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Ichiro Yabe

Showing results (61-70 of 301) with videos related to

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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.
Internal Medicine (Tokyo, Japan)|July 5, 2017
Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial HemorrhageHiroaki Yaguchi, Yasunori Mito, Ikkei Ohashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 2, 2018
[A retrospective study of the effects of 3,4-diaminopyridine treatment in Lambert-Eaton myasthenic syndrome]Ryoji Naganuma, Ichiro Yabe, Ikuko Takahashi, et al.
Internal Medicine (Tokyo, Japan)|August 5, 2014
Reliability of the Japanese version of the Berg balance scaleMasaaki Matsushima, Ichiro Yabe, Hisashi Uwatoko, et al.
International Journal of Urology : Official Journal of the Japanese Urological Association|July 9, 2016
Clinical efficacy of istradefylline on lower urinary tract symptoms in Parkinson's diseaseTakeya Kitta, Ichiro Yabe, Ikuko Takahashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 22, 2025
[Questionnaire survey regarding pediatric to adult transitional medical care targeting members of Japanese Society of Neurology]Toshio Saito, Yoshio Sakiyama, Katsuhisa Ogata, et al.
Internal Medicine (Tokyo, Japan)|September 26, 2017
Amyloid Polyneuropathy and Myocardial Amyloidosis 10 Years after Domino Liver Transplantation from a Patient with a Transthyretin Ser50Arg MutationMasaaki Matsushima, Ichiro Yabe, Masaya Tsuda, et al.
Journal of Neurology|April 23, 2002
Late onset ataxia phenotype in dentatorubro-pallidoluysian atrophy (DRPLA)Ichiro Yabe, Hidenao Sasaki, Seiji Kikuchi, et al.
Journal of the Neurological Sciences|July 11, 2006
MSA-C is the predominant clinical phenotype of MSA in Japan: analysis of 142 patients with probable MSAIchiro Yabe, Hiroyuki Soma, Asako Takei, et al.
Pageof 31

Showing results (61-70 of 301) with videos related to

Sort By:
Pageof 31
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.
Internal Medicine (Tokyo, Japan)|July 5, 2017
Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial HemorrhageHiroaki Yaguchi, Yasunori Mito, Ikkei Ohashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 2, 2018
[A retrospective study of the effects of 3,4-diaminopyridine treatment in Lambert-Eaton myasthenic syndrome]Ryoji Naganuma, Ichiro Yabe, Ikuko Takahashi, et al.
Internal Medicine (Tokyo, Japan)|August 5, 2014
Reliability of the Japanese version of the Berg balance scaleMasaaki Matsushima, Ichiro Yabe, Hisashi Uwatoko, et al.
International Journal of Urology : Official Journal of the Japanese Urological Association|July 9, 2016
Clinical efficacy of istradefylline on lower urinary tract symptoms in Parkinson's diseaseTakeya Kitta, Ichiro Yabe, Ikuko Takahashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 22, 2025
[Questionnaire survey regarding pediatric to adult transitional medical care targeting members of Japanese Society of Neurology]Toshio Saito, Yoshio Sakiyama, Katsuhisa Ogata, et al.
Internal Medicine (Tokyo, Japan)|September 26, 2017
Amyloid Polyneuropathy and Myocardial Amyloidosis 10 Years after Domino Liver Transplantation from a Patient with a Transthyretin Ser50Arg MutationMasaaki Matsushima, Ichiro Yabe, Masaya Tsuda, et al.
Journal of Neurology|April 23, 2002
Late onset ataxia phenotype in dentatorubro-pallidoluysian atrophy (DRPLA)Ichiro Yabe, Hidenao Sasaki, Seiji Kikuchi, et al.
Journal of the Neurological Sciences|July 11, 2006
MSA-C is the predominant clinical phenotype of MSA in Japan: analysis of 142 patients with probable MSAIchiro Yabe, Hiroyuki Soma, Asako Takei, et al.
Pageof 31