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N Tachi

Showing results (31-40 of 98) with videos related to

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No to Hattatsu = Brain and Development|January 1, 1993
[A case of multiple sclerosis associated with chronic inflammatory demyelinating polyradiculoneuropathy]Y Watanabe, Y Ishikawa, S Wakai, et al.
Pediatric Neurology|January 1, 1990
Mosaic pattern of dystrophins in Duchenne muscular dystrophyN Tachi, K Sasaki, T Yamada, et al.
European Neurology|February 25, 2000
Hereditary cerebellar ataxia with peripheral neuropathy and mental retardationN Tachi, N Kozuka, K Ohya, et al.
Pediatric Neurology|July 1, 1993
Infantile neuroaxonal dystrophy: axonal changes in biopsied muscle tissueS Wakai, H Asanuma, N Tachi, et al.
Journal of the Neurological Sciences|February 10, 1998
Tomaculous neuropathy in Charcot-Marie-Tooth disease with myelin protein zero gene mutationN Tachi, N Kozuka, K Ohya, et al.
Pediatric Neurology|July 1, 1990
Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophyN Tachi, M Tachi, K Sasaki, et al.
Histology and Histopathology|October 1, 1996
Immunocytochemical localization of myotonin protein kinase on muscle from patients with congenital myotonic dystrophyN Tachi, N Kozuka, K Ohya, et al.
Pediatric Neurology|May 1, 1993
Asymptomatic Becker muscular dystrophy: expression of dystrophin and dystrophin-related proteinN Tachi, S Wakai, Y Watanabe, et al.
Journal of the Neurological Sciences|September 1, 1995
Expression of myotonic dystrophy protein kinase in biopsied musclesN Tachi, N Kozuka, K Ohya, et al.
Journal of Child Neurology|November 1, 1996
CTG repeat size and histologic findings of skeletal muscle from patients with congenital myotonic dystrophyN Tachi, N Kozuka, K Ohya, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
No to Hattatsu = Brain and Development|January 1, 1993
[A case of multiple sclerosis associated with chronic inflammatory demyelinating polyradiculoneuropathy]Y Watanabe, Y Ishikawa, S Wakai, et al.
Pediatric Neurology|January 1, 1990
Mosaic pattern of dystrophins in Duchenne muscular dystrophyN Tachi, K Sasaki, T Yamada, et al.
European Neurology|February 25, 2000
Hereditary cerebellar ataxia with peripheral neuropathy and mental retardationN Tachi, N Kozuka, K Ohya, et al.
Pediatric Neurology|July 1, 1993
Infantile neuroaxonal dystrophy: axonal changes in biopsied muscle tissueS Wakai, H Asanuma, N Tachi, et al.
Journal of the Neurological Sciences|February 10, 1998
Tomaculous neuropathy in Charcot-Marie-Tooth disease with myelin protein zero gene mutationN Tachi, N Kozuka, K Ohya, et al.
Pediatric Neurology|July 1, 1990
Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophyN Tachi, M Tachi, K Sasaki, et al.
Histology and Histopathology|October 1, 1996
Immunocytochemical localization of myotonin protein kinase on muscle from patients with congenital myotonic dystrophyN Tachi, N Kozuka, K Ohya, et al.
Pediatric Neurology|May 1, 1993
Asymptomatic Becker muscular dystrophy: expression of dystrophin and dystrophin-related proteinN Tachi, S Wakai, Y Watanabe, et al.
Journal of the Neurological Sciences|September 1, 1995
Expression of myotonic dystrophy protein kinase in biopsied musclesN Tachi, N Kozuka, K Ohya, et al.
Journal of Child Neurology|November 1, 1996
CTG repeat size and histologic findings of skeletal muscle from patients with congenital myotonic dystrophyN Tachi, N Kozuka, K Ohya, et al.
Pageof 10