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Yushi Inoue

Showing results (171-180 of 183) with videos related to

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Brain Communications|November 16, 2022
Ictal direct current shifts contribute to defining the core ictal focus in epilepsy surgeryMitsuyoshi Nakatani, Morito Inouchi, Masako Daifu-Kobayashi, et al.
Molecular Medicine (Cambridge, Mass.)|March 1, 2019
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypesAnaïs Begemann, Mario A Acuña, Markus Zweier, et al.
Nature Communications|July 23, 2014
Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizuresNaoko H Tomioka, Hiroki Yasuda, Hiroyuki Miyamoto, et al.
Brain & Development|March 16, 2013
Clinical analysis of catastrophic epilepsy in infancy and early childhood: results of the Far-East Asia Catastrophic Epilepsy (FACE) study groupHirokazu Oguni, Taisuke Otsuki, Katsuhiro Kobayashi, et al.
Communications Biology|September 4, 2018
Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in miceIkuo Ogiwara, Hiroyuki Miyamoto, Tetsuya Tatsukawa, et al.
Scientific Reports|May 17, 2022
CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainateToshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo, et al.
Annals of Clinical and Translational Neurology|June 13, 2020
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disordersToshimitsu Suzuki, Toshifumi Suzuki, Matthieu Raveau, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 4, 2022
Burden of seizures and comorbidities in patients with epilepsy: a survey based on the tertiary hospital-based Epilepsy Syndrome Registry in JapanYushi Inoue, Shin-Ichiro Hamano, Masaharu Hayashi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 16, 2021
Current medico-psycho-social conditions of patients with West syndrome in JapanShinsaku Yoshitomi, Shin-Ichiro Hamano, Masaharu Hayashi, et al.
Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.
Pageof 19

Showing results (171-180 of 183) with videos related to

Sort By:
Pageof 19
Brain Communications|November 16, 2022
Ictal direct current shifts contribute to defining the core ictal focus in epilepsy surgeryMitsuyoshi Nakatani, Morito Inouchi, Masako Daifu-Kobayashi, et al.
Molecular Medicine (Cambridge, Mass.)|March 1, 2019
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypesAnaïs Begemann, Mario A Acuña, Markus Zweier, et al.
Nature Communications|July 23, 2014
Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizuresNaoko H Tomioka, Hiroki Yasuda, Hiroyuki Miyamoto, et al.
Brain & Development|March 16, 2013
Clinical analysis of catastrophic epilepsy in infancy and early childhood: results of the Far-East Asia Catastrophic Epilepsy (FACE) study groupHirokazu Oguni, Taisuke Otsuki, Katsuhiro Kobayashi, et al.
Communications Biology|September 4, 2018
Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in miceIkuo Ogiwara, Hiroyuki Miyamoto, Tetsuya Tatsukawa, et al.
Scientific Reports|May 17, 2022
CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainateToshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo, et al.
Annals of Clinical and Translational Neurology|June 13, 2020
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disordersToshimitsu Suzuki, Toshifumi Suzuki, Matthieu Raveau, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 4, 2022
Burden of seizures and comorbidities in patients with epilepsy: a survey based on the tertiary hospital-based Epilepsy Syndrome Registry in JapanYushi Inoue, Shin-Ichiro Hamano, Masaharu Hayashi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 16, 2021
Current medico-psycho-social conditions of patients with West syndrome in JapanShinsaku Yoshitomi, Shin-Ichiro Hamano, Masaharu Hayashi, et al.
Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.
Pageof 19