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I Nonaka

Showing results (91-100 of 503) with videos related to

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Lancet (London, England)|February 27, 1993
Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophyK Matsumura, I Nonaka, K P Campbell
Journal of the Neurological Sciences|December 1, 1988
Perifascicular atrophic fibers in childhood dermatomyositis with particular reference to mitochondrial changesM Woo, S J Chung, I Nonaka
Acta Neuropathologica|January 1, 1984
Muscle fiber type differentiation and satellite cell populations in normally grown and neonatally denervated muscles in the ratS Okada, I Nonaka, S M Chou
Neurology|August 1, 1982
Involvement of the Onuf nucleus in Werdnig-Hoffmann diseaseS M Chou, S Kuzuhara, I Nonaka
Rinsho Shinkeigaku = Clinical Neurology|January 1, 1992
[Reducing body myopathy--a case report]Y Kobayashi, K Nihei, K Kuwajima, et al.
Muscle & Nerve|February 1, 1992
Segmental cytochrome c-oxidase deficiency in CPEO: teased muscle fiber analysisT Matsuoka, Y Goto, H Hasegawa, et al.
Journal of Human Genetics|March 18, 2000
Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implicationsM Makino, S Horai, Y Goto, et al.
Cellular Signalling|August 1, 1996
Activation of Ras and protection from apoptotic cell death by BDNF in PC12 cells expressing TrkBZ Jian, I Nonaka, S Hattori, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunochemical study of connectin (titin) in neuromuscular diseases using a monoclonal antibody: connectin is degraded extensively in Duchenne muscular dystrophyK Matsumura, T Shimizu, I Nonaka, et al.
Journal of the Neurological Sciences|July 1, 1981
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formationI Nonaka, N Sunohara, S Ishiura, et al.
Pageof 51

Showing results (91-100 of 503) with videos related to

Sort By:
Pageof 51
Lancet (London, England)|February 27, 1993
Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophyK Matsumura, I Nonaka, K P Campbell
Journal of the Neurological Sciences|December 1, 1988
Perifascicular atrophic fibers in childhood dermatomyositis with particular reference to mitochondrial changesM Woo, S J Chung, I Nonaka
Acta Neuropathologica|January 1, 1984
Muscle fiber type differentiation and satellite cell populations in normally grown and neonatally denervated muscles in the ratS Okada, I Nonaka, S M Chou
Neurology|August 1, 1982
Involvement of the Onuf nucleus in Werdnig-Hoffmann diseaseS M Chou, S Kuzuhara, I Nonaka
Rinsho Shinkeigaku = Clinical Neurology|January 1, 1992
[Reducing body myopathy--a case report]Y Kobayashi, K Nihei, K Kuwajima, et al.
Muscle & Nerve|February 1, 1992
Segmental cytochrome c-oxidase deficiency in CPEO: teased muscle fiber analysisT Matsuoka, Y Goto, H Hasegawa, et al.
Journal of Human Genetics|March 18, 2000
Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implicationsM Makino, S Horai, Y Goto, et al.
Cellular Signalling|August 1, 1996
Activation of Ras and protection from apoptotic cell death by BDNF in PC12 cells expressing TrkBZ Jian, I Nonaka, S Hattori, et al.
Journal of the Neurological Sciences|November 1, 1989
Immunochemical study of connectin (titin) in neuromuscular diseases using a monoclonal antibody: connectin is degraded extensively in Duchenne muscular dystrophyK Matsumura, T Shimizu, I Nonaka, et al.
Journal of the Neurological Sciences|July 1, 1981
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formationI Nonaka, N Sunohara, S Ishiura, et al.
Pageof 51