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I Nonaka

Showing results (311-320 of 503) with videos related to

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Muscle & Nerve. Supplement|January 1, 1995
Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)J H Lee, K Goto, K Sahashi, et al.
Journal of Neuropathology and Experimental Neurology|August 5, 1998
Accumulation of tau in autophagic vacuoles in chloroquine myopathyN Murakami, F Oyama, Y Gu, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 19, 2002
[Recent advances in limb-girdle muscular dystrophy research]I Nonaka, N Minami, J Chae, et al.
Journal of the Neurological Sciences|September 1, 1990
Degradation of connectin (titin) in Fukuyama type congenital muscular dystrophy: immunochemical study with monoclonal antibodiesK Matsumura, T Shimizu, Y Sunada, et al.
Biochemical and Biophysical Research Communications|November 14, 1991
Dystrophin-related protein in the fetal and denervated skeletal muscles of normal and mdx miceM Takemitsu, S Ishiura, R Koga, et al.
Brain & Development|January 1, 1982
Basilar artery occlusion in a case of Duchenne muscular dystrophyT Matsuishi, E Yano, K Terasawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Deficiency of subunits of complex I or IV in mitochondrial myopathies: immunochemical and immunohistochemical studyM Tanaka, M Nishikimi, H Suzuki, et al.
Neurology|July 9, 2003
A novel form of autophagic vacuolar myopathy with late-onset and multiorgan involvementD Kaneda, K Sugie, A Yamamoto, et al.
Neuromuscular Disorders : NMD|November 26, 1998
MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathyI Nishino, N Minami, O Kobayashi, et al.
Neuromuscular Disorders : NMD|January 1, 1994
Selective defect in dystrophin-associated glycoproteins 50DAG (A2) and 35DAG (A4) in the dystrophic hamster: an animal model for severe childhood autosomal recessive muscular dystrophy (SCARMD)Y Yamanouchi, Y Mizuno, H Yamamoto, et al.
Pageof 51

Showing results (311-320 of 503) with videos related to

Sort By:
Pageof 51
Muscle & Nerve. Supplement|January 1, 1995
Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)J H Lee, K Goto, K Sahashi, et al.
Journal of Neuropathology and Experimental Neurology|August 5, 1998
Accumulation of tau in autophagic vacuoles in chloroquine myopathyN Murakami, F Oyama, Y Gu, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 19, 2002
[Recent advances in limb-girdle muscular dystrophy research]I Nonaka, N Minami, J Chae, et al.
Journal of the Neurological Sciences|September 1, 1990
Degradation of connectin (titin) in Fukuyama type congenital muscular dystrophy: immunochemical study with monoclonal antibodiesK Matsumura, T Shimizu, Y Sunada, et al.
Biochemical and Biophysical Research Communications|November 14, 1991
Dystrophin-related protein in the fetal and denervated skeletal muscles of normal and mdx miceM Takemitsu, S Ishiura, R Koga, et al.
Brain & Development|January 1, 1982
Basilar artery occlusion in a case of Duchenne muscular dystrophyT Matsuishi, E Yano, K Terasawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Deficiency of subunits of complex I or IV in mitochondrial myopathies: immunochemical and immunohistochemical studyM Tanaka, M Nishikimi, H Suzuki, et al.
Neurology|July 9, 2003
A novel form of autophagic vacuolar myopathy with late-onset and multiorgan involvementD Kaneda, K Sugie, A Yamamoto, et al.
Neuromuscular Disorders : NMD|November 26, 1998
MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathyI Nishino, N Minami, O Kobayashi, et al.
Neuromuscular Disorders : NMD|January 1, 1994
Selective defect in dystrophin-associated glycoproteins 50DAG (A2) and 35DAG (A4) in the dystrophic hamster: an animal model for severe childhood autosomal recessive muscular dystrophy (SCARMD)Y Yamanouchi, Y Mizuno, H Yamamoto, et al.
Pageof 51