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Yoko Aoki

Showing results (171-180 of 255) with videos related to

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Emerging Infectious Diseases|October 26, 2012
Epidemic myalgia in adults associated with human parechovirus type 3 infection, Yamagata, Japan, 2008Katsumi Mizuta, Makoto Kuroda, Masayuki Kurimura, et al.
Brain & Development|February 4, 2018
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutationHaruhiko Nakamura, Mitsugu Uematsu, Yurika Numata-Uematsu, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 25, 2013
Epidemic myalgia associated with human parechovirus type 3 infection among adults occurs during an outbreak among children: findings from Yamagata, Japan, in 2011Katsumi Mizuta, Tatsushi Yamakawa, Hikaru Nagasawa, et al.
Medicine|February 11, 2022
A rare pediatric case of McCune-Albright syndrome with acute visual disturbance: Case reportHiroshi Ninomiya, Michio Ozeki, Akifumi Nozawa, et al.
Clinical Neurology and Neurosurgery|August 21, 2016
Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutationAyumi Nishiyama, Hitoshi Warita, Toshiaki Takahashi, et al.
Blood Advances|January 12, 2022
Phenotypic heterogeneity in individuals with MECOM variants in 2 familiesTetsuya Niihori, Reo Tanoshima, Yoji Sasahara, et al.
Human Mutation|February 2, 2006
Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemiaShigeo Kure, Kumi Kato, Agirios Dinopoulos, et al.
Pediatric Research|April 17, 2008
Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptorKanako Kojima-ishii, Shigeo Kure, Akiko Ichinohe, et al.
International Cancer Conference Journal|March 31, 2025
Coexisting germline variants of <i>MLH1</i> and <i>MSH6</i> in a patient with Lynch syndrome who had uterine and ovarian cancerSho Umegaki, Masanobu Takahashi, Junko Hasegawa-Minato, et al.
Molecular Genetics and Metabolism|April 3, 2004
Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemiaXue Yang, Osamu Sakamoto, Yoichi Matsubara, et al.
Pageof 26

Showing results (171-180 of 255) with videos related to

Sort By:
Pageof 26
Emerging Infectious Diseases|October 26, 2012
Epidemic myalgia in adults associated with human parechovirus type 3 infection, Yamagata, Japan, 2008Katsumi Mizuta, Makoto Kuroda, Masayuki Kurimura, et al.
Brain & Development|February 4, 2018
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutationHaruhiko Nakamura, Mitsugu Uematsu, Yurika Numata-Uematsu, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 25, 2013
Epidemic myalgia associated with human parechovirus type 3 infection among adults occurs during an outbreak among children: findings from Yamagata, Japan, in 2011Katsumi Mizuta, Tatsushi Yamakawa, Hikaru Nagasawa, et al.
Medicine|February 11, 2022
A rare pediatric case of McCune-Albright syndrome with acute visual disturbance: Case reportHiroshi Ninomiya, Michio Ozeki, Akifumi Nozawa, et al.
Clinical Neurology and Neurosurgery|August 21, 2016
Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutationAyumi Nishiyama, Hitoshi Warita, Toshiaki Takahashi, et al.
Blood Advances|January 12, 2022
Phenotypic heterogeneity in individuals with MECOM variants in 2 familiesTetsuya Niihori, Reo Tanoshima, Yoji Sasahara, et al.
Human Mutation|February 2, 2006
Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemiaShigeo Kure, Kumi Kato, Agirios Dinopoulos, et al.
Pediatric Research|April 17, 2008
Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptorKanako Kojima-ishii, Shigeo Kure, Akiko Ichinohe, et al.
International Cancer Conference Journal|March 31, 2025
Coexisting germline variants of <i>MLH1</i> and <i>MSH6</i> in a patient with Lynch syndrome who had uterine and ovarian cancerSho Umegaki, Masanobu Takahashi, Junko Hasegawa-Minato, et al.
Molecular Genetics and Metabolism|April 3, 2004
Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemiaXue Yang, Osamu Sakamoto, Yoichi Matsubara, et al.
Pageof 26