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Hiroyuki Soma

Showing results (1-10 of 21) with videos related to

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Rinsho Shinkeigaku = Clinical Neurology|December 4, 2008
[Progressive cerebellar ataxia with euthyroid Hashimoto's disease--implication of autoantibodies associated with Hashimoto's disease in progressive cerebellar ataxia]Ichiro Yabe, Kazunori Sato, Hiroyuki Soma, et al.
Journal of Human Genetics|September 7, 2007
Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese familiesRehana Basri, Ichiro Yabe, Hiroyuki Soma, et al.
Journal of Neurology|December 14, 2004
No association between FMR1 premutations and multiple system atrophyIchiro Yabe, Hiroyuki Soma, Asako Takei, et al.
Cognitive Neuropsychology|December 3, 2016
A case of pure autotopagnosia following Creutzfeldt-Jakob diseaseItaru Tamura, Shinsuke Hamada, Hiroyuki Soma, et al.
Journal of the Neurological Sciences|October 24, 2007
Usefulness of the Scale for Assessment and Rating of Ataxia (SARA)Ichiro Yabe, Masaaki Matsushima, Hiroyuki Soma, et al.
Journal of the Neurological Sciences|November 26, 2005
Heredity in multiple system atrophyHiroyuki Soma, Ichiro Yabe, Asako Takei, et al.
Internal Medicine (Tokyo, Japan)|July 3, 2007
X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matterRehana Basri, Ichiro Yabe, Hiroyuki Soma, et al.
Internal Medicine (Tokyo, Japan)|March 22, 2022
Cat Scratch Disease-associated Encephalitis Followed by ParkinsonismMasakazu Nakamura, Shigehisa Ura, Ichiro Yabe, et al.
Brain and Nerve = Shinkei Kenkyu No Shinpo|March 1, 2008
[Spastic paraplegia caused by a novel mutation in the spastin gene (1207C-->G, P361R)--clinical features of a patient without family history]Yuka Machino, Yasumasa Kokubo, Hiroyuki Soma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 30, 2008
Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genesHiroyuki Soma, Ichiro Yabe, Asako Takei, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Rinsho Shinkeigaku = Clinical Neurology|December 4, 2008
[Progressive cerebellar ataxia with euthyroid Hashimoto's disease--implication of autoantibodies associated with Hashimoto's disease in progressive cerebellar ataxia]Ichiro Yabe, Kazunori Sato, Hiroyuki Soma, et al.
Journal of Human Genetics|September 7, 2007
Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese familiesRehana Basri, Ichiro Yabe, Hiroyuki Soma, et al.
Journal of Neurology|December 14, 2004
No association between FMR1 premutations and multiple system atrophyIchiro Yabe, Hiroyuki Soma, Asako Takei, et al.
Cognitive Neuropsychology|December 3, 2016
A case of pure autotopagnosia following Creutzfeldt-Jakob diseaseItaru Tamura, Shinsuke Hamada, Hiroyuki Soma, et al.
Journal of the Neurological Sciences|October 24, 2007
Usefulness of the Scale for Assessment and Rating of Ataxia (SARA)Ichiro Yabe, Masaaki Matsushima, Hiroyuki Soma, et al.
Journal of the Neurological Sciences|November 26, 2005
Heredity in multiple system atrophyHiroyuki Soma, Ichiro Yabe, Asako Takei, et al.
Internal Medicine (Tokyo, Japan)|July 3, 2007
X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matterRehana Basri, Ichiro Yabe, Hiroyuki Soma, et al.
Internal Medicine (Tokyo, Japan)|March 22, 2022
Cat Scratch Disease-associated Encephalitis Followed by ParkinsonismMasakazu Nakamura, Shigehisa Ura, Ichiro Yabe, et al.
Brain and Nerve = Shinkei Kenkyu No Shinpo|March 1, 2008
[Spastic paraplegia caused by a novel mutation in the spastin gene (1207C-->G, P361R)--clinical features of a patient without family history]Yuka Machino, Yasumasa Kokubo, Hiroyuki Soma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 30, 2008
Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genesHiroyuki Soma, Ichiro Yabe, Asako Takei, et al.
Pageof 3