 2018
Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in <i>NF1</i> and <i>MAGEL2</i>Satoshi Akamine, Noriaki Sagata, Yasunari Sakai, et al.
Brain & Development|November 28, 2009
Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, JapanHiroyuki Torisu, Ryutaro Kira, Yoshito Ishizaki, et al.
Clinical Immunology (Orlando, Fla.)|September 7, 2023
Heterogeneity and mitochondrial vulnerability configurate the divergent immunoreactivity of human induced microglia-like cellsKousuke Yonemoto, Fumihiko Fujii, Ryoji Taira, et al.
Seizure|June 3, 2019
PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesiaAkihisa Okumura, Keiko Shimojima, Hirokazu Kurahashi, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
Pageof 7