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Ken Inoue

Showing results (131-140 of 486) with videos related to

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Clinical Endoscopy|June 12, 2026
MANTIS closure device-based rotate-suturing technique by both the operator and assistant for colorectal endoscopic submucosal dissection defectsNaohisa Yoshida, Hardesh Dhillon, Ken Inoue, et al.
Gut and Liver|December 6, 2018
Blue Laser Imaging, Blue Light Imaging, and Linked Color Imaging for the Detection and Characterization of Colorectal TumorsNaohisa Yoshida, Osamu Dohi, Ken Inoue, et al.
Brain & Development|April 13, 2015
Comment on "delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: report of a new case and review of the literature" by Azzolini S et al. Brain & Development 2014;36:716-720Toshiyuki Yamamoto, Jun-Ichi Takanashi, Kenji Kurosawa, et al.
Frontiers in Neuroscience|August 4, 2018
Implications of Systemic Inflammation and Periodontitis for Major DepressionSadayuki Hashioka, Ken Inoue, Maiko Hayashida, et al.
European Journal of Medical Genetics|February 8, 2022
A familial 2p14 microdeletion disrupting actin-related protein 2 and Ras-related protein Rab-1A genes with intellectual disability and language impairmentKenshiro Tabata, Akihiko Ishiyama, Yoko Nakamura, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 6, 2009
The P86L common allele of CALHM1 does not influence risk for Alzheimer disease in Japanese cohortsKen Inoue, Noriko Tanaka, Fumio Yamashita, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2007
A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese familyKyoko Takano, Eiji Nakagawa, Ken Inoue, et al.
International Maritime Health|April 8, 2021
The realities of a new era featuring truly international lectures during the prolonged COVID-19 pandemic: international collaboration and advances in medical educationKen Inoue, Nailya Chaizhunusova, Nursultan Seksenbayev, et al.
Genomics|August 6, 2002
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autismTakanori Yamagata, Swaroop Aradhya, Masato Mori, et al.
Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica|October 16, 2009
[Causative factors as cues for addressing the rapid increase in suicide in Mie Prefecture, Japan: comparison of trends between 1996-2002 and 1989-1995]Ken Inoue, Tatsushige Fukunaga, Shuntaro Abe, et al.
Pageof 49

Showing results (131-140 of 486) with videos related to

Sort By:
Pageof 49
Clinical Endoscopy|June 12, 2026
MANTIS closure device-based rotate-suturing technique by both the operator and assistant for colorectal endoscopic submucosal dissection defectsNaohisa Yoshida, Hardesh Dhillon, Ken Inoue, et al.
Gut and Liver|December 6, 2018
Blue Laser Imaging, Blue Light Imaging, and Linked Color Imaging for the Detection and Characterization of Colorectal TumorsNaohisa Yoshida, Osamu Dohi, Ken Inoue, et al.
Brain & Development|April 13, 2015
Comment on "delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: report of a new case and review of the literature" by Azzolini S et al. Brain & Development 2014;36:716-720Toshiyuki Yamamoto, Jun-Ichi Takanashi, Kenji Kurosawa, et al.
Frontiers in Neuroscience|August 4, 2018
Implications of Systemic Inflammation and Periodontitis for Major DepressionSadayuki Hashioka, Ken Inoue, Maiko Hayashida, et al.
European Journal of Medical Genetics|February 8, 2022
A familial 2p14 microdeletion disrupting actin-related protein 2 and Ras-related protein Rab-1A genes with intellectual disability and language impairmentKenshiro Tabata, Akihiko Ishiyama, Yoko Nakamura, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 6, 2009
The P86L common allele of CALHM1 does not influence risk for Alzheimer disease in Japanese cohortsKen Inoue, Noriko Tanaka, Fumio Yamashita, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2007
A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese familyKyoko Takano, Eiji Nakagawa, Ken Inoue, et al.
International Maritime Health|April 8, 2021
The realities of a new era featuring truly international lectures during the prolonged COVID-19 pandemic: international collaboration and advances in medical educationKen Inoue, Nailya Chaizhunusova, Nursultan Seksenbayev, et al.
Genomics|August 6, 2002
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autismTakanori Yamagata, Swaroop Aradhya, Masato Mori, et al.
Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica|October 16, 2009
[Causative factors as cues for addressing the rapid increase in suicide in Mie Prefecture, Japan: comparison of trends between 1996-2002 and 1989-1995]Ken Inoue, Tatsushige Fukunaga, Shuntaro Abe, et al.
Pageof 49