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Tohru Ibi

Showing results (1-10 of 14) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Dysphagia]Tohru Ibi, Naoki Nakao, Ko Sahashi
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Liver failure]Tohru Ibi, Naoki Nakao, Ko Sahashi
Rinsho Shinkeigaku = Clinical Neurology|March 20, 2015
[Dyskinesia-hyperpyrexia syndrome in a patient with Parkinson's disease: a case report]Soutarou Taguchi, Jun-ichi Niwa, Tohru Ibi, et al.
Medical Gas Research|December 8, 2011
Open-label trial and randomized, double-blind, placebo-controlled, crossover trial of hydrogen-enriched water for mitochondrial and inflammatory myopathiesMikako Ito, Tohru Ibi, Ko Sahashi, et al.
Mitochondrion|September 21, 2007
Therapeutic potential of pyruvate therapy for mitochondrial diseasesMasashi Tanaka, Yutaka Nishigaki, Noriyuki Fuku, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|August 10, 2004
[Markedly improving sarcoid cervical myelopathy after the diagnostic treatment of prednisolone, associated with highly spondylotic spines]Kazunori Hirose, Akira Hoshino, Takaaki Fukuoka, et al.
Neurobiology of Disease|June 1, 2014
LDB3 splicing abnormalities are specific to skeletal muscles of patients with myotonic dystrophy type 1 and alter its PKC binding affinityYoshihiro Yamashita, Tohru Matsuura, Tatsuaki Kurosaki, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 6, 2008
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathologyAkira Hoshino, Yasushi Iwasaki, Masayuki Izumi, et al.
Neuroscience Letters|May 24, 2012
A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravisYosuke Kokunai, Keigo Goto, Tomoya Kubota, et al.
Internal Medicine (Tokyo, Japan)|January 14, 2005
Gastric dysmotility associated with accumulation of mitochondrial A3243G mutation in the stomachAkihiro Fujii, Makoto Yoneda, Masahiro Ohtani, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Dysphagia]Tohru Ibi, Naoki Nakao, Ko Sahashi
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Liver failure]Tohru Ibi, Naoki Nakao, Ko Sahashi
Rinsho Shinkeigaku = Clinical Neurology|March 20, 2015
[Dyskinesia-hyperpyrexia syndrome in a patient with Parkinson's disease: a case report]Soutarou Taguchi, Jun-ichi Niwa, Tohru Ibi, et al.
Medical Gas Research|December 8, 2011
Open-label trial and randomized, double-blind, placebo-controlled, crossover trial of hydrogen-enriched water for mitochondrial and inflammatory myopathiesMikako Ito, Tohru Ibi, Ko Sahashi, et al.
Mitochondrion|September 21, 2007
Therapeutic potential of pyruvate therapy for mitochondrial diseasesMasashi Tanaka, Yutaka Nishigaki, Noriyuki Fuku, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|August 10, 2004
[Markedly improving sarcoid cervical myelopathy after the diagnostic treatment of prednisolone, associated with highly spondylotic spines]Kazunori Hirose, Akira Hoshino, Takaaki Fukuoka, et al.
Neurobiology of Disease|June 1, 2014
LDB3 splicing abnormalities are specific to skeletal muscles of patients with myotonic dystrophy type 1 and alter its PKC binding affinityYoshihiro Yamashita, Tohru Matsuura, Tatsuaki Kurosaki, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 6, 2008
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathologyAkira Hoshino, Yasushi Iwasaki, Masayuki Izumi, et al.
Neuroscience Letters|May 24, 2012
A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravisYosuke Kokunai, Keigo Goto, Tomoya Kubota, et al.
Internal Medicine (Tokyo, Japan)|January 14, 2005
Gastric dysmotility associated with accumulation of mitochondrial A3243G mutation in the stomachAkihiro Fujii, Makoto Yoneda, Masahiro Ohtani, et al.
Pageof 2