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 Nonaka

Showing results (341-350 of 503) with videos related to

Pageof 51
Sort By:
Neuromuscular Disorders : NMD|March 1, 1995
Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathyN Murakami, Y Goto, M Itoh, et al.
Neuropathology and Applied Neurobiology|April 1, 1997
A comparative freeze-fracture study of plasma membrane of dystrophic skeletal muscles in dy/dy mice with merosin (laminin 2) deficiency and mdx mice with dystrophin deficiencyS Shibuya, Y Wakayama, H Oniki, et al.
Annals of Neurology|October 1, 1992
Mitochondrial DNA mutation and Leigh's syndromeR Sakuta, Y Goto, S Horai, et al.
Brain & Development|January 1, 1990
Complete external ophthalmoplegia in a patient with congenital myopathy without specific features (minimal change myopathy)E Ohtaki, Y Yamaguchi, Y Yamashita, et al.
Neurology|August 23, 2000
Psychosis and progressing dementia: presenting features of a mitochondriopathyS Amemiya, M Hamamoto, Y Goto, et al.
Brain & Development|May 18, 2000
A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiencyJ Sugimoto, M Shimohira, Y Osawa, et al.
The American Journal of Pathology|February 1, 1995
Sarcoglycan complex is selectively lost in dystrophic hamster muscleY Mizuno, S Noguchi, H Yamamoto, et al.
Muscle & Nerve. Supplement|April 12, 2013
Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)J H Lee, K Goto, K O Sahashi, et al.
No to Hattatsu = Brain and Development|December 9, 1998
[X-linked recessive myotubular myopathy with a splice-site mutation in the myotubularin gene]T Watanabe, M Watanabe, T Saito, et al.
Neuromuscular Disorders : NMD|July 1, 1993
Monomelic muscle atrophyM Takemitsu, K Murayama, T Saga, et al.
Pageof 51

Showing results (341-350 of 503) with videos related to

Sort By:
Pageof 51
Neuromuscular Disorders : NMD|March 1, 1995
Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathyN Murakami, Y Goto, M Itoh, et al.
Neuropathology and Applied Neurobiology|April 1, 1997
A comparative freeze-fracture study of plasma membrane of dystrophic skeletal muscles in dy/dy mice with merosin (laminin 2) deficiency and mdx mice with dystrophin deficiencyS Shibuya, Y Wakayama, H Oniki, et al.
Annals of Neurology|October 1, 1992
Mitochondrial DNA mutation and Leigh's syndromeR Sakuta, Y Goto, S Horai, et al.
Brain & Development|January 1, 1990
Complete external ophthalmoplegia in a patient with congenital myopathy without specific features (minimal change myopathy)E Ohtaki, Y Yamaguchi, Y Yamashita, et al.
Neurology|August 23, 2000
Psychosis and progressing dementia: presenting features of a mitochondriopathyS Amemiya, M Hamamoto, Y Goto, et al.
Brain & Development|May 18, 2000
A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiencyJ Sugimoto, M Shimohira, Y Osawa, et al.
The American Journal of Pathology|February 1, 1995
Sarcoglycan complex is selectively lost in dystrophic hamster muscleY Mizuno, S Noguchi, H Yamamoto, et al.
Muscle & Nerve. Supplement|April 12, 2013
Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)J H Lee, K Goto, K O Sahashi, et al.
No to Hattatsu = Brain and Development|December 9, 1998
[X-linked recessive myotubular myopathy with a splice-site mutation in the myotubularin gene]T Watanabe, M Watanabe, T Saito, et al.
Neuromuscular Disorders : NMD|July 1, 1993
Monomelic muscle atrophyM Takemitsu, K Murayama, T Saga, et al.
Pageof 51