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Hitoshi Osaka

Showing results (51-60 of 218) with videos related to

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The Journal of Comparative Neurology|October 24, 2003
Nicotinic acetylcholine receptor distribution in relation to spinal neurotransmission pathwaysImran Khan, Hitoshi Osaka, Shanaka Stanislaus, et al.
Brain & Development|December 3, 2019
Serum and cerebrospinal fluid cytokines in children with acute encephalopathyYuta Kawahara, Akira Morimoto, Yukiko Oh, et al.
Human Genome Variation|June 6, 2022
A TUBB4A Met363Thr variant in pediatric hypomyelination without atrophy of the basal gangliaMarina Hashiguchi, Yukifumi Monden, Yasuyuki Nozaki, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|April 8, 2017
Severe demyelination in a patient with a late infantile form of Niemann-Pick disease type CTsuyoshi Kodachi, Shizuko Matsumoto, Masashi Mizuguchi, et al.
Journal of Human Genetics|June 27, 2014
Causative novel PNKP mutations and concomitant PCDH15 mutations in a patient with microcephaly with early-onset seizures and developmental delay syndrome and hearing lossMitsuko Nakashima, Kyoko Takano, Hitoshi Osaka, et al.
Human Genome Variation|September 14, 2018
Mitochondrial DNA 3243A>T mutation in a patient with MELAS syndromeTakahiro Ikeda, Hitoshi Osaka, Hiroko Shimbo, et al.
Journal of Neurology|March 22, 2015
Sporadic infantile-onset spinocerebellar ataxia caused by missense mutations of the inositol 1,4,5-triphosphate receptor type 1 geneMasayuki Sasaki, Chihiro Ohba, Mizue Iai, et al.
Brain & Development|December 11, 2007
Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matterJun Tohyama, Noriyuki Akasaka, Hitoshi Osaka, et al.
JIMD Reports|July 13, 2013
A Japanese adult case of guanidinoacetate methyltransferase deficiencyTomoyuki Akiyama, Hitoshi Osaka, Hiroko Shimbo, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 15, 2015
Japanese familial case of myoclonus-dystonia syndrome with a splicing mutation in SGCETakahito Wada, Kyoko Takano, Yoshinori Tsurusaki, et al.
Pageof 22

Showing results (51-60 of 218) with videos related to

Sort By:
Pageof 22
The Journal of Comparative Neurology|October 24, 2003
Nicotinic acetylcholine receptor distribution in relation to spinal neurotransmission pathwaysImran Khan, Hitoshi Osaka, Shanaka Stanislaus, et al.
Brain & Development|December 3, 2019
Serum and cerebrospinal fluid cytokines in children with acute encephalopathyYuta Kawahara, Akira Morimoto, Yukiko Oh, et al.
Human Genome Variation|June 6, 2022
A TUBB4A Met363Thr variant in pediatric hypomyelination without atrophy of the basal gangliaMarina Hashiguchi, Yukifumi Monden, Yasuyuki Nozaki, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|April 8, 2017
Severe demyelination in a patient with a late infantile form of Niemann-Pick disease type CTsuyoshi Kodachi, Shizuko Matsumoto, Masashi Mizuguchi, et al.
Journal of Human Genetics|June 27, 2014
Causative novel PNKP mutations and concomitant PCDH15 mutations in a patient with microcephaly with early-onset seizures and developmental delay syndrome and hearing lossMitsuko Nakashima, Kyoko Takano, Hitoshi Osaka, et al.
Human Genome Variation|September 14, 2018
Mitochondrial DNA 3243A>T mutation in a patient with MELAS syndromeTakahiro Ikeda, Hitoshi Osaka, Hiroko Shimbo, et al.
Journal of Neurology|March 22, 2015
Sporadic infantile-onset spinocerebellar ataxia caused by missense mutations of the inositol 1,4,5-triphosphate receptor type 1 geneMasayuki Sasaki, Chihiro Ohba, Mizue Iai, et al.
Brain & Development|December 11, 2007
Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matterJun Tohyama, Noriyuki Akasaka, Hitoshi Osaka, et al.
JIMD Reports|July 13, 2013
A Japanese adult case of guanidinoacetate methyltransferase deficiencyTomoyuki Akiyama, Hitoshi Osaka, Hiroko Shimbo, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 15, 2015
Japanese familial case of myoclonus-dystonia syndrome with a splicing mutation in SGCETakahito Wada, Kyoko Takano, Yoshinori Tsurusaki, et al.
Pageof 22