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I Nonaka

Showing results (141-150 of 503) with videos related to

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Muscle & Nerve|November 1, 1987
Immunohistochemical localization of AMP deaminase in rimmed vacuoles in human skeletal muscleI Higuchi, S Ishiura, I Nonaka, et al.
No to Hattatsu = Brain and Development|September 1, 1987
[An atypical form of juvenile myasthenia gravis associated with severe emaciation, muscle atrophy, ophthalmoplegia, bulbar signs and joint contracture]M Tojo, N Sakuragawa, I Nonaka, et al.
Journal of Neurocytology|April 1, 1985
Internodal microvillus-like Schwann cell fingers in myelinated fibres in mouse spinal rootsH Ishii, K Suzuki, H Aikawa, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Distal myopathy with rimmed vacuolesI Nonaka, N Murakami, Y Suzuki, et al.
Experimental Neurology|March 1, 1986
Hereditary peroneal muscular atrophy in the mouse: an experimental model for congenital contractures (arthrogryposis)I Nonaka, A Kikuchi, T Suzuki, et al.
Journal of Neuroimmunology|February 1, 1988
Semi-quantitative immunohistochemical studies on Thy-1 antigen expressed by thymic myoid cellsA Kikuchi, I Kamo, K Fujisawa, et al.
Journal of the Neurological Sciences|December 1, 1991
Muscle histopathology in myoclonus epilepsy with ragged-red fibers (MERRF)T Matsuoka, Y Goto, M Yoneda, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 1, 1993
[The significance of cytoplasmic body in neuromuscular diseases]C Akiyama, R Sakuta, T Matsuoka, et al.
Archives of Neurology|January 1, 1984
Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patientsT Matsuishi, M Yoshino, K Terasawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methodsN Ninomiya, T Iwamasa, I Matsuda, et al.
Pageof 51

Showing results (141-150 of 503) with videos related to

Sort By:
Pageof 51
Muscle & Nerve|November 1, 1987
Immunohistochemical localization of AMP deaminase in rimmed vacuoles in human skeletal muscleI Higuchi, S Ishiura, I Nonaka, et al.
No to Hattatsu = Brain and Development|September 1, 1987
[An atypical form of juvenile myasthenia gravis associated with severe emaciation, muscle atrophy, ophthalmoplegia, bulbar signs and joint contracture]M Tojo, N Sakuragawa, I Nonaka, et al.
Journal of Neurocytology|April 1, 1985
Internodal microvillus-like Schwann cell fingers in myelinated fibres in mouse spinal rootsH Ishii, K Suzuki, H Aikawa, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Distal myopathy with rimmed vacuolesI Nonaka, N Murakami, Y Suzuki, et al.
Experimental Neurology|March 1, 1986
Hereditary peroneal muscular atrophy in the mouse: an experimental model for congenital contractures (arthrogryposis)I Nonaka, A Kikuchi, T Suzuki, et al.
Journal of Neuroimmunology|February 1, 1988
Semi-quantitative immunohistochemical studies on Thy-1 antigen expressed by thymic myoid cellsA Kikuchi, I Kamo, K Fujisawa, et al.
Journal of the Neurological Sciences|December 1, 1991
Muscle histopathology in myoclonus epilepsy with ragged-red fibers (MERRF)T Matsuoka, Y Goto, M Yoneda, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 1, 1993
[The significance of cytoplasmic body in neuromuscular diseases]C Akiyama, R Sakuta, T Matsuoka, et al.
Archives of Neurology|January 1, 1984
Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patientsT Matsuishi, M Yoshino, K Terasawa, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methodsN Ninomiya, T Iwamasa, I Matsuda, et al.
Pageof 51