Search research articles
Contact Us
Filters
Showing results (21-30 of 51) with videos related to
Page
of 6
Sort By:
Brain : a Journal of Neurology
|
July 13, 2006
Selective COX-2 inhibitor celecoxib prevents experimental autoimmune encephalomyelitis through COX-2-independent pathway
Katsuichi 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 Immunoglobulin
Ryosuke Fukazawa, Hiroki Takeuchi, Nobuyuki Oka, et al.
The Neurologist
|
March 15, 2006
HTLV-I-associated peripheral neuropathy with smoldering-type adult T-cell leukemia
Hideaki 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 disease
Toshiyuki Yamanishi, Hisao Tachibana, Miyako Oguru, et al.
Internal Medicine (Tokyo, Japan)
|
April 23, 2003
Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2
Kotaro Mizutani, Nobuyuki Oka, Susumu Kusunoki, et al.
Acta Haematologica
|
September 17, 2003
Idiopathic thrombocytopenic purpura and mononeuropathy multiplex
Toshiharu Ijichi, Manabu Muranishi, Kazuo Shimura, et al.
Clinical Neurology and Neurosurgery
|
November 21, 2013
Clinical correlates of anhedonia in patients with Parkinson's disease
Kiyohiro 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 phenotype
Akiko Abe, Chikahiko Numakura, Kayoko Saito, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 51) with videos related to
Sort By:
Page
of 6
Brain : a Journal of Neurology
|
July 13, 2006
Selective COX-2 inhibitor celecoxib prevents experimental autoimmune encephalomyelitis through COX-2-independent pathway
Katsuichi 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 Immunoglobulin
Ryosuke Fukazawa, Hiroki Takeuchi, Nobuyuki Oka, et al.
The Neurologist
|
March 15, 2006
HTLV-I-associated peripheral neuropathy with smoldering-type adult T-cell leukemia
Hideaki 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 disease
Toshiyuki Yamanishi, Hisao Tachibana, Miyako Oguru, et al.
Internal Medicine (Tokyo, Japan)
|
April 23, 2003
Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2
Kotaro Mizutani, Nobuyuki Oka, Susumu Kusunoki, et al.
Acta Haematologica
|
September 17, 2003
Idiopathic thrombocytopenic purpura and mononeuropathy multiplex
Toshiharu Ijichi, Manabu Muranishi, Kazuo Shimura, et al.
Clinical Neurology and Neurosurgery
|
November 21, 2013
Clinical correlates of anhedonia in patients with Parkinson's disease
Kiyohiro 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 phenotype
Akiko Abe, Chikahiko Numakura, Kayoko Saito, et al.
Page
of 6