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Iori Ohmori

Showing results (1-10 of 48) with videos related to

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Neurochemistry International|October 12, 2020
Scn1a and Cacna1a mutations mutually alter their original phenotypes in ratsIori Ohmori, Kiyoka Kobayashi, Mamoru Ouchida
Epileptic Disorders : International Epilepsy Journal with Videotape|August 26, 2011
Dravet syndrome with an exceptionally good seizure outcome in two adolescentsKatsuhiro Kobayashi, Iori Ohmori, Mamoru Ouchida, et al.
Brain & Development|July 29, 2019
Action of antiepileptic drugs on neuronsKatsuhiro Kobayashi, Fumika Endoh, Iori Ohmori, et al.
Experimental Animals|November 15, 2019
Poor mother-offspring relationships in rats with Cacna1a mutationNozomi Kawakami, Kiyoka Kobayashi, Ayumu Nishimura, et al.
Neuroscience Letters|June 16, 2005
Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizuresMinako Ito, Iori Ohmori, Tomoyuki Nakahori, et al.
Biochemical and Biophysical Research Communications|June 27, 2002
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancyIori Ohmori, Mamoru Ouchida, Yoko Ohtsuka, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 21, 2014
Action potentials contribute to epileptic high-frequency oscillations recorded with electrodes remote from neuronsKatsuhiro Kobayashi, Tomoyuki Akiyama, Iori Ohmori, et al.
Epilepsia|May 9, 2022
Novel animal model of combined generalized and focal epilepsyIori Ohmori, Mamoru Ouchida, Masakazu Shinohara, et al.
Brain & Development|August 9, 2003
Paroxysmal movement disorders in severe myoclonic epilepsy in infancyYoko Ohtsuka, Iori Ohmori, Tatsuya Ogino, et al.
Neurobiology of Disease|November 13, 2022
Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrainIori Ohmori, Mamoru Ouchida, Hirohiko Imai, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Neurochemistry International|October 12, 2020
Scn1a and Cacna1a mutations mutually alter their original phenotypes in ratsIori Ohmori, Kiyoka Kobayashi, Mamoru Ouchida
Epileptic Disorders : International Epilepsy Journal with Videotape|August 26, 2011
Dravet syndrome with an exceptionally good seizure outcome in two adolescentsKatsuhiro Kobayashi, Iori Ohmori, Mamoru Ouchida, et al.
Brain & Development|July 29, 2019
Action of antiepileptic drugs on neuronsKatsuhiro Kobayashi, Fumika Endoh, Iori Ohmori, et al.
Experimental Animals|November 15, 2019
Poor mother-offspring relationships in rats with Cacna1a mutationNozomi Kawakami, Kiyoka Kobayashi, Ayumu Nishimura, et al.
Neuroscience Letters|June 16, 2005
Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizuresMinako Ito, Iori Ohmori, Tomoyuki Nakahori, et al.
Biochemical and Biophysical Research Communications|June 27, 2002
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancyIori Ohmori, Mamoru Ouchida, Yoko Ohtsuka, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 21, 2014
Action potentials contribute to epileptic high-frequency oscillations recorded with electrodes remote from neuronsKatsuhiro Kobayashi, Tomoyuki Akiyama, Iori Ohmori, et al.
Epilepsia|May 9, 2022
Novel animal model of combined generalized and focal epilepsyIori Ohmori, Mamoru Ouchida, Masakazu Shinohara, et al.
Brain & Development|August 9, 2003
Paroxysmal movement disorders in severe myoclonic epilepsy in infancyYoko Ohtsuka, Iori Ohmori, Tatsuya Ogino, et al.
Neurobiology of Disease|November 13, 2022
Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrainIori Ohmori, Mamoru Ouchida, Hirohiko Imai, et al.
Pageof 5