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

M Suehara

Showing results (21-30 of 33) with videos related to

Pageof 4
Sort By:
Annals of Neurology|August 17, 2001
Frameshift mutation in the collagen VI gene causes Ullrich's diseaseI Higuchi, T Shiraishi, T Hashiguchi, et al.
Acta Neuropathologica|January 1, 1989
Germanium myopathy: clinical and experimental pathological studiesI Higuchi, S Izumo, M Kuriyama, et al.
AIDS Research and Human Retroviruses|June 1, 1993
Limited sequence divergence of HTLV-I of Indian HAM/TSP patients from a prototype Japanese isolateK Hashimoto, J Lalkaka, J Fujisawa, et al.
Neuroepidemiology|January 1, 1991
Epidemiology of progressive muscular dystrophy in Okinawa, Japan. Classification with molecular biological techniquesM Nakagawa, K Nakahara, H Yoshidome, et al.
Journal of the Neurological Sciences|March 7, 2001
Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin geneM Nakagawa, T Matsuzaki, M Suehara, et al.
Muscle & Nerve|March 1, 1997
Antibodies to potassium channels of PC12 in serum of Isaacs' syndrome: Western blot and immunohistochemical studiesK Arimura, O Watanabe, I Kitajima, et al.
European Journal of Immunology|July 1, 1990
Association of a particular amino acid sequence of the HLA-DR beta 1 chain with HTLV-I-associated myelopathyK Usuku, M Nishizawa, K Matsuki, et al.
Acta Neuropathologica|August 31, 2000
Histopathological analysis of four autopsy cases of HTLV-I-associated myelopathy/tropical spastic paraparesis: inflammatory changes occur simultaneously in the entire central nervous systemM M Aye, E Matsuoka, T Moritoyo, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1H Takashima, M Nakagawa, M Suehara, et al.
Annals of Neurology|June 1, 1997
A new type of hereditary motor and sensory neuropathy linked to chromosome 3H Takashima, M Nakagawa, K Nakahara, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Annals of Neurology|August 17, 2001
Frameshift mutation in the collagen VI gene causes Ullrich's diseaseI Higuchi, T Shiraishi, T Hashiguchi, et al.
Acta Neuropathologica|January 1, 1989
Germanium myopathy: clinical and experimental pathological studiesI Higuchi, S Izumo, M Kuriyama, et al.
AIDS Research and Human Retroviruses|June 1, 1993
Limited sequence divergence of HTLV-I of Indian HAM/TSP patients from a prototype Japanese isolateK Hashimoto, J Lalkaka, J Fujisawa, et al.
Neuroepidemiology|January 1, 1991
Epidemiology of progressive muscular dystrophy in Okinawa, Japan. Classification with molecular biological techniquesM Nakagawa, K Nakahara, H Yoshidome, et al.
Journal of the Neurological Sciences|March 7, 2001
Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin geneM Nakagawa, T Matsuzaki, M Suehara, et al.
Muscle & Nerve|March 1, 1997
Antibodies to potassium channels of PC12 in serum of Isaacs' syndrome: Western blot and immunohistochemical studiesK Arimura, O Watanabe, I Kitajima, et al.
European Journal of Immunology|July 1, 1990
Association of a particular amino acid sequence of the HLA-DR beta 1 chain with HTLV-I-associated myelopathyK Usuku, M Nishizawa, K Matsuki, et al.
Acta Neuropathologica|August 31, 2000
Histopathological analysis of four autopsy cases of HTLV-I-associated myelopathy/tropical spastic paraparesis: inflammatory changes occur simultaneously in the entire central nervous systemM M Aye, E Matsuoka, T Moritoyo, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1H Takashima, M Nakagawa, M Suehara, et al.
Annals of Neurology|June 1, 1997
A new type of hereditary motor and sensory neuropathy linked to chromosome 3H Takashima, M Nakagawa, K Nakahara, et al.
Pageof 4