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

P Takahashi

Showing results (41-50 of 148) with videos related to

Pageof 15
Sort By:
Rinsho Shinkeigaku = Clinical Neurology|March 26, 2013
[A case of progressive ataxia and palatal tremor (PAPT) with ear clicks]Hiroyuki Sumikura, Tatsusada Okuno, Masanori P Takahashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 30, 2015
[A case of new-onset refractory status epilepticus (NORSE) with an autoimmune etiology]Teruyuki Ishikura, Tatsusada Okuno, Katsuya Araki, et al.
European Journal of Biochemistry|July 4, 2001
S1 proteins C2 and D2 are novel hnRNPs similar to the transcriptional repressor, CArG box motif-binding factor AA Inoue, A Omori, S Ichinose, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 28, 2011
[A survey of cardiologists, diabetologists, gynecologists and ophthalmologists practicing in Osaka on the medical consultation behaviors of myotonic dystrophy patients]Tsuyoshi Matsumura, Takashi Kimura, Yosuke Kokunai, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 24, 2015
[A case of Möbius syndrome with congenital facial palsy and supranuclear oculomotor palsy]Mitsuru Furuta, Masahito Mihara, Yasuyoshi Kimura, et al.
Cell Structure and Function|April 1, 1997
Association of hnRNP S1 proteins C2 and D2 with vimentin intermediate filamentsK Tsugawa, K P Takahashi, T Watanabe, et al.
Journal of the Neurological Sciences|April 3, 2020
Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patientsMaki Nakaza, Yuri Kitamura, Mitsuru Furuta, et al.
Neuromuscular Disorders : NMD|July 15, 2020
Mutation spectrum and health status in skeletal muscle channelopathies in JapanRyogen Sasaki, Maki Nakaza, Mitsuru Furuta, et al.
BMC Neurology|February 15, 2022
Quality of life and subjective symptom impact in Japanese patients with myotonic dystrophy type 1Haruo Fujino, Toshio Saito, Masanori P Takahashi, et al.
Neuroscience Letters|November 25, 2000
The expression of ion channel mRNAs in skeletal muscles from patients with myotonic muscular dystrophyT Kimura, M P Takahashi, Y Okuda, et al.
Pageof 15

Showing results (41-50 of 148) with videos related to

Sort By:
Pageof 15
Rinsho Shinkeigaku = Clinical Neurology|March 26, 2013
[A case of progressive ataxia and palatal tremor (PAPT) with ear clicks]Hiroyuki Sumikura, Tatsusada Okuno, Masanori P Takahashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 30, 2015
[A case of new-onset refractory status epilepticus (NORSE) with an autoimmune etiology]Teruyuki Ishikura, Tatsusada Okuno, Katsuya Araki, et al.
European Journal of Biochemistry|July 4, 2001
S1 proteins C2 and D2 are novel hnRNPs similar to the transcriptional repressor, CArG box motif-binding factor AA Inoue, A Omori, S Ichinose, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 28, 2011
[A survey of cardiologists, diabetologists, gynecologists and ophthalmologists practicing in Osaka on the medical consultation behaviors of myotonic dystrophy patients]Tsuyoshi Matsumura, Takashi Kimura, Yosuke Kokunai, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 24, 2015
[A case of Möbius syndrome with congenital facial palsy and supranuclear oculomotor palsy]Mitsuru Furuta, Masahito Mihara, Yasuyoshi Kimura, et al.
Cell Structure and Function|April 1, 1997
Association of hnRNP S1 proteins C2 and D2 with vimentin intermediate filamentsK Tsugawa, K P Takahashi, T Watanabe, et al.
Journal of the Neurological Sciences|April 3, 2020
Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patientsMaki Nakaza, Yuri Kitamura, Mitsuru Furuta, et al.
Neuromuscular Disorders : NMD|July 15, 2020
Mutation spectrum and health status in skeletal muscle channelopathies in JapanRyogen Sasaki, Maki Nakaza, Mitsuru Furuta, et al.
BMC Neurology|February 15, 2022
Quality of life and subjective symptom impact in Japanese patients with myotonic dystrophy type 1Haruo Fujino, Toshio Saito, Masanori P Takahashi, et al.
Neuroscience Letters|November 25, 2000
The expression of ion channel mRNAs in skeletal muscles from patients with myotonic muscular dystrophyT Kimura, M P Takahashi, Y Okuda, et al.
Pageof 15