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T Miike

Showing results (51-60 of 95) with videos related to

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Neurology|August 1, 1982
Infantile glycogen storage myopathy in a girl with phosphorylase kinase deficiencyY Ohtani, I Matsuda, T Iwamasa, et al.
Brain & Development|March 1, 1994
Central nervous system disorders and possible brain type carnitine palmitoyltransferase II deficiencyY Ohtani, A Tomoda, T Miike, et al.
Biochemical and Biophysical Research Communications|September 7, 2000
Targeted and stable gene delivery into muscle cells by a two-step transfer systemI Fujii, S Suzuki, T Igarashi, et al.
Brain & Development|June 17, 1998
Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysisM Ikezawa, N Minami, M Takahashi, et al.
Neuropediatrics|May 1, 1982
Glycogen storage myopathy with abnormal lactate dehydrogenaseN Nagata, T Miike, I Matsuda, et al.
Brain & Development|January 1, 1991
Vascular alterations in Fukuyama type congenital muscular dystrophyS Sugino, M Miyatake, Y Ohtani, et al.
Journal of the Neurological Sciences|October 1, 1989
Possible systemic smooth muscle layer dysfunction due to a deficiency of dystrophin in Duchenne muscular dystrophyM Miyatake, T Miike, J Zhao, et al.
Pediatric Neurology|March 1, 1986
Carnitine prevents Reye-like syndrome in atypical carnitine deficiencyT Matsubasa, Y Ohtani, T Miike, et al.
Muscle & Nerve|February 1, 1991
Dystrophin: localization and presumed functionM Miyatake, T Miike, J E Zhao, et al.
Brain & Development|January 1, 1994
Two patients with distal muscular dystrophy and autonomic nerve dysfunctionA Tomoda, J E Zhao, Y Ohtani, et al.
Pageof 10

Showing results (51-60 of 95) with videos related to

Sort By:
Pageof 10
Neurology|August 1, 1982
Infantile glycogen storage myopathy in a girl with phosphorylase kinase deficiencyY Ohtani, I Matsuda, T Iwamasa, et al.
Brain & Development|March 1, 1994
Central nervous system disorders and possible brain type carnitine palmitoyltransferase II deficiencyY Ohtani, A Tomoda, T Miike, et al.
Biochemical and Biophysical Research Communications|September 7, 2000
Targeted and stable gene delivery into muscle cells by a two-step transfer systemI Fujii, S Suzuki, T Igarashi, et al.
Brain & Development|June 17, 1998
Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysisM Ikezawa, N Minami, M Takahashi, et al.
Neuropediatrics|May 1, 1982
Glycogen storage myopathy with abnormal lactate dehydrogenaseN Nagata, T Miike, I Matsuda, et al.
Brain & Development|January 1, 1991
Vascular alterations in Fukuyama type congenital muscular dystrophyS Sugino, M Miyatake, Y Ohtani, et al.
Journal of the Neurological Sciences|October 1, 1989
Possible systemic smooth muscle layer dysfunction due to a deficiency of dystrophin in Duchenne muscular dystrophyM Miyatake, T Miike, J Zhao, et al.
Pediatric Neurology|March 1, 1986
Carnitine prevents Reye-like syndrome in atypical carnitine deficiencyT Matsubasa, Y Ohtani, T Miike, et al.
Muscle & Nerve|February 1, 1991
Dystrophin: localization and presumed functionM Miyatake, T Miike, J E Zhao, et al.
Brain & Development|January 1, 1994
Two patients with distal muscular dystrophy and autonomic nerve dysfunctionA Tomoda, J E Zhao, Y Ohtani, et al.
Pageof 10