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Gen Sobue

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Journal of Neurology, Neurosurgery, and Psychiatry|December 18, 2012
Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2BToshiaki Takahashi, Masashi Aoki, Naoki Suzuki, et al.
Human Molecular Genetics|June 14, 2011
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Atsushi Takahashi, Michiaki Kubo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTNHazuki Watanabe, Naoki Atsuta, Akihiro Hirakawa, et al.
Journal of Neurology|January 20, 2020
Cognitive and behavioral status in Japanese ALS patients: a multicenter studyYasuhiro Watanabe, Joost Raaphorst, Yuishin Izumi, et al.
Neurobiology of Aging|January 18, 2022
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Naoki Atsuta, et al.
Nature Genetics|July 24, 2019
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion diseaseJun Sone, Satomi Mitsuhashi, Atsushi Fujita, et al.
International Psychogeriatrics|May 1, 2025
Nation-wide Japanese FTD consortium FTLD-J: Utility of case review meetingsShunsuke Sato, Kohji Mori, Michihito Masuda, et al.
Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.
The Lancet Regional Health. Western Pacific|September 29, 2025
Pan-Asian consortium for treatment and research in ALS (PACTALS) guidelines for management of amyotrophic lateral sclerosisSteve Vucic, Nortina Shahrizaila, Osamu Kano, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Pageof 58

Showing results (561-570 of 576) with videos related to

Sort By:
Pageof 58
Journal of Neurology, Neurosurgery, and Psychiatry|December 18, 2012
Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2BToshiaki Takahashi, Masashi Aoki, Naoki Suzuki, et al.
Human Molecular Genetics|June 14, 2011
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Atsushi Takahashi, Michiaki Kubo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2016
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTNHazuki Watanabe, Naoki Atsuta, Akihiro Hirakawa, et al.
Journal of Neurology|January 20, 2020
Cognitive and behavioral status in Japanese ALS patients: a multicenter studyYasuhiro Watanabe, Joost Raaphorst, Yuishin Izumi, et al.
Neurobiology of Aging|January 18, 2022
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Naoki Atsuta, et al.
Nature Genetics|July 24, 2019
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion diseaseJun Sone, Satomi Mitsuhashi, Atsushi Fujita, et al.
International Psychogeriatrics|May 1, 2025
Nation-wide Japanese FTD consortium FTLD-J: Utility of case review meetingsShunsuke Sato, Kohji Mori, Michihito Masuda, et al.
Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.
The Lancet Regional Health. Western Pacific|September 29, 2025
Pan-Asian consortium for treatment and research in ALS (PACTALS) guidelines for management of amyotrophic lateral sclerosisSteve Vucic, Nortina Shahrizaila, Osamu Kano, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Pageof 58