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Experimental and Therapeutic Medicine
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February 4, 2020
Successful treatment of a 12-year-old boy with Guillain-Barré syndrome requiring tracheostomy due to respiratory muscle paralysis: A case report
Manabu Miyamoto, George Imataka, Go Ichikawa, et al.
Brain & Development
|
July 19, 2005
An analysis of epilepsy with chromosomal abnormalities
Hideo Yamanouchi, George Imataka, Eiji Nakagawa, et al.
Brain & Development
|
August 25, 2020
Guidelines for the diagnosis and treatment of acute encephalopathy in childhood
Masashi Mizuguchi, Takashi Ichiyama, George Imataka, et al.
Brain & Development
|
May 6, 2008
Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin
Akihisa Okumura, Masashi Mizuguchi, Hiroyuki Kidokoro, et al.
Modern Rheumatology Case Reports
|
November 24, 2025
Rapidly progressive glucocorticoid-resistant childhood-primary angiitis of the central nervous system positive for HLA-B51 and A26: a case report
Yuji Fujita, Kei Ikeda, Sayumi Saida, et al.
Human Genome Variation
|
June 12, 2026
A novel truncating FBN1 variant in a family with Marfan syndrome
Yuka Ito, Hiroshi Suzumura, Yuko Tanaka, et al.
Epilepsia
|
November 19, 2011
Acute encephalopathy in children with Dravet syndrome
Akihisa Okumura, Mitsugu Uematsu, George Imataka, et al.
Neurology. Genetics
|
September 24, 2016
Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndrome
Thanes Termglinchan, Seito Hisamatsu, Junko Ohmori, et al.
Neuromuscular Disorders : NMD
|
June 3, 2011
Inflammatory changes in infantile-onset LMNA-associated myopathy
Hirofumi Komaki, Yukiko K Hayashi, Rie Tsuburaya, et al.
American Journal of Medical Genetics. Part A
|
April 10, 2014
The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations
Yasukazu Yamada, Noriko Nomura, Kenichiro Yamada, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 61) with videos related to
Sort By:
Page
of 7
Experimental and Therapeutic Medicine
|
February 4, 2020
Successful treatment of a 12-year-old boy with Guillain-Barré syndrome requiring tracheostomy due to respiratory muscle paralysis: A case report
Manabu Miyamoto, George Imataka, Go Ichikawa, et al.
Brain & Development
|
July 19, 2005
An analysis of epilepsy with chromosomal abnormalities
Hideo Yamanouchi, George Imataka, Eiji Nakagawa, et al.
Brain & Development
|
August 25, 2020
Guidelines for the diagnosis and treatment of acute encephalopathy in childhood
Masashi Mizuguchi, Takashi Ichiyama, George Imataka, et al.
Brain & Development
|
May 6, 2008
Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin
Akihisa Okumura, Masashi Mizuguchi, Hiroyuki Kidokoro, et al.
Modern Rheumatology Case Reports
|
November 24, 2025
Rapidly progressive glucocorticoid-resistant childhood-primary angiitis of the central nervous system positive for HLA-B51 and A26: a case report
Yuji Fujita, Kei Ikeda, Sayumi Saida, et al.
Human Genome Variation
|
June 12, 2026
A novel truncating FBN1 variant in a family with Marfan syndrome
Yuka Ito, Hiroshi Suzumura, Yuko Tanaka, et al.
Epilepsia
|
November 19, 2011
Acute encephalopathy in children with Dravet syndrome
Akihisa Okumura, Mitsugu Uematsu, George Imataka, et al.
Neurology. Genetics
|
September 24, 2016
Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndrome
Thanes Termglinchan, Seito Hisamatsu, Junko Ohmori, et al.
Neuromuscular Disorders : NMD
|
June 3, 2011
Inflammatory changes in infantile-onset LMNA-associated myopathy
Hirofumi Komaki, Yukiko K Hayashi, Rie Tsuburaya, et al.
American Journal of Medical Genetics. Part A
|
April 10, 2014
The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations
Yasukazu Yamada, Noriko Nomura, Kenichiro Yamada, et al.
Page
of 7