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Hiroyuki Murai

Showing results (61-70 of 163) with videos related to

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Journal of the Neurological Sciences|July 9, 2004
Time-dependent cytokine deviation toward the Th2 side in Japanese multiple sclerosis patients with interferon beta-1bHirofumi Ochi, Mei Feng-Jun, Manabu Osoegawa, et al.
Journal of the Neurological Sciences|December 21, 2004
Th2 shift in juvenile muscular atrophy of distal upper extremity: a combined allergological and flow cytometric analysisManabu Osoegawa, Hirofumi Ochi, Feng-Jun Mei, et al.
Prion|March 3, 2015
Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imagingYuko Amano, Noriyuki Kimura, Takuya Hanaoka, et al.
Journal of the Neurological Sciences|December 21, 2004
Th1 shift in CIDP versus Th2 shift in vasculitic neuropathy in CSFFeng-Jun Mei, Takaaki Ishizu, Hiroyuki Murai, et al.
Journal of the Neurological Sciences|June 5, 2004
HTLV-1-associated myelopathy/tropical spastic paraparesis accompanied with psoriasisAkihiro Watanabe, Masakazu Kawajiri, Koji Ikezoe, et al.
Internal Medicine (Tokyo, Japan)|September 27, 2002
High incidence of subclinical peripheral neuropathy in myelitis with hyperIgEaemia and mite antigen-specific IgE (atopic myelitis): an electrophysiological studyManabu Osoegawa, Hirofumi Ochi, Takeshi Yamada, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 23, 2013
A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathyWataru Shiraishi, Shintaro Hayashi, Takashi Kamada, et al.
Journal of the Neurological Sciences|April 11, 2003
Myelitis with atopic diathesis: a nationwide survey of 79 cases in JapanManabu Osoegawa, Hirofumi Ochi, Motozumi Minohara, et al.
Clinical Neurology and Neurosurgery|November 18, 2005
A case of late-onset Segawa syndrome (autosomal dominant dopa-responsive dystonia) with a novel mutation of the GTP-cyclohydrase I (GCH1) geneHirokazu Furuya, Hiroyuki Murai, Kazuo Takasugi, et al.
Plos One|May 3, 2013
Characteristic cerebrospinal fluid cytokine/chemokine profiles in neuromyelitis optica, relapsing remitting or primary progressive multiple sclerosisTakuya Matsushita, Takahisa Tateishi, Noriko Isobe, et al.
Pageof 17

Showing results (61-70 of 163) with videos related to

Sort By:
Pageof 17
Journal of the Neurological Sciences|July 9, 2004
Time-dependent cytokine deviation toward the Th2 side in Japanese multiple sclerosis patients with interferon beta-1bHirofumi Ochi, Mei Feng-Jun, Manabu Osoegawa, et al.
Journal of the Neurological Sciences|December 21, 2004
Th2 shift in juvenile muscular atrophy of distal upper extremity: a combined allergological and flow cytometric analysisManabu Osoegawa, Hirofumi Ochi, Feng-Jun Mei, et al.
Prion|March 3, 2015
Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imagingYuko Amano, Noriyuki Kimura, Takuya Hanaoka, et al.
Journal of the Neurological Sciences|December 21, 2004
Th1 shift in CIDP versus Th2 shift in vasculitic neuropathy in CSFFeng-Jun Mei, Takaaki Ishizu, Hiroyuki Murai, et al.
Journal of the Neurological Sciences|June 5, 2004
HTLV-1-associated myelopathy/tropical spastic paraparesis accompanied with psoriasisAkihiro Watanabe, Masakazu Kawajiri, Koji Ikezoe, et al.
Internal Medicine (Tokyo, Japan)|September 27, 2002
High incidence of subclinical peripheral neuropathy in myelitis with hyperIgEaemia and mite antigen-specific IgE (atopic myelitis): an electrophysiological studyManabu Osoegawa, Hirofumi Ochi, Takeshi Yamada, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 23, 2013
A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathyWataru Shiraishi, Shintaro Hayashi, Takashi Kamada, et al.
Journal of the Neurological Sciences|April 11, 2003
Myelitis with atopic diathesis: a nationwide survey of 79 cases in JapanManabu Osoegawa, Hirofumi Ochi, Motozumi Minohara, et al.
Clinical Neurology and Neurosurgery|November 18, 2005
A case of late-onset Segawa syndrome (autosomal dominant dopa-responsive dystonia) with a novel mutation of the GTP-cyclohydrase I (GCH1) geneHirokazu Furuya, Hiroyuki Murai, Kazuo Takasugi, et al.
Plos One|May 3, 2013
Characteristic cerebrospinal fluid cytokine/chemokine profiles in neuromyelitis optica, relapsing remitting or primary progressive multiple sclerosisTakuya Matsushita, Takahisa Tateishi, Noriko Isobe, et al.
Pageof 17