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

Yusuke Sakiyama

Showing results (11-20 of 58) with videos related to

Pageof 6
Sort By:
Annals of Neurology|September 10, 2011
A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emiaYuji Okamoto, Itsuro Higuchi, Yusuke Sakiyama, et al.
Clinical Neurology and Neurosurgery|December 21, 2012
DYSF mutation analysis in a group of Chinese patients with dysferlinopathyZhe Zhao, Jing Hu, Yusuke Sakiyama, et al.
Journal of Neurology|July 30, 2022
Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series studyJun-Hui Yuan, Yujiro Higuchi, Akihiro Hashiguchi, et al.
ACS Nano|October 13, 2017
High-Speed Atomic Force Microscopy Visualization of the Dynamics of the Multienzyme Fatty Acid SynthaseFriederike M C Benning, Yusuke Sakiyama, Adam Mazur, et al.
Internal Medicine (Tokyo, Japan)|December 16, 2015
Clinical and Electron Microscopic Findings in Two Patients with Mitochondrial Myopathy Associated with Episodic Hyper-creatine Kinase-emiaSatoshi Nozuma, Yuji Okamoto, Itsuro Higuchi, et al.
ACS Central Science|August 31, 2018
Gating Protein Transport in Solid State Nanopores by Single Molecule RecognitionGustav Emilsson, Yusuke Sakiyama, Bita Malekian, et al.
Frontiers in Neurology|February 13, 2023
Gene panel analysis of 119 index patients with suspected periodic paralysis in JapanJun-Hui Yuan, Yujiro Higuchi, Akihiro Hashiguchi, et al.
Journal of Clinical Pathology|April 6, 2013
Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutationJun-Hui Yuan, Yusuke Sakiyama, Itsuro Higuchi, et al.
Journal of the Peripheral Nervous System : JPNS|March 26, 2013
Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IEJunhui Yuan, Yujiro Higuchi, Tatsui Nagado, et al.
Neurology|April 19, 2013
Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutationJunhui Yuan, Eiji Matsuura, Yujiro Higuchi, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Annals of Neurology|September 10, 2011
A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emiaYuji Okamoto, Itsuro Higuchi, Yusuke Sakiyama, et al.
Clinical Neurology and Neurosurgery|December 21, 2012
DYSF mutation analysis in a group of Chinese patients with dysferlinopathyZhe Zhao, Jing Hu, Yusuke Sakiyama, et al.
Journal of Neurology|July 30, 2022
Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series studyJun-Hui Yuan, Yujiro Higuchi, Akihiro Hashiguchi, et al.
ACS Nano|October 13, 2017
High-Speed Atomic Force Microscopy Visualization of the Dynamics of the Multienzyme Fatty Acid SynthaseFriederike M C Benning, Yusuke Sakiyama, Adam Mazur, et al.
Internal Medicine (Tokyo, Japan)|December 16, 2015
Clinical and Electron Microscopic Findings in Two Patients with Mitochondrial Myopathy Associated with Episodic Hyper-creatine Kinase-emiaSatoshi Nozuma, Yuji Okamoto, Itsuro Higuchi, et al.
ACS Central Science|August 31, 2018
Gating Protein Transport in Solid State Nanopores by Single Molecule RecognitionGustav Emilsson, Yusuke Sakiyama, Bita Malekian, et al.
Frontiers in Neurology|February 13, 2023
Gene panel analysis of 119 index patients with suspected periodic paralysis in JapanJun-Hui Yuan, Yujiro Higuchi, Akihiro Hashiguchi, et al.
Journal of Clinical Pathology|April 6, 2013
Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutationJun-Hui Yuan, Yusuke Sakiyama, Itsuro Higuchi, et al.
Journal of the Peripheral Nervous System : JPNS|March 26, 2013
Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IEJunhui Yuan, Yujiro Higuchi, Tatsui Nagado, et al.
Neurology|April 19, 2013
Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutationJunhui Yuan, Eiji Matsuura, Yujiro Higuchi, et al.
Pageof 6