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

I Yabe

Showing results (21-30 of 51) with videos related to

Pageof 6
Sort By:
Journal of Medical Genetics|November 6, 2001
Twenty CAG repeats are sufficient to cause the SCA6 phenotypeK Komeichi, H Sasaki, I Yabe, et al.
Journal of Neuroimmunology|August 11, 2001
Genetic polymorphisms of IL-1beta and IL-1 receptor antagonist in association with multiple sclerosis in Japanese patientsM Niino, S Kikuchi, T Fukazawa, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 12, 2002
An examination of the association between beta2 adrenergic receptor polymorphisms and multiple sclerosisM Niino, S Kikuchi, R Miyagishi, et al.
Journal of Medical Genetics|August 6, 2002
Spastin gene mutation in Japanese with hereditary spastic paraplegiaI Yabe, H Sasaki, K Tashiro, et al.
Neurology|February 26, 2000
Dissociation of smooth pursuit and vestibulo-ocular reflex cancellation in SCA-6N Takeichi, K Fukushima, H Sasaki, et al.
Journal of the Neurological Sciences|September 1, 2000
Vitamin D receptor gene polymorphism in multiple sclerosis and the association with HLA class II allelesM Niino, T Fukazawa, I Yabe, et al.
Nihon Igaku Hoshasen Gakkai Zasshi. Nippon Acta Radiologica|January 1, 1980
[Radiotherapy for carcinoma of the uterine cervix (author's transl)]Y Takegawa, H Kohnoike, N Watanabe, et al.
Nihon Igaku Hoshasen Gakkai Zasshi. Nippon Acta Radiologica|January 1, 1980
[Postoperative radiotherapy for carcinoma of the uterine cervix (author's transl)]Y Takegawa, N Watanabe, F Kohrai, et al.
Acta Radiologica. Oncology|January 1, 1981
Hodgkin's disease irradiated with the inverted-Y techniqueC E Mercke, I Yabe, T G Landberg, et al.
Journal of Medical Genetics|July 9, 2010
MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genesM Nakamura, I Yabe, A Sudo, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|November 6, 2001
Twenty CAG repeats are sufficient to cause the SCA6 phenotypeK Komeichi, H Sasaki, I Yabe, et al.
Journal of Neuroimmunology|August 11, 2001
Genetic polymorphisms of IL-1beta and IL-1 receptor antagonist in association with multiple sclerosis in Japanese patientsM Niino, S Kikuchi, T Fukazawa, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 12, 2002
An examination of the association between beta2 adrenergic receptor polymorphisms and multiple sclerosisM Niino, S Kikuchi, R Miyagishi, et al.
Journal of Medical Genetics|August 6, 2002
Spastin gene mutation in Japanese with hereditary spastic paraplegiaI Yabe, H Sasaki, K Tashiro, et al.
Neurology|February 26, 2000
Dissociation of smooth pursuit and vestibulo-ocular reflex cancellation in SCA-6N Takeichi, K Fukushima, H Sasaki, et al.
Journal of the Neurological Sciences|September 1, 2000
Vitamin D receptor gene polymorphism in multiple sclerosis and the association with HLA class II allelesM Niino, T Fukazawa, I Yabe, et al.
Nihon Igaku Hoshasen Gakkai Zasshi. Nippon Acta Radiologica|January 1, 1980
[Radiotherapy for carcinoma of the uterine cervix (author's transl)]Y Takegawa, H Kohnoike, N Watanabe, et al.
Nihon Igaku Hoshasen Gakkai Zasshi. Nippon Acta Radiologica|January 1, 1980
[Postoperative radiotherapy for carcinoma of the uterine cervix (author's transl)]Y Takegawa, N Watanabe, F Kohrai, et al.
Acta Radiologica. Oncology|January 1, 1981
Hodgkin's disease irradiated with the inverted-Y techniqueC E Mercke, I Yabe, T G Landberg, et al.
Journal of Medical Genetics|July 9, 2010
MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genesM Nakamura, I Yabe, A Sudo, et al.
Pageof 6