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Nobuyuki Oka

Showing results (21-30 of 51) with videos related to

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Brain : a Journal of Neurology|July 13, 2006
Selective COX-2 inhibitor celecoxib prevents experimental autoimmune encephalomyelitis through COX-2-independent pathwayKatsuichi Miyamoto, Sachiko Miyake, Miho Mizuno, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 22, 2014
[A case of demyelinating polyneuropathy associated with anti-myelin-associated glycoprotein antibodies with progressive quadriparesis and respiratory failure]Natsuko Yuki, Akira Yoshioka, Reiko Horio, et al.
Internal Medicine (Tokyo, Japan)|November 16, 2020
Adult Krabbe Disease That Was Successfully Treated with Intravenous ImmunoglobulinRyosuke Fukazawa, Hiroki Takeuchi, Nobuyuki Oka, et al.
The Neurologist|March 15, 2006
HTLV-I-associated peripheral neuropathy with smoldering-type adult T-cell leukemiaHideaki Matsui, Fukashi Udaka, Tamotsu Kubori, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 26, 2014
[A novel mutation in glycyl-tRNA synthetase caused Charcot-Marie-Tooth disease type 2D with facial and respiratory muscle involvement]Nobuko Kawakami, Kenichi Komatsu, Hirofumi Yamashita, et al.
Internal Medicine (Tokyo, Japan)|March 2, 2013
Anxiety and depression in patients with Parkinson's diseaseToshiyuki Yamanishi, Hisao Tachibana, Miyako Oguru, et al.
Internal Medicine (Tokyo, Japan)|April 23, 2003
Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2Kotaro Mizutani, Nobuyuki Oka, Susumu Kusunoki, et al.
Acta Haematologica|September 17, 2003
Idiopathic thrombocytopenic purpura and mononeuropathy multiplexToshiharu Ijichi, Manabu Muranishi, Kazuo Shimura, et al.
Clinical Neurology and Neurosurgery|November 21, 2013
Clinical correlates of anhedonia in patients with Parkinson's diseaseKiyohiro Matsui, Hisao Tachibana, Toshiyuki Yamanishi, et al.
Journal of Human Genetics|January 23, 2009
Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotypeAkiko Abe, Chikahiko Numakura, Kayoko Saito, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Brain : a Journal of Neurology|July 13, 2006
Selective COX-2 inhibitor celecoxib prevents experimental autoimmune encephalomyelitis through COX-2-independent pathwayKatsuichi Miyamoto, Sachiko Miyake, Miho Mizuno, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 22, 2014
[A case of demyelinating polyneuropathy associated with anti-myelin-associated glycoprotein antibodies with progressive quadriparesis and respiratory failure]Natsuko Yuki, Akira Yoshioka, Reiko Horio, et al.
Internal Medicine (Tokyo, Japan)|November 16, 2020
Adult Krabbe Disease That Was Successfully Treated with Intravenous ImmunoglobulinRyosuke Fukazawa, Hiroki Takeuchi, Nobuyuki Oka, et al.
The Neurologist|March 15, 2006
HTLV-I-associated peripheral neuropathy with smoldering-type adult T-cell leukemiaHideaki Matsui, Fukashi Udaka, Tamotsu Kubori, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 26, 2014
[A novel mutation in glycyl-tRNA synthetase caused Charcot-Marie-Tooth disease type 2D with facial and respiratory muscle involvement]Nobuko Kawakami, Kenichi Komatsu, Hirofumi Yamashita, et al.
Internal Medicine (Tokyo, Japan)|March 2, 2013
Anxiety and depression in patients with Parkinson's diseaseToshiyuki Yamanishi, Hisao Tachibana, Miyako Oguru, et al.
Internal Medicine (Tokyo, Japan)|April 23, 2003
Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2Kotaro Mizutani, Nobuyuki Oka, Susumu Kusunoki, et al.
Acta Haematologica|September 17, 2003
Idiopathic thrombocytopenic purpura and mononeuropathy multiplexToshiharu Ijichi, Manabu Muranishi, Kazuo Shimura, et al.
Clinical Neurology and Neurosurgery|November 21, 2013
Clinical correlates of anhedonia in patients with Parkinson's diseaseKiyohiro Matsui, Hisao Tachibana, Toshiyuki Yamanishi, et al.
Journal of Human Genetics|January 23, 2009
Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotypeAkiko Abe, Chikahiko Numakura, Kayoko Saito, et al.
Pageof 6