Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ko Sahashi

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|August 10, 2004
[Markedly improving sarcoid cervical myelopathy after the diagnostic treatment of prednisolone, associated with highly spondylotic spines]Kazunori Hirose, Akira Hoshino, Takaaki Fukuoka, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 23, 2013
[Compound heterozygous mutations in the muscle chloride channel gene (CLCN1) in a Japanese family with Thomsen's disease]Ryogen Sasaki, Masanori P Takahashi, Yosuke Kokunai, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 6, 2008
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathologyAkira Hoshino, Yasushi Iwasaki, Masayuki Izumi, et al.
Neuroscience Letters|May 24, 2012
A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravisYosuke Kokunai, Keigo Goto, Tomoya Kubota, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|November 5, 2010
Abnormal myocardial energy-production state in mitochondrial cardiomyopathy and acute response to L-arginine infusion. C-11 acetate kinetics revealed by positron emission tomographyKenichiro Arakawa, Takashi Kudo, Masamichi Ikawa, et al.
Scientific Reports|September 11, 2015
Collagen Q and anti-MuSK autoantibody competitively suppress agrin/LRP4/MuSK signalingKenji Otsuka, Mikako Ito, Bisei Ohkawara, et al.
Internal Medicine (Tokyo, Japan)|January 14, 2005
Gastric dysmotility associated with accumulation of mitochondrial A3243G mutation in the stomachAkihiro Fujii, Makoto Yoneda, Masahiro Ohtani, et al.
Journal of Human Genetics|April 20, 2012
Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophyYoshihiro Yamashita, Tohru Matsuura, Jun Shinmi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2007
Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese populationHiroaki Nozaki, Takeshi Ikeuchi, Akio Kawakami, et al.
Mitochondrion|January 13, 2010
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutationsYutaka Nishigaki, Hitomi Ueno, Jorida Coku, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|August 10, 2004
[Markedly improving sarcoid cervical myelopathy after the diagnostic treatment of prednisolone, associated with highly spondylotic spines]Kazunori Hirose, Akira Hoshino, Takaaki Fukuoka, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 23, 2013
[Compound heterozygous mutations in the muscle chloride channel gene (CLCN1) in a Japanese family with Thomsen's disease]Ryogen Sasaki, Masanori P Takahashi, Yosuke Kokunai, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 6, 2008
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathologyAkira Hoshino, Yasushi Iwasaki, Masayuki Izumi, et al.
Neuroscience Letters|May 24, 2012
A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravisYosuke Kokunai, Keigo Goto, Tomoya Kubota, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|November 5, 2010
Abnormal myocardial energy-production state in mitochondrial cardiomyopathy and acute response to L-arginine infusion. C-11 acetate kinetics revealed by positron emission tomographyKenichiro Arakawa, Takashi Kudo, Masamichi Ikawa, et al.
Scientific Reports|September 11, 2015
Collagen Q and anti-MuSK autoantibody competitively suppress agrin/LRP4/MuSK signalingKenji Otsuka, Mikako Ito, Bisei Ohkawara, et al.
Internal Medicine (Tokyo, Japan)|January 14, 2005
Gastric dysmotility associated with accumulation of mitochondrial A3243G mutation in the stomachAkihiro Fujii, Makoto Yoneda, Masahiro Ohtani, et al.
Journal of Human Genetics|April 20, 2012
Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophyYoshihiro Yamashita, Tohru Matsuura, Jun Shinmi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2007
Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese populationHiroaki Nozaki, Takeshi Ikeuchi, Akio Kawakami, et al.
Mitochondrion|January 13, 2010
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutationsYutaka Nishigaki, Hitomi Ueno, Jorida Coku, et al.
Pageof 3